Osamu Ohara
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Computer Science
Osamu Ohara'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)Osamu Ohara'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
- Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells (2013) (3424)
- The Transcriptional Landscape of the Mammalian Genome (2005) (3394)
- Chemotherapy-resistant human AML stem cells home to and engraft within the bone-marrow endosteal region (2007) (901)
- Complete sequencing and characterization of 21,243 full-length human cDNAs (2004) (879)
- Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro. (1997) (707)
- Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome (2001) (537)
- NetPath: a public resource of curated signal transduction pathways (2010) (449)
- Identification of Therapeutic Targets for Quiescent, Chemotherapy-Resistant Human Leukemia Stem Cells (2010) (384)
- Let-7 microRNA-mediated mRNA deadenylation and translational repression in a mammalian cell-free system. (2007) (353)
- A Mass Spectrometry-based Proteomic Approach for Identification of Serine/Threonine-phosphorylated Proteins by Enrichment with Phospho-specific Antibodies (2002) (352)
- Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004) (346)
- Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain. (1996) (342)
- Polycomb group proteins Ring1A/B are functionally linked to the core transcriptional regulatory circuitry to maintain ES cell identity (2008) (318)
- Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (1998) (304)
- IκB kinase-α is critical for interferon-α production induced by Toll-like receptors 7 and 9 (2006) (286)
- Basophil-derived interleukin-4 controls the function of natural helper cells, a member of ILC2s, in lung inflammation. (2014) (271)
- High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study. (2011) (253)
- Histone H2A Mono-Ubiquitination Is a Crucial Step to Mediate PRC1-Dependent Repression of Developmental Genes to Maintain ES Cell Identity (2012) (247)
- The Zinc Transporter SLC39A13/ZIP13 Is Required for Connective Tissue Development; Its Involvement in BMP/TGF-β Signaling Pathways (2008) (232)
- Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene (1993) (232)
- Distinct cellular pathways select germline-encoded and somatically mutated antibodies into immunological memory (2012) (227)
- Plasmacytoid dendritic cells are crucial for the initiation of inflammation and T cell immunity in vivo. (2011) (225)
- One-sided polymerase chain reaction: the amplification of cDNA. (1989) (225)
- Direct observation of DNA rotation during transcription by Escherichia coli RNA polymerase (2001) (219)
- IkappaB kinase-alpha is critical for interferon-alpha production induced by Toll-like receptors 7 and 9. (2006) (209)
- Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (1999) (206)
- Glucocorticoids suppress group II phospholipase A2 production by blocking mRNA synthesis and post-transcriptional expression. (1990) (203)
- Obesity Drives STAT-1-Dependent NASH and STAT-3-Dependent HCC (2018) (200)
- Vascular Smooth Muscle Cell-derived, Gla-containing Growth-potentiating Factor for Ca-mobilizing Growth Factors (*) (1995) (187)
- Identification of high-molecular-weight proteins with multiple EGF-like motifs by motif-trap screening. (1998) (184)
- Discriminating gene expression profiles of memory B cell subpopulations (2008) (184)
- Molecular cloning of pancreatic group I phospholipase A2 receptor. (1994) (183)
- Novel Subset of CD8α+ Dendritic Cells Localized in the Marginal Zone Is Responsible for Tolerance to Cell-Associated Antigens1 (2009) (181)
- Group II phospholipase A2 mRNA synthesis is stimulated by two distinct mechanisms in rat vascular smooth muscle cells (1990) (181)
- Novel regulation of MHC class II function in B cells (2007) (176)
- Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (1998) (173)
- Aicardi-Goutières syndrome is caused by IFIH1 mutations. (2014) (170)
- Characterization of human Smg5/7a: a protein with similarities to Caenorhabditis elegans SMG5 and SMG7 that functions in the dephosphorylation of Upf1. (2003) (167)
- Human Proteinpedia enables sharing of human protein data (2008) (164)
- Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (2001) (150)
- Intracellular cell-autonomous association of Notch and its ligands: a novel mechanism of Notch signal modification. (2002) (148)
- The epigenetic regulator Uhrf1 facilitates the proliferation and maturation of colonic regulatory T cells (2014) (147)
- Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (1999) (143)
- Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (1999) (142)
- Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro. (2000) (139)
- Protein 4.1B associates with both Caspr/paranodin and Caspr2 at paranodes and juxtaparanodes of myelinated fibres (2003) (135)
- Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro. (1998) (134)
- Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (2000) (134)
- The completion of the Mammalian Gene Collection (MGC). (2009) (132)
- Single-cell imaging of caspase-1 dynamics reveals an all-or-none inflammasome signaling response. (2014) (129)
- Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency (2016) (123)
- IL-21–induced Bɛ cell apoptosis mediated by natural killer T cells suppresses IgE responses (2006) (121)
- Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro. (1998) (119)
- DomCut: prediction of inter-domain linker regions in amino acid sequences (2003) (117)
- Construction and characterization of human brain cDNA libraries suitable for analysis of cDNA clones encoding relatively large proteins. (1997) (113)
- Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs. (2002) (112)
- Mina, an Il4 repressor, controls T helper type 2 bias (2009) (109)
- Chronic Mucocutaneous Candidiasis Caused by a Gain-of-Function Mutation in the STAT1 DNA-Binding Domain (2012) (105)
- Sox5 and c-Maf cooperatively induce Th17 cell differentiation via RORγt induction as downstream targets of Stat3 (2014) (105)
- Prediction of the coding sequences of unidentified human genes. XVIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (2000) (103)
- An Immunogram for the Cancer‐Immunity Cycle: Towards Personalized Immunotherapy of Lung Cancer (2017) (103)
- Zinc transporter SLC39A10/ZIP10 facilitates antiapoptotic signaling during early B-cell development (2014) (101)
- Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro. (1997) (101)
- Zinc transporter SLC39A10/ZIP10 controls humoral immunity by modulating B-cell receptor signal strength (2014) (100)
- Vα14 NK T cell–triggered IFN-γ production by Gr-1+CD11b+ cells mediates early graft loss of syngeneic transplanted islets (2005) (100)
- PCGF6-PRC1 suppresses premature differentiation of mouse embryonic stem cells by regulating germ cell-related genes (2017) (100)
- The CAP-Gly domain of CYLD associates with the proline-rich sequence in NEMO/IKKgamma. (2004) (98)
- Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes. (2015) (98)
- Prediction of the coding sequences of unidentified human genes. XIX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (2000) (98)
- HUGE: a database for human large proteins identified in the Kazusa cDNA sequencing project. (2000) (96)
- HUGE: a database for human large proteins identified by Kazusa cDNA sequencing project (1999) (93)
- Obesity-associated autoantibody production requires AIM to retain the immunoglobulin M immune complex on follicular dendritic cells. (2013) (92)
- Protective neutralizing influenza antibody response in the absence of T follicular helper cells (2016) (92)
- Real-time single-cell imaging of protein secretion (2014) (91)
- Identification of a High‐Frequency Somatic NLRC4 Mutation as a Cause of Autoinflammation by Pluripotent Cell–Based Phenotype Dissection (2017) (90)
- cDNA cloning and sequence determination of rat membrane-associated phospholipase A2. (1989) (90)
- Membrane-bound human SCF/KL promotes in vivo human hematopoietic engraftment and myeloid differentiation. (2012) (89)
- The ORFeome Collaboration: a genome-scale human ORF-clone resource (2016) (89)
- Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders. (2017) (86)
- Construction of an open-access database that integrates cross-reference information from the transcriptome and proteome of immune cells (2007) (84)
- Distinctive four promoters collectively direct expression of brain-derived neurotrophic factor gene. (1994) (83)
- Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects. (2011) (82)
- Mammalian Polycomb-Like Pcl2/Mtf2 Is a Novel Regulatory Component of PRC2 That Can Differentially Modulate Polycomb Activity both at the Hox Gene Cluster and at Cdkn2a Genes (2010) (82)
- Prediction of Therapeutic Responses to Tocilizumab in Patients With Rheumatoid Arthritis: Biomarkers Identified by Analysis of Gene Expression in Peripheral Blood Mononuclear Cells Using Genome‐Wide DNA Microarray (2014) (82)
- Structural comparison of phospholipase-A2-binding regions in phospholipase-A2 receptors from various mammals. (1994) (81)
- HUGE: a database for human KIAA proteins, a 2004 update integrating HUGEppi and ROUGE (2004) (81)
- Dog and rat pancreatic phospholipases A2: complete amino acid sequences deduced from complementary DNAs. (1986) (79)
- The Menin–Bach2 axis is critical for regulating CD4 T-cell senescence and cytokine homeostasis (2014) (77)
- Apoptosis inhibitor of macrophage (AIM) is required for obesity-associated recruitment of inflammatory macrophages into adipose tissue (2011) (75)
- Type II brain 4.1 (4.1B/KIAA0987), a member of the protein 4.1 family, is localized to neuronal paranodes. (2000) (73)
- Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency. (2016) (73)
- Generation of orthotopically functional salivary gland from embryonic stem cells (2018) (73)
- Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection (2018) (72)
- A Pyrrolo-Pyrimidine Derivative Targets Human Primary AML Stem Cells in Vivo (2013) (71)
- Activation of Endogenous Retroviruses in Dnmt1(-/-) ESCs Involves Disruption of SETDB1-Mediated Repression by NP95 Binding to Hemimethylated DNA. (2016) (71)
- Zinc Transporter SLC39A7/ZIP7 Promotes Intestinal Epithelial Self-Renewal by Resolving ER Stress (2016) (70)
- Pancreatic-type phospholipase A2 induces group II phospholipase A2 expression and prostaglandin biosynthesis in rat mesangial cells. (1994) (70)
- Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21. (1997) (68)
- Unique activation status of peripheral blood mononuclear cells at acute phase of Kawasaki disease (2009) (68)
- The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts* (2007) (66)
- Acetate differentially regulates IgA reactivity to commensal bacteria (2021) (65)
- Characterization of a new beta-spectrin gene which is predominantly expressed in brain. (1998) (65)
- Two brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma. (2009) (65)
- Cyano2Dbase updated: linkage of 234 protein spots to corresponding genes through N-terminal microsequencing. (1999) (64)
- Cutting Edge: Requirement of MARCH-I-Mediated MHC II Ubiquitination for the Maintenance of Conventional Dendritic Cells1 (2009) (63)
- Conditional ablation of CD205+ conventional dendritic cells impacts the regulation of T-cell immunity and homeostasis in vivo (2012) (63)
- Solution structure of the SWIRM domain of human histone demethylase LSD1. (2006) (62)
- Phosphorylation of clock protein PER1 regulates its circadian degradation in normal human fibroblasts. (2004) (60)
- Cytotoxic T Lymphocytes Block Tumor Growth Both by Lytic Activity and IFNγ-Dependent Cell-Cycle Arrest (2014) (59)
- Mammalian Polycomb Scmh1 mediates exclusion of Polycomb complexes from the XY body in the pachytene spermatocytes (2006) (59)
- A novel mucosal vaccine targeting Peyer's patch M cells induces protective antigen-specific IgA responses. (2014) (59)
- Bach2–Batf interactions control Th2-type immune response by regulating the IL-4 amplification loop (2016) (59)
- Murine induced pluripotent stem cells can be derived from and differentiate into natural killer T cells. (2010) (58)
- Exploration of Human ORFeome: High-Throughput Preparation of ORF Clones and Efficient Characterization of Their Protein Products (2008) (57)
- Autosomal-Dominant Chronic Mucocutaneous Candidiasis with STAT1-Mutation can be Complicated with Chronic Active Hepatitis and Hypothyroidism (2012) (57)
- BREK/LMTK2 is a myosin VI‐binding protein involved in endosomal membrane trafficking (2008) (56)
- Identification of three novel non-classical cadherin genes through comprehensive analysis of large cDNAs. (2001) (56)
- Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain. (1999) (56)
- MEGF1/fat2 Proteins Containing Extraordinarily Large Extracellular Domains Are Localized to Thin Parallel Fibers of Cerebellar Granule Cells (2002) (56)
- Prediction and prioritization of neoantigens: integration of RNA sequencing data with whole‐exome sequencing (2017) (56)
- Single-cell chemical lysis method for analyses of intracellular molecules using an array of picoliter-scale microwells. (2008) (55)
- Circulating AIM prevents hepatocellular carcinoma through complement activation. (2014) (54)
- Mammalian fat3: a large protein that contains multiple cadherin and EGF-like motifs. (2002) (53)
- Characterization of cDNA clones in size-fractionated cDNA libraries from human brain. (1997) (53)
- Detection of Base Substitution-Type Somatic Mosaicism of the NLRP3 Gene with >99.9% Statistical Confidence by Massively Parallel Sequencing (2012) (53)
- Towards a proteome project of cyanobacterium Synechocystis sp. strain PCC6803: Linking 130 protein spots with their respective genes (1997) (53)
- Generation of safe and therapeutically effective human induced pluripotent stem cell‐derived hepatocyte‐like cells for regenerative medicine (2017) (53)
- Micro–adhesion rings surrounding TCR microclusters are essential for T cell activation (2016) (53)
- Isolation from Cochlea of a Novel Human Intronless Gene with Predominant Fetal Expression (2004) (52)
- Characterization of mammalian synemin, an intermediate filament protein present in all four classes of muscle cells and some neuroglial cells: co-localization and interaction with type III intermediate filament proteins and keratins (2003) (52)
- SigC, the Group 2 Sigma Factor of RNA Polymerase, Contributes to the Late-stage Gene Expression and Nitrogen Promoter Recognition in the Cyanobacterium Synechocystis sp. Strain PCC 6803 (2004) (52)
- Prediction of the coding sequences of mouse homologues of FLJ genes: the complete nucleotide sequences of 110 mouse FLJ-homologous cDnas identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries. (2004) (51)
- Directional cDNA library construction assisted by the in vitro recombination reaction. (2001) (51)
- Prediction of the coding sequences of unidentified human genes. XXII. The complete sequences of 50 new cDNA clones which code for large proteins. (2001) (51)
- Smurf1 directly targets hPEM-2, a GEF for Cdc42, via a novel combination of protein interaction modules in the ubiquitin-proteasome pathway (2008) (50)
- Chronic Granulomatous Disease: Two Decades of Experience From a Tertiary Care Centre in North West India (2013) (50)
- Novel Alternative Splicings of BPAG1 (Bullous Pemphigoid Antigen 1) Including the Domain Structure Closely Related to MACF (Microtubule Actin Cross-linking Factor)* (2002) (49)
- Prediction of the coding sequences of unidentified human genes. XXI. The complete sequences of 60 new cDNA clones from brain which code for large proteins. (2001) (49)
- PAD4 regulates proliferation of multipotent haematopoietic cells by controlling c-myc expression (2013) (49)
- Single molecular assay of individual ATP turnover by a myosin‐GFP fusion protein expressed in vitro (1997) (49)
- Cyano2Dbase updated: Linkage of 234 protein spots to corresponding genes through N‐terminal microsequencing (1999) (49)
- Optimization of Data-Independent Acquisition Mass Spectrometry for Deep and Highly Sensitive Proteomic Analysis (2019) (48)
- Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles. (2013) (47)
- Sequence features surrounding the translation initiation sites assigned on the genome sequence of Synechocystis sp. strain PCC6803 by amino-terminal protein sequencing. (1996) (47)
- Human ATP-binding cassette transporter ABCC10: expression profile and p53-dependent upregulation. (2004) (47)
- A novel RING-H2 motif protein downregulated by axotomy: its characteristic localization at the postsynaptic density of axosomatic synapse (1995) (47)
- Identification of CD34+ and CD34- leukemia-initiating cells in MLL-rearranged human acute lymphoblastic leukemia. (2015) (47)
- Efficient Regeneration of Human Vα24+ Invariant Natural Killer T Cells and Their Anti‐Tumor Activity In Vivo (2016) (47)
- Alternative pathway for the development of Vα14+ NKT cells directly from CD4–CD8– thymocytes that bypasses the CD4+CD8+ stage (2017) (46)
- Heterotrimeric G Protein βγ Subunits Stimulate FLJ00018, a Guanine Nucleotide Exchange Factor for Rac1 and Cdc42* (2008) (46)
- Structural and functional differences of SWIRM domain subtypes. (2007) (46)
- Absence of DNA polymerase theta results in decreased somatic hypermutation frequency and altered mutation patterns in Ig genes. (2006) (45)
- RAPID: Resource of Asian Primary Immunodeficiency Diseases (2008) (44)
- Cloning of a novel phosphotyrosine binding domain containing molecule, Odin, involved in signaling by receptor tyrosine kinases (2002) (44)
- The N-terminal domain of MYO18A has an ATP-insensitive actin-binding site. (2005) (44)
- CNOT3 contributes to early B cell development by controlling Igh rearrangement and p53 mRNA stability (2015) (44)
- Alanine‐scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss‐ or gain‐of‐function variants (2017) (42)
- The FLS (Fatty liver Shionogi) mouse reveals local expressions of lipocalin-2, CXCL1 and CXCL9 in the liver with non-alcoholic steatohepatitis (2013) (42)
- Naturally occurring regulatory dendritic cells regulate murine cutaneous chronic graft-versus-host disease. (2009) (42)
- Infection Profile in Chronic Granulomatous Disease: a 23-Year Experience from a Tertiary Care Center in North India (2017) (42)
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis (2017) (42)
- A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation. (2017) (42)
- Hyperactivation of JAK1 tyrosine kinase induces stepwise, progressive pruritic dermatitis. (2016) (41)
- Dysregulated fatty acid metabolism in nasal polyp‐derived eosinophils from patients with chronic rhinosinusitis (2019) (40)
- Biallelic GALM pathogenic variants cause a novel type of galactosemia (2018) (39)
- A Novel Src Homology 2 Domain-containing Molecule, Src-like Adapter Protein-2 (SLAP-2), Which Negatively Regulates T Cell Receptor Signaling* (2002) (38)
- Data-Independent Acquisition Mass Spectrometry-Based Deep Proteome Analysis for Hydrophobic Proteins from Dried Blood Spots Enriched by Sodium Carbonate Precipitation. (2021) (37)
- Rapid diagnosis of FHL3 by flow cytometric detection of intraplatelet Munc13-4 protein. (2011) (36)
- Expression of protein 4.1G in Schwann cells of the peripheral nervous system (2006) (36)
- Induction of WT1-specific human CD8+ T cells from human HSCs in HLA class I Tg NOD/SCID/IL2rgKO mice. (2016) (36)
- Characterization of multiple alternative forms of heterogeneous nuclear ribonucleoprotein K by phosphate‐affinity electrophoresis (2010) (36)
- Pulse-chase experiment for the analysis of protein stability in cultured mammalian cells by covalent fluorescent labeling of fusion proteins. (2009) (36)
- Kinetic profiles of sequential gene expressions for chemokines in mice with contact hypersensitivity. (2003) (35)
- Molecular characterization of a new member of the protein 4.1 family (brain 4.1) in rat brain. (1999) (35)
- Comparison of mRNA and protein levels of four members of the protein 4.1 family: the type II brain 4.1/4.1B/KIAA0987 is the most predominant member of the protein 4.1 family in rat brain. (2000) (34)
- NetSlim: high-confidence curated signaling maps (2011) (34)
- The novel protein complex with SMARCAD1/KIAA1122 binds to the vicinity of TSS. (2008) (34)
- A Patient with CTLA-4 Haploinsufficiency Presenting Gastric Cancer (2015) (34)
- KLRG+ invariant natural killer T cells are long-lived effectors (2014) (34)
- AT‐Rich–Interactive Domain–Containing Protein 5A Functions as a Negative Regulator of Retinoic Acid Receptor–Related Orphan Nuclear Receptor γt–Induced Th17 Cell Differentiation (2014) (34)
- Correction: The Zinc Transporter SLC39A13/ZIP13 Is Required for Connective Tissue Development; Its Involvement in BMP/TGF-β Signaling Pathways (2008) (34)
- Mitochonic Acid 5 (MA-5) Facilitates ATP Synthase Oligomerization and Cell Survival in Various Mitochondrial Diseases (2017) (33)
- Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones. (2002) (33)
- Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency (2007) (32)
- Rescue of recurrent deep intronic mutation underlying cell type–dependent quantitative NEMO deficiency (2018) (32)
- RAG1 Deficiency May Present Clinically as Selective IgA Deficiency (2015) (32)
- Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome. (2010) (31)
- XXIV World Allergy Congress 2015 (2016) (31)
- Germline mutations of MEK in cardio-facio-cutaneous syndrome are sensitive to MEK and RAF inhibition: implications for therapeutic options. (2007) (31)
- Enhanced Chondrogenesis of Induced Pluripotent Stem Cells From Patients With Neonatal‐Onset Multisystem Inflammatory Disease Occurs via the Caspase 1–Independent cAMP/Protein Kinase A/CREB Pathway (2015) (31)
- Ubiquitin‐specific protease 2‐69 in macrophages potentially modulates metainflammation (2013) (31)
- A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study. (2014) (30)
- Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis (2015) (30)
- Sequence-dependent DNA separation by anion-exchange high-performance liquid chromatography. (1996) (30)
- Immunolocalization of protein 4.1B/DAL-1 during neoplastic transformation of mouse and human intestinal epithelium (2004) (30)
- Human NK cell development in hIL-7 and hIL-15 knockin NOD/SCID/IL2rgKO mice (2019) (30)
- Deficiency of the oxidative damage-specific DNA glycosylase NEIL1 leads to reduced germinal center B cell expansion. (2009) (29)
- Pancreatic-type phospholipase A2 activates prostaglandin E2 production in rat mesangial cells by receptor binding reaction. (1995) (29)
- PCDH24‐induced contact inhibition involves downregulation of β‐catenin signaling (2009) (29)
- Direct genomic sequencing of bacterial DNA: the pyruvate kinase I gene of Escherichia coli. (1989) (29)
- Purification and characterization of recombinant murine immune interferon (1986) (28)
- Identification of a New Pathway for Th1 Cell Development Induced by Cooperative Stimulation with IL-4 and TGF-β (2012) (28)
- A comprehensive approach for establishment of the platform to analyze functions of KIAA proteins II: public release of inaugural version of InGaP database containing gene/protein expression profiles for 127 mouse KIAA genes/proteins. (2004) (27)
- EPC1/TIP60-Mediated Histone Acetylation Facilitates Spermiogenesis in Mice (2017) (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)
- Structural and functional characterization of the NHR1 domain of the Drosophila neuralized E3 ligase in the notch signaling pathway. (2009) (27)
- Mast cells play role in wound healing through the ZnT2/GPR39/IL-6 axis (2019) (27)
- Genetic and transcriptional landscape of plasma cells in POEMS syndrome (2019) (27)
- ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era. (2020) (27)
- A gene‐targeting approach for functional characterization of KIAA genes encoding extremely large proteins (2006) (27)
- Erratum: Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells (2014) (27)
- Dynamic and coordinated expression profile of dbl-family guanine nucleotide exchange factors in the developing mouse brain. (2003) (27)
- Down-regulation of CD5 expression on activated CD8+ T cells in familial hemophagocytic lymphohistiocytosis with perforin gene mutations. (2013) (26)
- Identification of Individual Cancer‐Specific Somatic Mutations for Neoantigen‐Based Immunotherapy of Lung Cancer (2016) (26)
- The RIKEN integrated database of mammals (2010) (26)
- A comprehensive approach for establishment of the platform to analyze functions of KIAA proteins: Generation and evaluation of anti‐mKIAA antibodies (2004) (26)
- Detection of spurious interruptions of protein-coding regions in cloned cDNA sequences by GeneMark analysis. (2000) (26)
- Post‐transcriptional effects of phorbol 12‐myristate 13‐acetate on transcriptome of U937 cells (2004) (26)
- Deregulated Mucosal Immune Surveillance through Gut-Associated Regulatory T Cells and PD-1+ T Cells in Human Colorectal Cancer (2018) (26)
- Immunohistochemical Study of Protein 4.1B in the Normal and W/Wv Mouse Seminiferous Epithelium (2004) (26)
- Clinical and Host Genetic Characteristics of Mendelian Susceptibility to Mycobacterial Diseases in Japan (2011) (26)
- Systemic DC Activation Modulates the Tumor Microenvironment and Shapes the Long-Lived Tumor-Specific Memory Mediated by CD8+ T Cells. (2016) (26)
- Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation (2020) (26)
- Mutation@A Glance: An Integrative Web Application for Analysing Mutations from Human Genetic Diseases (2010) (25)
- A simple and sensitive method for determining transcription initiation site: identification of two transcription initiation sites in rat group II phospholipase A2 gene. (1990) (25)
- Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency. (2015) (25)
- Characterization of size-fractionated cDNA libraries generated by the in vitro recombination-assisted method. (2002) (25)
- NK cell and IFN signatures are positive prognostic biomarkers for resectable pancreatic cancer. (2018) (25)
- Generation of Novel Traj18-Deficient Mice Lacking Vα14 Natural Killer T Cells with an Undisturbed T Cell Receptor α-Chain Repertoire (2016) (25)
- Mutations affecting thymus organogenesis in Medaka, Oryzias latipes (2004) (24)
- Anomalous behavior of human leukocyte interferon subtypes on polyacrylamide gel electrophoresis in the presence of dodecyl sulfate (1987) (24)
- Development of a molecular diagnostic test for Retinitis Pigmentosa in the Japanese population (2018) (24)
- Characterization of a human homolog (BACH1) of the mouse Bach1 gene encoding a BTB-basic leucine zipper transcription factor and its mapping to chromosome 21q22.1. (1998) (24)
- Rbm10 regulates inflammation development via alternative splicing of Dnmt3b (2017) (24)
- Genome-wide identification and characterization of transcripts translationally regulated by bacterial lipopolysaccharide in macrophage-like J774.1 cells. (2008) (24)
- Prediction of Candidate Primary Immunodeficiency Disease Genes Using a Support Vector Machine Learning Approach (2009) (24)
- Identification of novel transcribed sequences on human chromosome 22 by expressed sequence tag mapping. (2001) (23)
- PLD4 is a genetic determinant to systemic lupus erythematosus and involved in murine autoimmune phenotypes (2019) (23)
- Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function (2015) (23)
- Protein 4.1B in mouse islets of Langerhans and β-cell tumorigenesis (2003) (23)
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- SH3 domain of Hypothetical protein BAA76854.1 (2003) (0)
- 2P194 Single molecule observation of ATP hydrolysis of Myosin V (2005) (0)
- An improved cosmid vector for the nested deletion method using the bacteriophage T3 DNA packaging system. (1996) (0)
- [Structure and function of pancreatic group I phospholipase A2 receptor]. (1994) (0)
- Proteomic analysis reveals the gut microbiota as a novel regulator of host trypsin protease (2019) (0)
- Measurement of inflammatory cytokine secretion from human monocytes after inflammasome activation (2012) (0)
- Targeting critical kinases and anti-apoptotic molecules overcomes steroid resistance in MLL-rearranged leukaemia. (2021) (0)
- Hematopoietic stem cells (+iPS) (WS-010) Chairpersons: Hiromitsu Nakauchi, Haruhiko Koseki (2010) (0)
- 1P324 Kinetic analysis of LPS-activation in macrophage-like cells based on a quantification system for gene expression level in a single cell(Measurements,The 48th Annual Meeting of the Biophysical Society of Japan) (2010) (0)
- PW02-029 - Single cell fluorescent immunoassay of CINCA/NOMID (2013) (0)
- A method for amplification of nucleic acid, kit for amplification of nucleic acid, methods for detecting single nucleotide polymorphism and reagent kit for the detection of single nucleotide polymorphism (2003) (0)
- 1P293 The construction of measurement system for simultaneous observation of myosin V(9. Molecular motor (I),Poster Session,Abstract,Meeting Program of EABS & BSJ 2006) (2006) (0)
- Mosaicism of an ELANE Mutation in an Asymptomatic Mother (2019) (0)
- AB076. Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis (2017) (0)
- Infection Profile in Chronic Granulomatous Disease: a 23-Year Experience from a Tertiary Care Center in North India (2017) (0)
- Solution structure of RNP domain in Synaptojanin 2 (2003) (0)
- Title Enhanced Chondrogenesis of Induced Pluripotent Stem Cells From Patients With Neonatal-Onset Multisystem Inflammatory Disease Occurs via the Caspase 1-Independent cAMP / Protein Kinase (2019) (0)
- Multiomic technologies for analyses of inborn errors of immunity: from snapshot of the average cell to dynamic temporal picture at single-cell resolution (2021) (0)
- Clinical and Genetic Characterization of Japanese Sporadic Cases of Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis Syndrome from a Single Medical Center in Japan (2014) (0)
- A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients (2016) (0)
- X-Linked Agammaglobulinemia Associated with B-Precursor Acute Lymphoblastic Leukemia (2015) (0)
- 1PT202 Effects of the cell-cell communication on the populational variability of mRNA levels among clonal macrophages after LPS stimulation(The 50th Annual Meeting of the Biophysical Society of Japan) (2012) (0)
- Decoding Activation of ILC2 using Time-Dependent Cell-State Selection (2021) (0)
- Molecular pathological analysis on neurofilament deficient quail “quiver” (1992) (0)
- Meningoencephalitis in Children with Primary Antibody Deficiency: A Single-Center Experience From Northwest India and Review of Literature (2021) (0)
- Inhibition of immunoglobulin class-switching prevents pemphigus onset in desmoglein 3-specific B cell receptor knock-in mouse (2021) (0)
- Systems immunology (WS-086) Chairpersons: Osamu Ohara, Arup Chakraborty (2010) (0)
- Serum ‘alpha-hydroxybutyrate dehydrogenase’ in hepatobiliary and other diseases (1966) (0)
- A Complement Factor B Mutation in a Large Kindred with Atypical Hemolytic Uremic Syndrome (2014) (0)
- 015 Interleukin-27 alleviates psoriatic inflammation by suppressing Interleukin-17A production from T17 cells (2020) (0)
- Common Variable Immunodeficiency Caused by FANC Mutations (2017) (0)
- RAG1 Deficiency May Present Clinically as Selective IgA Deficiency (2015) (0)
- Allergy and the rules of cell society: An approach by using omics measurements (2020) (0)
- A complementary approach for genetic diagnosis of inborn errors of immunity using proteogenomic analysis. (2023) (0)
- Is Caused by IFIH1 Mutations (2020) (0)
- OP0120 Roles of B Cell Leukemia/Lymphoma 3 in The Development of T Follicular Helper Cells and the Pathogenesis of Rheumatoid Arthritis (2015) (0)
- P03-023 – Autoinflammatory diseases database in Japan (2013) (0)
- 2P442 RefDIC : Construction of an open-access database of the quantitative transcriptome and proteome data of immune cells(48. Bioinformatics, genomics and proteomics (II),Poster Session,Abstract,Meeting Program of EABS & BSJ 2006) (2006) (0)
- Roles of a macrophage molecule M‐mod in type 2 diabetes (2012) (0)
- FRI0208 Prediction of treatment response of tocilizumab for rheumatoid arthritis with comprehensive gene expression analysis in peripheral blood mononuclear cells (2013) (0)
- 3P329 Development of a microscopic platform for analyses of secretory protein at single-cell level using picoliter microwell array(Bioimaging,Poster Presentations) (2007) (0)
- A Patient with CTLA-4 Haploinsufficiency Presenting Gastric Cancer (2015) (0)
- 3PS031 Live-cell secretion imaging assay of the inflammatory cytokine from human monocytes(The 50th Annual Meeting of the Biophysical Society of Japan) (2012) (0)
- 1P-325 Mammalian cells sorting with thermal gelation polymer solution on a PDMS chip fabricated using one step 3D casting technique(The 46th Annual Meeting of the Biophysical Society of Japan) (2008) (0)
- Development Induced by Cooperative Identification of a New Pathway for Th1 Cell (2012) (0)
- Rapid Detection of Intracellular p47phox and p67phox by Flow Cytometry; Useful Screening Tests for Chronic Granulomatous Disease (2013) (0)
- Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiency (2020) (0)
- Reply (2014) (0)
- 1P306 Analysis of non-classical secretion of IL-1β using real-time single-cell secretion imaging(27. Bioimaging,Poster,The 52nd Annual Meeting of the Biophysical Society of Japan(BSJ2014)) (2014) (0)
- Solution structure of the first C2 domain of synaptotagmin IV from human fetal brain (KIAA1342) (2003) (0)
- Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiency. (2020) (0)
- Diagnosis of NLRP3 somatic mosaicism in CINCA/NOMID patients using next-generation sequencing (2011) (0)
- Serum carboxypeptidase—b activity in various liver diseases (1967) (0)
- Title A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis (2018) (0)
- A Novel Application of GeneMark-RC to the Analysis of Prokaryotic Genomes and Human cDNAs:Sequence Data with Statistical Deviations Are Rich in Important Biological Information (1998) (0)
- SCD2-mediated monounsaturated fatty acid metabolism regulates cGAS-STING-dependent type I IFN responses in CD4+ T cells (2021) (0)
- Solution structure of the second PDZ domain of human KIAA1526 protein (2003) (0)
- Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (2020) (0)
- The origin and minimization of band compression atrifacts on DNA sequencing. (1998) (0)
- Serum leucine aminopeptidase and its isozyme in various diseases (1966) (0)
- Membrane-Bound Human Stem Cell Factor Promotes Differentiation of Human Granulocytes and Mast Cells In Vivo, (2011) (0)
- Targeting Critical Kinases and Anti-Apoptotic Molecules Overcomes Steroid Resistance in Infant MLL-Rearranged Leukemia (2019) (0)
- Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan (2022) (0)
- EP1182: PATHOGENESIS OF PRIMARY SCLEROSING CHOLANGITIS BY BILE PROTEOME ANALYSIS USING HIGH-PRECISION MASS SPECTROMETRY (2022) (0)
- Real-time single-cell imaging of protein (2014) (0)
- Qualitative change monitoring of heterogeneous nuclear ribonucleoprotein K (2015) (0)
- Serum alpha-hydroxybutyrate dehydrogenase activity in cancer of digestive organs (1966) (0)
- An Integrated in Silico Approach to Deduce Interacting Domains of Primary Immunodeficiency Disease Causing Genes (0)
- Solution structure of SH3 domain in Rac/Cdc42 guanine nucleotide exchange factor(GEF) 6 (2004) (0)
- NEXAFS and XPS studies of VUV/O3 treated aromatic polyurea for high-speed electrophoresis microchips (2011) (0)
- Autosomal-Dominant Chronic Mucocutaneous Candidiasis with STAT1-Mutation can be Complicated with Chronic Active Hepatitis and Hypothyroidism (2012) (0)
- 3P300 Structural basis for impairment of genes in human inherited disorders(Bioinformatics: Functional genomics,The 48th Annual Meeting of the Biophysical Society of Japan) (2010) (0)
- Mina53, an IL4 repressor controlling TH2-bias (136.42) (2009) (0)
- AB017. Gene panel study for target metabolic diseases of newborn screening in Japan. (2017) (0)
- γ-Glutamyl transpeptidase isozyme pattern on patients with hepatobiliary disease (1969) (0)
- Cell therapy (DC, Treg, NKT) (WS-040) Chairpersons: Toshinori Nakayama, Jay Berzofsky (2010) (0)
- LB788 Development of a novel three-dimensional human epidermal model from plucked hair follicle-derived keratinocytes (2016) (0)
- Reply: To PMID 24591094. (2014) (0)
- HP1 deficiency results in De-Repression of Endogenous Retroviruses and Induction of Neurodegeneration via Complement (2022) (0)
- Chronic Granulomatous Disease: Two Decades of Experience From a Tertiary Care Centre in North West India (2013) (0)
- Design and application of a target capture sequencing of exons and conserved non-coding sequences for the rat (2016) (0)
- Clinical and Immunological Characterization of ICF Syndrome in Japan (2018) (0)
- [A new direction of comprehensive analysis of human cDNAs: complete sequencing of relatively long human cDNA clones which encode large proteins]. (1997) (0)
- Multiomic technologies for analyses of inborn errors of immunity: from snapshot of the average cell to dynamic temporal picture at single-cell resolution (2021) (0)
- Generating a transgenic mouse line stably expressing human MHC surface antigen from a HAC carrying multiple genomic BACs (2014) (0)
- Dendritic Cells for the Maintenance of Conventional MARCH-I-Mediated MHC II Ubiquitination Cutting Edge: Requirement of (2009) (0)
- IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation (2020) (0)
- 013 Fcγ receptor IIb-dependent blockade of immunoglobulin class-switch is crucial to prevent pemphigus onset in desmoglein 3-sepecific B cell receptor knock-in mouse (2020) (0)
- [Rapid cDNA sequencing method using the polymerase chain reaction]. (1990) (0)
- Structural characterization of pancreatic group I phospholipase A2 receptor. (1995) (0)
- Exome-wide benchmark of difficult-to-sequence regions using short-read next-generation DNA sequencing (2022) (0)
- SCD2-mediated monounsaturated fatty acid metabolism regulates cGAS-STING-dependent type I IFN in CD4+ T cells (2021) (0)
- Uterine epithelial Gp130 orchestrates hormone response and epithelial remodeling for successful embryo attachment in mice (2023) (0)
- Primary immunodeficiency (WS-051) Chairpersons: Toshio Miyawaki, Michelle Letarte (2010) (0)
- [Molecular aspects of mammalian phospholipases A2 from the standpoint of arachidonic acid release]. (1992) (0)
- Th1/Th2 (PP-015) (2010) (0)
- Real-time secretion analysis revealed correlation of IL-1β release and loss of cell membrane integrity (2013) (0)
- Quantitative live-cell imaging of secretion activity reveals dynamic immune responses (2022) (0)
- Solution structure of the SH3 domain of human olygophrein-1 like protein (KIAA0621) (2003) (0)
- Nature Butyrate Supplementary Information (2013) (0)
- STAT1 DNA-Binding Domain by a Gain-of-Function Mutation in the Chronic Mucocutaneous Candidiasis Caused (2012) (0)
- Mosaicism of an ELANE Mutation in an Asymptomatic Mother in a Familial Case of Cyclic Neutropenia (2015) (0)
- [MULTIOMICS ANALYSIS OF HUMAN EOSINOPHILS REVEALED MOLECULAR MECHANISM OF EOSINOPHILIC RHINOSINUSITIS AND SEVERE ASTHMA]. (2019) (0)
- Correction to: Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3 (2021) (0)
- Novel mutation of IL2RG gene in a Korean boy with X-linked severe combined immunodeficiency. (2013) (0)
- Analysis of the gene-deficient strain of the cyanobacterial sigma factor (1998) (0)
- Mast cells play role in wound healing through the ZnT2/GPR39/IL-6 axis (2019) (0)
- 717 Molecular characterization of transcriptional apparatus of brain-derived neurotrophic factor gene (1993) (0)
- Cancer T Cells in Human Colorectal + and PD-1 through Gut-Associated Regulatory T Cells Deregulated Mucosal Immune Surveillance (2018) (0)
- ETV6-related thrombocytopenia associated with a transient decrease in von Willebrand factor (2021) (0)
- Erratum à l'article / Erratum to the article “The Kazusa cDNA project for identification of unknown human transcripts” [C. R. Biologies 326 (2004) 959–966] (2004) (0)
- Molecular mechanism and structural basis of STAT 1 GOF Molecular Mechanism and Structural Basis of Gain of Function of STAT 1 Caused by Pathogenic R 274 Q Mutation (2017) (0)
- Differential Transcriptome of Peripheral Mononuclear Blood Cells in Pulmonary Sarcoidosis (2022) (0)
- Inhibitory effect of plasma and ascitic fluid from ehrlich ascites tumor mouse upon cytotoxic activities of fatty acids. Abstr. (1960) (0)
- Time evolution of microenvironment around cells regulated by the secretion activity and culture density of the cells (2017) (0)
- Identification and characterization of human myosin VI-interacting proteins (2003) (0)
- Iconography : Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders (2018) (0)
- Evaluation of the Suitability of Dried Saliva Spots for In-Depth Proteome Analyses for Clinical Applications. (2022) (0)
- Solution structure of WWE domain in BAB28015 (2004) (0)
- Immunodeficiency in Two Female Patients with Incontinentia Pigmenti with Heterozygous NEMO Mutation Diagnosed by LPS Unresponsiveness (2017) (0)
- Title A deletion in the intergenic region upstream of Ednrb causeshead spot in the rat strain (2018) (0)
- Role of JNK in global translation under normal growth conditions (2008) (0)
- BTNL2 germline variants may be involved in the pathogenesis of renal granuloma (2019) (0)
- Potential Functional Roles for CD26/Dipeptidyl Peptidase-4 in Mediating Responses of Human Lung Microvascular Endothelial Cells (2022) (0)
- ADA‐SCID with ‘WAZA‐ARI’ mutations that synergistically abolished ADA protein stability (2011) (0)
- Proteome analysis of cyanobacterium: Synechocystis sp. strain PCC6803. (1998) (0)
- 2P332 Quantitative measurement of protein secretion from a single cell in real time(The 48th Annual Meeting of the Biophysical Society of Japan) (2010) (0)
- S3e1-1 A Perspective of Immunogenomics from A Biophysical Viewpoint(S3-e1: "Dynamic Features in Immune System",Symposia,Abstract,Meeting Program of EABS & BSJ 2006) (2006) (0)
- PDMS-CYTOP hybrid structure microwell array chip for total internal reflection fluorescence microscopy (2013) (0)
- Deficient Mice Zfp 35 Allergen-Induced Airway Inflammation in Enhanced Th 2 Cell Differentiation and Ohara (2009) (0)
- PCGF1-PRC1 links chromatin repression with DNA replication during hematopoietic cell lineage commitment (2022) (0)
- Fanctional analysis of Myo18A (2003) (0)
- Efficient regeneration of Human Vα24(+) invariant NKT cells and their anti-tumor activity in vivo. (2016) (0)
- A Novel Protein Array Using Microbeads Aligned In A Microfluidic Chip (2009) (0)
- Uterine epithelial Gp130 orchestrate embryo implantation via increased Snail family transcriptional repressor 1 and attenuated estrogen response in mice. (2021) (0)
- In-depth proteomic analysis of juvenile dermatomyositis serum reveals protein expression associated with muscle-specific autoantibodies. (2023) (0)
- Abstract 3965: Killing and IFN-γ-dependent G1 cell cycle arrest are the mechanisms of regulation of tumor growth by cytotoxic T lymphocytes. (2013) (0)
- 3P-054 A novel protein array using microbeads aligned in a microfluidic chip(The 46th Annual Meeting of the Biophysical Society of Japan) (2008) (0)
- Identification of Differentially Expressed Proteins in the Serum for Systemic Juvenile Idiopathic Arthritis Using Next-generation Proteomics (2021) (0)
- 2P278 Development of the molecular interaction analysis system using microbeads array (2004) (0)
- A deletion in the intergenic region upstream of Ednrb causes head spot in the rat strain KFRS4/Kyo (2017) (0)
- 1P333 Protein expression profiling for single-cell using microbead array technology (2005) (0)
- Erratum: Mina, an I14 repressor, controls T helper type 2 bias (Nature Immunology 10.1038/ni.1747) (2009) (0)
- Genomic Analysis of Diffuse Large B Cell Lymphoma in a Japanese Cohort Using Targeted DNA Sequencing (2020) (0)
- Desmoglein-specific B-cell-targeted single-cell analysis revealing unique gene regulation in pemphigus patients. (2023) (0)
- Whole-exome sequencing in unresectable pancreatic cancer patients with long-term survival. (2019) (0)
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What Schools Are Affiliated With Osamu Ohara?
Osamu Ohara is affiliated with the following schools:
