Seishi Ogawa
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Computer Science
Seishi Ogawa's Degrees
- PhD Computer Science University of Tokyo
- Masters Computer Science University of Tokyo
- Bachelors Computer Science University of Tokyo
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(Suggest an Edit or Addition)Seishi Ogawa's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Frequent pathway mutations of splicing machinery in myelodysplasia (2011) (1799)
- Landscape of genetic lesions in 944 patients with myelodysplastic syndromes (2013) (1219)
- Integrated molecular analysis of clear-cell renal cell carcinoma (2013) (909)
- Oncogenic mutations of ALK kinase in neuroblastoma (2008) (861)
- KIF5B-RET fusions in lung adenocarcinoma (2012) (736)
- A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. (2005) (694)
- Mutational landscape and clonal architecture in grade II and III gliomas (2015) (676)
- AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis (2004) (651)
- Autologous Induced Stem‐Cell–Derived Retinal Cells for Macular Degeneration: Brief Report (2017) (604)
- Integrated molecular analysis of adult T cell leukemia/lymphoma (2015) (600)
- Frequent inactivation of A20 in B-cell lymphomas (2009) (559)
- Somatic RHOA mutation in angioimmunoblastic T cell lymphoma (2014) (508)
- Notch1 but not Notch2 is essential for generating hematopoietic stem cells from endothelial cells. (2003) (493)
- Genomic and molecular characterization of esophageal squamous cell carcinoma (2014) (493)
- Aberrant PD-L1 expression through 3′-UTR disruption in multiple cancers (2016) (489)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms (2009) (415)
- Age-related remodelling of oesophageal epithelia by mutated cancer drivers (2019) (372)
- Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms (2012) (325)
- Clinical significance of somatic mutation in unexplained blood cytopenia. (2017) (322)
- Dynamics of clonal evolution in myelodysplastic syndromes (2016) (311)
- Polycomb-mediated loss of miR-31 activates NIK-dependent NF-κB pathway in adult T cell leukemia and other cancers. (2012) (304)
- Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms. (2015) (299)
- The landscape of somatic mutations in Down syndrome–related myeloid disorders (2013) (295)
- Prospective Comparison of the Diagnostic Potential of Real-Time PCR, Double-Sandwich Enzyme-Linked Immunosorbent Assay for Galactomannan, and a (1→3)-β-d-Glucan Test in Weekly Screening for Invasive Aspergillosis in Patients with Hematological Disorders (2004) (290)
- SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML). (2012) (285)
- The genomic landscape of nasopharyngeal carcinoma (2014) (275)
- Monitoring and robust induction of nephrogenic intermediate mesoderm from human pluripotent stem cells (2013) (272)
- Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays. (2007) (264)
- Evi-1 is a critical regulator for hematopoietic stem cells and transformed leukemic cells. (2008) (261)
- Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk (2010) (253)
- Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia. (2015) (253)
- International Consensus Classification of Myeloid Neoplasms and Acute Leukemia: Integrating Morphological, Clinical, and Genomic Data. (2022) (249)
- Genomic Landscape of Esophageal Squamous Cell Carcinoma in a Japanese Population. (2016) (244)
- Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (2019) (237)
- Acquired initiating mutations in early hematopoietic cells of CLL patients. (2014) (230)
- Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation. (2017) (226)
- Somatic SETBP1 mutations in myeloid malignancies (2013) (225)
- Therapy of relapsed leukemia after allogeneic hematopoietic cell transplantation with T cells specific for minor histocompatibility antigens. (2010) (222)
- Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. (2007) (222)
- Comprehensive analysis of genetic alterations and their prognostic impacts in adult acute myeloid leukemia patients (2014) (205)
- Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia (2013) (201)
- Generation of Alveolar Epithelial Spheroids via Isolated Progenitor Cells from Human Pluripotent Stem Cells (2014) (198)
- ACTN1 mutations cause congenital macrothrombocytopenia. (2013) (190)
- BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders. (2013) (184)
- Aberrant splicing of U12-type introns is the hallmark of ZRSR2 mutant myelodysplastic syndrome (2014) (184)
- Prognostic relevance of genetic alterations in diffuse lower-grade gliomas (2018) (183)
- Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents (2016) (175)
- Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders (2013) (174)
- Genetics of MDS. (2019) (173)
- Recurrent somatic mutations underlie corticotropin-independent Cushing’s syndrome (2014) (170)
- An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data (2013) (170)
- Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells (2014) (169)
- Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse. (2015) (166)
- Gain‐of‐function mutations and copy number increases of Notch2 in diffuse large B‐cell lymphoma (2009) (160)
- Real-Time Automated PCR for Early Diagnosis and Monitoring of Cytomegalovirus Infection after Bone Marrow Transplantation (2000) (149)
- Clonal hematopoiesis in acquired aplastic anemia. (2016) (148)
- Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma (2015) (148)
- Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients. (2013) (148)
- Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia. (2011) (144)
- TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups (2019) (141)
- Inactivation of multiple tumor-suppressor genes involved in negative regulation of the cell cycle, MTS1/p16INK4A/CDKN2, MTS2/p15INK4B, p53, and Rb genes in primary lymphoid malignancies. (1996) (135)
- Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution (2016) (130)
- MICAL, a Novel CasL Interacting Molecule, Associates with Vimentin* (2002) (130)
- Splicing factor mutations and cancer (2014) (128)
- Loss of the cyclin-dependent kinase 4-inhibitor (p16; MTS1) gene is frequent in and highly specific to lymphoid tumors in primary human hematopoietic malignancies. (1995) (126)
- Two susceptibility loci to Takayasu arteritis reveal a synergistic role of the IL12B and HLA-B regions in a Japanese population. (2013) (125)
- Clinical value of the wild-type estrogen receptor β expression in breast cancer (2001) (125)
- Molecular heterogeneity in peripheral T-cell lymphoma, not otherwise specified revealed by comprehensive genetic profiling (2019) (124)
- Role of Donor Clonal Hematopoiesis in Allogeneic Hematopoietic Stem-Cell Transplantation. (2019) (123)
- HLA mismatch combinations associated with decreased risk of relapse: implications for the molecular mechanism. (2009) (122)
- Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms. (2009) (121)
- Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis (2018) (120)
- Evaluation of oestrogen receptor beta wild-type and variant protein expression, and relationship with clinicopathological factors in breast cancers. (2002) (118)
- Effects of HLA allele and killer immunoglobulin-like receptor ligand matching on clinical outcome in leukemia patients undergoing transplantation with T-cell-replete marrow from an unrelated donor. (2007) (118)
- Cell Therapy Using Human Induced Pluripotent Stem Cell‐Derived Renal Progenitors Ameliorates Acute Kidney Injury in Mice (2015) (118)
- CIZ, a Zinc Finger Protein That Interacts with p130cas and Activates the Expression of Matrix Metalloproteinases (2000) (116)
- Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia (2018) (115)
- The Evi‐1 oncoprotein inhibits c‐Jun N‐terminal kinase and prevents stress‐induced cell death (2000) (113)
- Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis (2019) (112)
- Clonal evolution in myelodysplastic syndromes (2017) (111)
- Defective Epstein–Barr virus in chronic active infection and haematological malignancy (2019) (110)
- Genome-wide identification of genes with amplification and/or fusion in small cell lung cancer (2013) (108)
- Alternative splicing due to an intronic SNP in HMSD generates a novel minor histocompatibility antigen. (2007) (108)
- Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia. (2015) (107)
- TCEB1-mutated Renal Cell Carcinoma: A Distinct Genomic and Morphologic Subtype (2014) (107)
- miR-34a functions as a tumor suppressor modulating EGFR in glioblastoma multiforme (2013) (106)
- High-Resolution Genomic Copy Number Profiling of Glioblastoma Multiforme by Single Nucleotide Polymorphism DNA Microarray (2009) (105)
- Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria. (2014) (104)
- AML1/Runx1 rescues Notch1-null mutation-induced deficiency of para-aortic splanchnopleural hematopoiesis. (2006) (104)
- Prognostic relevance of integrated genetic profiling in adult T-cell leukemia/lymphoma. (2015) (103)
- PRPF8 Defects Cause Missplicing in Myeloid Malignancies (2013) (102)
- SF3B1-mutant MDS as a distinct disease subtype: a proposal from the International Working Group for the Prognosis of MDS (2020) (98)
- Somatic Mutations in MDS Patients Are Associated with Clinical Features and Predict Prognosis Independent of the IPSS-R: Analysis of Combined Datasets from the International Working Group for Prognosis in MDS-Molecular Committee (2015) (95)
- Relapse of leukemia with loss of mismatched HLA resulting from uniparental disomy after haploidentical hematopoietic stem cell transplantation. (2010) (94)
- AML1/Runx1 Negatively Regulates Quiescent Hematopoietic Stem Cells in Adult Hematopoiesis1 (2008) (93)
- AML1 Is Functionally Regulated through p300-mediated Acetylation on Specific Lysine Residues* (2004) (92)
- A TLR3-Specific Adjuvant Relieves Innate Resistance to PD-L1 Blockade without Cytokine Toxicity in Tumor Vaccine Immunotherapy. (2017) (91)
- Highly Efficient Ex Vivo Expansion of Human Hematopoietic Stem Cells Using Delta1‐Fc Chimeric Protein (2006) (90)
- Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia (2017) (90)
- Molecular allelokaryotyping of early‐stage, untreated chronic lymphocytic leukemia (2008) (89)
- Genomic landscape of liposarcoma (2015) (89)
- Variegated RHOA mutations in adult T-cell leukemia/lymphoma. (2016) (88)
- Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia (2016) (88)
- Mutations of the Smad4 gene in acute myelogeneous leukemia and their functional implications in leukemogenesis (2001) (87)
- Frequent structural variations involving programmed death ligands in Epstein-Barr virus-associated lymphomas (2019) (84)
- Genome-wide, high-resolution detection of copy number, loss of heterozygosity, and genotypes from formalin-fixed, paraffin-embedded tumor tissue using microarrays. (2007) (82)
- Clonal expansion in non-cancer tissues (2021) (82)
- Loss of function mutations in RPL27 and RPS27 identified by whole‐exome sequencing in Diamond‐Blackfan anaemia (2015) (81)
- Cloning of genes involved in chromosomal translocations by high-resolution single nucleotide polymorphism genomic microarray (2008) (80)
- Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations (2017) (80)
- Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype (2009) (80)
- Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome (2017) (80)
- MYC Amplification as a Prognostic Marker of Early-Stage Lung Adenocarcinoma Identified by Whole Genome Copy Number Analysis (2010) (80)
- Impact of highly conserved HLA haplotype on acute graft-versus-host disease. (2010) (78)
- Genomic determinants of chronic myelomonocytic leukemia (2017) (78)
- Genomic landscape and clonal evolution of acute myeloid leukemia with t(8;21): an international study on 331 patients. (2019) (77)
- Runx1/AML-1 Ranks as a Master Regulator of Adult Hematopoiesis (2004) (77)
- Both Notch1 and Notch2 contribute to the regulation of melanocyte homeostasis (2007) (76)
- Mutational Landscape of Pediatric Acute Lymphoblastic Leukemia. (2017) (76)
- Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma. (2016) (73)
- CLINICAL AND BIOLOGICAL IMPLICATIONS OF ANCESTRAL AND NON-ANCESTRAL IDH1 AND IDH2 MUTATIONS IN MYELOID NEOPLASMS (2015) (73)
- Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency. (2016) (73)
- Gastric cancer cell line Hs746T harbors a splice site mutation of c-Met causing juxtamembrane domain deletion. (2010) (73)
- Influence of glutathione S-transferase A1 polymorphism on the pharmacokinetics of busulfan. (2006) (72)
- Notch1 oncoprotein antagonizes TGF‐β/Smad‐mediated cell growth suppression via sequestration of coactivator p300 (2005) (72)
- A temporal shift of the evolutionary principle shaping intratumor heterogeneity in colorectal cancer (2018) (72)
- ERCC5 is a novel biomarker of ovarian cancer prognosis. (2008) (71)
- Host-Residual Invariant NK T Cells Attenuate Graft-versus-Host Immunity1 (2005) (70)
- Reduced TET2 function leads to T-cell lymphoma with follicular helper T-cell-like features in mice (2014) (70)
- SF3B1-mutant myelodysplastic syndrome as a distinct disease subtype - A Proposal of the International Working Group for the Prognosis of Myelodysplastic Syndromes (IWG-PM). (2020) (68)
- The E‐Id Protein Axis Specifies Adaptive Lymphoid Cell Identity and Suppresses Thymic Innate Lymphoid Cell Development (2017) (67)
- Neoantigen Load, Antigen Presentation Machinery, and Immune Signatures Determine Prognosis in Clear Cell Renal Cell Carcinoma (2016) (67)
- Regeneration of CD8αβ T Cells from T-cell-Derived iPSC Imparts Potent Tumor Antigen-Specific Cytotoxicity. (2016) (67)
- Telomere attrition and candidate gene mutations preceding monosomy 7 in aplastic anemia. (2015) (67)
- Integrated molecular profiling of juvenile myelomonocytic leukemia. (2018) (67)
- Mutations and loss of expression of a mismatch repair gene, hMLH1, in leukemia and lymphoma cell lines. (1997) (66)
- Ordering of mutations in acute myeloid leukemia with partial tandem duplication of MLL (MLL-PTD) (2016) (65)
- KLF5 regulates the integrity and oncogenicity of intestinal stem cells. (2014) (65)
- Induced pluripotent stem cells from CINCA syndrome patients as a model for dissecting somatic mosaicism and drug discovery. (2012) (64)
- Gain of GRHL2 is associated with early recurrence of hepatocellular carcinoma. (2008) (64)
- Donor killer immunoglobulin-like receptor (KIR) genotype-patient cognate KIR ligand combination and antithymocyte globulin preadministration are critical factors in outcome of HLA-C-KIR ligand-mismatched T cell-replete unrelated bone marrow transplantation. (2008) (63)
- Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma. (2014) (63)
- Crk-Associated Substrate Lymphocyte Type Is Required for Lymphocyte Trafficking and Marginal Zone B Cell Maintenance1 (2005) (62)
- In Vivo Alemtuzumab Enables Haploidentical Human Leukocyte Antigen-Mismatched Hematopoietic Stem-Cell Transplantation Without Ex Vivo Graft Manipulation (2005) (61)
- Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML. (2012) (60)
- Coordinated regulation of transcription factors through Notch2 is an important mediator of mast cell fate (2008) (60)
- Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome. (2019) (60)
- Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations. (2009) (59)
- North American ATLL has a distinct mutational and transcriptional profile and responds to epigenetic therapies. (2018) (59)
- Oncogenic mutations of ALK in neuroblastoma (2011) (59)
- Whole‐exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia (2016) (58)
- Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia (2010) (57)
- Gene expression and risk of leukemic transformation in myelodysplasia. (2017) (56)
- Extensive gene deletions in Japanese patients with Diamond-Blackfan anemia. (2012) (56)
