「Cryptic insertion of CBFB into MYH11 leading to a type D fusion in acute myeloid leukemia with normal karyotype」の関連論文
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Usefulness of functional splicing analysis to confirm precise disease pathogenesis in Diamond-Blackfan anemia caused by intronic variants in RPS19
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Project 1 Analyzing Tumor Microenvironment and Exploiting its Characteristics in Search of Optimizing Cancer Therapy Including Neutron Capture Therapy (R2P1)
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Human metaphase chromosome consists of randomly arranged chromatin fibres with up to 30-nm diameter
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6. Life Science and Medical Science
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Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
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Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
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Circulatory C-type natriuretic peptide reduces mucopolysaccharidosis-associated craniofacial hypoplasia in vivo
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Sarcomatoid mesothelioma diagnosed in a patient with mesothelioma in situ: a case report on morphologic differences after 9-month interval with details analysis of cytology in early-stage mesothelioma
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TDO2 Overexpression Is Associated with Cancer Stem Cells and Poor Prognosis in Esophageal Squamous Cell Carcinoma
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TDO2 Overexpression Is Associated with Cancer Stem Cells and Poor Prognosis in Esophageal Squamous Cell Carcinoma
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Acyl-CoA synthetase 6 regulates long-chain polyunsaturated fatty acid composition of membrane phospholipids in spermatids and supports normal spermatogenic processes in mice
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MYCL promotes iPSC-like colony formation via MYC Box 0 and 2 domains
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Increased expression of programmed cell death ligand 1 and galectin 9 in transplant recipients who achieved tolerance after immunosuppression withdrawal
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Compromised anti-tumor–immune features of myeloid cell components in chronic myeloid leukemia patients
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精巣高発現タンパク質の精子形成における機能と応用
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A systemic form chronic active Epstein-Barr virus infection diagnosed from erythema nodosum-like skin lesions
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Prophylactic treatment of rapamycin ameliorates naturally developing and episode -induced heterotopic ossification in mice expressing human mutant ACVR1
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Promising SARS-CoV-2 main protease inhibitor ligand-binding modes evaluated using LB-PaCS-MD/FMO
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Thiopurine Use During Pregnancy Has Deleterious Effects on Offspring in Nudt15 R138C Knock-In Mice.
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St8sia1-deficiency in mice alters tumor environments of gliomas, leading to reduced disease severity
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CEBPγ facilitates lamellipodia formation and cancer cell migration through CERS6 upregulation
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Myelin protein zero (P0)- and Wnt1-Cre marked muscle resident neural crest-derived mesenchymal progenitor cells give rise to heterotopic ossification in mouse models
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MafB is important for pancreatic β-cell maintenance under a MafA deficient condition
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Establishment and Application of Anti-CD20 Monoclonal Antibodies using the Cell-based Immunization and Screening Method for the Detection of B Cells
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Immunobiochemical, molecular biological, and reverse genetical studies on vitellogenin receptor candidates in medaka, Oryzias latipes [an abstract of entire text]
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A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia
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Pathogenic mutation of TDP-43 impairs RNA processing in a cell type-specific manner : implications for the pathogenesis of ALS/FTLD (本文)
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高純度間葉系幹細胞は機能的ミトコンドリア投入に優れている
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Self-assembling small-molecule adjuvants as antigen nano-carriers
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Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population
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Comparative Plastid Genomics of Green-Colored Dinoflagellates Unveils Parallel Genome Compaction and RNA Editing
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Molecular genetic study of the FMR1 CGG repeat configurations in the Japanese population and patients with Fragile X-Associated Tremor/Ataxia Syndrome
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Clinical Significance of Serum Galectin-9 and Soluble CD155 Levels in Patients with Systemic Sclerosis
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Prenatal diagnosis of severe mitochondrial disease caused by nuclear gene defects: a study in Japan
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Glycan profile of signet ring cell gastric cancer and potential applicability of lectin drug conjugate therapy
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胎仔ライディッヒ前駆細胞の解析
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Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia
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Conserved Double Translation Initiation Site for Δ160p53 Protein Hints at Isoform’s Key Role in Mammalian Physiology
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大気圧酸素プラズマ照射によるT細胞の活性制御に関する研究
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New Horizons in Electromagnetics in Medicine and Biology
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Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous CPLANE1 Variant
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Pharmacogenomic study of anti-tuberculosis drugs-induced liver injury in Thais
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Confluent and reticulated papillomatosis with eruptions on the trunk and extremities
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Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers
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MDM4 as a prognostic factor for patients with gastric cancer with low expression of p53:immunohistochemical study of p53, MDM2, and MDM4
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Re-generation of cytotoxic γδT cells with distinctive signatures from human γδT-derived iPSCs
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MAGI-2 orchestrates the localization of backbone proteins in the slit diaphragm of podocytes
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Autoantibodies against the plakin family proteins as a novel marker for chronic graft-versus-host disease of the lung
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The landscape of genetic aberrations in myxofibrosarcoma
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Research for elucidation of immune evasion mechanisms and development of a novel immunotherapy for cancer in dogs [an abstract of entire text]