Kenichi Yoshida
#170,108
Most Influential Person Now
Researcher
Kenichi Yoshida's AcademicInfluence.com Rankings
Kenichi Yoshidacomputer-science Degrees
Computer Science
#10396
World Rank
#10916
Historical Rank
Computational Linguistics
#2621
World Rank
#2647
Historical Rank
Machine Learning
#4750
World Rank
#4804
Historical Rank
Artificial Intelligence
#5122
World Rank
#5189
Historical Rank
Download Badge
Computer Science
Kenichi Yoshida's Degrees
- PhD Computer Science University of Tokyo
- Masters Computer Science University of Tokyo
- Bachelors Computer Science University of Tokyo
Similar Degrees You Can Earn
Why Is Kenichi Yoshida Influential?
(Suggest an Edit or Addition)Kenichi Yoshida'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)
- Mutational landscape and clonal architecture in grade II and III gliomas (2015) (676)
- 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)
- Somatic RHOA mutation in angioimmunoblastic T cell lymphoma (2014) (508)
- Aberrant PD-L1 expression through 3′-UTR disruption in multiple cancers (2016) (489)
- 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)
- ANGPTL3 Decreases Very Low Density Lipoprotein Triglyceride Clearance by Inhibition of Lipoprotein Lipase* (2002) (320)
- Dynamics of clonal evolution in myelodysplastic syndromes (2016) (311)
- Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms. (2015) (299)
- The landscape of somatic mutations in Down syndrome–related myeloid disorders (2013) (295)
- Replication from oriP of Epstein-Barr Virus Requires Human ORC and Is Inhibited by Geminin (2001) (292)
- SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML). (2012) (285)
- Angiopoietin-like protein 4 is a potent hyperlipidemia-inducing factor in mice and inhibitor of lipoprotein lipase Published, JLR Papers in Press, September 16, 2002. DOI 10.1194/jlr.C200010-JLR200 (2002) (259)
- Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia. (2015) (253)
- 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)
- Tobacco exposure and somatic mutations in normal human bronchial epithelium (2019) (203)
- Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia (2013) (201)
- ACTN1 mutations cause congenital macrothrombocytopenia. (2013) (190)
- BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders. (2013) (184)
- Protein Region Important for Regulation of Lipid Metabolism in Angiopoietin-like 3 (ANGPTL3) (2003) (176)
- Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents (2016) (175)
- 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)
- Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse. (2015) (166)
- Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients. (2013) (148)
- Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma (2015) (148)
- TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups (2019) (141)
- Genomewide linkage and linkage disequilibrium analyses identify COL6A1, on chromosome 21, as the locus for ossification of the posterior longitudinal ligament of the spine. (2003) (138)
- Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution (2016) (130)
- Splicing factor mutations and cancer (2014) (128)
- 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)
- Integration of hepatitis B virus DNA into the myeloid/lymphoid or mixed‐lineage leukemia (MLL4) gene and rearrangements of MLL4 in human hepatocellular carcinoma (2008) (120)
- Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis (2018) (120)
- Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia (2018) (115)
- Polymorphisms in the prostaglandin E2 receptor subtype 2 gene confer susceptibility to aspirin-intolerant asthma: a candidate gene approach. (2004) (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)
- Regulation of Geminin and Cdt1 expression by E2F transcription factors (2004) (108)
- Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia. (2015) (107)
- Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria. (2014) (104)
- Prognostic relevance of integrated genetic profiling in adult T-cell leukemia/lymphoma. (2015) (103)
- PRPF8 Defects Cause Missplicing in Myeloid Malignancies (2013) (102)
- IGF-I induces senescence of hepatic stellate cells and limits fibrosis in a p53-dependent manner (2016) (95)
- Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia (2017) (90)
- Genomic landscape of liposarcoma (2015) (89)
- Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia (2016) (88)
- Variegated RHOA mutations in adult T-cell leukemia/lymphoma. (2016) (88)
- Frequent structural variations involving programmed death ligands in Epstein-Barr virus-associated lymphomas (2019) (84)
- Loss of function mutations in RPL27 and RPS27 identified by whole‐exome sequencing in Diamond‐Blackfan anaemia (2015) (81)
- Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations (2017) (80)
- The Promyelotic Leukemia Zinc Finger Promotes Osteoblastic Differentiation of Human Mesenchymal Stem Cells as an Upstream Regulator of CBFA1*[boxs] (2005) (80)
- Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome (2017) (80)
- Genomic landscape and clonal evolution of acute myeloid leukemia with t(8;21): an international study on 331 patients. (2019) (77)
- Gene regulatory network of unfolded protein response genes in endoplasmic reticulum stress (2012) (74)
- CDCA4 Is an E2F Transcription Factor Family-induced Nuclear Factor That Regulates E2F-dependent Transcriptional Activation and Cell Proliferation* (2006) (73)
- Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma. (2016) (73)
- Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency. (2016) (73)
- Reduced TET2 function leads to T-cell lymphoma with follicular helper T-cell-like features in mice (2014) (70)
- The E‐Id Protein Axis Specifies Adaptive Lymphoid Cell Identity and Suppresses Thymic Innate Lymphoid Cell Development (2017) (67)
- ANRIL is implicated in the regulation of nucleus and potential transcriptional target of E2F1. (2010) (67)
- Integrated molecular profiling of juvenile myelomonocytic leukemia. (2018) (67)
- Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma. (2014) (63)
- Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome. (2019) (60)
- Whole‐exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia (2016) (58)
- Gene expression and risk of leukemic transformation in myelodysplasia. (2017) (56)
- Identification of epigallocatechin-3-gallate in green tea polyphenols as a potent inducer of p53-dependent apoptosis in the human lung cancer cell line A549. (2009) (56)
- 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)
- Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice. (2018) (55)
- Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans (2020) (55)
- Novel recurrent mutations in the RAS-like GTP-binding gene RIT1 in myeloid malignancies (2012) (53)
- GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies (2015) (53)
- Identification of a novel cell-cycle-induced MCM family protein MCM9. (2005) (52)
- Detection of WIPI1 mRNA as an indicator of autophagosome formation (2014) (52)
- Expression of MCM10 and TopBP1 is regulated by cell proliferation and UV irradiation via the E2F transcription factor (2004) (50)
- Lineage tracing of human development through somatic mutations (2021) (50)
- Comprehensive analysis of expression pattern and promoter regulation of human autophagy-related genes (2009) (50)
- Gain-of-function IKBKB mutation causes human combined immune deficiency (2018) (49)
- Frequent somatic mutations in epigenetic regulators in newly diagnosed chronic myeloid leukemia (2017) (48)
- ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia (2016) (48)
- Ischemia-reperfusion induces myocardial infarction through mitochondrial Ca²⁺ overload. (2012) (46)
- Haploinsufficiency of Sf3b1 leads to compromised stem cell function but not to myelodysplasia (2014) (44)
- Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma. (2019) (44)
- Fibroblast cell shape and adhesion in vitro is altered by overexpression of the 7a and 7b isoforms of protocadherin 7, but not the 7c isoform. (2003) (43)
- Tumour necrosis factor alpha-stimulated gene-6 inhibits osteoblastic differentiation of human mesenchymal stem cells induced by osteogenic differentiation medium and BMP-2. (2006) (43)
- The destruction box of human Geminin is critical for proliferation and tumor growth in human colon cancer cells (2004) (41)
- Recurrent genetic defects on chromosome 7q in myeloid neoplasms (2014) (41)
- JPO1/CDCA7, a novel transcription factor E2F1-induced protein, possesses intrinsic transcriptional regulator activity. (2006) (40)
- Acute loss of transcription factor E2F1 induces mitochondrial biogenesis in Hela cells (2006) (40)
- Invariant patterns of clonal succession determine specific clinical features of myelodysplastic syndromes (2019) (39)
- Loss of DNA Damage Response in Neuroblastoma and Utility of a PARP Inhibitor (2017) (39)
- Variations in infection sites and mortality rates among patients in intensive care units with severe sepsis and septic shock in Japan (2019) (38)
- Recurrent genetic defects on chromosome 5q in myeloid neoplasms (2016) (38)
- Long-term outcome of 6-month maintenance chemotherapy for acute lymphoblastic leukemia in children (2017) (37)
- Two Cases of Atezolizumab-Induced Hypophysitis (2017) (37)
- Single-cell analysis based dissection of clonality in myelofibrosis (2019) (37)
- Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoter (2003) (35)
- Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia. (2019) (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)
- Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes. (2018) (34)
- Ischemia enhances translocation of connexin43 and gap junction intercellular communication, thereby propagating contraction band necrosis after reperfusion. (2009) (33)
- TERT promoter mutations and chromosome 8p loss are characteristic of nonalcoholic fatty liver disease‐related hepatocellular carcinoma (2016) (33)
- Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele (2016) (32)
- Olanzapine orally disintegrating tablet vs. risperidone oral solution in the treatment of acutely agitated psychotic patients. (2008) (32)
- Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia (2015) (32)
- Frequent Genetic Alterations in Immune Checkpoint-Related Genes in Intravascular Large B-Cell Lymphoma. (2020) (32)
- Molecular classification and diagnostics of upper urinary tract urothelial carcinoma. (2021) (32)
- Comprehensive analysis of genetic aberrations linked to tumorigenesis in regenerative nodules of liver cirrhosis (2019) (30)
- Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia (2017) (30)
- Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms (2016) (30)
- Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia (2021) (29)
- Transcriptional co-factor CDCA4 participates in the regulation of JUN oncogene expression. (2008) (29)
- Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases (2015) (28)
- Cell‐cycle‐dependent regulation of the human and mouse Tome‐1 promoters (2005) (28)
- Adverse prognostic effect of homozygous TET2 mutation on the relapse risk of acute myeloid leukemia in patients of normal karyotype (2015) (28)
- Early detection and evolution of preleukemic clones in therapy-related myeloid neoplasms following autologous SCT. (2018) (28)
- Oxidative stress augments pulmonary hypertension in chronically hypoxic mice overexpressing the oxidized LDL receptor. (2013) (28)
- Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol‐3‐OH kinase &dgr; syndrome type 1 (2019) (27)
- Genetic and transcriptional landscape of plasma cells in POEMS syndrome (2019) (27)
- Genomon ITDetector: a tool for somatic internal tandem duplication detection from cancer genome sequencing data (2015) (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)
- Exacerbating factors of radiation-induced myeloid leukemogenesis. (1993) (27)
- Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia (2015) (26)
- Clonal dynamics in a single AML case tracked for 9 years reveals the complexity of leukemia progression (2016) (26)
- Tracing the development of acute myeloid leukemia in CBL syndrome. (2014) (26)
- De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome. (2018) (26)
- Deep sequencing in cancer research. (2013) (25)
- Profiling of molecular pathways regulated by microRNA 601 (2009) (25)
- Accelerated Telomere Shortening in Acromegaly; IGF-I Induces Telomere Shortening and Cellular Senescence (2015) (25)
- Detection of the G17V RHOA Mutation in Angioimmunoblastic T-Cell Lymphoma and Related Lymphomas Using Quantitative Allele-Specific PCR (2014) (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)
- Increased levels of the oxidative stress marker, nitrotyrosine in patients with provocation test-induced coronary vasospasm. (2014) (23)
- PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus (2016) (23)
- Conditional expression of MCM7 increases tumor growth without altering DNA replication activity (2003) (22)
- Transcriptional regulation of human chromatin assembly factor ASF1. (2007) (22)
- Molecular pathogenesis of disease progression in MLL-rearranged AML (2018) (22)
- Genetic and clinical characteristics of Japanese patients with sporadic somatotropinoma. (2016) (22)
- A diagnostic pitfall in IgG4-related hypophysitis: infiltration of IgG4-positive cells in the pituitary of granulomatosis with polyangiitis (2015) (22)
- Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome. (2013) (21)
- Identification of the genetic and clinical characteristics of neuroblastomas using genome-wide analysis (2017) (21)
- Recombinant Human-Soluble Thrombomodulin Contributes to Reduced Mortality in Sepsis Patients With Severe Respiratory Failure: A Retrospective Observational Study Using a Multicenter Dataset (2019) (21)
- BCL6 locus is hypermethylated in angioimmunoblastic T-cell lymphoma (2017) (21)
- BRCC3 mutations in myeloid neoplasms (2015) (21)
- Autonomous feedback loop of RUNX1-p53-CBFB in acute myeloid leukemia cells (2017) (21)
- Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan (2015) (20)
- 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)
- NOTCH1 pathway activating mutations and clonal evolution in pediatric T‐cell acute lymphoblastic leukemia (2019) (20)
- The quality of life in acromegalic patients with biochemical remission by surgery alone is superior to that in those with pharmaceutical therapy without radiotherapy, using the newly developed Japanese version of the AcroQoL (2015) (20)
- Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children (2015) (20)
- The small heat shock protein alphaB-crystallin inhibits differentiation-induced caspase 3 activation and myogenic differentiation. (2006) (20)
- Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients (2019) (20)
- Characterization of estrogen-induced F-box protein FBXO45. (2005) (19)
- Hyperosmotic stress up-regulates the expression of major vault protein in SW620 human colon cancer cells. (2008) (19)
- Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia. (2020) (19)