- Chromosomal abnormalities and novel disease‐related regions in progression from Barrett's esophagus to esophageal adenocarcinoma (2009) (56)
- The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias. (2010) (55)
- Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans (2020) (55)
- Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice. (2018) (55)
- Identification of cell-type-specific mutations in nodal T-cell lymphomas (2017) (55)
- Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes (2017) (55)
- Novel recurrent mutations in the RAS-like GTP-binding gene RIT1 in myeloid malignancies (2012) (53)
- Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO ‘MDS-U’ designation (2012) (53)
- GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies (2015) (53)
- Identification of human minor histocompatibility antigens based on genetic association with highly parallel genotyping of pooled DNA. (2008) (53)
- Genetic profiling of myeloproliferative disorders by single-nucleotide polymorphism oligonucleotide microarray. (2006) (52)
- Notch Activation Induces the Generation of Functional NK Cells from Human Cord Blood CD34-Positive Cells Devoid of IL-151 (2009) (51)
- Derivation of functional mature neutrophils from human embryonic stem cells. (2009) (51)
- CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML). (2012) (50)
- Gain-of-function IKBKB mutation causes human combined immune deficiency (2018) (49)
- A comprehensive characterization of cis-acting splicing-associated variants in human cancer (2017) (49)
- ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia (2016) (48)
- Frequent somatic mutations in epigenetic regulators in newly diagnosed chronic myeloid leukemia (2017) (48)
- Oligomerization of Evi-1 regulated by the PR domain contributes to recruitment of corepressor CtBP (2005) (48)
- Genomewide screening of DNA copy number changes in chronic myelogenous leukemia with the use of high‐resolution array‐based comparative genomic hybridization (2006) (47)
- The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (2017) (47)
- Origins of myelodysplastic syndromes after aplastic anemia. (2017) (46)
- EED mutants impair polycomb repressive complex 2 in myelodysplastic syndrome and related neoplasms (2012) (45)
- Biochemical and Epigenetic Insights into L-2-Hydroxyglutarate, a Potential Therapeutic Target in Renal Cancer (2018) (45)
- Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations (2014) (45)
- The transcriptionally active form of AML1 is required for hematopoietic rescue of the AML1-deficient embryonic para-aortic splanchnopleural (P-Sp) region. (2004) (45)
- Haploinsufficiency of Sf3b1 leads to compromised stem cell function but not to myelodysplasia (2014) (44)
- CD1d expression level in tumor cells is an important determinant for anti-tumor immunity by natural killer T cells (2006) (44)
- Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma. (2019) (44)
- Mutations of Chk2 in primary hematopoietic neoplasms. (2002) (44)
- Disruption of SF 3 B 1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells (2015) (43)
- Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis (2021) (42)
- Recurrent genetic defects on chromosome 7q in myeloid neoplasms (2014) (41)
- The BRG1/SOX9 axis is critical for acinar cell–derived pancreatic tumorigenesis (2018) (41)
- SNP array analysis of tyrosine kinase inhibitor-resistant chronic myeloid leukemia identifies heterogeneous secondary genomic alterations. (2010) (40)
- Functional Domains of Runx1 Are Differentially Required for CD4 Repression, TCRβ Expression, and CD4/8 Double-Negative to CD4/8 Double-Positive Transition in Thymocyte Development1 (2005) (40)
- Splicing factor mutations in myelodysplasia (2012) (40)
- Genome-Wide Loss of Heterozygosity and Uniparental Disomy in BRCA1/2-Associated Ovarian Carcinomas (2008) (40)
- Loss of DNA Damage Response in Neuroblastoma and Utility of a PARP Inhibitor (2017) (39)
- Invariant patterns of clonal succession determine specific clinical features of myelodysplastic syndromes (2019) (39)
- Molecular allelokaryotyping of relapsed pediatric acute lymphoblastic leukemia. (2009) (39)
- Identified hidden genomic changes in mantle cell lymphoma using high-resolution single nucleotide polymorphism genomic array. (2009) (39)
- Recurrent genetic defects on chromosome 5q in myeloid neoplasms (2016) (38)
- Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells (2015) (38)
- Prognostic analysis according to the 2017 ELN risk stratification by genetics in adult acute myeloid leukemia patients treated in the Japan Adult Leukemia Study Group (JALSG) AML201 study. (2018) (38)
- The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes. (2017) (38)
- Long-term outcome of 6-month maintenance chemotherapy for acute lymphoblastic leukemia in children (2017) (37)
- Significance of perivascular tumour cells defined by CD109 expression in progression of glioma (2017) (37)
- Single-cell analysis based dissection of clonality in myelofibrosis (2019) (37)
- Hes1 immortalizes committed progenitors and plays a role in blast crisis transition in chronic myelogenous leukemia. (2010) (37)
- Aberrations of NEGR1 on 1p31 and MYEOV on 11q13 in neuroblastoma (2011) (37)
- HapMap scanning of novel human minor histocompatibility antigens. (2008) (36)
- Recurrent RARB Translocations in Acute Promyelocytic Leukemia Lacking RARA Translocation. (2018) (36)
- The AML1/ETO(MTG8) and AML1/Evi-1 Leukemia-Associated Chimeric Oncoproteins Accumulate PEBP2β(CBFβ) in the Nucleus More Efficiently Than Wild-Type AML1 (1998) (36)
- DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes (2013) (36)
- Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia. (2019) (35)
- Rapid diagnosis of invasive pulmonary aspergillosis by quantitative polymerase chain reaction using bronchial lavage fluid (2003) (35)
- Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how? (2012) (35)
- Combined Cohesin-Runx1 Deficiency Synergistically Perturbs Chromatin Looping and Causes Myelodysplastic Syndromes. (2020) (35)
- Clinical and genetic characteristics of congenital sideroblastic anemia: comparison with myelodysplastic syndrome with ring sideroblast (MDS-RS) (2012) (35)
- Deletion of the TNFAIP3/A20 gene detected by FICTION analysis in classical Hodgkin lymphoma (2012) (35)
- Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes. (2018) (34)
- Notch2 signaling is required for proper mast cell distribution and mucosal immunity in the intestine. (2011) (34)
- CBL mutations in juvenile myelomonocytic leukemia and pediatric myelodysplastic syndrome (2010) (33)
- TERT promoter mutations and chromosome 8p loss are characteristic of nonalcoholic fatty liver disease‐related hepatocellular carcinoma (2016) (33)
- Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia (2015) (32)
- Molecular classification and diagnostics of upper urinary tract urothelial carcinoma. (2021) (32)
- Characterization of genetic lesions in rhabdomyosarcoma using a high‐density single nucleotide polymorphism array (2013) (32)
- Frequent Genetic Alterations in Immune Checkpoint-Related Genes in Intravascular Large B-Cell Lymphoma. (2020) (32)
- Deregulated Intracellular Signaling by Mutated c-CBL in Myeloid Neoplasms (2010) (32)
- Identification of a SRC‐like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation (2005) (32)
- Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele (2016) (32)
- Integration of Recurrent Somatic Mutations with Clinical Outcomes: A Pooled Analysis of 1049 Patients with Clear Cell Renal Cell Carcinoma. (2016) (32)
- A prospective trial to evaluate the safety and efficacy of pravastatin for the treatment of refractory chronic graft-versus-host disease. (2005) (31)
- Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project. (2007) (31)
- Frequent false‐positive results of Aspergillus latex agglutination test (1999) (31)
- Highly immunogenic cancer cells require activation of the WNT pathway for immunological escape (2021) (31)
- Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia (2017) (30)
- Whole‐genome profiling of chromosomal aberrations in hepatoblastoma using high‐density single‐nucleotide polymorphism genotyping microarrays (2008) (30)
- Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms (2016) (30)
- Requirements for Localization of p130 cas to Focal Adhesions (1997) (30)
- Molecular characterization of the recurrent unbalanced translocation der(1;7)(q10;p10). (2003) (30)
- Comprehensive analysis of genetic aberrations linked to tumorigenesis in regenerative nodules of liver cirrhosis (2019) (30)
- Expression Profiling of Immature Thymocytes Revealed a Novel Homeobox Gene That Regulates Double-Negative Thymocyte Development1 (2007) (29)
- Molecular allelokaryotyping of T-cell prolymphocytic leukemia cells with high density single nucleotide polymorphism arrays identifies novel common genomic lesions and acquired uniparental disomy (2009) (29)
- Dual antitumor mechanisms of Notch signaling inhibitor in a T‐cell acute lymphoblastic leukemia xenograft model (2009) (29)
- Graft-versus-Tumor Effect Against Advanced Pancreatic Cancer after Allogeneic Reduced-Intensity Stem Cell Transplantation (2005) (29)
- Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia (2021) (29)
- CYP3A4*18: it is not rare allele in Japanese population. (2003) (29)
- The transcription factor E2A activates multiple enhancers that drive Rag expression in developing T and B cells (2020) (29)
- Novel CUX1 missense mutation in association with 7q− at leukemic transformation of MPN (2011) (29)
- Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases (2015) (28)
- Adverse prognostic effect of homozygous TET2 mutation on the relapse risk of acute myeloid leukemia in patients of normal karyotype (2015) (28)
- Immunotherapy against metastatic renal cell carcinoma with mature dendritic cells (2007) (28)
- Early detection and evolution of preleukemic clones in therapy-related myeloid neoplasms following autologous SCT. (2018) (28)
- Prognostic significance of genetic alterations detected by high‐density single nucleotide polymorphism array in gastric cancer (2010) (27)
- Adult T‐cell leukemia cells are characterized by abnormalities of Helios expression that promote T cell growth (2013) (27)
- Smap1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia. (2013) (27)
- Genomon ITDetector: a tool for somatic internal tandem duplication detection from cancer genome sequencing data (2015) (27)
- Somatic mutations in lymphocytes in patients with immune-mediated aplastic anemia (2021) (27)
- A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele (2015) (27)
- Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol‐3‐OH kinase &dgr; syndrome type 1 (2019) (27)
- Dasatinib Is an Effective Treatment for Angioimmunoblastic T-cell Lymphoma (2020) (27)
- Genetic and transcriptional landscape of plasma cells in POEMS syndrome (2019) (27)
- Genome-wide surveillance of mismatched alleles for graft-versus-host disease in stem cell transplantation. (2015) (26)
- De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome. (2018) (26)
- Evolutionary basis of HLA-DPB1 alleles affects acute GVHD in unrelated donor stem cell transplantation. (2018) (26)
- Clonal dynamics in a single AML case tracked for 9 years reveals the complexity of leukemia progression (2016) (26)
- High-resolution genomic copy number profiling of primary intraocular lymphoma by single nucleotide polymorphism microarrays (2014) (26)
- Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia (2015) (26)
- Prognostic value of genetic mutations in adolescent and young adults with acute myeloid leukemia (2018) (26)
- Tracing the development of acute myeloid leukemia in CBL syndrome. (2014) (26)
- Alterations of the genes involved in the PI3K and estrogen-receptor pathways influence outcome in human epidermal growth factor receptor 2-positive and hormone receptor-positive breast cancer patients treated with trastuzumab-containing neoadjuvant chemotherapy (2013) (26)
- Deep sequencing in cancer research. (2013) (25)
- A high occurrence of acquisition and/or expansion of C-CBL mutant clones in the progression of high-risk myelodysplastic syndrome to acute myeloid leukemia. (2011) (25)
- Whole-genome landscape of adult T-cell leukemia/lymphoma. (2021) (25)
- Detection of the G17V RHOA Mutation in Angioimmunoblastic T-Cell Lymphoma and Related Lymphomas Using Quantitative Allele-Specific PCR (2014) (24)
- Bernard–Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion (2013) (24)
- Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism (2015) (24)
- Hypoxic adaptation of leukemic cells infiltrating the CNS affords a therapeutic strategy targeting VEGFA. (2017) (24)
- Variegated RHOA mutations in human cancers. (2016) (24)
- Chronic phase of ETV6‐ABL1 positive CML responds to imatinib (2008) (24)
- Infection perturbs Bach2- and Bach1-dependent erythroid lineage ‘choice’ to cause anemia (2018) (23)
- PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus (2016) (23)
- Variegated clonality and rapid emergence of new molecular lesions in xenografts of acute lymphoblastic leukemia are associated with drug resistance. (2015) (22)
- Molecular pathogenesis of disease progression in MLL-rearranged AML (2018) (22)
- BRCC3 mutations in myeloid neoplasms (2015) (21)
- Autonomous feedback loop of RUNX1-p53-CBFB in acute myeloid leukemia cells (2017) (21)
- Identification of unbalanced genome copy number abnormalities in patients with multiple myeloma by single-nucleotide polymorphism genotyping microarray analysis (2012) (21)
- Hepatoblastoma in a patient with sotos syndrome. (2009) (21)
- HapMuC: somatic mutation calling using heterozygous germ line variants near candidate mutations (2014) (21)
- BCL6 locus is hypermethylated in angioimmunoblastic T-cell lymphoma (2017) (21)
- Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome. (2013) (21)
- RNA fusions involving CD28 are rare in peripheral T-cell lymphomas and concentrate mainly in those derived from follicular helper T cells (2018) (21)
- Identification of the genetic and clinical characteristics of neuroblastomas using genome-wide analysis (2017) (21)
- Differential expression of individual transcript variants of PD-1 and PD-L2 genes on Th-1/Th-2 status is guaranteed for prognosis prediction in PCNSL (2019) (20)
- Exploration of the genetic basis of GVHD by genetic association studies. (2009) (20)
- Clinical significance and origin of leukocytes that lack HLA-A allele expression in patients with acquired aplastic anemia. (2016) (20)
- DOCK2 is involved in the host genetics and biology of severe COVID-19 (2022) (20)
- Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients (2019) (20)
- Establishment and characterization of novel human primary and metastatic anaplastic thyroid cancer cell lines and their genomic evolution over a year as a primagraft. (2015) (20)
- NOTCH1 pathway activating mutations and clonal evolution in pediatric T‐cell acute lymphoblastic leukemia (2019) (20)
- Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan (2015) (20)
- Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy (2020) (20)
- Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia. (2020) (19)
- Contribution of germline mutations to PARK2 gene inactivation in lung adenocarcinoma (2012) (19)
- Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells (2009) (19)
- Aggressive transformation of juvenile myelomonocytic leukemia associated with duplication of oncogenic KRAS due to acquired uniparental disomy. (2013) (19)
- Sustained clonal hematopoiesis by HLA-lacking hematopoietic stem cells without driver mutations in aplastic anemia. (2018) (19)
- G17V RHOA: Genetic evidence of GTP-unbound RHOA playing a role in tumorigenesis in T cells (2015) (19)
- A nonsense mutation of IDH1 in myelodysplastic syndromes and related disorders (2011) (18)
- High-risk HLA alleles for severe acute graft-versus-host disease and mortality in unrelated donor bone marrow transplantation (2016) (18)
- Identification of Ki23819, a highly potent inhibitor of kinase activity of mutant FLT3 receptor tyrosine kinase (2005) (18)
- TP53 State Dictates Genome Stability, Clinical Presentation and Outcomes in Myelodysplastic Syndromes (2019) (18)
- Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome (2022) (18)
- LUBAC accelerates B-cell lymphomagenesis by conferring B cells resistance to genotoxic stress. (2020) (18)
- Paroxysmal nocturnal hemoglobinuria induced by the occurrence of BCR-ABL in a PIGA mutant hematopoietic progenitor cell (2016) (18)
- N‐ras and p53 gene mutations in Japanese patients with myeloproliferative disorders (2002) (18)
- Impact of SNP array karyotyping on the diagnosis and the outcome of chronic myelomonocytic leukemia with low risk cytogenetic features or no metaphases (2016) (18)
- Identification of a novel fusion gene, TTL, fused to ETV6 in acute lymphoblastic leukemia with t(12;13)(p13;q14), and its implication in leukemogenesis (2003) (18)
- Acquired expression of CblQ367P in mice induces dysplastic myelopoiesis mimicking chronic myelomonocytic leukemia. (2017) (18)
- PD-1 Inhibitor Therapy in Adult T-Cell Leukemia–Lymphoma. (2018) (18)
- Diagnostic challenge of Diamond–Blackfan anemia in mothers and children by whole-exome sequencing (2017) (17)
- Corrigendum: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia (Leukemia (2016) 30 (1672-1681) DOI: 10.1038/leu.2016.69) (2016) (17)
- Genetic analysis of a case of Helicobacter pylori-uninfected intramucosal gastric cancer in a family with hereditary diffuse gastric cancer (2018) (17)
- Integrated Molecular Characterization of the Lethal Pediatric Cancer Pancreatoblastoma. (2018) (17)
- Novel neuroblastoma amplified sequence (NBAS) mutations in a Japanese boy with fever-triggered recurrent acute liver failure (2019) (17)
- Integrated Analysis of Copy Number Alterations and Loss of Heterozygosity in Human Pancreatic Cancer Using a High-Resolution, Single Nucleotide Polymorphism Array (2008) (17)
- Hematopoietic stem cells expanded by fibroblast growth factor-1 are excellent targets for retrovirus-mediated gene delivery. (2005) (17)
- Genetic differences between Asian and Caucasian chronic lymphocytic leukemia (2013) (17)
- Genomic Profiling for Clinical Decision Making in Myeloid Neoplasms and Acute Leukemia. (2022) (16)
- Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer (2017) (16)
- Molecular characterization of the genomic breakpoints in a case of t(3;21)(q26;q22) (1999) (16)
- PAK Kinase Inhibition Has Therapeutic Activity in Novel Preclinical Models of Adult T-Cell Leukemia/Lymphoma (2019) (16)
- Crk‐associated substrate lymphocyte type regulates myeloid cell motility and suppresses the progression of leukemia induced by p210Bcr/Abl (2011) (16)
- Two novel high-risk adult B-cell acute lymphoblastic leukemia subtypes with high expression of CDX2 and IDH1/2 mutations. (2021) (16)
- Clinical significance of ASXL2 and ZBTB7A mutations and C-terminally truncated RUNX1-RUNX1T1 expression in AML patients with t(8;21) enrolled in the JALSG AML201 study (2018) (16)
- Cbl-family ubiquitin ligases and their recruitment of CIN85 are largely dispensable for epidermal growth factor receptor endocytosis. (2014) (15)
- Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays (2014) (15)
- Novel DDX41 variants in Thai patients with myeloid neoplasms (2019) (15)
- Frequent Loss of the Cyclin‐dependent Kinase‐4 Inhibitor Gene in Human Gliomas (1995) (15)
- Array CGH identifies copy number changes in 11% of 520 MDS patients with normal karyotype and uncovers prognostically relevant deletions (2016) (15)
- Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative (2022) (15)
- VAV1 mutations contribute to development of T-cell neoplasms in mice. (2020) (15)
- Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants (2020) (15)
- SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3 (2012) (15)
- Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets (2020) (15)
- Unbiased Detection of Driver Mutations in Extramammary Paget Disease (2020) (14)
- Genome-Wide Analysis of Ocular Adnexal Lymphoproliferative Disorders Using High-Resolution Single Nucleotide Polymorphism Array. (2015) (14)
- Reduced‐intensity bone marrow transplantation from an alternative unrelated donor for myelodysplastic syndrome of first‐donor origin (2003) (14)
- ASXL2 regulates hematopoiesis in mice and its deficiency promotes myeloid expansion (2018) (14)
- Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation (2018) (14)
- Whole-exome sequence analysis of ataxia telangiectasia-like phenotype (2014) (14)
- Recurrent CCND3 mutations in MLL-rearranged acute myeloid leukemia. (2018) (14)
- KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cells. (2019) (14)
- CBL mutations in infant acute lymphoblastic leukaemia (2012) (14)
- ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1‐RUNX1T1 and associated with a better prognosis (2017) (14)
- Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation (2018) (14)
- Somatic mosaicism in chronic myeloid leukemia in remission. (2016) (14)
- Common Variable Immunodeficiency Caused by FANC Mutations (2017) (13)
- Frameshift Mutations of the hMSH6 Gene in Human Leukemia Cell Lines (1998) (13)
- BRCA1 alterations with additional defects in DNA damage response genes may confer chemoresistance to BRCA‐like breast cancers treated with neoadjuvant chemotherapy (2017) (13)
- Single cell genotyping of exome sequencing-identified mutations to characterize the clonal composition and evolution of inv(16) AML in a CBL mutated clonal hematopoiesis. (2016) (13)
- Immune-Mediated Hematopoietic Failure after Allogeneic Hematopoietic Stem Cell Transplantation: A Common Cause of Late Graft Failure in Patients with Complete Donor Chimerism. (2018) (13)
- Induction of HLA‐B*40:02‐restricted T cells possessing cytotoxic and suppressive functions against haematopoietic progenitor cells from a patient with severe aplastic anaemia (2016) (13)
- DNA methylation-based classification reveals difference between pediatric T-cell acute lymphoblastic leukemia and normal thymocytes (2019) (13)
- A frequent nonsense mutation in exon 1 across certain HLA-A and HLA-B alleles in leukocytes of patients with acquired aplastic anemia (2020) (13)
- Metachronous anaplastic sarcoma of the kidney and thyroid follicular carcinoma as manifestations of DICER1 abnormalities. (2017) (12)
- A case of malignant rhabdoid tumor mimicking yolk sac tumor (2019) (12)
- Structural Determinants of the Gain-of-Function Phenotype of Human Leukemia-associated Mutant CBL Oncogene* (2017) (12)
- Proteogenomic identification of an immunogenic HLA class I neoantigen in mismatch repair–deficient colorectal cancer tissue (2021) (12)
- Double minute chromosomes containing MYB gene and NUP214-ABL1 fusion gene in T-cell leukemia detected by single nucleotide polymorphism DNA microarray and fluorescence in situ hybridization. (2009) (12)
- Copy number analysis identifies tumor suppressive lncRNAs in human osteosarcoma. (2017) (12)
- Japan COVID-19 Task Force: a nation-wide consortium to elucidate host genetics of COVID-19 pandemic in Japan (2021) (12)
- Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (2020) (12)
- Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency. (2021) (12)
- BCOR and BCORL 1 mutations in myelodysplastic syndromes and related disorders (2013) (12)
- Myelodysplastic Syndrome-Associated SRSF2 Mutations Cause Splicing Changes by Altering Binding Motif Sequences (2019) (12)
- Gain-of-function c-CBL mutations associated with uniparental disomy of 11q in myeloid neoplasms (2010) (12)
- Whole-Exome Sequencing-Based Approach for Germline Mutations in Patients with Inborn Errors of Immunity (2020) (11)
- RNAmut: robust identification of somatic mutations in acute myeloid leukemia using RNA-sequencing (2020) (11)
- Splicing factor mutations in AML. (2014) (11)
- A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India (2020) (11)
- Recurrent SPI 1 ( PU . 1 ) fusions in high-risk pediatric T cell acute lymphoblastic leukemia (2019) (11)
- Clonally related diffuse large B-cell lymphoma and interdigitating dendritic cell sarcoma sharing MYC translocation (2018) (11)
- Novel splicing-factor mutations in juvenile myelomonocytic leukemia (2012) (11)
- Rearrangement of retinoic acid receptor alpha and PML in promyelocytic blast crisis of Ph1 chromosome positive chronic myelocytic leukemia with normal copies of chromosome 15. (1993) (11)
- A histone modifier, ASXL1, interacts with NONO and is involved in paraspeckle formation in hematopoietic cells. (2021) (10)
- The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype (2016) (10)
- Clinical Characteristics of Patients with Coronavirus Disease (COVID-19): Preliminary Baseline Report of Japan COVID-19 Task Force, a Nationwide Consortium to Investigate Host Genetics of COVID-19 (2021) (10)
- The HTLV-1 viral oncoproteins Tax and HBZ reprogram the cellular mRNA splicing landscape (2021) (10)
- A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia (2018) (10)
- CTX-712, a Novel Clk Inhibitor Targeting Myeloid Neoplasms with SRSF2 Mutation (2019) (10)
- Ischemic colitis as a manifestation of thrombotic microangiopathy following bone marrow transplantation. (2003) (10)
- Escape hematopoiesis by HLA-B5401-lacking hematopoietic stem progenitor cells in men with acquired aplastic anemia (2019) (10)
- Distinct and convergent consequences of splice factor mutations in myelodysplastic syndromes (2020) (9)
- Genetic biomarkers for PD-1/PD-L1 blockade therapy (2016) (9)
- TP53 Mutation Status Divides MDS Patients with Complex Karyotypes into Distinct Prognostic Risk Groups: Analysis of Combined Datasets from the International Working Group for MDS-Molecular Prognosis Committee (2014) (9)
- Adults with germline CBL mutation complicated with juvenile myelomonocytic leukemia at infancy (2016) (9)
- Molecular Heterogeneity in Peripheral T-Cell Lymphoma Not Otherwise Specified Revealed By Comprehensive Mutational Profiling (2016) (9)
- Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets. (2020) (9)
- Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia (2018) (9)
- Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2P95-mutated neoplasms (2020) (9)
- Molecular pathogenesis of progression to myeloid leukemia from TET-insufficient status. (2020) (9)
- HLA class I allele-lacking leukocytes predict rare clonal evolution to MDS/AML in patients with acquired aplastic anemia. (2021) (9)
- Antineoplastic effect of a single oral dose of the novel Flt3 inhibitor KRN383 on xenografted human leukemic cells harboring Flt3-activating mutations. (2006) (9)
- Germline DDX41 mutations define a unique subtype of myeloid neoplasms. (2022) (9)
- Highly Efficient Ex Vivo Expansion of Human Hematopoietic Stem Cells Using Delta1-Fc Chimeric Protein. (2006) (9)
- Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome (2019) (9)
- RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior prognosis. (2018) (9)
- Older patients with normal karyotype acute myeloid leukemia have a higher rate of genomic changes compared to young patients as determined by SNP array analysis. (2012) (9)
- Somatic Mutations in Schinzel-Giedion Syndrome Gene SETBP1 Determine Progression in Myeloid Malignancies (2012) (8)
- Mutational Landscape of Pediatric Acute Lymphoblastic Leukemia (2016) (8)
- Aged healthy mice acquire clonal hematopoiesis mutations (2021) (8)
- Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia (2016) (8)
- Gain-of-Function Mutations and Copy Number Increases of Notch2 in Diffuse Large B-Cell Lymphoma. (2007) (8)
- Modification of cellular and humoral immunity by somatically reverted T cells in X-linked lymphoproliferative syndrome type 1. (2019) (8)
- Long-term sustained mixed chimerism after allogeneic stem cell transplantation in a patient with severe aplastic anemia. (2007) (8)
- Frequent mutations in HLA and related genes in extranodal NK/T cell lymphomas (2020) (8)
- Decreased RORC expression and downstream signaling in HTLV‐1‐associated adult T‐cell lymphoma/leukemia uncovers an antiproliferative IL17 link: A potential target for immunotherapy? (2018) (8)
- Fusion partner-specific mutation profiles and KRAS mutations as adverse prognostic factors in MLL-rearranged AML. (2020) (8)
- Glucagonoma With Necrolytic Migratory Erythema: Metabolic Profile and Detection of Biallelic Inactivation of DAXX Gene (2018) (8)
- Erratum: The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202) (2017) (8)
- Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia (2018) (8)
- Genome-wide copy number analysis on GeneChip platform using copy number analyzer for affymetrix GeneChip 2.0 software. (2007) (8)
- Genetic Predispositions to Myeloid Neoplasms Caused By Germline DDX41 Mutations (2015) (8)
- Aggressive transformation of anaplastic large cell lymphoma with increased number of ALK-translocated chromosomes (2015) (8)
- Discovery of Functional Alternatively Spliced PKM Transcripts in Human Cancers (2019) (8)
- Mutational Analyses of the AML1 Gene in Patients with Myelodysplastic Syndrome (2002) (8)
- Truncation and microdeletion of EVC/EVC2 with missense mutation of EFCAB7 in Ellis‐van Creveld syndrome (2016) (8)
- Erratum: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia (2016) (8)
- Genome-wide analysis of myelodysplastic syndromes. (2012) (8)
- Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia (2021) (7)
- Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia (2017) (7)
- Paraneoplastic hypereosinophilic syndrome associated with IL3‐IgH positive acute lymphoblastic leukemia (2018) (7)
- Identification of Chromosomal Abnormalities in Healthy Bone Marrow Using 250K SNP Arrays. (2006) (7)
- Noonan syndrome‐associated biallelic LZTR1 mutations cause cardiac hypertrophy and vascular malformations in zebrafish (2019) (7)
- Indolent feature of Helicobacter pylori-uninfected intramucosal signet ring cell carcinomas with CDH1 mutations (2021) (7)
- Classification of clear cell renal cell carcinoma based on PKM alternative splicing (2019) (7)
- Clinical utility of target capture‐based panel sequencing in hematological malignancies: A multicenter feasibility study (2020) (7)
- SRSF2 is Mutated in 47.2% (77/163) of Chronic Myelomonocytic Leukemia (CMML) and Prognostically Favorable in Cases with Concomitant RUNX1 mutations (2011) (7)
- Two patients with 19p13.2 deletion (Malan syndrome) involving NFIX and CACNA1A with overgrowth, developmental delay, and epilepsy (2017) (7)
- Comprehensive Analysis of Aberrant RNA Splicing in Myelodysplastic Syndromes (2014) (7)
- [A case with myositis as a manifestation of chronic graft-versus-host-disease (GVHD) with severe muscle swelling developed after aggressive muscular exercise]. (2003) (7)
- Toll-like receptor genetic variations in bone marrow transplantation (2017) (7)
- Absence of a common founder mutation in patients with co-occurring myelodysplastic syndrome and plasma cell disorder. (2020) (7)
- Potential curability of newly diagnosed acute promyelocytic leukemia without use of chemotherapy: the example of liposomal all-trans retinoic acid (2005) (7)
- Blastic plasmacytoid dendritic cell neoplasm arising from clonal hematopoiesis (2018) (6)
- TET2 haploinsufficiency alters reprogramming into induced pluripotent stem cells. (2020) (6)
- Allelotypes of lung adenocarcinomas featuring ALK fusion demonstrate fewer onco- and suppressor gene changes (2013) (6)
- Clonal hematopoiesis associates with improved survival in metastatic colorectal cancer patients from the FIRE-3 trial. (2021) (6)
- Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome (2020) (6)
- Hematopoietic stem progenitor cells lacking HLA differ from those lacking GPI-anchored proteins in the hierarchical stage and sensitivity to immune attack in patients with acquired aplastic anemia (2021) (6)
- Association of high-risk neuroblastoma classification based on expression profiles with differentiation and metabolism (2021) (6)
- The Evolving Genomic Landscape of Esophageal Squamous Cell Carcinoma Under Chemoradiotherapy (2021) (6)
- Molecular studies reveal MLL-MLLT10/AF10 and ARID5B-MLL gene fusions displaced in a case of infantile acute lymphoblastic leukemia with complex karyotype (2017) (6)
- Chronological Analysis of Clonal Evolution in Acquired Aplastic Anemia (2014) (6)
- Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets (2020) (6)
- Genetic basis of myelodysplastic syndromes (2020) (6)
- Clonal hematopoiesis in adult pure red cell aplasia (2021) (6)
- Hes 1 immortalizes committed progenitors and plays a role in blast crisis transition in chronic myelogenous leukemia (2010) (6)
- Pharmacokinetics of alemtuzumab after haploidentical HLA‐mismatched hematopoietic stem cell transplantation using in vivo alemtuzumab with or without CD52‐positive malignancies (2006) (6)
- Clinical Significance of Peripheral Blood Erythroblastosis after Hematopoietic Stem Cell Transplantation (2004) (6)
- Erratum: Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome (Cancer Cell (2019) 36(2) (123–138.e10), (S1535610819302983), (10.1016/j.ccell.2019.06.007)) (2019) (6)
- Stratification of patients with clear cell renal cell carcinoma to facilitate drug repositioning (2021) (5)
- Blastic transformation of juvenile myelomonocytic leukemia caused by the copy number gain of oncogenic KRAS (2017) (5)
- [Frequent inactivation of A20 through gene mutation in B-cell lymphomas]. (2011) (5)
- Prominence of nestin-expressing Schwann cells in bone marrow of patients with myelodysplastic syndromes with severe fibrosis (2019) (5)
- Predisposed genomic instability in pre-treatment bone marrow evolves to therapy-related myeloid neoplasms in malignant lymphoma (2019) (5)
- Clinical Impacts of Germline DDX41 Mutations on Myeloid Neoplasms (2020) (5)
- Single-Cell Analysis of the Multicellular Ecosystem in Viral Carcinogenesis by HTLV-1 (2021) (5)
- Soluble PD-L1 through alternative polyadenylation works as a decoy in lung cancer immunotherapy. (2021) (5)
- Correction: Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution (2017) (5)
- Feasibility and clinical utility of comprehensive genomic profiling of hematological malignancies (2022) (5)
- The landscape of genetic aberrations in myxofibrosarcoma (2022) (5)
- Prediction of drug candidates for clear cell renal cell carcinoma using a systems biology-based drug repositioning approach (2022) (5)
- Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient (2015) (5)
- Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia (2020) (5)
- Diagnosis and relapse: cytogenetically normal acute myelogenous leukemia without FLT3-ITD or MLL-PTD (2017) (5)
- HapMap SNP Scanner: an online program to mine SNPs responsible for cell phenotype. (2012) (5)
- MDS-related mutations in aplastic anemia. (2014) (4)
- Genetic Background of Chronic Active Epstein-Barr Virus Disease (2017) (4)
- Mutational Spectrum Analysis of Interesting Correlation and Interrelationship Between RNA Splicing Pathway and Commonly Targeted Genes in Myelodysplastic Syndrome (2011) (4)
- Genome-Wide Analysis of MDS/MPD Disclosed Frequent Homozygous C-Cbl mutations Tightly Associated with 11q-UPD (2008) (4)
- Distinct gene alterations with a high percentage of myeloperoxidase-positive leukemic blasts in de novo acute myeloid leukemia. (2018) (4)
- Effects of mild obesity on outcomes in Japanese patients with COVID-19: a nationwide consortium to investigate COVID-19 host genetics (2022) (4)
- Novel mechanism of immune evasion in cancer via structural variations of the PD-L1 gene. (2017) (4)
- Impact of genetic alterations in stem-cell transplantation for myelodysplasia and secondary acute myeloid leukemia Short title: Genetic alterations in myelodysplasia with HCT (2017) (4)
- Secondary Pulmonary Alveolar Proteinosis Following Treatment with Azacitidine for Myelodysplastic Syndrome (2019) (4)
- XPO1 inhibitors represent a novel therapeutic option in Adult T-cell Leukemia, triggering p53-mediated caspase-dependent apoptosis (2021) (4)
- Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma (2011) (4)
- In Analogy to AML, MDS Can be Sub-Classified By Ancestral Mutations (2014) (4)
- RARB Translocations in Acute Promyelocytic Leukemia without Rara translocation (2017) (4)
- Genetic Background of Idiopathic Bone Marrow Failure Syndromes in Children (2015) (4)
- Molecular hallmarks of adult T cell leukemia: miRNA, epigenetics, and emerging signaling abnormalities (2014) (4)
- Identification of Two New DBA Genes, RPS27 and RPL27, by Whole-Exome Sequencing in Diamond-Blackfan Anemia Patients (2012) (4)
- Genome analysis of myelodysplastic syndromes among atomic bomb survivors in Nagasaki (2019) (4)
- Progression to polythythemia vera from familial thrombocytosis with germline JAK2 R867Q mutation (2018) (4)
- Inactivation of Multiple Tumor-Suppressor Genes Involved in Negative Regulation of the CellCycle , MTSlip 16 ' NK 4 A / CDKN 2 , MTS 2 / plSXNKTB , p 53 , and Rb Genes in Primary Lymphoid Malignancies (2002) (4)
- Additional file 3: Figure S2 (2013) (4)
- PF532 INTEGRATED PROFILING OF DNA METHYLATION AND MUTATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES (2019) (4)
- Detection of Loss of A20 Gene by FICTION in Hodgkin's Lymphoma Cases. (2009) (4)
- High prevalence of myeloid malignancies in progeria with Werner syndrome is associated with p53 insufficiency. (2022) (4)
- Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome. (2019) (4)
- NGS-Based Copy Number Analysis in 1,185 Patients with Myeloid Neoplasms (2016) (4)
- Tracing the evolutionary history of blood cells to the unicellular ancestor of animals. (2022) (4)
- A Cure for Paroxysmal Nocturnal Hemoglobinuria Using Molecular Targeted Therapy Specific to a Driver Mutation (2015) (4)
- A Cryptic NUP214-ABL1 Fusion in B-cell Precursor Acute Lymphoblastic Leukemia (2017) (4)
- U-shaped association between abnormal serum uric acid levels and COVID-19 severity: reports from the Japan COVID-19 Task Force (2022) (3)
- Identification of enhancer of mRNA decapping 4 as a novel fusion partner of MLL in acute myeloid leukemia. (2019) (3)
- Different Mutant Splicing Factors Cause Distinct Missplicing Events and Give Rise to Different Clinical Phenotypes in Myelodysplastic Syndromes (2015) (3)
- A Possible Association Between a Nucleotide‐Binding Domain LRR‐Containing Protein Family PYD‐Containing Protein 1 Mutation and an Autoinflammatory Disease Involving Liver Cirrhosis (2021) (3)
- Abstract 5119: Frequent splicing pathway mutations and aberrant RNA splicing in myelodysplasia (2012) (3)
- Impact of Somatic Mutations on Outcome in Patients with MDS after Stem-Cell Transplantation (2015) (3)
- Molecular Profiling of Blastic Transformation in Chronic Myeloid Leukemia (2018) (3)
- Genome-Wide Analysis of B Cell Non-Hodgkin’s Lymphoma Disclosed Frequent Involvement of Genes in NFkB Pathway (2008) (3)
- Chromatin-Spliceosome Mutations in Acute Myeloid Leukemia (2021) (3)
- The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force (2022) (3)
- Aberrant MYCN expression drives oncogenic hijacking of EZH2 as a transcriptional activator in peripheral T cell lymphoma (2022) (3)
- Mathematical Modeling and Mutational Analysis Reveal Optimal Therapy to Prevent Malignant Transformation in Grade II IDH-Mutant Gliomas (2021) (3)
- Genome-wide DNA methylation analysis in pediatric acute myeloid leukemia (2022) (3)
- Novel mechanism of immune evasion involving PD-L1 in various cancers (2016) (3)
- Tumor heterogeneity. (2021) (3)
- Ring sideroblasts in AML are associated with adverse risk characteristics and have a distinct gene expression pattern. (2019) (3)
- Rearrangement and Deletion of the PAX5 Gene in Pediatric Acute B-Cell Lineage Lymphoblastic Leukemia. (2007) (3)
- Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia (2022) (3)
- Patient-specific MDS-RS iPSCs define the mis-spliced transcript repertoire and chromatin landscape of SF3B1-mutant HSPCs (2022) (3)
- Acute myeloid leukemia with a cryptic NUP98/PRRX2 rearrangement developing after low-dose methotrexate therapy for rheumatoid arthritis (2019) (3)
- Expressional changes of genes and miRNA in common megakaryocyte-erythroid progenitors from lower-risk myelodysplastic syndrome (2014) (3)
- Sudden Intracranial Hemorrhage in a Patient With Atypical Chronic Myeloid Leukemia in Chronic Phase. (2017) (3)
- Clinical “MUTATOME” Of Myelodysplastic Syndrome; Comparison To Primary Acute Myelogenous Leukemia (2013) (3)
- Hidden Abnormalities and Novel Classification of t(15;17) APL Based on Genomic Alterations. (2007) (3)
- Clonal Hematopoiesis: Cell of Origin, Lineage Repartition and Dynamic Evolution during Chemotherapy (2017) (3)
- Germline SAMD9 and SAMD9L Alterations in Adult Myelodysplastic Syndromes (2017) (3)
- Characteristics of hospitalized patients with COVID-19 during the first to fifth waves of infection: a report from the Japan COVID-19 Task Force (2022) (3)
- Pan-Myeloid Leukemia Analysis: Machine Learning-Based Approach to Predict Phenotype and Clinical Outcomes Using Mutation Data (2018) (3)
- Decreased RORC expression and downstream signaling in HTLV-1-associated Adult T-cell Lymphoma/Leukemia uncovers an antiproliferative IL17 link: a potential target for immunotherapy? (2018) (3)
- NUDT15 variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia (2021) (3)
- Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma (2019) (3)
- ZRSR2 Mutations Cause Dysregulated RNA Splicing in MDS (2014) (3)
- Clinical significance of prediabetes, undiagnosed diabetes and diagnosed diabetes on critical outcomes in COVID‐19: Integrative analysis from the Japan COVID‐19 task force (2022) (2)
- Acquired Aplastic Anemia: New Genetics, New Genomics (2014) (2)
- Impact of accumulative smoking exposure and chronic obstructive pulmonary disease on COVID-19 outcomes: report based on findings from the Japan COVID-19 task force (2022) (2)
- Corrigendum: The landscape of somatic mutations in Down syndrome–related myeloid disorders (2013) (2)
- Germline RUNX1 translocation in familial platelet disorder with propensity to myeloid malignancies (2021) (2)
- [Genetic analysis of hereditary hematological disorders: overview]. (2015) (2)
- Genotype-Phenotype Relationships and Therapeutic Targets in Acute Erythroid Leukemia (2020) (2)
- A Case of Tyrosine Kinase Inhibitor-Resistant Chronic Myeloid Leukemia, Chronic Phase with ASXL1 Mutation (2020) (2)
- Somatic G17V Rhoa Mutation Specifies Angioimmunoblastic T-Cell Lymphoma (2013) (2)
- Complete Bone Marrow Necrosis with Charcot-Leyden Crystals Caused by Myeloid Neoplasm with Mutated NPM1 and TET2 (2022) (2)
- Novel Molecular Pathogenesis and Therapeutic Target in Acute Erythroid Leukemia (2019) (2)
- Roles of TET2 and C-CBL Mutations In the Progression of De Novo Myelodysplastic Syndrome to Acute Myeloid Leukemia (2010) (2)
- Prognostic Relevance of Genetic Abnormalities in Blastic Transformation of Chronic Myeloid Leukemia (2020) (2)
- Dysregulation of DNA Methylation Involves in Progression of Myeloid Leukemia in Down Syndrome (2015) (2)
- High Density SNP Arrays Reveal That Distinct Clonal Lesions Including Uniparental Disomy Can Be Detected in a Proportion of Patients with Aplastic Anemia with Normal Metaphase Cytogenetics. (2006) (2)
- Genetic Basis of Myeloid Proliferation Related to Down Syndrome (2012) (2)
- In Vivo Effects of Notch Signaling Inhibitor on Tumor Growth and Its Mechanism of Action. (2006) (2)
- [Genetic landscape of adult T-cell leukemia/lymphoma]. (2016) (2)
- Revised version 2 ) Biallelic DICER 1 mutations in sporadic pleuropulmonary blastoma Running title Biallelic DICER 1 mutations in sporadic PPB (2014) (2)
- Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation (2018) (2)
- Srsf2 P95H Mutation Causes Impaired Stem Cell Repopulation and Hematopoietic Differentiation in Mice (2015) (2)
- Characterization of adenocarcinoma of the lung in a familial adenomatous polyposis patient (2008) (2)
- Predictive Value of Mutation Analysis in the Diagnostic Approach to Patients with Unexplained Cytopenia (2016) (2)
- MP23-16 TCEB1-MUTATED RENAL CELL CARCINOMA: A DISTINCT GENOMIC AND MORPHOLOGIC SUBTYPE (2014) (2)
- Adaptor Protein LNK Binds to and Is Phosphorylated by JAK3 and May Serve as a Scaffold for JAK3 Autophosphorylation In the Absence of An Appropriate Cytokine Receptor (2010) (2)
- Alteration of the immune environment in bone marrow from children with recurrent B cell precursor acute lymphoblastic leukemia (2021) (2)
- Frequent HLA-DR loss on hematopoietic stem progenitor cells in patients with cyclosporine-dependent aplastic anemia carrying HLA-DR15 (2022) (2)
- Lineage-Specific Aberrant mRNA Splicing By U2AF1 Mutation Alters Erythroid and Granulomonocytic Differentiation (2015) (2)
- Genetic analysis of pheochromocytoma and paraganglioma complicating cyanotic congenital heart disease. (2022) (2)
- SNP Karyotyping in Myelodysplastic Syndromes (MDS) Reveals the Presence of Cryptic Karyotypic Abnormalities, Including Uniparental Disomy, and Has Important Prognostic Implications. (2006) (2)
- Impact of upper and lower respiratory symptoms on COVID-19 outcomes: a multicenter retrospective cohort study (2022) (2)
- VEGFA- a New Therapeutic Target in CNS Leukemia (2016) (2)
- Should Young Patients with e19a2 Type BCR/ABL Rearrangement Undergo Stem Cell Transplantation? (2003) (2)
- Hypermethylation of Bcl6 Is a Potential Cause of Development of Lymphoma with Tfh Features in Tet2 Knockdown Mice (2013) (2)
- Multi-omics analysis defines highly refractory RAS burdened immature subgroup of infant acute lymphoblastic leukemia (2022) (2)
- Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma (2021) (2)
- DDX41 Is a Tumor Suppressor Gene Associated with Inherited and Acquired Mutations (2014) (2)
- Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (2021) (2)
- A robust molecular pattern for myelodysplastic syndromes in two independent cohorts investigated by next‐generation sequencing can be revealed by comparative bioinformatic analyses (2014) (2)
- Publisher Correction: Defective Epstein–Barr virus in chronic active infection and haematological malignancy (2019) (2)
- Atypical dyskeratosis congenita diagnosed using whole‐exome sequencing (2017) (2)
- Serial Sequencing in Myelodysplastic Syndromes Reveals Dynamic Changes in Clonal Architecture and Allows for a New Prognostic Assessment of Mutations Detected in Cross-Sectional Testing (2015) (2)
- Spectrum Of Genetic Alterations In Acquired Aplastic Anemia (2013) (2)
- Deciphering the Clonal Origin of Relapsed Acute Lymphoblastic Leukemia in Children. (2020) (2)
- Expansion of gastric intestinal metaplasia with copy number aberrations contributes to field cancerization. (2022) (2)
- PPM1D and DNMT3A Mutations in Myelodysplasia and Clonal Hematopoiesis (2019) (2)
- Landscape of Genetic Alterations in Adult T-Cell Leukemia/Lymphoma (2014) (2)
- Distinct, Ethnic, Clinical, and Genetic Characteristics of Myelodysplastic Syndromes with Der(1;7) (2019) (2)
- Clinical Effect of Genetic Alterations in Pediatric Patients with B-Progenitor Acute Lymphoblastic Leukemia (2017) (2)
- Abstract 94: Genomic landscape and clonal expansions of upper urinary tract urothelial carcinoma (2016) (2)
- Identification of a Novel Titin Variant Underlying Myocardial Involvement in Neurofibromatosis Type 1. (2018) (2)
- Ectopic neuroblastoma in monozygotic twins with different ages of onset: possible twin-to-twin metastasis in utero with distinct genetic alterations after birth. (2014) (1)
- Erratum: AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not maintenance of hematopoietic stem cells in adult hematopoiesis (2005) (1)
- The Impact of Clonal Architecture of IDH1 and IDH2 Mutant Cases on the Biology of Myeloid Malignancies (2014) (1)
- On the origin of gastric tumours: analysis of a case with intramucosal gastric carcinoma and oxyntic gland adenoma (2023) (1)
- Abstract 2147: Molecular allelokaryotyping to identify mechanism of development of Asian chronic lymphocytic leukemia (2010) (1)
- myeloproliferative neoplasms negative - leukemic transformation of Philadelphia chromosome Prevalence and prognostic impact of allelic imbalances associated with (2011) (1)
- Whole Exome Sequencing Reveals Clonal Evolution Pattern and Driver Mutations Of Relapsed Pediatric AML (2013) (1)
- Immature granulocyte fraction in the peripheral blood is a practical indicator for mobilization of CD34+ cells (2004) (1)
- Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia. (2015) (1)
- Description of longitudinal tumor evolution in a case of multiply relapsed clear cell sarcoma of the kidney (2021) (1)
- Emergence of t(3;21)(q26.2;q22) during eltrombopag treatment in a patient with relapsed aplastic anemia who received chemotherapy for angioimmunoblastic T-cell lymphoma (2022) (1)
- TAL1 Super Enhancer Aberration and Stil-TAL1 Fusion in Pediatric T Cell Acute Lymphoblastic Leukemia (2016) (1)
- Molecular Characteristics That Predict Response to Azacitidine Therapy (2019) (1)
- Maturing papillomatous nevoid melanoma in the scalp mimicking recurrent melanocytic nevus: A case report of previously undescribed subtype of nevoid melanoma (2021) (1)
- Molecular Signatures That Predict Response to Azacitidine Treatment for Myelodysplastic Syndromes (2017) (1)
- Genome-Wide Association Studies of Genetic Incompatibility That Is Relevant to the Development of GvHD in Unrelated Bone Marrow Transplantation (2008) (1)
- Childhood acute myeloid leukemia with 5q deletion and HNRNPH1-MLLT10 fusion: the first case report (2022) (1)
- Functional Analysis of SRSF2 Mutations in Myelodysplastic Syndromes and Related Disorders (2011) (1)
- The AML 1 / ETO ( MTG 8 ) and AML 1 / Evi1 Leukemia-Associated Chimeric (1998) (1)
- Two Novel Distinct Subtypes of Myeloid Neoplasms Molecularly Associated with Histone H3K36 Methylations (2015) (1)
- Abstract 4702: Genome-wide analysis of copy number alternations and gene mutations in renal cell carcinoma (2011) (1)
- Clinical Features and Prognostic Impact of RUNX1 and PTPN11 Mutations in Pediatric Acute Myeloid Leukemia—the Jccg Study, JPLSG AML-05- (2017) (1)
- Genetic features of B‐cell lymphoblastic lymphoma with TCF3‐PBX1 (2021) (1)
- Hidden FLT3-D835Y clone in FLT3-ITD-positive acute myeloid leukemia that evolved into very late relapse with T-lymphoblastic leukemia (2018) (1)
- Abstract 2225: Comprehensive molecular characterization of esophageal squamous cell carcinoma (2014) (1)
- Whole Exome Sequencing Reveals Spectrum of Gene Mutations in Pediatric AML (2012) (1)
- The landscape and clonal architecture in lower grade glioma. (2015) (1)
- Comprehensive Sequencing Analysis in Subcutaneous Panniculitis-like T-Cell Lymphoma (2017) (1)
- Whole-genome sequencing analysis of an atypical teratoid/rhabdoid tumor in a patient with Phelan–McDermid syndrome: a case report and systematic review (2022) (1)
- leukemia identifies heterogeneous secondary genomic alterations SNP array analysis of tyrosine kinase inhibitor-resistant chronic myeloid (2011) (1)
- Numerous Genomic Abnormalities in AML with Normal Karyotype. (2007) (1)
- The Tyrosine Kinase-Binding and Proline-Rich Domains of Mutant CBL Are Essential for Leukemogenesis (2015) (1)
- Whole-Genome Analysis of Adult T-Cell Leukemia/Lymphoma (2020) (1)
- Preclinical Evaluation of a Novel MALT1 Inhibitor CTX-177 for Relapse/Refractory Lymphomas (2020) (1)
- [IDH1/2 gene mutations in myelodysplastic syndromes]. (2012) (1)
- EPOR/JAK/STAT Signaling Pathway As Therapeutic Target of Acute Erythroid Leukemia (2021) (1)
- Next‐generation sequencing in two cases of de novo acute basophilic leukaemia (2021) (1)
- Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (2021) (1)
- Identification of an asymptomatic Shwachman–Bodian–Diamond syndrome mutation in a patient with acute myeloid leukemia (2021) (1)
- Novel Pathogenic Defects Of Dead/H-Box Helicases In Myeloid Neoplasms (2013) (1)
- Development of Philadelphia chromosome-negative acute myeloid leukemia with IDH2 and NPM1 mutations in a patient with chronic myeloid leukemia who showed a major molecular response to tyrosine kinase inhibitor therapy (2021) (1)
- Post-azacitidine clone size predicts outcome of patients with myelodysplastic syndromes and related myeloid neoplasms. (2023) (1)
- Reply to the letter: “Arima syndrome and bilateral retinoblastoma in interstitial deletion of 13q14.13–q32.3”: Where is the molar tooth sign? (2011) (1)
- G17V Rhoa Mutation in Circulating DNA Is a Useful Marker for Diagnosis of AITL and AITL-Related Lymphoma (2015) (1)
- Persistent clonal cytogenetic abnormality with del(20q) from an initial diagnosis of acute promyelocytic leukemia (2019) (1)
- Abstract 3294: Clonal evolution and integral analysis of hepatoblastoma (2015) (1)
- Novel TENM3–ALK fusion is an alternate mechanism for ALK activation in neuroblastoma (2022) (1)
- Donor cell-derived transient abnormal myelopoiesis as a specific complication of umbilical cord blood transplantation (2018) (1)
- Frequent Loss of HLA Alleles From Hematopoietic Stem Cells in Patients with Hepatitis-Associated Aplastic Anemia (2011) (1)
- Prognostic model of lower grade gliomas. (2015) (1)
- Long-Term Clonal Inversion in an MDS-RS Case with Dual SF3B1 Mutations (2022) (1)
- Spliceosomal Gene LUC7L2 Mutation Causes Missplicing and Alteration Of Gene Expression In Myeloid Neoplasms (2013) (1)
- TEMPORAL AND SPACIAL EVOLUTION OF CLONES IN 400 LOW GRADE GLIOMAS IN JAPAN (2014) (1)
- Biological Analysis of SRSF2 Mutations in Leukemogenesis (2012) (1)
- Biological Characterization of the U2af1 S34F Mutation in the Pathogenesis of Myelodysplasia (2018) (1)
- Distinctive Genetic Features of Plasma Cells in POEMS Syndrome (2016) (1)
- ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan (2015) (1)
- Molecular Defects In BRCC3 Complex, a Novel Pathogenic Pathway In MDS (2013) (1)
- Whole-Genome Sequencing of Primary Central Nervous System Lymphoma and Diffuse Large B-Cell Lymphoma (2016) (1)
- Immunologically-Selected Hematopoiesis Caused by HLA Allelic Loss In Patients with Aplastic Anemia (2010) (1)
- The viral oncoproteins Tax and HBZ reprogram the cellular mRNA splicing landscape (2021) (1)
- Soluble PD-L1 works as a decoy in lung cancer immunotherapy via alternative polyadenylation (2022) (1)
- Partial monosomy of 10p and duplication of another chromosome in two patients (2017) (1)
- Remission clone in acute myeloid leukemia shows growth advantage after chemotherapy but is distinct from leukemic clone. (2019) (1)
- Differential expression of individual transcript variants of PD-1 and PD-L2 genes on Th-1/Th-2 status is guaranteed for prognosis prediction in PCNSL (2019) (1)
- Genetic Basis of Primary Central Nervous System Lymphoma (2015) (1)
- Coexistence and Prognostic Significance of EVI1 Expression and Driver Mutations in KMT2A-Rearranged Acute Myeloid Leukemia (2019) (1)
- Array CGH Identifies Copy Number Changes In 10% Of 520 MDS Patients With Normal Karyotype: Deletions Encompass The Genes TET2, DNMT3A, ETV6, NF1, RUNX1, and STAG2 and Are Associated With Shorter Survival (2013) (1)
- Comprehensive Analysis of 343 Genes Using Targeted Sequencing Panel By Next-Generation Sequencer in 77 Pediatric AML Patients with Normal and Complex Karyotypes: Jccg Study, JPLSG AML-05 (2018) (1)
- Novel and Significant Impact of Germline Variants Predisposed to Pathogenic Somatic Mutations and Loss of Heterozygosity (LOH) in Myelodysplastic Syndromes (MDS) and Clonal Hematopoiesis of Indeterminate Potential (CHIP) (2018) (1)
- Recurrent VAV1 Abnormalities in Angioimmunoblastic T Cell Lymphoma (2016) (1)
- Poor Myocardial Compaction in a Patient with Recessive MYL2 Myopathy. (2021) (1)
- Dramatic response to encorafenib in a patient with Erdheim–Chester disease harboring the BRAFV600E mutation (2021) (1)
- Tumor and Stem Cell Biology KLF 5 Regulates the Integrity and Oncogenicity of Intestinal Stem Cells (2014) (1)
- Various Germline Congenital Disorder Genes Are Somatically Mutated in Myeloid Malignancies (2012) (1)
- Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations (2020) (1)
- Genetic and epigenetic loss of miR-31 activates NIK-dependent NF-κB pathway in Adult T-cell Leukemia (2011) (1)
- Whole Exome Sequencing to Predict Response to Hypomethylating Agents in MDS (2012) (1)
- The first Japanese biobank of patient‐derived pediatric acute lymphoblastic leukemia xenograft models (2022) (1)
- Clonal evidence for the development of neuroblastoma with extensive copy‐neutral loss of heterozygosity arising in a mature teratoma (2021) (1)
- Targeted deep next generation sequencing identifies potential somatic and germline variants for predisposition to familial Burkitt lymphoma (2021) (1)
- Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia (2022) (1)
- Preclinical Translational Research Suggests a Clinical Trial Strategy for a Novel MALT1 Inhibitor ONO-7018/CTX-177 Against Malignant Lymphomas (2022) (1)
- Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients (2020) (1)
- Deletion of the TNFAIP3/A20gene detected by FICTION analysis in classical Hodgkin lymphoma (2012) (1)
- UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia (2022) (1)
- Epigenetic Memory Enables the Dominant Generation of Adult-Type Erythrocytes From Human Induced Pluripotent Stem Cells (2010) (1)
- Mutation Screening Associated with Chromosome 7 Abnormalities Using Next Generation Whole Exome Sequencing (2012) (1)
- ASXL1 Mutations Predict a Poor Response to Darbepoetin Alfa in Anemic Patients with Low-Risk MDS: A Multicenter, Phase II Study (2020) (1)
- Frequent Alterations of Driver Genes in Chromosome X and Their Clinical Relevance in Extranodal NK/T-Cell Lymphoma (2022) (1)
- Drug Repositioning for Clear Cell Renal Cell Carcinoma Based on Stratification of Patients (2021) (1)
- Optimization of prediction methods for risk assessment of pathogenic germline variants in the Japanese population (2021) (1)
- Der(1;7)(q10;p10) Presents with a Unique Genetic Profile and Frequent ETNK1 Mutations in Myeloid Neoplasms (2021) (1)
- High-Resolution Genomic Copy Number Profiling of Primary Intraocular Lymphomas Using SNP Microarrays (2011) (1)
- [Successful treatment of pure red cell aplasia with cyclosporin in a patient with T-cell large granular lymphocytic leukemia harboring the STAT3 D661V mutation]. (2019) (1)
- Frequent Activating Somatic Alterations in T-Cell Receptor / NF-κb Signaling in Adult T-Cell Leukemia/Lymphoma (2015) (1)
- Detection of Novel Pathogenic Gene Rearrangements in Pediatric Acute Myeloid Leukemia By RNA Sequencing (2015) (1)
- Determinants of Phenotypic Commitment and Clonal Progression--Conclusions from the Study of Clonal Architecture in CMML (2015) (1)
- Cooperative Effects of SRSF2 and STAG2 mutations on Development of Myelodysplastic Syndrome and Its Related Disorders (2022) (0)
- Abstract 3401: Comprehensive analysis of genetic alterations and intratumor heterogeneity in myxofibrosarcoma (2018) (0)
- XPO1 inhibitors represent a novel therapeutic option in Adult T-cell Leukemia, triggering p53-mediated caspase-dependent apoptosis (2021) (0)
- Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort (2020) (0)
- Identification of a novel causative gene for Diamond-Blackfan anemia using zebrafish (2015) (0)
- Use of the neutrophil-to-lymphocyte ratio and an oxygen requirement to predict disease severity in patients with COVID-19 (2023) (0)
- O1-18-3EXOME SEQUENCING AND SNP ARRAY REVEAL EPIGENOME MODIFIER DEFECTS IN NASOPHARYNGEAL CARCINOMA (2014) (0)
- Chronic Myelomonocytic Leukemia (CMML) Can be Categorized By Ancestral Mutational Events (2014) (0)
- Clinical and Genetic Characteristics of Patients with Shwachman-Diamond Syndrome in Japan (2018) (0)
- 1766P Longitudinal alteration of cytokine profile in the peripheral blood and clinical response for neoadjuvant chemotherapy in triple-negative breast cancer patients (translational research of the JBCRG-22 trial) (2021) (0)
- Abstract 5126: Genetic analysis of metachronous pancreatic cancers (2019) (0)
- Combined DNA and Transcriptome Sequencing Reveals Discrete Subtypes of Myelodysplasia (2016) (0)
- Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations (2020) (0)
- MP28-19 GENOME-WIDE ANALYSIS OF COPY NUMBER ALTERATIONS IN RENAL-PELVIC AND URETERAL CANCERS (2012) (0)
- Abstract 3184: Integrative analysis of clear cell renal cell carcinoma. (2013) (0)
- Novel translocation of POGZ/STK11 in de novo mast cell leukemia with KIT D816H mutation (2022) (0)
- [108th Scientific Meeting of the Japanese Society of Internal Medicine: educational lecture: 17. Molecular pathogenesis of B cell lymphoma]. (2011) (0)
- Landscape of DNA Methylation and Genetic Profiles in 291 Patients with Myelodysplastic Syndromes (2015) (0)
- Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia (2018) (0)
- Whole Exome Analysis of Myelodysplastic Syndromes Using Next-Generation Resequencing Technology (2010) (0)
- 49 Male predominance among Japanese adult patients with late-onset hemorrhagic cystitis (HC) after hematopoietic stem cell transplantation (HSCT) (2003) (0)
- TET2 Haploinsufficiency Alters Reprogramming into Induced Pluripotent Stem Cells (2020) (0)
- Non-Random Interactions between Founder and Subclonal Mutations Shape the Clinical and Morphological Features of MDS (2017) (0)
- Landscape of Driver Mutations and Their Clinical Impacts in Pediatric Acute Lymphoblastic Leukemia (2016) (0)
- DISTINCT GENOMIC LANDSCAPE OF UPPER URINARY TRACT UROTHELIAL CARCINOMA: MP71‐02 (2017) (0)
- The 79 th Annual Meeting of the Japanese Cancer Association Day 2 October 2 ( Friday ) (2020) (0)
- mutations in adult T-cell leukemia / lymphoma (2015) (0)
- Prognostic Analysis According to the 2017 ELN Risk Stratification by Genetics in Adult Acute Myeloid Leukemia Patients Treated in The Japan Adult Leukemia Study Group (JALSG) AML201 study: AML‐052 (2018) (0)
- Transcriptome Analysis Revealed the Entire Genetic Understanding of Pediatric Acute Myeloid Leukemia with a Normal Karyotype (2016) (0)
- Aberrations of Genes Regulating NF Kappa B Pathway in B-Cell Malignant Lymphoma. (2009) (0)
- Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations (2021) (0)
- Utility of SNP Arrays in Chronic Myelomonocytic Leukemia with Low Risk Cytogenetic Features or No Metaphases (2014) (0)
- Abstract 1437: Differential role of mutations in clonal evolution in esophageal mucosa at risk for cancer (2017) (0)
- Abstract P2-10-12: Relationship between predicted risks of carrying breast cancer susceptibility genes and the presence of germline variants in Japanese patients with primary breast cancer (2020) (0)
- Abstract 1309: Distinct molecular subtypes and a high diagnostic urinary biomarker of upper urinary tract urothelial carcinoma (2020) (0)
- Autonomous feedback loop of RUNX1-p53-CBFB in acute myeloid leukemia cells (2017) (0)
- Invariant Patterns of Clonal Succession Determines Specific Phenotypic and Clinical Features of Myelodysplastic Syndromes (MDS) (2018) (0)
- Abstract 1002: Epigenetic and genetic characteristics and their association with prognosis of follicular lymphoma: Analysis at a Japanese single institution (2023) (0)
- New targetes and biomarkers in hematological malignancies (2018) (0)
- Implication of AML1/RUNX1 Function in the Homeostasis and Leukemic Transformation of Hematopoietic Stem Cells. (2007) (0)
- Reduced Tet2 Function Contributes to Development of Peripheral T-Cell Lymphoma with Follicular Helper T-Cell-Like Features in Mice (2012) (0)
- ATRT-11. PREVALENCE OF GERMLINE VARIANTS IN SMARCB1 INCLUDING SOMATIC MOSAICISM IN AT/RT AND OTHER RHABDOID TUMORS (2020) (0)
- 48 Next-generation sequencing technology combined with multiplexed barcoded samples of myelodysplastic syndromes reveals an abundance of target gene mutations (2011) (0)
- Prognosis of Pediatric Acute Myeloid Leukemia with KMT2A-MLLT3 According to DNA Methylation Patterns: Jccg JPLSG AML-05 Study (2022) (0)
- P-030 Novel mutations in spliceosomal gene PRPF8 show ring sideroblast phenotype in patients with myeloid neoplasms (2013) (0)
- Abstract 3384: Comprehensive genetic analysis of myxofibrosarcoma and comparison with other soft tissue sarcomas (2017) (0)
- Successful azacitidine therapy for myelodysplastic syndrome associated with VEXAS syndrome. (2023) (0)
- Gene mutations in myelodysplastic syndromes. (2016) (0)
- Transition in Thymocyte Development Double-Negative to CD 4 / 8 Double-Positive Expression , and CD 4 / 8 β TCR Differentially Required for CD 4 Repression , Functional Domains of Runx 1 Are Kurokawa (2005) (0)
- Abstract 71: Mutational analysis for IDH1 and IDH2 in pediatric leukemia (2012) (0)
- Adult Low-Hypodiploid Acute Lymphoblastic Leukemia Evolves from TP53-Mutated Clonal Hematopoiesis. (2023) (0)
- Tokuda Akihiro Tomida Shinya Toyokuni Hitoshi Tsuda Shoichiro Tsugane Tatsuhiko Tsunoda Heiichiro Udono Koji Ueda Yoshimasa Uehara Hiroo Ueno Kazuo Umezawa Toshikazu Ushijima Toshihiko Wakabayashi Kenji Wakai Tetsuro Watabe (2016) (0)
- PS983 NOVEL MOLECULAR PATHOGENESIS AND THERAPEUTIC TARGET IN ACUTE ERYTHROID LEUKEMIA (2019) (0)
- Incidence, Clinical Associations, and Co-Mutation Patterns of UBA1 Mutations in MDS (2022) (0)
- Abstract 5117: Mutations of cohesin genes in myeloid malignancy (2012) (0)
- Anti-COX-2 autoantibody is a novel biomarker of immune aplastic anemia (2022) (0)
- Abstract 225: Frequent abnormalities in TP53 and increased genetic instability in myxofibrosarcoma (2020) (0)
- Mutations of the Spliceosome Complex Genes Occur In Adult Patients but Are Very Rare In Children with Myeloid Neoplasia (2011) (0)
- Title Generation of Alveolar Epithelial Spheroids via Isolated Progenitor Cells from Human Pluripotent Stem Cells( (2017) (0)
- Single-cell analysis based dissection of clonality in myelofibrosis (2020) (0)
- [Genetic analysis of hematopoietic neoplasms]. (2005) (0)
- Unrelated hematopoietic stem cell transplantation for familial platelet disorder/acute myeloid leukemia with germline RUNX1 mutations. (2023) (0)
- T‐cell lymphoma, B‐cell lymphoma, and myelodysplastic syndrome harboring common mutations: Trilineage tumorigenesis from a common founder clone (2021) (0)
- Abstract 2223: Genome-wide analysis of copy number alterations and gene mutations in testicular germ cell cancer (2014) (0)
- COL4A1 is a Novel Causative Gene Responsible for Congenital Hemolytic Anemia, Representing Characteristic Clinical Course in Infants (2015) (0)
- Clinical clustering with prognostic implications in Japanese COVID-19 patients: report from Japan COVID-19 Task Force, a nation-wide consortium to investigate COVID-19 host genetics (2022) (0)
- Integrated Molecular Analysis of Myelodysplastic Syndromes Using Whole Genome Sequencing (2016) (0)
- A Novel Diagnostic Method For AITL By Detecting RHOA G17V Hotspot Mutation Using Allele-Specific Real-Time PCR (2013) (0)
- Abstract 5877: Genetic analysis of metachronous pancreatic cancers (2020) (0)
- Molecular Landscape of Myeloid Neoplasms with Der(1;7)(q10;p10) (2022) (0)
- Novel neuroblastoma amplified sequence (NBAS) mutations in a Japanese boy with fever-triggered recurrent acute liver failure (2019) (0)
- Mutational Type and Configuration of an Individual Gene May Differentially Impact the Clinical and Phenotypic Features (2019) (0)
- Abstract 2092: Integrated genetic analysis of clear cell renal cell carcionoma (2012) (0)
- TET2 Mutation Associated with Organ Infiltrations in ATLL (2018) (0)
- Unique Gain-of-Function of Mutated c-CBL Tumor Suppresor in Myeloid Neoplasms. (2009) (0)
- 270 FOUNDER AND SUBCLONAL SOMATIC MUTATIONS CONTRIBUTING TO LEUKEMIC EVOLUTION IN MYELODYSPLASTIC SYNDROMES AND RELATED MYELOID NEOPLASMS (2015) (0)
- implications for the molecular mechanism HLA mismatch combinations associated with decreased risk of relapse : (2009) (0)
- GE-34THE MUTATIONAL LANDSCAPE AND TEMPORAL AND SPATIAL CLONAL EVOLUTION TO PROGRESSION IN 351 LOW-GRADE GLIOMAS. (2014) (0)
- I-003 Splicing factor mutations in myelodysplastic syndrome and other myeloid neoplasms (2013) (0)
- Older Patients with Normal Cytogenetics AML Have a Higher Rate of Genomic Changes Compared to Young Patients as Determined by SNP Chip Analysis (2010) (0)
- A case of vasculogenic mesenchymal tumor in the mediastinum: whole-exome sequencing reveals origin from pre-existing germ cell tumor (2023) (0)
- Whole Exome and Transcriptome Analyses in Pediatric T-Cell Acute Lymphoblastic Leukemia (2014) (0)
- Abstract 3803: Genome-wide approach to identify gene targets of pleuropulmonary blastoma. (2013) (0)
- anemia Extensive gene deletions in Japanese patients with Diamond-Blackfan (2012) (0)
- VAV1 Mutations Contributes to the Development of T-Cell Malignancies in Mice (2019) (0)
- [Bone marrow failure syndrome (idiopathic hematopoietic disorders): progress in diagnosis and treatment. Topics: IV. Recent topics of hematopoiesis; 1. Novel molecular mechanism of myelodysplastic syndromes]. (2012) (0)
- Impact of Highly Conserved HLA Haplotype on Acute Graft-Versus-Host Disease in Unrelated Bone Marrow Transplantation (2008) (0)
- Integrated molecular analysis of upper urinary tract urothelial carcinoma (2018) (0)
- Evidence of Common Mechanisms Underlying the Survival Advantage of the PIG-A mutant and 13q- Hematopoietic Stem Cell Clones In Patients with Immune-Mediated Bone Marrow Failure (2010) (0)
- Impact of respiratory bacterial infections on mortality in Japanese patients with COVID-19: a retrospective cohort study (2023) (0)
- Abstract 2450: Mutational profiling of MLL-PTD acute myeloid leukemia (2017) (0)
- Identification of Recurrent Submicroscopic Deletions of chromosome1q31.3 As Possible Molecular Prognostic Markers in Acute Promyelocytic Leukemia (APL) (2011) (0)
- Genetic Profiling of Adult Acute Lymphoblastic Leukemia Cells by Single Nucleotide Polymorphism Oligonucleotide Microarray. (2007) (0)
- Molecular hallmarks of adult T cell leukemia: miRNA, epigenetics, and emerging signaling abnormalities (2014) (0)
- Escape Hematopoiesis By HLA-B5401-Lacking Hematopoietic Stem Progenitor Cells in Male Patients with Acquired Aplastic Anemia (2018) (0)
- The effect of CARD11 mutation and HBZ expression accelerated lymphoproliferative diseases and formed the pathological basis for adult T-cell leukemia/lymphoma (2022) (0)
- Mutations in Triple-Negative Patients with Myeloproliferative Neoplasms (2019) (0)
- Mutational Analysis for IDH1 and IDH2 In Pediatric Leukemia (2010) (0)
- Ancestral Events Including Germline and Somatic Mutations Determine Subclonal Events and Affect Phenotype of Progression in MDS (2017) (0)
- Myelodysplastic Syndrome (MDS)-Determining Clonal Events at Presentation of Aplastic Anemia (AA) (2015) (0)
- 67 SUBCLASSIFICATION OF CHRONIC MYELOMONOCYTIC LEUKEMIA BY ANCESTRAL MUTATIONAL EVENTS (2015) (0)
- The Presence Of Leukemogenic Mutational Events In Paroxysmal Nocturnal Hemoglobinuria Suggests That Clonal Architecture Of Bone Marrow Failure Is Similar To Myelodysplastic Syndrome (2013) (0)
- News Release Title Publication of frequent genetic abnormalities of immune checkpoint-related genes in intravascular large B-cell lymphoma ~Detection of genetic alterations using cell-free DNA in a rare type of malignant lymphoma~ (2020) (0)
- Diagnostic Efficacy of Whole-Exome Sequencing in 250 Patients with Congenital Bone Marrow Failure (2014) (0)
- S135 NGS-BASED COPY-NUMBER ANALYSIS IN MORE THAN 2,000 PATIENTS WITH MYELOID NEOPLASMS (2019) (0)
- Notch Signaling-Dependant Expulsion of Parasites through Mast Cell-Mediated Immunity. (2004) (0)
- promyelocytic leukemia (APL) based on genomic alterations Hidden abnormalities and novel classification of t(15;17) acute (2013) (0)
- [The correlation between alterations of cell cycle-regulating, tumor-suppressor genes and the clinical prognosis in adult ALL patients]. (1997) (0)
- Afoundervariant in theSouthAsianpopulation leads toahigh prevalence of FANCL Fanconi anemia cases in India (2019) (0)
- Abstract 6085: Clonal evolution of mammary epithelial cells into breast cancers (2022) (0)
- Novel Biological Effects and Distinct Patterns of Rhoa Mutations in Adult T-Cell Leukemia/Lymphoma and Angioimmunoblastic T Cell Lymphoma (2014) (0)
- Biallelic DICER 1 mutations in sporadic PPB 2 Financial support (2014) (0)
- Advanced Neuroblastoma: Role of ALK Mutations (2012) (0)
- Genomic analysis of two rare cases of pediatric Ph‐positive T‐ALL (2021) (0)
- Erythroid differentiation intensifies RNA mis-splicing in SF3B1-mutant myelodysplastic syndromes with ring sideroblasts (2023) (0)
- Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma Biallelic DICER1 mutations in sporadic PPB (2014) (0)
- [Genome-wide analysis of AML and MDS]. (2012) (0)
- Characteristics and Clinical Effectiveness of COVID-19 Vaccination in Hospitalized Patients in Omicron-dominated Epidemic Wave – A Nationwide Study in Japan (2023) (0)
- [Leukemia and lymphoma]. (2010) (0)
- Clinical Features of Patients with ASXL1 and ASXL2 Mutations in Pediatric Acute Myeloid Leukemia (2014) (0)
- Elderly‐onset systemic Epstein–Barr virus‐positive T‐cell lymphoma of childhood (2022) (0)
- Molecular Characterization Of Adult T-Cell Leukemia/Lymphoma (2013) (0)
- Cas-L Suppresses Progression of Leukemia Induced by p210Bcr/Abl. (2006) (0)
- Significant Features of DNA Methylation at Bivalent Promotor and Repressed Polycomb Regions in Pediatric AML-the Jccg Study, JPLSG AML-05- (2019) (0)
- Distinct molecular subtypes and a high diagnostic urinary biomarker of upper urinary tract urothelial carcinoma (2020) (0)
- Whole Exome Analysis Of Germline Alterations Associated With Myelodysplastic Syndrome (2013) (0)
- Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis (2019) (0)
- Abstract 164: Clonal evolution in noncancerous esophageal mucosa in normal and cancer-bearing individuals (2016) (0)
- Novel Mechanism of Post-Transcriptional Regulation of PD-L1 Expression By 3'-UTR Binding Proteins (2017) (0)
- 18 CANDIDATE GENE MUTATIONS IN ACQUIRED APLASTIC ANEMIA CORRELATION WITH SURVIVAL AND CLONAL EVOLUTION TO MYELODYSPLASTIC SYNDROME (2015) (0)
- A Knowledge-Based Approach for Clinical Annotation of Oncogenic Variants to Support Patient-Tailored Diagnosis in Myeloid Disease (2017) (0)
- Abstract 5482: L-2HG/ L2HGDH axis as therapeutic target for kidney cancer (2018) (0)
- [Molecular profiling of myelodysplastic syndromes]. (2014) (0)
- High Resolution Melt Analysis for Rapid and Cost-Effective Screening of TP53 Mutations in Patients with Myeloid Malignancies (2018) (0)
- Comment on Taskesen et al , page 3327 Splicing factor mutations in AML (2014) (0)
- Title Single nucleotide polymorphism genomic arrays analysis of t ( 8 ; 21 ) acutemyeloid leukemia cells (2017) (0)
- 1. Novel Molecular Mechanism of Myelodysplastic Syndromes (2012) (0)
- Genomic Profiling of Different Subtypes of B-Cell Non-Hodgkin’s Lymphoma Using High-Density Single Nucleotide Polymorphism (SNP) Microarrays. (2007) (0)
- Basal cell carcinoma on the ventral site of the finger with an intronic deletion of SUFU gene. (2021) (0)
- Gene Expression Profiles and Methylation Analysis in Down Syndrome Related Acute Lymphoblastic Leukemia (2016) (0)
- Ki23819 (KRN383•HCl) Inhibits Kinase Activity of Wild Type and Mutant FLT3 Receptor Tyrosine Kinase In Vitro . (2004) (0)
- PS998 JANUS KINASE AND CYTOKINE RECEPTOR MUTATIONS IN TRANSIENT ABNORMAL MYELOPOIESIS AND MYELOID LEUKEMIA IN CHILDREN WITH TRISOMY 21 (2019) (0)
- Attenuate Graft-versus-Host Immunity Host-Residual Invariant NK T Cells (2005) (0)
- Abstract 2154: Molecular allelo-karyotyping of pulmonary adenocarcinoma using high resolution single nucleotide polymorphism genomic arrays (2010) (0)
- Distinct Bone Marrow Microenvironment Abnormalities in MDS and MPN with Fibrosis (2019) (0)
- Abstract 4994: Association of protein inhibitor of activated STAT protein 4 with the development of pancreatic ductal adenocarcinoma identified by chromosomal analysis from single nucleotide polymorphism arrays (2010) (0)
- Evidence That GPI-AP-Specific CTLs Are Not Involved In The “escape” Of Piga mutant Hematopoietic Stem Cells In Aplastic Anemia (2013) (0)
- model for dissecting somatic mosaicism and drug discovery Induced pluripotent stem cells from CINCA syndrome patients as a (2013) (0)
- Two new studies published in Nature shed light on somatic muta tions that occur in ulcerative colitis, providing insights into mutagenesis in the inflamed intes- tinal epithelium and mutational profiles in colitis-associated cancer (2020) (0)
- Impact Of HLA Allele and Haplotype On Acute Graft-Versus-Host Disease and Survival After Hematopoietic Stem Cell Transplantation From Unrelated Donor (2013) (0)
- Comprehensive Profiling of Somatic Mutations Which Define Primary Disease and Relapse in Various Acute Leukemia Subtypes (2012) (0)
- Title Splicing factor mutations and cancer (2018) (0)
- Abstract 741: Clonal evolution of non-malignant proliferative lesions into breast cancers (2019) (0)
- Alterations of the genes involved in the PI3K and estrogen-receptor pathways influence outcome in human epidermal growth factor receptor 2-positive and hormone receptor-positive breast cancer patients treated with trastuzumab-containing neoadjuvant chemotherapy (2013) (0)
- Identification of candidate tumor suppressor genes from critical deletions of long arm of chromosome 6 in hematopoietic neoplasm (2002) (0)
- Mutational Spectrum of Myelodysplastic Syndrome Malignancies Revealed by Whole Exome Sequencing (2012) (0)
- Abstract 3429: Genetic analysis of pancreatic neuroendocrine neoplasms grade 3 (2019) (0)
- Abstract 4751: Genetic subtype-specific prognostic significance of genetic alterations in lower-grade gliomas (2016) (0)
- Exploring Genetic Basis of GVHD by Whole-Genome Association Studies in a Large Series from the Japan Marrow Donation Program (JMDP). (2007) (0)
- Tumor-promoting function and regulatory landscape of PD-L2 in B-cell lymphoma (2022) (0)
- Abstract 3933: The landscape and clonal architecture in lower grade glioma (2015) (0)
- Post-Treatment Clone Size Predicts Survival Independently of IPSS-R and Response after Azacitidine Therapy for MDS. (2020) (0)
- Evi-1 Is Essential for Expansion and Maintenance of Hematopoietic Stem Cells. (2006) (0)
- High-Resolution Analyses of Epigenetic Aberrations in Myelodysplastic Syndrome. (2007) (0)
- High Density SNP Array Analysis of Tyrosine Kinase Inhibitor (TKI) Resistant Chronic Myeloid Leukemia (CML) Shows Secondary Genomic Alterations (2008) (0)
- Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets (2020) (0)
- [Acquired platelet dysfunction with severe bleeding tendency in triple-negative myelofibrosis]. (2021) (0)
- Hematopoietic stem progenitor cells with malignancy‐related gene mutations in patients with acquired aplastic anemia are characterized by the increased expression of CXCR4 (2022) (0)
- (P-Sp) region rescue of the AML1-deficient embryonic para-aortic splanchnopleural The transcriptionally active form of AML1 is required for hematopoietic (2013) (0)
- Abstract 4353: Integrated molecular analysis of upper urinary tract urothelial carcinoma (2018) (0)
- Abstract 4791: Prognostic model of lower grade gliomas (2015) (0)
- High Risk HLA Allele for Severe Acute Graft-Versus-Host-Disease and Mortality in Unrelated Donor Hematopoietic Stem Cell Transplantation (2016) (0)
- Molecular Cytogenetic Analyses of HIG, a Novel Human Cell Line Carrying t(1;3)(p36.3;q25.3) Established from a Patient with Chronic Myelogenous Leukemia in Blastic Crisis (2003) (0)
- PD3-05 RECURRENT SOMATIC MUTATIONS UNDERLIE CORTICOTROPIN-INDEPENDENT CUSHING'S SYNDROME (2015) (0)
- 0168: Whole Genome Copy Number Analysis of Advanced Ovarian Cancer Identifies Patterns Associated with Prolonged Survival (2006) (0)
- CLINICAL AND MOLECULAR CHARACTERISTICS OF SRSF2-MUTATED NEOPLASMS (2019) (0)
- Molecular allelokaryotyping of mantle cell lymphoma (2008) (0)
- Successful treatment of hepatosplenic T-cell lymphoma with fludarabine, high-dose cytarabine and subsequent unrelated umbilical cord blood transplantation (2021) (0)
- Assessment of the International Prognostic Scoring System for Determining Chemotherapeutic Indications in Myelodysplastic Syndrome: Japanese Retrospective Multicenter Study (2005) (0)
- Resistance of Hematopoietic Stem Cells Lacking the KIR Ligand to Autologous NK Cell Attacks in Patients with Acquired Aplastic Anemia (2014) (0)
- Profiling of Multiple Gene Mutations In Myelodysplastic Syndromes Using High-Throughput Resequenceing Combined with Barcode Labeling (2010) (0)
- Hidden abnormalities and novel disease-related genomic changes during development of esophageal adenocarcinomas (2008) (0)
- Recurrent Genomic Aberrations of D-Type Cyclins Are Therapeutic Targets of CDK4/6 Inhibitors in t(8;21) and MLL-Rearranged Acute Myeloid Leukemia (2018) (0)
- Abstract 2456: Distinct genomic landscape of upper urinary tract urothelial carcinoma (2017) (0)
- Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases (2015) (0)
- Whole Genome 250K SNP Array Allows for Detection of Previously Unidentified Lesions in Chromosome 5 in Patients with MDS. (2006) (0)
- Molecular Diversity Detected by Whole Exome Sequencing in Chronic Myelomonocytic Leukemia (2012) (0)
- Whole-Exome Sequencing Reveals a Paucity of Somatic Gene Mutations in Aplastic Anemia and Refractory Cytopenia of Childhood (2014) (0)
- Transcription elongation defects link oncogenic splicing factor mutations to targetable alterations in chromatin landscape (2023) (0)
- Analysis of Clonal Evolution of AML Using Simultaneous Single-Cell DNA/RNA Analysis (2020) (0)
- Abstract 3389: Clonal evolution of atypical proliferative lesions into breast cancers (2018) (0)
- Abstract 6066: Genomic analysis of end-stage renal disease (2023) (0)
- Next-Generation Sequencing Reveal Proviral Genome and Transcriptome in Adult T-Cell Leukemia/Lymphoma (2015) (0)
- Abstract B93: Gene fusions detected by whole transcriptome sequencing of lung adenocarcinoma. (2011) (0)
- [Genetic abnormalities in myelodysplastic syndrome]. (2005) (0)
- TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia. (2023) (0)
- High-Resolution Analyses of Genetic and Epigenetic Aberrations in Infant Leukemia with MLL Rearrangement. (2007) (0)
- Abstract 2101:GBM: miR-34aacts as a tumor suppressor and prognosis maker as well as modulating EGFR (2010) (0)
- Clonal Hematopoiesis By HLA Class I Allele-Lacking Hematopoietic Stem Cells and Concomitant Aberrant Stem Cells Is Rarely Associated with Clonal Evolution to Secondary Myelodysplastic Syndrome and Acute Myeloid Leukemia in Patients with Acquired Aplastic Anemia (2020) (0)
- Genomic Microarray Alterations Add Prognostic Power to the IPSS-R in MDS with Normal Karyotype (2014) (0)
- Genotype-Resultant Morphology of Myelodysplastic Syndromes (MDS) (2018) (0)
- Prevalence of pathogenic variants in cancer-predisposing genes in second cancer after childhood solid cancers. (2023) (0)
- Impact and Function of Somatic PHF6 Mutations in Myeloid Neoplasms (2014) (0)
- Identification of Cell-Type-Specific Mutations in Angioimmunoblastic T-Cell Lymphoma (2014) (0)
- Abstract 1683: Mutational landscape of colorectal cancer with POLE gene mutation (2019) (0)
- Functional Characterization of Compound DDX41 Germline and Somatic R525H Mutations in the Development of Myeloid Malignancies (2020) (0)
- The Presence of Defective Epstein-Barr Virus (EBV) Infection in Patients with EBV-Associated Hematological Malignancy (2018) (0)
- Abstract 801: Clinical application of genomic signature includingALKmutation to the new tumor risk classification for neuroblastoma (2010) (0)
- PS1308 TARGETING T-CELL RECEPTOR SIGNALING PATHWAY BY DASATINIB IN RELAPSED/REFRACTORY ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA (2019) (0)
- DNA Methylation and Genetic Profiles in 320 Patients with Myelodysplastic Syndromes (2018) (0)
- Abstract 3322: Chronology and risk-dependence of age-related remodelling of oesophageal epithelia (2019) (0)
- Contribution of MIR9 on Disease Progression of Chronic Myelogenous Leukemia (2017) (0)
- Abstract 6198: Genetic analysis of synchronous or metachronous multiple pancreatic cancers (2022) (0)
- Genetic Landscape of BPDCN Arising in CML Remission (2022) (0)
- Karyotypic and Genetic Abnormalities Associated with Clonal Evolution in Paroxysmal Nocturnal Hemoglobinuria. (2012) (0)
- TAL1 and MYB Abnormalities in Childhood T-Cell Acute Lymphoblastic Leukemia (2015) (0)
- C021 SNP-array karyotyping complements routine metaphase cytogenetics in the detection of chromosomal aberrations including uniparental disomy in MDS (2007) (0)
- Relapse of Leukemia with Loss of Mismatched HLA Due to Uniparentaldisomy Follwing Haploidentical Hematopoietic Transplantation. (2009) (0)
- Abstract P5-13-04: Clonal evolution of mammary epithelial cells into breast cancers (2023) (0)
- Abstract 4602: Recurrent pathway mutations of multiple components of cohesin complex in myeloid neoplasms. (2013) (0)
- AML1/Runx1 Negatively Regulates the Number of Quiescent Hematopoietic Stem Cells in Adult Hematopoiesis. (2006) (0)
- Mechanisms Underlying Augmented Lymphomagenesis by LUBAC; Possible Accumulation of AID-Mediated Somatic Mutations (2018) (0)
- Title Integrated genetic and epigenetic analysis defines novelmolecular subgroups in rhabdomyosarcoma (2019) (0)
- [Hematopoietic recovery by ASXL1-mutated clones after immune suppressive therapy in a patient with severe aplastic anemia]. (2023) (0)
- Abstract SY09-02: A novel genetic mechanism of evading antitumor immunity in multiple human cancers (2017) (0)
- Abstract 3405: Integrated analysis of urothelial carcinoma (2019) (0)
- A temporal shift of the evolutionary principle shaping intratumor heterogeneity in colorectal cancer (2018) (0)
- Cyclophosphamide^|^mdash;associated cardiomyopathy after allogeneic hematopoietic stem cell transplantation from a sibling donor for refractory cytopenia of childhood (2014) (0)
- Resistance of KIR ligand-missing leukocytes to natural killer cells in vivo in patients with acquired aplastic anemia (2020) (0)
- Clinical and Molecular Significance of Peripheral Blood Cell-Free DNA in B-Cell Lymphomas for Detection of Genetic Mutations and Correlation with Disease Status (2014) (0)
- Abstract 3547: Frequent genomic alterations to evade the immune system in colorectal cancer with POLE gene mutation (2020) (0)
- Abstract 1184: Prognostic significance of genetic alterations detected by high-density single nucleotide polymorphism (SNP) array in gastrointestinal cancer (2010) (0)
- O-007 BCOR and BCORL1 mutations in myelodysplasia: Prevalence, prognosis and clonal hierarchy (2013) (0)
- [Essential thrombocythemia correctly diagnosed through the guidance of comprehensive genomic profiling]. (2019) (0)
- Whole-Exome Analysis of Autoimmune Lymphoproliferative Syndrome-like Diseases (2015) (0)
- Optimization of R/W and Thermal Stability of Exchange Coupled Composite Media for Perpendicular Magnetic Recording (2007) (0)
- THALIDOMIDE FOR CHRONIC GVHD. AUTHORS' REPLY (1998) (0)
- Opposing Pathogenesis of Germline SAMD9/SAMD9L Variants in Adult Myelodysplastic Syndrome (MDS) (2018) (0)
- Abstract 3802: Genetic basis of myeloid leukemogenesis in Down syndrome. (2013) (0)
- Title Genetic basis of myeloid transformation in familial platelet disorder / acute myeloid leukemia patients with haploinsufficient RUNX 1 allele (2019) (0)
- Regeneration of Tumor Antigen Specific CTLs Utilizing iPSC Technology for Off-the-Shelf Immunotherapy (2016) (0)
- 764 Integrative analysis of clear cell renal cell carcinoma (2013) (0)
- [Gain-of-function mutation of c-CBL tumor suppressor gene in myeloid neoplasms]. (2011) (0)
- Common Variable Immunodeficiency Caused by FANC Mutations (2017) (0)
- Age-related remodelling of oesophageal epithelia by mutated cancer drivers (2019) (0)
- Detailed Analysis of the Impact of Clonal Hematopoiesis on the Risk of Severe COVID-19 Infection (2022) (0)
- High-grade CMV antigenemia after hematopoietic stem cell transplantation Risk factor and outcome (2003) (0)
- High Frequency of Loss of Heterozygosity Due to Uniparental Disomy or Allele Deletion of Ocular Adnexal MALT-Type Lymphoma. (2007) (0)
- Abstract P3-06-04: Clonal evolution of non-malignant proliferative lesions into breast cancers (2019) (0)
- Somatic PHF6 Mutations In Myeloid Malignancies (2013) (0)
- Abstract 3853: Unique pattern of copy number changes including chromothripsis in pulmonary adenocarcinoma with EML4-ALK fusion (2015) (0)
- P-145 Sequential gain of SETBP1 mutations in severe aplastic anemia evolving into acute myeloid leukemia with monosomy 7 (2013) (0)
- Whole-Exome Sequencing in a Pediatric Patient with Relapsed/Refractory Burkitt Leukemia Resistant to Conventional Chemotherapy (2017) (0)
- Genome-Wide Analysis of Non-Coding Alterations in Pan-Myeloid Cancers Using Whole Genome Sequencing (2018) (0)
- Resistance of KIR Ligand–Missing Leukocytes to NK Cells In Vivo in Patients with Acquired Aplastic Anemia (2020) (0)
- [How Does Aging Contribute to Cancer?] (2020) (0)
- Role Of Sf3b1 On Hematopoiesis (2013) (0)
- Germline Risks and Clinical Impacts of DDX41 Mutations in Myeloid Malignancies (2022) (0)
- A Comprehensive, Multiomics Analysis of Natural Killer-Cell Malignancies (2022) (0)
- Abstract 6734: Identification of the novel TENM3-ALK fusion in an AYA case with ALK rearranged neuroblastoma (2023) (0)
- Abstract 3939: The genomic landscape of nasopharyngeal carcinoma (2015) (0)
- [Deregulated splicing machinery in myelodysplastic syndromes]. (2012) (0)
- Integrated Analysis of Copy-Number Alterations and Gene Mutations in 2,000 Patients with Myeloid Neoplasms (2019) (0)
- Abstract 4902: Clonal evolution of proliferative lesions into breast cancers (2020) (0)
- marrow failure in Japanese Fanconi anemia patients Variant ALDH2 is associated with accelerated progression of bone (2013) (0)
- Allelotypes of lung adenocarcinomas featuring ALK fusion demonstrate fewer onco- and suppressor gene changes (2013) (0)
- Identification of the ultrahigh-risk subgroup in neuroblastoma cases through DNA methylation analysis and its treatment exploiting cancer metabolism (2022) (0)
- 66 SUBCLINICAL ANCESTRAL EVENTS FOR PROGRESSION TO MANIFEST CLONAL MYELODYSPLASIA ARE PRESENT IN APLASTIC ANEMIA AT PRESENTATION: COMPARISON OF DE NOVO AND POST AA MDS (2015) (0)
- Abstract 3403: Genetic analysis of pheochromocytoma (2019) (0)
- Molecular Allelo-Karyotyping of Adult T-Cell Leukemia Using High SNP Genotyping Microarrays. (2007) (0)
- Abstract 3088: Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma (2014) (0)
- Characterization of Pathogenic Variants and Clinical Phenotypes in 117 Japanese Fanconi Anemia Patients (2018) (0)
- Distinct Pathogenesis of Clonal Hematopoiesis Revealed By Single Cell RNA Sequencing Integrated with Highly Sensitive Genotyping Method (2020) (0)
- Myelodysplastic Syndrome Patients Show Mutation-Specific DNA Methylation Patterns (2015) (0)
- Cas-L/Hef1 Is Required for Marginal Zone B Cell Maintenance and Lymphocyte Trafficking. (2005) (0)
- PD18-11 DISTINCT MOLECULAR SUBTYPES AND A HIGH DIAGNOSTIC URINARY BIOMARKER OF UPPER URINARY TRACT UROTHELIAL CARCINOMA (2020) (0)
- Genomic Analysis of Myelodysplastic Syndromes Among Nagasaki Atomic Bomb Survivors (2018) (0)
- Abstract 2675: Clonal expansion of skin keratinocyte (2021) (0)
- Distribution and Clinical Features of NOTCH1 Signaling Activating Alterations in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL) (2018) (0)
- A possible association between a novel NLRP1 mutation and an autoinflammatory disease involving liver cirrhosis. (2021) (0)
- A Moderate Increase in the WT1 mRNA Copy Number in Peripheral Blood of Patients with Long-Standing Acquired Aplastic Anemia without Apparent Signs of Myelodysplastic Syndrome (2017) (0)
- the Impact of Clonal Dynamics on Prognosis and Outcome in Myelodysplastic Syndromes (2016) (0)
- TET2 Mutations Revealed by Whole Genome Sequencing in Adult T-Cell Leukemia. (2012) (0)
- Defective Epstein–Barr virus in chronic active infection and haematological malignancy (2019) (0)
- Functional Roles of DDX41 Mutations in the Development of Myeloid Malignancies (2021) (0)
- Bone Marrow Failure with 13q Deletion: A Distinct Clinicopathological Entity with Immune Pathophysiology, (2011) (0)
- Genetic Landscapes Of Childhood T-Cell Acute Lymphoblastic Leukemia (2013) (0)
- O-23 Cytogenetic and clinical features of unbalanced translocation der(1;7)(g10;p10) in myelodysplastic syndromes (2005) (0)
- 3064 – COMBINATION OF ASXL1 MUTATION AND STAG2 LOSS LEADS TO DEVELOPMENT OF MYELODYSPLASTIC SYNDROMES (2021) (0)
- PS1367 COMPREHENSIVE GENETIC ANALYSIS OF MULTIPLE MYELOMA IN JAPAN (2019) (0)
- CARD11 mutation and HBZ expression induce lymphoproliferative disease and adult T-cell leukemia/lymphoma (2022) (0)
- MPTH-18. COMPREHENSIVE MUTATIONAL AND CYTOGENETIC ANALYSIS REVEALED GENETIC PROGNOSTIC FACTORS IN GRADE II AND III GLIOMAS (2016) (0)
- NGS Evaluation of the Eqol-MDS Trial: Preliminary Analysis of Eltrombopag for Thrombocytopenia of Low-Risk MDS (2021) (0)
- Genetic basis of progression and relapse in Clear Cell Sarcoma of the Kidney (2020) (0)
- Genomic Changes Associated with Leukemic Transformation of Myeloproliferative Disorders. (2008) (0)
- ["Domino" transplantation]. (2001) (0)
- INTEGRATED PROFILING OF DNA METHYLATION AND MUTATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES (2019) (0)
- [Oncogenic mutations of ALK are associated with tumorigenesis of neuroblastoma]. (2009) (0)
- Network-Based Analysis of Exome Sequencing Mutations Identifies Molecular Subtypes of Myelodysplastic Syndromes (2015) (0)
- Abstract 92: Clonal evolution of proliferative lesions into breast cancers (2021) (0)
- Clinical and Genetic Characterization Of Patients With C-CBL Mutated Juvenile Myelomonocytic Leukemia By Whole-Exome/Deep Sequencing (2013) (0)
- Studies on the Molecular Diagnosis of Mowat ‒ Wilson Syndrome : The Role of Chromosomal Microarray in Approaching Syndromic Congenital Heart Defects (2018) (0)
- Biological and genetic characterization of the role of SRSF2 mutations in the pathogenesis of myelodysplastic syndromes (2015) (0)
- Abstract P1-10-15:BRCA1alterations with additional defects in DNA damage repair genes may confer chemoresistance to BRCA-like breast cancers treated with neoadjuvant chemotherapy (2020) (0)
- Pathway Mutations in the Splicing Machinery in Myeloid Neoplasms (2012) (0)
- Expression of Gata1s Followed By Stag2 Deficiency Promotes Abnormal Megakaryocytopoiesis and Induces Lethal Myelofibrosis (2022) (0)
- Development of an Online Tool to Scan Single Nucleotide Polymorphisms for Identification of Novel Minor Histocompatibility Antigens (2011) (0)
- S132 BIOLOGICAL CHARACTERIZATION OF THE U2AF1 S34F MUTATION IN THE PATHOGENESIS OF MYELODYSPLASIA (2019) (0)
- Abstract 2185: Genetic analysis of metachronous pancreatic cancers (2021) (0)
- A growing genetic tree in the soil of prostate. (2021) (0)
- Abstract 738: Myxofibrosarcoma is characterized by frequent abnormalities in TP53 and increased genetic instability (2019) (0)
- Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia (2015) (0)
- High Density SNP Array Analysis of Acute Promyelocytic Leukemia (APL) Detects New Common Genomic Copy Number Alterations as Possible Cooperating Lesions (2010) (0)
- Expression of PD-1 and PD-L2 associated with Th1/Th2 helper T cell balance enables prognosis prediction in primary central nervous system lymphoma (2019) (0)
- Analysis of Clonal Evolution/Heterogeneity of MDS By Simultaneous Detection of Both Mutation and Gene Expression By Single Cell Sequencing (2018) (0)
- Evolutionary basis of HLA-DPB 1 alleles affects acute GVHD in unrelated donor stem cell transplantation Running title : Evolutionary basis of HLA-DPB 1 and acute GVHD (2017) (0)
- Progression to B acute lymphoblastic leukemia in 8p11 myeloproliferative syndrome with t(6;8)(q27;p12). (2023) (0)
- Abstract 5875: Analysis of clonal expansion in epithelium affected by ulcerative colitis reveals frequent mutations affecting IL-17 signaling pathway and novel cancer vulnerability (2020) (0)
- GENO-03PROGNOSTIC SIGNIFICANCE OF GENETIC ALTERATIONS FROM COMPREHENSIVE ANALYSIS IN LOWER-GRADE GLIOMAS. (2015) (0)
- SNP Chip Analysis of Myelodysplastic Syndromes Disclosed High Frequency of Uniparental Disomy and a Novel Dominant Mutation as the Target of 11q UPD. (2007) (0)
- A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele (2015) (0)
- Clinical Features of Pediatric Acute Myeloid Leukemia with TP53 and CDKN2A/2B copy Number Alterations (2019) (0)
- Abstract 4385: Landscape of driver gene mutations in stage II and stage III colorectal cancer (2017) (0)
- JS1-1MOLECULAR PATHOGENESIS OF MYELODYSPLASTIC SYNDROMES (2014) (0)
- Clonal Evolution Pattern and Prognostic Significance of Clonal Architecture in KMT2A-Rearranged Acute Myeloid Leukemia (2021) (0)
- Oligomerization of Evi-1 Contributes to Recruitment of Transcriptional Corepressor CtBP and Repression of TGF-β Signaling. (2004) (0)
- ATP11C Encodes a Major Flippase in Human Erythrocyte and Its Genetic Defect Causes Congenital Non-Spherocytic Hemolytic Anemia (2015) (0)
- Author's response to reviews Title: Alterations of the genes involved in the PI3K and estrogen-receptor pathways influence outcome in human epidermal growth factor receptor 2-positive and hormone receptor-positive breast cancer patients treated with trastuzumab-containing neoadjuvant chemotherapy Au (2013) (0)
- Infection perturbs Bach2- and Bach1-dependent erythroid lineage ‘choice’ to cause anemia (2018) (0)
- Abstract 1511: Origin of synchronous or metachronous multiple pancreatic cancers (2023) (0)
- Mass Cytometric Analysis Revealed Dynamic Alteration of the Tumor Immune Environment in Bone Marrow from Children with Recurrent B Cell Precursor Acute Lymphoblastic Leukemia (2021) (0)
- COMPREHENSIVE ANALYSIS OF UPPER URINARY TRACT UROTHELIAL CARCINOMA: MP58‐09 (2018) (0)
- Deregulated RNA Splicing Machinery in Myelodysplastic Syndromes (2012) (0)
- Abstract 5759: Molecular classification and risk stratification of colorectal cancer (2022) (0)
- Single Oral Administration of KRN383, a Novel Flt3 Inhibitor, Induces Eradication of the Xenograft Tumor Harboring Flt3 Mutation in Mice. (2004) (0)
- Mutant ASXL1 Disrupts Paraspeckle Formation through Aberrant Interaction with Nono in Hematopoietic Cells (2019) (0)
- An Adverse Prognostic Effect of Homozygous TET2 Mutational Status on the Relapse Risk of Acute Myeloid Leukemia Patients of Normal Karyotype (2014) (0)
- Balance of Transcription Factors Downstream of Notch Signaling Determines the Fate of Myeloid Progenitors toward Differentiation to Mast Cells or Immortalization without Differentiation. (2006) (0)
- Whole Exome Sequencing Shows a Paucity Of Somatic Gene Mutations In Pediatric Idiopathic Bone Marrow Failure Syndrome (2013) (0)
- Whole Exome Sequencing Detecting Kinesin Family Gene Defects In Myeloid Neoplasm (2013) (0)
- Hypoxic adaptation of leukemic cells infiltrating the CNS affords a therapeutic strategy targeting VEGF Running Title: Hypoxic adaptation of leukemic cells in the CNS Authors and affiliations (2017) (0)
- Genome-Wide Analysis of Copy Number Alterations/LOH/Allelic Imbalances in Non-Hodgkin Lymphoma Using Ultrahigh-Density SNP-Genotyping Microarrays with the Robust CNAG Algorithms. (2005) (0)
- Frequent but Reversible and Manageable Cardiac Complications after Successful Haploidentical HLA-Mismatched Hematopoietic Stem Cell Transplantation (HSCT) without Ex Vivo Graft Manipulation. (2004) (0)
- C-Cbl Regulates Interaction of Immature Hematopoietic Cells with the Bone Marrow Microenvironment by Rac GTPase-Mediated Cytoskeletal Signals. (2009) (0)
- Abstract 925: Whole exome analysis of myelodysplastic syndromes (2011) (0)
- Abstract 978: Genomic characterization and risk stratification of colorectal cancer (2023) (0)
- 714 Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome (2015) (0)
- The Clinical and Genetic Features of Dyskeratosis Congenita, Cryptic Dyskeratosis Congenita, and Hoyeraal-Hreidarsson Syndrome in Japan (2014) (0)
- 24 COMPREHENSIVE ANALYSIS OF ALTERNATIVE RNA SPLICING IN MYELODYSPLASTIC SYNDROMES (2015) (0)
- An eltrombopag‐induced remission of bone‐marrow aplasia accompanied by marked leukoerythroblastosis and splenomegaly (2022) (0)
- Title Aberrant splicing and defective mRNA production induced bysomatic spliceosome mutations in myelodysplasia (2019) (0)
- Abstract 4721: Novel lincRNA SLINKY is a prognostic biomarker in kidney cancer (2017) (0)
- PD03-02 NOVEL STRUCTURAL VARIANTS IN CTNNB1 AND MOLECULAR CLASSIFICATION IN CORTISOL-PRODUCING ADENOMA (2023) (0)
- Comprehensive genomic analysis of upper urinary tract urothelial carcinoma (2019) (0)
- The XPO7/Npat Axis Is a Potential Therapeutic Target for TP53-Mutated AML (2022) (0)
- Loss of HLA Class-I Expression In Leukemic Cells That Relapsed After HLA-Matched and -Mismatched SCT (2010) (0)
- Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism (2015) (0)
- P-146 Clinical and genetic characterization of 17 juvenile myelomonocytic leukemia patients with c-CBL mutations (2013) (0)
- Comprehensive Analysis of Methylation of CpG Islands on the Long Arm of Chromosome 7. (2004) (0)
- P-001 Next generation whole exome sequencing for recurrent somatic mutations on chromosome 7 (2013) (0)
- Recurrent Gene Mutations in Pediatric Patients with AML By Targeted Sequencing ―the Jccg Study, JPLSG AML-05― (2019) (0)
- A novel SREBF1::NACC1 gene fusion in an unclassifiable intracranial tumour (2022) (0)
- Publisher Correction: Defective Epstein–Barr virus in chronic active infection and haematological malignancy (2019) (0)
- Somatic Mutations and Loss-Of-Heterozygosity Impair The DNA Repair Functions Of CUX1 in Myelodysplastic Syndromes (MDS) (2013) (0)
- KRAS mutations Frequently Coexist with High-Risk MLL Fusions and Are Independent Adverse Prognostic Factors in MLL-Rearranged Acute Myeloid Leukemia (2020) (0)
- Stag2 regulates Hematopoietic Differentiation and Self-Renewal (2017) (0)
- Analysis of Genomic Predispositions to Sporadic Myeloid Neoplasms Mediated By DDX41 in Japan (2018) (0)
- SNP Array Analysis in Refractory Anemia with Ringed Sideroblast Allows for Detection of a High Frequency of Previously Cryptic Chromosomal Defects with Possible Clinical Significance. (2006) (0)
- [New insight into myelodysplastic syndromes and related myeloid disorders]. (2013) (0)
- Whole-Exome Resequencing Identifies Somatic Mutations Of BCOR and BCORL1 Transcriptional Corepressor Genes and Major Cohesin Complex Component Genes In Pediatric Acute Myeloid Leukemia (2013) (0)
- A novel prognostic model incorporating genetic profiling for myelodysplastic syndromes. (2017) (0)
- Mis-Splicing Due to Somatic U2AF 2 Mutations in Myeloid Neoplasms (2022) (0)
- Correction: Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia (2020) (0)
- Array-Based Comparative Genomic Hybridization for Genome-Wide Analysis of DNA Copy Number in Myelodysplastic Syndromes. (2004) (0)
- Frequent somatic mutations in epigenetic regulators in newly diagnosed chronic myeloid leukemia (2017) (0)
- Post-azacitidine clone size predicts long-term clinical outcome of patients with myelodysplastic syndromes and related myeloid neoplasms (2021) (0)
- RNA Sequencing Illustrates the Genetic Backgrounds of Pediatric Acute Myeloid Leukemia (2017) (0)
- The Prognostic Value of TP53 Mutations Depends on Clinical Backgrounds in Pediatric Patients with Acute Lymphoblastic Leukemia (2018) (0)
- Comprehensive Genomic Analysis Identified Acute Lymphoblastic Leukemia in Down Syndrome Was Highly Heterogeneous with the High Prevalence of Ph-like Signature (2018) (0)
- O-29 Genome-wide high-resolution analysis of DNA copy number changes in myelodysplastic syndromes using high-density oligonucleotide SNP genotyping arrays (2005) (0)
- Essential thrombocythaemia with aggressive megakaryocytosis after myelofibrotic transformation (2021) (0)
- TRANSPLANTATION Genome-wide surveillance of mismatched alleles for graft-versus-host disease in stem cell transplantation (2015) (0)
- Abstract 2019: Whole exome analysis reveals spectrum of gene mutations in adult T-cell leukemia/lymphoma. (2013) (0)
- 17. Molecular Pathogenesis of B Cell Lymphoma (2011) (0)
- Analysis of Mechanisms Underlying Clonal Evolution of AML By a New Single-Cell Sequencing Platform (2019) (0)
- Abstract 4849: Profiling of multiple gene mutations in myelodysplastic syndromes using high-throughput resequenceing combined with barcode labeling (2011) (0)
- Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (2021) (0)
- Genomic landscape of upper urinary tract urothelial carcinoma (2017) (0)
- Clinical significance of the increased expression of the WT1 gene in peripheral blood of patients with acquired aplastic anemia (2022) (0)
- Abstract 1426: Targeted sequencing of colorectal cancer in search for prognostic biomarkers (2018) (0)
- Comprehensive Genetic Analysis in Cases of Juvenile Myelomonocytic Leukemia for Prognostic Estimation (2016) (0)
- Corrigendum to “Antineoplastic effect of a single oral dose of the novel Flt3 inhibitor KRN383 on xenografted human leukemic cells harboring Flt3-activating mutations” [Leuk. Res. 30 (2006) 1541–1546] (2007) (0)
- Whole Exome Analysis Reveals Spectrum of Gene Mutations in Juvenile Myelomonocytic Leukemia (2012) (0)
- Single Cell Genotyping of Inv(16) AML in CBL Mutated Clonal Hematopoiesis Characterizes Clonal Architecture and Evolution of Exome Sequencing-Identified Mutations in the Protein Tyrosine Phosphatase Ptprt and Other Genes (2015) (0)
- Abstract 3132: Tumorigenesis of MEN2 pheochromocytoma (2021) (0)
- Abstract 6168: Implementation and adoption of a web tool to support precision diagnostic and treatment decisions for patient with myelodysplastic syndromes (2023) (0)
- LYMPHOID NEOPLASIA Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma (2016) (0)
- Genetic Landscape and Clonal Evolution Following 5-Aza Therapy in Patients with High-Risk Myelodysplastic Syndromes (2016) (0)
- Abstract 482: Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma (2015) (0)
- 435 GENOME-WIDE ANALYSIS OF COPY NUMBER ALTERATIONS AND GENE MUTATIONS IN RENAL CELL CARCINOMA (2012) (0)
- Degree of Aberrant Antigen Expression in Myelodysplastic Syndromes Correlates with the Number of Molecular Mutations (2015) (0)
- 219 RELATION BETWEEN MOLECULAR MUTATIONS AND ABERRANTLY EXPRESSED ANTIGENS IN MYELODYSPLASTIC SYNDROMES (2015) (0)
- High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors (2020) (0)
- [Relationship between clinical features and somatic gene mutations in myelodysplastic syndrome]. (2018) (0)
- Integrated genetic and clinical prognostic factors for aggressive adult T-cell leukemia/lymphoma. (2023) (0)
- ASXL1 mutations with serum EPO levels predict poor response to darbepoetin alfa in lower-risk MDS: W-JHS MDS01 trial (2021) (0)
- Abstract 2229: Whole exome sequencing reveals the landscape of gene mutations and evolution in low-grade glioma (2014) (0)
- Abstract 2276: Genetic classification of colorectal cancer (2021) (0)
- Abstract 5122: Integral view of copy number alteration and commonly targeted genes in MDS found a new aspect of correlation and interrelationship with mutated components of the RNA splicing machinery (2012) (0)
- Abstract 5754: The genetic aberrations in carcinogenic sequence of colitis-associated cancer (2017) (0)
- Structural Variations Involving Programmed Death Ligands in B-Cell and T-Cell Lymphomas (2016) (0)
- Abstract 5494: CTX-712, a novel splicing modulator targeting myeloid neoplasms (2022) (0)
- Abstract 3902: Comparison of allelic profiles of EGFR-mutated and ALK-translocated female adenocarcinomas of the lung by CGH microarrays: Implications for two distinct carcinogenesis pathways in non-smokers (2011) (0)
- Corrigendum: Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells (vol 29, pg 1092, 2015) (2015) (0)
- Targeting lineage plasticity overcomes chemoresistance. (2022) (0)
- Genetic Profile of Acute Erythroid Leukemia (2016) (0)
- Inhibition of dopamine receptor D1 signaling promotes human bile duct cancer progression via WNT signaling (2022) (0)
- Clinical Significance of Mutations and Copy Number Lesions on Prognosis of Patients with MDS after Unrelated Bone Marrow Transplantation (2016) (0)
- Identifications of Highly Aggressive Phenotype with SPI1 Overexpression in Pediatric T Cell Acute Lymphoblastic Leukemia/Lymphoma (2016) (0)
- Abstract A2-20: Integrative study of genomic alterations in liposarcoma (2015) (0)
- ASXL2 Is Recurrently Mutated in t(8;21) AML and Regulates Hematopoietic Development (2016) (0)
- Prevalence, Clone Size and Lineage Diversity Of HLA-A Allele-Lacking Leukocytes In Patients With Acquired Aplastic Anemia (2013) (0)
- Genome-Wide Mutational Landscape of Infant Acute Lymphoblastic Leukemia (2016) (0)
- Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2‐mutation carriers (2022) (0)
- Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants (2020) (0)
- A case of vasoactive intestinal peptide-secreting tumor (VIPoma) arising from MEN1 inactivation which recurred 15 years after the initial resection. (2023) (0)
- Distinct Features of Chip-Derived and De Novo MDS (2018) (0)
- Long-term outcome of six months maintenance chemotherapy for ALL in children: TCCSG L92-13E study. (2015) (0)
- Identification of a Novel Chromosomal Translocation t(11;16)(q23;q22) Fusing MLL to Enhancer of mRNA Decapping (EDC)-4 in Smoldering Acute Myeloid Leukemia (2016) (0)
- Genetic Differences Between BRCA-Associated and Sporadic Ovarian Cancer DNA (2007) (0)
- Identi fi cation of enhancer of mRNA decapping 4 as a novel fusion partner of MLL in acute myeloid leukemia (2019) (0)
- Abstract #1413: Allele-specific copy number analysis of human osteosarcoma by single nucleotide polymorphism (SNP) array identifies several monoallelic amplicons independent of MYC in chromosome 8 q-arm (8q) (2009) (0)
- Genome-Wide Analysis of Copy Number Analysis of Myelodysplastic Syndromes Using High-Density SNP-Genotyping Microarrays. (2005) (0)
- Abstract P4-05-15: Clonal evolution of proliferative lesions into breast cancers (2020) (0)
- [Significance of A20 in B-cell lymphomas]. (2011) (0)
- Haematological malignancies in relatives of patients affected with myeloproliferative neoplasms (2022) (0)
- Diagnostic significance of secondary bacteremia in patients with COVID-19 (2023) (0)
- SETBP1 and Schinzel-Giedion Syndrome (2016) (0)
- Whole Exome Sequencing (“mutatome”) Of Deletion 5q (2013) (0)
- Molecular and Cellular Pathobiology Biallelic DICER 1 Mutations in Sporadic Pleuropulmonary Blastoma (2014) (0)
- Landscape of Subclonal Mutations in Myelodysplastic Syndromes (MDS) Allows for a Novel Hierarchy of Clonal Advantage By Combining Germline and Somatic Mutations (2016) (0)
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What Schools Are Affiliated With Seishi Ogawa?
Seishi Ogawa is affiliated with the following schools:
