「Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma」の関連論文
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Genetic and Epigenetic Pathogenesis of Acromegaly
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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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St8sia1-deficiency in mice alters tumor environments of gliomas, leading to reduced disease severity
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Identification of novel mutations and reassignment of archival xeroderma pigmentosum group C cell strains from Japanese patients
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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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Efficacious Combination Drug Treatment for Colorectal Cancer that Overcomes Resistance to KRAS G12C Inhibitors
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Mineralocorticoid and glucocorticoid receptors and 11beta-hydroxysteroid dehydrogenases in human breast lesions
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Partial Epithelial-Mesenchymal Transition Was Observed Under p63 Expression in Acquired Middle Ear Cholesteatoma and Congenital Cholesteatoma.
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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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Malfunctioning CD106-positive, short-term hematopoietic stem cells trigger diabetic neuropathy in mice by cell fusion.
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Genotype-phenotype mapping of a patient-derived lung cancer organoid biobank identifies NKX2-1-defined Wnt dependency in lung adenocarcinoma (本文)
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Cryptic insertion of CBFB into MYH11 leading to a type D fusion in acute myeloid leukemia with normal karyotype
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The role of H3K27 demethylation in retinal development
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Lionheart LincRNA alleviates cardiac systolic dysfunction under pressure overload
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Relationship between gene mutations and clinicopathological features in nonampullary duodenal epithelial tumors
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Identification and monitoring of mutations in circulating cell-free tumor DNA in hepatocellular carcinoma treated with lenvatinib
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Identification and monitoring of mutations in circulating cell-free tumor DNA in hepatocellular carcinoma treated with lenvatinib
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Circulating microRNA/isomiRs as novel biomarkers of esophageal squamous cell carcinoma
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Circulating microRNA/isomiRs as novel biomarkers of esophageal squamous cell carcinoma
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Hes1 is essential in proliferating ductal cell-mediated development of intrahepatic cholangiocarcinoma
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GPR64, Screened from Ewing Sarcoma Cells, Is a Potential Target for Antibody-Based Therapy for Various Sarcomas
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BMP and activin membrane-bound inhibitor (BAMBI) regulates mesothelioma cell proliferation and clinical outcome
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BMP and activin membrane-bound inhibitor (BAMBI) regulates mesothelioma cell proliferation and clinical outcome
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Involvement of Transcription Factor 21 in the Pathogenesis of Fibrosis in Endometriosis
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Tumour-immune microenvironment in duodenal-type follicular lymphoma
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Mutation burden-orthogonal tumor genomic subtypes delineate responses to immune checkpoint therapy
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Simple, Frequent Indicator for Personal Identification-Postmortem and Antemortem Abdominal Computed Tomography Findings of a Charred Body.
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RUNX1 rearrangement in mature B-cell acute lymphoblastic leukemia with non-L3 morphology
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Combined Hypophysitis and Type 1 Diabetes Mellitus Related to Immune Checkpoint Inhibitors
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MicroRNA-124a Inhibits Endoderm Lineage Commitment in Mouse Embryonic Stem Cells
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Distinctive roles of syntaxin binding protein 4 and its action target, TP63, in lung squamous cell carcinoma: a theranostic study for the precision medicine
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Single-cell transcriptome atlas of Drosophila gastrula 2.0
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A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease
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CEBPγ facilitates lamellipodia formation and cancer cell migration through CERS6 upregulation
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Utility of plasma circulating tumor DNA and tumor DNA profiles in head and neck squamous cell carcinoma
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Long-Read-Resolved, Ecosystem-Wide Exploration of Nucleotide and Structural Microdiversity of Lake Bacterioplankton Genomes
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Combination of RERG and ZNF671 methylation rates in circulating cell-free DNA: A novel biomarker for screening of nasopharyngeal carcinoma
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ミスマッチ修復機能欠損のtype2子宮体癌における免疫チェックポイント阻害剤の有用性の検討
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Studies on multifunctional genome elements functioning in mouse spermatogenesis [an abstract of entire text]
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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]
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Quality assessment tests for tumorigenicity of human iPS cell-derived cartilage
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Microbiota of Severe Early Childhood Caries (S-ECC): Their Preponderance,Site-specificity,and Clinical Control with Silver Diamine Fluoride
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p53 expression in repair/reactive renal tubular cells: A potential pitfall leading to a false-positive diagnosis of urine cytology
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Multi-stain to Multi-stain Transformation of High-Resolution Renal Biopsy Images by Generative Adversarial Networks Highlights Glomerular and Interstitial Abnormalities with a Virtual Single-section View
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Stanniocalcin-1 mRNA expression in soft-tissue tumors
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Harnessing Deep Learning to Analyze Cryptic Morphological Variability of Marchantia polymorpha
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Genome-scale CRISPR/Cas9 screening for gemcitabine modulators in pancreatic cancer
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SPC18 expression is an independent prognostic indicator of patients with esophageal squamous cell carcinoma
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SPC18 expression is an independent prognostic indicator of patients with esophageal squamous cell carcinoma