- Quantitative structure-property relationships for the calculation of the soil adsorption coefficient using machine learning algorithms with calculated chemical properties from open-source software. (2020) (18)
- A nonsense mutation of IDH1 in myelodysplastic syndromes and related disorders (2011) (18)
- Thymidine phosphorylase inhibits the expression of proapoptotic protein BNIP3. (2008) (17)
- Novel neuroblastoma amplified sequence (NBAS) mutations in a Japanese boy with fever-triggered recurrent acute liver failure (2019) (17)
- Integrated Molecular Characterization of the Lethal Pediatric Cancer Pancreatoblastoma. (2018) (17)
- Diagnostic challenge of Diamond–Blackfan anemia in mothers and children by whole-exome sequencing (2017) (17)
- Transcriptional Regulation of an Evolutionary Conserved Intergenic Region of CDT2-INTS7 (2008) (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)
- Acromegaly caused by a somatotroph adenoma in patient with neurofibromatosis type 1. (2019) (16)
- Isolated adrenocorticotropic hormone deficiency as a form of paraneoplastic syndrome (2018) (16)
- Delphinidin Induces Autolysosome as well as Autophagosome Formation and Delphinidin‐Induced Autophagy Exerts a Cell Protective Role (2012) (16)
- A Combined Computational and Experimental Study on the Structure-Regulation Relationships of Putative Mammalian DNA Replication Initiator GINS (2006) (16)
- Bullous exudative retinal detachment due to infiltration of leukemic cells in a child with acute lymphoblastic leukemia (2010) (16)
- A novel thymoma-associated autoimmune disease: Anti-PIT-1 antibody syndrome (2017) (15)
- Array CGH identifies copy number changes in 11% of 520 MDS patients with normal karyotype and uncovers prognostically relevant deletions (2016) (15)
- Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets (2020) (15)
- Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants (2020) (15)
- Novel DDX41 variants in Thai patients with myeloid neoplasms (2019) (15)
- Somatic mosaicism in chronic myeloid leukemia in remission. (2016) (14)
- Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation (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)
- Whole-exome sequence analysis of ataxia telangiectasia-like phenotype (2014) (14)
- Recurrent CCND3 mutations in MLL-rearranged acute myeloid leukemia. (2018) (14)
- Tobacco smoking and somatic mutations in human bronchial epithelium (2020) (14)
- Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation (2018) (14)
- Characteristics and outcomes of bacteremia among ICU-admitted patients with severe sepsis (2020) (14)
- ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1‐RUNX1T1 and associated with a better prognosis (2017) (14)
- Unbiased Detection of Driver Mutations in Extramammary Paget Disease (2020) (14)
- FBXL16 is a novel E2F1-regulated gene commonly upregulated in p16INK4A- and p14ARF-silenced HeLa cells. (2009) (13)
- Systems Biology-Based Identification of Crosstalk between E2F Transcription Factors and the Fanconi Anemia Pathway (2007) (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)
- Significance of body temperature in elderly patients with sepsis (2020) (13)
- DNA methylation-based classification reveals difference between pediatric T-cell acute lymphoblastic leukemia and normal thymocytes (2019) (13)
- The ex vivo production of ammonia predicts l-asparaginase biological activity in children with acute lymphoblastic leukemia (2009) (13)
- Pathogenesis of Anti–PIT-1 Antibody Syndrome: PIT-1 Presentation by HLA Class I on Anterior Pituitary Cells (2019) (13)
- Common Variable Immunodeficiency Caused by FANC Mutations (2017) (13)
- Normal neutrophil myosin IIA localization in an immunofluorescence analysis can rule out MYH9 disorders (2013) (12)
- Metachronous anaplastic sarcoma of the kidney and thyroid follicular carcinoma as manifestations of DICER1 abnormalities. (2017) (12)
- BCOR and BCORL 1 mutations in myelodysplastic syndromes and related disorders (2013) (12)
- Multiple Salivary Cortisol Measurements Are a Useful Tool to Optimize Metyrapone Treatment in Patients with Cushing’s Syndromes Treatment: Case Presentations (2018) (12)
- Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency. (2021) (12)
- Radiation-induced myeloid leukemia in mice under calorie restriction. (1997) (11)
- Novel splicing-factor mutations in juvenile myelomonocytic leukemia (2012) (11)
- Recurrent SPI 1 ( PU . 1 ) fusions in high-risk pediatric T cell acute lymphoblastic leukemia (2019) (11)
- Prediction of Soil Adsorption Coefficient in Pesticides Using Physicochemical Properties and Molecular Descriptors by Machine Learning Models (2020) (11)
- Case of type 1 diabetes mellitus following interferon β-1a treatment for multiple sclerosis. (2012) (11)
- Clonally related diffuse large B-cell lymphoma and interdigitating dendritic cell sarcoma sharing MYC translocation (2018) (11)
- The influence of type 2 diabetes on serum GH and IGF-I levels in hospitalized Japanese patients. (2016) (11)
- A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India (2020) (11)
- Gene Expression Changes During the Chondrogenic Differentiation of Human Mesenchymal Stem Cells (2007) (10)
- The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype (2016) (10)
- A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia (2018) (10)
- A subset of microRNAs potentially acts as a convergent hub for upstream transcription factors in cancer cells. (2010) (9)
- Germline DDX41 mutations define a unique subtype of myeloid neoplasms. (2022) (9)
- Molecular Heterogeneity in Peripheral T-Cell Lymphoma Not Otherwise Specified Revealed By Comprehensive Mutational Profiling (2016) (9)
- Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia (2018) (9)
- Myeloproliferative disorder due to abnormal production of hematopoietic stimulators. (1987) (9)
- IgG4-related hypophysitis in patients with autoimmune pancreatitis (2019) (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)
- Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets. (2020) (9)
- Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia (2016) (8)
- P53 labeling index in cholangioscopic biopsies is useful for determining spread of bile duct carcinomas. (2002) (8)
- Fusion partner-specific mutation profiles and KRAS mutations as adverse prognostic factors in MLL-rearranged AML. (2020) (8)
- Gene expression levels of human shelterin complex and shelterin-associated factors regulated by the topoisomerase II inhibitors doxorubicin and etoposide in human cultured cells (2013) (8)
- Erratum: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia (2016) (8)
- Aggressive transformation of anaplastic large cell lymphoma with increased number of ALK-translocated chromosomes (2015) (8)
- Somatic Mutations in Schinzel-Giedion Syndrome Gene SETBP1 Determine Progression in Myeloid Malignancies (2012) (8)
- Frequent mutations in HLA and related genes in extranodal NK/T cell lymphomas (2020) (8)
- Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia (2018) (8)
- Modification of cellular and humoral immunity by somatically reverted T cells in X-linked lymphoproliferative syndrome type 1. (2019) (8)
- Genetic Predispositions to Myeloid Neoplasms Caused By Germline DDX41 Mutations (2015) (8)
- Comprehensive Analysis of Aberrant RNA Splicing in Myelodysplastic Syndromes (2014) (7)
- Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia (2017) (7)
- Identification and characterization of a novel kelch-like gene KLHL15 in silico. (2005) (7)
- Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia (2021) (7)
- Peptide binding to Geminin and inhibitory for DNA replication. (2004) (7)
- Clinical utility of target capture‐based panel sequencing in hematological malignancies: A multicenter feasibility study (2020) (7)
- Comparative genomics on MCM8 orthologous genes reveals the transcriptional regulation by transcription factor E2F. (2006) (7)
- Paraneoplastic hypereosinophilic syndrome associated with IL3‐IgH positive acute lymphoblastic leukemia (2018) (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)
- Development of QSAR models for prediction of fish bioconcentration factors using physicochemical properties and molecular descriptors with machine learning algorithms (2021) (7)
- Factors correlated with serum insulin-like growth factor-I levels in health check-up subjects. (2018) (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)
- Procedure for Liquid Chromatographic Determination of Thiamphenicol in Bovine Serum and Milk (1994) (6)
- Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets (2020) (6)
- Dendritic Cells Pre-Pulsed with Wilms’ Tumor 1 in Optimized Culture for Cancer Vaccination (2020) (6)
- Association of high-risk neuroblastoma classification based on expression profiles with differentiation and metabolism (2021) (6)
- Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome (2020) (6)
- Chronological Analysis of Clonal Evolution in Acquired Aplastic Anemia (2014) (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)
- Geminin organizes the molecular platform to balance cellular proliferation and differentiation. (2007) (6)
- Expression and tissue distribution of human X-linked armadillo repeat containing-6. (2010) (5)
- Correction: Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution (2017) (5)
- Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia (2020) (5)
- Identification of FAZF as a novel BMP2‐induced transcription factor during osteoblastic differentiation (2007) (5)
- Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient (2015) (5)
- Studies on the Mechanisms of Pollen Embryogenesis (III) : Mitotic Responses of the Pollen to Varied Sucrose Concentrations and the Process of Embryoid Formation in Tobacco Anther Culture (1979) (5)
- [A case of jejunal perforation in gallstone ileus]. (2008) (5)
- Clinical Impacts of Germline DDX41 Mutations on Myeloid Neoplasms (2020) (5)
- The landscape of genetic aberrations in myxofibrosarcoma (2022) (5)
- 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)
- Mutational Spectrum Analysis of Interesting Correlation and Interrelationship Between RNA Splicing Pathway and Commonly Targeted Genes in Myelodysplastic Syndrome (2011) (4)
- NGS-Based Copy Number Analysis in 1,185 Patients with Myeloid Neoplasms (2016) (4)
- Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome. (2019) (4)
- Acute loss of DP1, but not DP2, induces p53 mRNA and augments p21Waf1/Cip1 and senescence (2012) (4)
- Genetic Background of Idiopathic Bone Marrow Failure Syndromes in Children (2015) (4)
- In Analogy to AML, MDS Can be Sub-Classified By Ancestral Mutations (2014) (4)
- Identification of Two New DBA Genes, RPS27 and RPL27, by Whole-Exome Sequencing in Diamond-Blackfan Anemia Patients (2012) (4)
- Augmentation of the ubiquitin-mediated proteolytic system by F-box and additional motif-containing proteins (Review). (2010) (4)
- Transcription of the Geminin gene is regulated by a negative-feedback loop (2014) (4)
- PF532 INTEGRATED PROFILING OF DNA METHYLATION AND MUTATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES (2019) (4)
- Genetic Background of Chronic Active Epstein-Barr Virus Disease (2017) (4)
- Production of interleukin-3 from a T-cell neoplasm. (1988) (4)
- Localization and mechanism of nephrocalcinosis in pseudo-Bartter's syndrome. (2010) (3)
- Clinical “MUTATOME” Of Myelodysplastic Syndrome; Comparison To Primary Acute Myelogenous Leukemia (2013) (3)
- Identification and characterization of human ZNF18 gene in silico. (2005) (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)
- Clonal Hematopoiesis: Cell of Origin, Lineage Repartition and Dynamic Evolution during Chemotherapy (2017) (3)
- Acceleration of a murine T-cell leukemia associated with loss of interleukin-3 producing activity. (1989) (3)
- FBXL 16 is a novel E 2 F 1-regulated gene commonly upregulated in p 16 INK 4 Aand p 14 ARF-silenced HeLa cells (3)
- Quality Verification with a Cluster−Controlled Manufacturing System to Generate Monocyte−Derived Dendritic Cells (2021) (3)
- Puma is a novel target of soy isoflavone genistein but is dispensable for genistein-induced cell fate determination. (2008) (3)
- Geminin as a molecular target for the development of new anticancer drugs. (2006) (3)
- Impact of Somatic Mutations on Outcome in Patients with MDS after Stem-Cell Transplantation (2015) (3)
- Pan-Myeloid Leukemia Analysis: Machine Learning-Based Approach to Predict Phenotype and Clinical Outcomes Using Mutation Data (2018) (3)
- Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia (2022) (3)
- Ring sideroblasts in AML are associated with adverse risk characteristics and have a distinct gene expression pattern. (2019) (3)
- Proof of Evidence: PPAR-induced ANGPTL4 in Lipid and Glucose Metabolism (2007) (3)
- Abstract 5119: Frequent splicing pathway mutations and aberrant RNA splicing in myelodysplasia (2012) (3)
- Sudden Intracranial Hemorrhage in a Patient With Atypical Chronic Myeloid Leukemia in Chronic Phase. (2017) (3)
- Molecular Profiling of Blastic Transformation in Chronic Myeloid Leukemia (2018) (3)
- A prospective naturalistic multicentre study of intravenous medications in behavioural emergencies: Haloperidol versus flunitrazepam (2010) (3)
- Different Mutant Splicing Factors Cause Distinct Missplicing Events and Give Rise to Different Clinical Phenotypes in Myelodysplastic Syndromes (2015) (3)
- Germline SAMD9 and SAMD9L Alterations in Adult Myelodysplastic Syndromes (2017) (3)
- Genome-wide DNA methylation analysis in pediatric acute myeloid leukemia (2022) (3)
- Genotype-Phenotype Relationships and Therapeutic Targets in Acute Erythroid Leukemia (2020) (2)
- PPM1D and DNMT3A Mutations in Myelodysplasia and Clonal Hematopoiesis (2019) (2)
- Revised version 2 ) Biallelic DICER 1 mutations in sporadic pleuropulmonary blastoma Running title Biallelic DICER 1 mutations in sporadic PPB (2014) (2)
- [Genetic analysis of hereditary hematological disorders: overview]. (2015) (2)
- Distinct, Ethnic, Clinical, and Genetic Characteristics of Myelodysplastic Syndromes with Der(1;7) (2019) (2)
- Spectrum Of Genetic Alterations In Acquired Aplastic Anemia (2013) (2)
- Publisher Correction: Defective Epstein–Barr virus in chronic active infection and haematological malignancy (2019) (2)
- Identification and characterization of ankyrin repeat and SOCS box-containing gene ASB15 in silico. (2005) (2)
- Corrigendum: The landscape of somatic mutations in Down syndrome–related myeloid disorders (2013) (2)
- Genetic Basis of Myeloid Proliferation Related to Down Syndrome (2012) (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)
- Clinical Effect of Genetic Alterations in Pediatric Patients with B-Progenitor Acute Lymphoblastic Leukemia (2017) (2)
- Dysregulation of DNA Methylation Involves in Progression of Myeloid Leukemia in Down Syndrome (2015) (2)
- Molecular and Functional Diversities of Cadherin and Protocadherin (2010) (2)
- Prognostic Relevance of Genetic Abnormalities in Blastic Transformation of Chronic Myeloid Leukemia (2020) (2)
- A CASE OF ADULT ILEAL DUPLICATION WITH HETEROTOPIC PANCREAS PRESENTING WITH PERITONITIS (2009) (2)
- A CASE OF LEPTOMENINGEAL CARCINOMATOSIS OCCURRING 9 YEARS AFTER SURGERY FOR EARLY GASTRIC CANCER (2009) (2)
- Landscape of Genetic Alterations in Adult T-Cell Leukemia/Lymphoma (2014) (2)
- Srsf2 P95H Mutation Causes Impaired Stem Cell Repopulation and Hematopoietic Differentiation in Mice (2015) (2)
- VEGFA- a New Therapeutic Target in CNS Leukemia (2016) (2)
- DDX41 Is a Tumor Suppressor Gene Associated with Inherited and Acquired Mutations (2014) (2)
- Atypical dyskeratosis congenita diagnosed using whole‐exome sequencing (2017) (2)
- Somatic G17V Rhoa Mutation Specifies Angioimmunoblastic T-Cell Lymphoma (2013) (2)
- Clinical Heterogeneity of Acquired Idiopathic Isolated Adrenocorticotropic Hormone Deficiency (2021) (2)
- Droplet digital polymerase chain reaction assay for the detection of the minor clone of KIT D816V in paediatric acute myeloid leukaemia especially showing RUNX1‐RUNX1T1 transcripts (2021) (2)
- Multi-omics analysis defines highly refractory RAS burdened immature subgroup of infant acute lymphoblastic leukemia (2022) (2)
- Novel Molecular Pathogenesis and Therapeutic Target in Acute Erythroid Leukemia (2019) (2)
- Abstract 94: Genomic landscape and clonal expansions of upper urinary tract urothelial carcinoma (2016) (2)
- ACTIVATION OF RHOA‐VAV1 SIGNALING IN ANGIOIMMUNOBLASTIC T‐CELL LYMPHOMA (2017) (2)
- Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation (2018) (2)
- Abstract 4702: Genome-wide analysis of copy number alternations and gene mutations in renal cell carcinoma (2011) (1)
- Signal Transduction Pathway Regulated by Genistein and its Therapeutic Use (2008) (1)
- Detection of Novel Pathogenic Gene Rearrangements in Pediatric Acute Myeloid Leukemia By RNA Sequencing (2015) (1)
- Clonal evidence for the development of neuroblastoma with extensive copy‐neutral loss of heterozygosity arising in a mature teratoma (2021) (1)
- [IDH1/2 gene mutations in myelodysplastic syndromes]. (2012) (1)
- Frequent Activating Somatic Alterations in T-Cell Receptor / NF-κb Signaling in Adult T-Cell Leukemia/Lymphoma (2015) (1)
- Der(1;7)(q10;p10) Presents with a Unique Genetic Profile and Frequent ETNK1 Mutations in Myeloid Neoplasms (2021) (1)
- Novel TENM3–ALK fusion is an alternate mechanism for ALK activation in neuroblastoma (2022) (1)
- Whole Exome Sequencing Reveals Spectrum of Gene Mutations in Pediatric AML (2012) (1)
- Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations (2020) (1)
- Molecular Defects In BRCC3 Complex, a Novel Pathogenic Pathway In MDS (2013) (1)
- Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia (2022) (1)
- Distinctive Genetic Features of Plasma Cells in POEMS Syndrome (2016) (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)
- Current Awareness and Status of Transthoracic Echocardiography in Kumamoto Prefecture ― A Report of the Kumamoto Cardiovascular Echocardiography Standardization Project ― (2020) (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)
- Biological Analysis of SRSF2 Mutations in Leukemogenesis (2012) (1)
- MicroRNA as a Modulator of Cell Proliferation and Senescence: Role in Lung Cancer Cells (2013) (1)
- Whole Exome Sequencing Reveals Clonal Evolution Pattern and Driver Mutations Of Relapsed Pediatric AML (2013) (1)
- Whole-Genome Sequencing of Primary Central Nervous System Lymphoma and Diffuse Large B-Cell Lymphoma (2016) (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)
- Hidden FLT3-D835Y clone in FLT3-ITD-positive acute myeloid leukemia that evolved into very late relapse with T-lymphoblastic leukemia (2018) (1)
- ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan (2015) (1)
- Molecular Signatures That Predict Response to Azacitidine Treatment for Myelodysplastic Syndromes (2017) (1)
- Poor Myocardial Compaction in a Patient with Recessive MYL2 Myopathy. (2021) (1)
- Spliceosomal Gene LUC7L2 Mutation Causes Missplicing and Alteration Of Gene Expression In Myeloid Neoplasms (2013) (1)
- Abstract 3294: Clonal evolution and integral analysis of hepatoblastoma (2015) (1)
- UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia (2022) (1)
- TAL1 Super Enhancer Aberration and Stil-TAL1 Fusion in Pediatric T Cell Acute Lymphoblastic Leukemia (2016) (1)
- EPOR/JAK/STAT Signaling Pathway As Therapeutic Target of Acute Erythroid Leukemia (2021) (1)
- Genetic abnormalities associated with the relapse of childhood leukemia. (2016) (1)
- Post-azacitidine clone size predicts outcome of patients with myelodysplastic syndromes and related myeloid neoplasms. (2023) (1)
- Coexistence and Prognostic Significance of EVI1 Expression and Driver Mutations in KMT2A-Rearranged Acute Myeloid Leukemia (2019) (1)
- Novel Pathogenic Defects Of Dead/H-Box Helicases In Myeloid Neoplasms (2013) (1)
- Various Germline Congenital Disorder Genes Are Somatically Mutated in Myeloid Malignancies (2012) (1)
- Whole Exome Sequencing to Predict Response to Hypomethylating Agents in MDS (2012) (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)
- Comprehensive Sequencing Analysis in Subcutaneous Panniculitis-like T-Cell Lymphoma (2017) (1)
- Optimization of prediction methods for risk assessment of pathogenic germline variants in the Japanese population (2021) (1)
- Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients (2020) (1)
- Two Novel Distinct Subtypes of Myeloid Neoplasms Molecularly Associated with Histone H3K36 Methylations (2015) (1)
- Recurrent VAV1 Abnormalities in Angioimmunoblastic T Cell Lymphoma (2016) (1)
- Functional Analysis of SRSF2 Mutations in Myelodysplastic Syndromes and Related Disorders (2011) (1)
- A CASE OF RECTOVESICAL FISTULA DUE TO PROSTATITIS (2009) (1)
- Description of longitudinal tumor evolution in a case of multiply relapsed clear cell sarcoma of the kidney (2021) (1)
- A case of von Meyenburg complex simulating multiple liver abscesses (2007) (1)
- A Case of Neuroendocrine Cell Carcinoma of Barrett's Esophagus (2011) (1)
- A CASE OF SPIGELIAN HERNIA REPAIRED USING THE MESH-PLUG METHOD (2010) (1)
- Molecular Characteristics That Predict Response to Azacitidine Therapy (2019) (1)
- Donor cell-derived transient abnormal myelopoiesis as a specific complication of umbilical cord blood transplantation (2018) (1)
- Childhood acute myeloid leukemia with 5q deletion and HNRNPH1-MLLT10 fusion: the first case report (2022) (1)
- Remission clone in acute myeloid leukemia shows growth advantage after chemotherapy but is distinct from leukemic clone. (2019) (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 Basis of Primary Central Nervous System Lymphoma (2015) (1)
- Cross-sectional prevalence of pancreatic cystic lesions in patients with acromegaly, a single-center experience (2017) (1)
- 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)
- Abstract 6734: Identification of the novel TENM3-ALK fusion in an AYA case with ALK rearranged neuroblastoma (2023) (0)
- Characterization of Pathogenic Variants and Clinical Phenotypes in 117 Japanese Fanconi Anemia Patients (2018) (0)
- Abstract 3403: Genetic analysis of pheochromocytoma (2019) (0)
- Abstract P5-13-04: Clonal evolution of mammary epithelial cells into breast cancers (2023) (0)
- Simplified Classification Method for Residual Antibiotics by Microbiological Assay Using Drug-Resistant Bacteria (1994) (0)
- A possible association between a novel NLRP1 mutation and an autoinflammatory disease involving liver cirrhosis. (2021) (0)
- PD18-11 DISTINCT MOLECULAR SUBTYPES AND A HIGH DIAGNOSTIC URINARY BIOMARKER OF UPPER URINARY TRACT UROTHELIAL CARCINOMA (2020) (0)
- Distribution and Clinical Features of NOTCH1 Signaling Activating Alterations in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL) (2018) (0)
- Genetic basis of progression and relapse in Clear Cell Sarcoma of the Kidney (2020) (0)
- PS1367 COMPREHENSIVE GENETIC ANALYSIS OF MULTIPLE MYELOMA IN JAPAN (2019) (0)
- Whole-Exome Analysis of Autoimmune Lymphoproliferative Syndrome-like Diseases (2015) (0)
- Genetic Landscapes Of Childhood T-Cell Acute Lymphoblastic Leukemia (2013) (0)
- INTEGRATED PROFILING OF DNA METHYLATION AND MUTATIONS IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES (2019) (0)
- Abstract 92: Clonal evolution of proliferative lesions into breast cancers (2021) (0)
- COMPREHENSIVE ANALYSIS OF UPPER URINARY TRACT UROTHELIAL CARCINOMA: MP58‐09 (2018) (0)
- Whole Exome Sequencing Detecting Kinesin Family Gene Defects In Myeloid Neoplasm (2013) (0)
- Clinical and Genetic Characterization Of Patients With C-CBL Mutated Juvenile Myelomonocytic Leukemia By Whole-Exome/Deep Sequencing (2013) (0)
- Clonal evolution in myelodysplastic syndromes. (2016) (0)
- Genome-Wide Analysis of Non-Coding Alterations in Pan-Myeloid Cancers Using Whole Genome Sequencing (2018) (0)
- Role Of Sf3b1 On Hematopoiesis (2013) (0)
- Title Splicing factor mutations and cancer (2018) (0)
- The Clinical and Genetic Features of Dyskeratosis Congenita, Cryptic Dyskeratosis Congenita, and Hoyeraal-Hreidarsson Syndrome in Japan (2014) (0)
- the Impact of Clonal Dynamics on Prognosis and Outcome in Myelodysplastic Syndromes (2016) (0)
- PS998 JANUS KINASE AND CYTOKINE RECEPTOR MUTATIONS IN TRANSIENT ABNORMAL MYELOPOIESIS AND MYELOID LEUKEMIA IN CHILDREN WITH TRISOMY 21 (2019) (0)
- O-007 BCOR and BCORL1 mutations in myelodysplasia: Prevalence, prognosis and clonal hierarchy (2013) (0)
- Abstract 3088: Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma (2014) (0)
- Development of Four-legged Vehicle for an Intelligent Robot (1985) (0)
- Frequent somatic mutations in epigenetic regulators in newly diagnosed chronic myeloid leukemia (2017) (0)
- Title Genetic basis of myeloid transformation in familial platelet disorder / acute myeloid leukemia patients with haploinsufficient RUNX 1 allele (2019) (0)
- S101: GENETIC AND EPIGENETIC FACTORS DRIVING PRIMARY MEDIASTINAL B-CELL LYMPHOMA PATHOGENESIS AND OUTCOME (2022) (0)
- Defective Epstein–Barr virus in chronic active infection and haematological malignancy (2019) (0)
- POST-AZACITIDINE CLONE SIZE PREDICTS LONG-TERM OUTCOME OF PATIENTS WITH MYELODYSPLASTIC SYNDROMES AND RELATED MYELOID NEOPLASMS (2023) (0)
- Abstract 2019: Whole exome analysis reveals spectrum of gene mutations in adult T-cell leukemia/lymphoma. (2013) (0)
- Abstract 5759: Molecular classification and risk stratification of colorectal cancer (2022) (0)
- [Progress in research of the pathogenesis of childhood MDS/MPN]. (2018) (0)
- Germline Risks and Clinical Impacts of DDX41 Mutations in Myeloid Malignancies (2022) (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)
- P-145 Sequential gain of SETBP1 mutations in severe aplastic anemia evolving into acute myeloid leukemia with monosomy 7 (2013) (0)
- 764 Integrative analysis of clear cell renal cell carcinoma (2013) (0)
- Landscape of Driver Mutations and Their Clinical Impacts in Pediatric Acute Lymphoblastic Leukemia (2016) (0)
- Expression and functional analysis of the largest human microRNA cluster C19MC (2016) (0)
- Abstract 1002: Epigenetic and genetic characteristics and their association with prognosis of follicular lymphoma: Analysis at a Japanese single institution (2023) (0)
- TET2 Mutations Revealed by Whole Genome Sequencing in Adult T-Cell Leukemia. (2012) (0)
- Abstract P3-06-04: Clonal evolution of non-malignant proliferative lesions into breast cancers (2019) (0)
- A Case of Double Cortex : Cortical Dysplasia due to Neuronal Migration Disosrder (1995) (0)
- Biological and genetic characterization of the role of SRSF2 mutations in the pathogenesis of myelodysplastic syndromes (2015) (0)
- Next-Generation Sequencing Reveal Proviral Genome and Transcriptome in Adult T-Cell Leukemia/Lymphoma (2015) (0)
- Cyclophosphamide^|^mdash;associated cardiomyopathy after allogeneic hematopoietic stem cell transplantation from a sibling donor for refractory cytopenia of childhood (2014) (0)
- Karyotypic and Genetic Abnormalities Associated with Clonal Evolution in Paroxysmal Nocturnal Hemoglobinuria. (2012) (0)
- Whole-Exome Sequencing Reveals a Paucity of Somatic Gene Mutations in Aplastic Anemia and Refractory Cytopenia of Childhood (2014) (0)
- Ancestral Events Including Germline and Somatic Mutations Determine Subclonal Events and Affect Phenotype of Progression in MDS (2017) (0)
- Abstract 1309: Distinct molecular subtypes and a high diagnostic urinary biomarker of upper urinary tract urothelial carcinoma (2020) (0)
- Frequent mutations that converge on the NFKBIZ pathway in ulcerative colitis (2019) (0)
- 435 GENOME-WIDE ANALYSIS OF COPY NUMBER ALTERATIONS AND GENE MUTATIONS IN RENAL CELL CARCINOMA (2012) (0)
- Abstract 164: Clonal evolution in noncancerous esophageal mucosa in normal and cancer-bearing individuals (2016) (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)
- Prognosis of Pediatric Acute Myeloid Leukemia with KMT2A-MLLT3 According to DNA Methylation Patterns: Jccg JPLSG AML-05 Study (2022) (0)
- Abstract 2342: Tobacco exposure and somatic mutations in normal bronchial epithelia (2020) (0)
- COL4A1 is a Novel Causative Gene Responsible for Congenital Hemolytic Anemia, Representing Characteristic Clinical Course in Infants (2015) (0)
- Mutations of the Spliceosome Complex Genes Occur In Adult Patients but Are Very Rare In Children with Myeloid Neoplasia (2011) (0)
- A Novel Diagnostic Method For AITL By Detecting RHOA G17V Hotspot Mutation Using Allele-Specific Real-Time PCR (2013) (0)
- 1. Novel Molecular Mechanism of Myelodysplastic Syndromes (2012) (0)
- Clinical Significance of Mutations and Copy Number Lesions on Prognosis of Patients with MDS after Unrelated Bone Marrow Transplantation (2016) (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)
- Identifications of Highly Aggressive Phenotype with SPI1 Overexpression in Pediatric T Cell Acute Lymphoblastic Leukemia/Lymphoma (2016) (0)
- Abstract 3401: Comprehensive analysis of genetic alterations and intratumor heterogeneity in myxofibrosarcoma (2018) (0)
- An Adverse Prognostic Effect of Homozygous TET2 Mutational Status on the Relapse Risk of Acute Myeloid Leukemia Patients of Normal Karyotype (2014) (0)
- 48 Next-generation sequencing technology combined with multiplexed barcoded samples of myelodysplastic syndromes reveals an abundance of target gene mutations (2011) (0)
- Whole Exome Analysis of Myelodysplastic Syndromes Using Next-Generation Resequencing Technology (2010) (0)
- Landscape of DNA Methylation and Genetic Profiles in 291 Patients with Myelodysplastic Syndromes (2015) (0)
- In Vitro Analysis of Genomic Heterogeneity in Pre-Invasive Lung Cancer (2019) (0)
- Expression and functional analysis of miRNA-370 in the human and mouse conserved cluster region (2016) (0)
- Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia (2015) (0)
- Epigenetic regulation of MAP1LC3 gene family on human cervical cancer cells (2016) (0)
- Abstract 4385: Landscape of driver gene mutations in stage II and stage III colorectal cancer (2017) (0)
- Different In Vitro-Generated MUTZ-3-Derived Dendritic Cell Types Secrete Dexosomes with Distinct Phenotypes and Antigen Presentation Potencies (2022) (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)
- 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)
- Whole Exome Sequencing Shows a Paucity Of Somatic Gene Mutations In Pediatric Idiopathic Bone Marrow Failure Syndrome (2013) (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)
- Abstract 738: Myxofibrosarcoma is characterized by frequent abnormalities in TP53 and increased genetic instability (2019) (0)
- Clinical Features of Pediatric Acute Myeloid Leukemia with TP53 and CDKN2A/2B copy Number Alterations (2019) (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)
- Abstract 925: Whole exome analysis of myelodysplastic syndromes (2011) (0)
- P-146 Clinical and genetic characterization of 17 juvenile myelomonocytic leukemia patients with c-CBL mutations (2013) (0)
- Abstract 978: Genomic characterization and risk stratification of colorectal cancer (2023) (0)
- How do experiments in animal models complement experiments in human subjects (2001) (0)
- 24 COMPREHENSIVE ANALYSIS OF ALTERNATIVE RNA SPLICING IN MYELODYSPLASTIC SYNDROMES (2015) (0)
- Comprehensive genomic analysis of upper urinary tract urothelial carcinoma (2019) (0)
- Clonal Evolution Pattern and Prognostic Significance of Clonal Architecture in KMT2A-Rearranged Acute Myeloid Leukemia (2021) (0)
- P-001 Next generation whole exome sequencing for recurrent somatic mutations on chromosome 7 (2013) (0)
- Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism (2015) (0)
- Correction: Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia (2020) (0)
- The Prognostic Value of TP53 Mutations Depends on Clinical Backgrounds in Pediatric Patients with Acute Lymphoblastic Leukemia (2018) (0)
- KRAS mutations Frequently Coexist with High-Risk MLL Fusions and Are Independent Adverse Prognostic Factors in MLL-Rearranged Acute Myeloid Leukemia (2020) (0)
- Post-azacitidine clone size predicts long-term clinical outcome of patients with myelodysplastic syndromes and related myeloid neoplasms (2021) (0)
- Analysis of Genomic Predispositions to Sporadic Myeloid Neoplasms Mediated By DDX41 in Japan (2018) (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)
- RNA Sequencing Illustrates the Genetic Backgrounds of Pediatric Acute Myeloid Leukemia (2017) (0)
- Publisher Correction: Defective Epstein–Barr virus in chronic active infection and haematological malignancy (2019) (0)
- Abstract 3158: Defining the mechanisms that lead to mutational heterogeneity in the normal respiratory epithelium (2022) (0)
- Whole Exome Analysis Reveals Spectrum of Gene Mutations in Juvenile Myelomonocytic Leukemia (2012) (0)
- Genetic Landscape and Clonal Evolution Following 5-Aza Therapy in Patients with High-Risk Myelodysplastic Syndromes (2016) (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)
- Genomic landscape of upper urinary tract urothelial carcinoma (2017) (0)
- Comprehensive Genomic Analysis Identified Acute Lymphoblastic Leukemia in Down Syndrome Was Highly Heterogeneous with the High Prevalence of Ph-like Signature (2018) (0)
- Abstract 2229: Whole exome sequencing reveals the landscape of gene mutations and evolution in low-grade glioma (2014) (0)
- Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma Biallelic DICER1 mutations in sporadic PPB (2014) (0)
- Abstract 5754: The genetic aberrations in carcinogenic sequence of colitis-associated cancer (2017) (0)
- Genetic Profile of Acute Erythroid Leukemia (2016) (0)
- Structural Variations Involving Programmed Death Ligands in B-Cell and T-Cell Lymphomas (2016) (0)
- Distinct Features of Chip-Derived and De Novo MDS (2018) (0)
- Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants (2020) (0)
- Recurrent Gene Mutations in Pediatric Patients with AML By Targeted Sequencing ―the Jccg Study, JPLSG AML-05― (2019) (0)
- MON-268 Factors Associated With QoL Impairment In Patients With Acromegaly In The Elderly (2020) (0)
- The Detection of Minor Clones with Somatic KIT D816V Mutations Using Droplet Digital PCR in Pediatric De Novo AML: AML-05 Trial from the Japanese Pediatric Leukemia/Lymphoma Study Group (2019) (0)
- SETBP1 and Schinzel-Giedion Syndrome (2016) (0)
- Whole Exome Sequencing (“mutatome”) Of Deletion 5q (2013) (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)
- Stag2 regulates Hematopoietic Differentiation and Self-Renewal (2017) (0)
- Identification of a novel causative gene for Diamond-Blackfan anemia using zebrafish (2015) (0)
- Title Aberrant splicing and defective mRNA production induced bysomatic spliceosome mutations in myelodysplasia (2019) (0)
- Molecular and Cellular Pathobiology Biallelic DICER 1 Mutations in Sporadic Pleuropulmonary Blastoma (2014) (0)
- Abstract P4-05-15: Clonal evolution of proliferative lesions into breast cancers (2020) (0)
- Somatic Mutations and Loss-Of-Heterozygosity Impair The DNA Repair Functions Of CUX1 in Myelodysplastic Syndromes (MDS) (2013) (0)
- PD03-02 NOVEL STRUCTURAL VARIANTS IN CTNNB1 AND MOLECULAR CLASSIFICATION IN CORTISOL-PRODUCING ADENOMA (2023) (0)
- Clinical and Genetic Characteristics of Patients with Shwachman-Diamond Syndrome in Japan (2018) (0)
- Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia (2018) (0)
- Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations (2020) (0)
- Combined DNA and Transcriptome Sequencing Reveals Discrete Subtypes of Myelodysplasia (2016) (0)
- DISTINCT GENOMIC LANDSCAPE OF UPPER URINARY TRACT UROTHELIAL CARCINOMA: MP71‐02 (2017) (0)
- Non-Random Interactions between Founder and Subclonal Mutations Shape the Clinical and Morphological Features of MDS (2017) (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)
- Autonomous feedback loop of RUNX1-p53-CBFB in acute myeloid leukemia cells (2017) (0)
- Abstract 2276: Genetic classification of colorectal cancer (2021) (0)
- Abstract 482: Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma (2015) (0)
- Abstract 1437: Differential role of mutations in clonal evolution in esophageal mucosa at risk for cancer (2017) (0)
- Single-cell analysis based dissection of clonality in myelofibrosis (2020) (0)
- LYMPHOID NEOPLASIA Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma (2016) (0)
- PS983 NOVEL MOLECULAR PATHOGENESIS AND THERAPEUTIC TARGET IN ACUTE ERYTHROID LEUKEMIA (2019) (0)
- Abstract 225: Frequent abnormalities in TP53 and increased genetic instability in myxofibrosarcoma (2020) (0)
- Abstract 5117: Mutations of cohesin genes in myeloid malignancy (2012) (0)
- Elucidation of gene function based on the animal genomics (2005) (0)
- Abstract 2092: Integrated genetic analysis of clear cell renal cell carcionoma (2012) (0)
- Cancer Vaccination Trial with Novel Multiple Peptides in Previously Treated Advanced Non-Small-Cell Lung Cancer (2012) (0)
- Abstract 2223: Genome-wide analysis of copy number alterations and gene mutations in testicular germ cell cancer (2014) (0)
- 270 FOUNDER AND SUBCLONAL SOMATIC MUTATIONS CONTRIBUTING TO LEUKEMIC EVOLUTION IN MYELODYSPLASTIC SYNDROMES AND RELATED MYELOID NEOPLASMS (2015) (0)
- Recent Advances in MicroRNA Expression Profiling towards a Molecular Anatomy of Tumorigenesis and Applications for Diagnosis, Prognosis, and Therapeutics (2011) (0)
- Novel neuroblastoma amplified sequence (NBAS) mutations in a Japanese boy with fever-triggered recurrent acute liver failure (2019) (0)
- Integrated molecular analysis of upper urinary tract urothelial carcinoma (2018) (0)
- Abstract 4849: Profiling of multiple gene mutations in myelodysplastic syndromes using high-throughput resequenceing combined with barcode labeling (2011) (0)
- Whole Exome and Transcriptome Analyses in Pediatric T-Cell Acute Lymphoblastic Leukemia (2014) (0)
- Long-term outcome of six months maintenance chemotherapy for ALL in children: TCCSG L92-13E study. (2015) (0)
- Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort (2020) (0)
- Aprospectivenaturalisticmulticentrestudyofintravenousmedicationsinbehavioural emergencies: Haloperidol versus flunitrazepam☆ (2010) (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)
- 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)
- Afoundervariant in theSouthAsianpopulation leads toahigh prevalence of FANCL Fanconi anemia cases in India (2019) (0)
- Topic: AS04-MDS Biology and Pathogenesis/AS04b-Clonal diversity & evolution (2021) (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)
- Genome-Wide Mutational Landscape of Infant Acute Lymphoblastic Leukemia (2016) (0)
- Cooperative Effects of SRSF2 and STAG2 mutations on Development of Myelodysplastic Syndrome and Its Related Disorders (2022) (0)
- Abstract 3184: Integrative analysis of clear cell renal cell carcinoma. (2013) (0)
- The Detection of Immunity against WT1 and SMAD4P130L of EpCAM+ Cancer Cells in Malignant Pleural Effusion (2022) (0)
- Transcriptome Analysis Revealed the Entire Genetic Understanding of Pediatric Acute Myeloid Leukemia with a Normal Karyotype (2016) (0)
- Clinical Features of Patients with ASXL1 and ASXL2 Mutations in Pediatric Acute Myeloid Leukemia (2014) (0)
- Novel Mechanism of Post-Transcriptional Regulation of PD-L1 Expression By 3'-UTR Binding Proteins (2017) (0)
- Gene Expression Profiles and Methylation Analysis in Down Syndrome Related Acute Lymphoblastic Leukemia (2016) (0)
- mutations in adult T-cell leukemia / lymphoma (2015) (0)
- Abstract 3384: Comprehensive genetic analysis of myxofibrosarcoma and comparison with other soft tissue sarcomas (2017) (0)
- Invariant Patterns of Clonal Succession Determines Specific Phenotypic and Clinical Features of Myelodysplastic Syndromes (MDS) (2018) (0)
- P-030 Novel mutations in spliceosomal gene PRPF8 show ring sideroblast phenotype in patients with myeloid neoplasms (2013) (0)
- Comprehensive Profiling of Somatic Mutations Which Define Primary Disease and Relapse in Various Acute Leukemia Subtypes (2012) (0)
- Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets (2020) (0)
- Post-Treatment Clone Size Predicts Survival Independently of IPSS-R and Response after Azacitidine Therapy for MDS. (2020) (0)
- Abstract 3429: Genetic analysis of pancreatic neuroendocrine neoplasms grade 3 (2019) (0)
- Mutational Spectrum of Myelodysplastic Syndrome Malignancies Revealed by Whole Exome Sequencing (2012) (0)
- Abstract 3803: Genome-wide approach to identify gene targets of pleuropulmonary blastoma. (2013) (0)
- NEUROENDOCRINOLOGY AND PITUITARY Factors Associated With QoL Impairment In Patients With Acromegaly In The Elderly (2020) (0)
- Molecular Characterization Of Adult T-Cell Leukemia/Lymphoma (2013) (0)
- A Knowledge-Based Approach for Clinical Annotation of Oncogenic Variants to Support Patient-Tailored Diagnosis in Myeloid Disease (2017) (0)
- Profiling of Multiple Gene Mutations In Myelodysplastic Syndromes Using High-Throughput Resequenceing Combined with Barcode Labeling (2010) (0)
- Somatic Mosaicism for a NRAS Mutation Associates with Disparate Clinical Features in RAS-associated Leukoproliferative Disease: a Report of Two Cases (2015) (0)
- Significant Features of DNA Methylation at Bivalent Promotor and Repressed Polycomb Regions in Pediatric AML-the Jccg Study, JPLSG AML-05- (2019) (0)
- TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia. (2023) (0)
- Whole Exome Analysis Of Germline Alterations Associated With Myelodysplastic Syndrome (2013) (0)
- Abstract 2456: Distinct genomic landscape of upper urinary tract urothelial carcinoma (2017) (0)
- 18 CANDIDATE GENE MUTATIONS IN ACQUIRED APLASTIC ANEMIA CORRELATION WITH SURVIVAL AND CLONAL EVOLUTION TO MYELODYSPLASTIC SYNDROME (2015) (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)
- Abstract 741: Clonal evolution of non-malignant proliferative lesions into breast cancers (2019) (0)
- Abstract 4353: Integrated molecular analysis of upper urinary tract urothelial carcinoma (2018) (0)
- Identification of Cell-Type-Specific Mutations in Angioimmunoblastic T-Cell Lymphoma (2014) (0)
- Impact and Function of Somatic PHF6 Mutations in Myeloid Neoplasms (2014) (0)
- Abstract 1683: Mutational landscape of colorectal cancer with POLE gene mutation (2019) (0)
- Abstract 3322: Chronology and risk-dependence of age-related remodelling of oesophageal epithelia (2019) (0)
- TAL1 and MYB Abnormalities in Childhood T-Cell Acute Lymphoblastic Leukemia (2015) (0)
- Contribution of MIR9 on Disease Progression of Chronic Myelogenous Leukemia (2017) (0)
- DNA Methylation and Genetic Profiles in 320 Patients with Myelodysplastic Syndromes (2018) (0)
- The Presence of Defective Epstein-Barr Virus (EBV) Infection in Patients with EBV-Associated Hematological Malignancy (2018) (0)
- Abstract 3547: Frequent genomic alterations to evade the immune system in colorectal cancer with POLE gene mutation (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)
- Title Integrated genetic and epigenetic analysis defines novelmolecular subgroups in rhabdomyosarcoma (2019) (0)
- Abstract 4602: Recurrent pathway mutations of multiple components of cohesin complex in myeloid neoplasms. (2013) (0)
- Abstract 3405: Integrated analysis of urothelial carcinoma (2019) (0)
- Molecular Diversity Detected by Whole Exome Sequencing in Chronic Myelomonocytic Leukemia (2012) (0)
- Chapter 7:Recent Advances in the Multivariate Chemometric Analysis of Cancer Metabolic Profiling (2014) (0)
- Opposing Pathogenesis of Germline SAMD9/SAMD9L Variants in Adult Myelodysplastic Syndrome (MDS) (2018) (0)
- Common Variable Immunodeficiency Caused by FANC Mutations (2017) (0)
- Abstract 3802: Genetic basis of myeloid leukemogenesis in Down syndrome. (2013) (0)
- Abstract 3389: Clonal evolution of atypical proliferative lesions into breast cancers (2018) (0)
- Patients with pheochromocytoma exhibit low aldosterone renin ratio-preliminary reports (2020) (0)
- Successful treatment of hepatosplenic T-cell lymphoma with fludarabine, high-dose cytarabine and subsequent unrelated umbilical cord blood transplantation (2021) (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)
- Expression analysis of autophagy-related genes by transcription factor CHOP (2017) (0)
- Age-related remodelling of oesophageal epithelia by mutated cancer drivers (2019) (0)
- Somatic PHF6 Mutations In Myeloid Malignancies (2013) (0)
- marrow failure in Japanese Fanconi anemia patients Variant ALDH2 is associated with accelerated progression of bone (2013) (0)
- Identification of the ultrahigh-risk subgroup in neuroblastoma cases through DNA methylation analysis and its treatment exploiting cancer metabolism (2022) (0)
- Prevalence of i.v. thiopental use in psychiatric emergency settings in Japan (2009) (0)
- Genotype-Resultant Morphology of Myelodysplastic Syndromes (MDS) (2018) (0)
This paper list is powered by the following services:
What Schools Are Affiliated With Kenichi Yoshida?
Kenichi Yoshida is affiliated with the following schools:
