「EVI1 and GATA2 misexpression induced by inv(3)(q21q26) contribute to megakaryocyte-lineage skewing and leukemogenesis.」の関連論文
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Identification of novel genes associated with dysregulation of B cells in patients with primary Sjögren's syndrome (本文)
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Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias.
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A Single RET Mutation in Hirschsprung Disease Induces Intestinal Aganglionosis Via a Dominant-Negative Mechanism
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Epigenomic dysregulation in AFP-producing gastric cancer
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Development of TCR-T cell therapy targeting mismatched HLA-DPB1 for relapsed leukemia after allogeneic transplantation
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T cell receptor-engineered T cells derived from target human leukocyte antigen-DPB1-specific T cell can be a potential tool for therapy against leukemia relapse following allogeneic hematopoietic cell transplantation
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Genomic stability of mouse spermatogonial stem cells in vitro
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The landscape of genetic aberrations in myxofibrosarcoma
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Neural Isoforms of Agrin Are Generated by Reduced PTBP1−RNA Interaction Network Spanning the Neuron−Specific Splicing Regions in AGRN
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An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome
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Hippo-TAZ signaling is the master regulator of the onset of triple-negative basal-like breast cancers
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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
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Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2‐mutation carriers
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Genome-wide association studies on hepatocellular carcinoma after eradication of hepatitis C virus in Japanese and on chronic hepatitis B in Thai
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Studies on multifunctional genome elements functioning in mouse spermatogenesis [an abstract of entire text]
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TEAD1 trapping by the Q353R–Lamin A/C causes dilated cardiomyopathy
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Incontinentia pigmenti in a female infant with somatic mosaicism due to the IKBKG variant
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Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing
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The pluripotent stem cell-specific transcript ESRG is dispensable for human pluripotency
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ILF2 enhances the DNA cytosine deaminase activity of tumor mutator APOBEC3B in multiple myeloma cells
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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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Recapitulation of pro-inflammatory signature of monocytes with ACVR1A mutation using FOP patient-derived iPSCs
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CEBPγ facilitates lamellipodia formation and cancer cell migration through CERS6 upregulation
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The role of H3K27 demethylation in retinal development
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胎仔ライディッヒ前駆細胞の解析
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Autism-associated mutation in Hevin/Sparcl1 induces endoplasmic reticulum stress through structural instability
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Three-dimensional human placenta-like bud synthesized from induced pluripotent stem cells
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Gene Editing in Murine Hematopoietic Stem Cells Using a Novel Ex Vivo Expansion System
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Beta-1,4-galactosyltransferase-3 deficiency suppresses the growth of immunogenic tumors in mice
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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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Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
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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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Wilson’s disease model establishment from human induced pluripotent stem cells
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Osteogenic cocktail induces calcifications in human breast cancer cell line via placental alkaline phosphatase expression.
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Identification of CXCL12-abundant reticular cells in human adult bone marrow
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UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
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Post-induction MRD by FCM and GATA1-PCR are significant prognostic factors for myeloid leukemia of Down syndrome.
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Patient-derived ovarian cancer organoids capture the genomic profiles of primary tumours applicable for drug sensitivity and resistance testing (本文)
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Re-generation of cytotoxic γδT cells with distinctive signatures from human γδT-derived iPSCs
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Analyses of genetic and retinal lesions in Ccdc85c knockout rats: a rat model of genetic hydrocephalus
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Comprehensive genomics in androgen receptor-dependent castration-resistant prostate cancer identifies an adaptation pathway mediated by opioid receptor kappa 1
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Inhibition of heat shock protein 90 destabilizes receptor tyrosine kinase ROR1 in lung adenocarcinoma
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DDIT4 Facilitates Lymph Node Metastasis via the Activation of NF-κB Pathway and Epithelial-Mesenchymal Transition
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Disrupted Cav1.2 Selectivity Causes Overlapping Long QT and Brugada Syndrome Phenotypes in CACNA1C-E1115K iPS Cell Model
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Comprehensive analysis of TCR function using a novel system reveals the multiple unconventional tumor-reactive T cells in breast cancer-infiltrating lymphocytes
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Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous CPLANE1 Variant
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Phosphorylation of the anaphase promoting complex activator FZR1/CDH1 is required for meiosis II entry in mouse male germ cell (本文)
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β-Cell senescence in the pathogenesis of type 2 diabetes.
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St8sia1-deficiency in mice alters tumor environments of gliomas, leading to reduced disease severity