「An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome」の関連論文
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Molecular Mechanism of Quinclorac Resistance in Multiple-Herbicide Resistant Echinochloa phyllopogon
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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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Morphea in a Crohn's disease patient undergoing ustekinumab treatment
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Impairment of DYRK2 by DNMT1-mediated transcription augments carcinogenesis in human colorectal cancer
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Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ
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Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ
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RUNX1 rearrangement in mature B-cell acute lymphoblastic leukemia with non-L3 morphology
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Latest classification of ependymoma in the molecular era and advances in its treatment: a review
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Studies on DNA methylation changes in canine malignant melanoma [an abstract of entire text]
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Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7
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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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Usefulness of interleukin-18 as a diagnostic biomarker to differentiate adult-onset Still’s disease with/without macrophage activation syndrome from other secondary hemophagocytic lymphohistiocytosis in adults
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A pipeline for complete characterization of complex germline rearrangements from long DNA reads
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Investigation of the current situation regarding diagnosis and treatment of Alport syndrome in Asian countries: results of survey of the Asian Paediatric Nephrology association (AsPNA) tubular and inherited working group
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JNK and Yorkie drive tumor malignancy by inducing L-amino acid transporter 1 in Drosophila
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Chronic Active Epstein–Barr Virus Infection Indistinguishable from Autoimmune Hepatitis: A Case Report
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Elucidation of cause and natural feature of cheating rhizobia, and host defense mechanism against them
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Steroid profiling for assessing adrenal hepatic syndrome in canine hepatocellular carcinoma
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A Case Report of an Accessory and Cavitated Uterine Mass Treated with Total Laparoscopic Hysterectomy
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Natural genetic transformation mediates MRSA emergence
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Molecular analysis of drug resistance associating gene mutations in Mycobacterium tuberculosis clinical isolates in Nepal [an abstract of entire text]
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Neonatal Pseudohypoaldosteronism Type-1 in Japan
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Real-life progression of the use of a genetic panel in to diagnose neonatal cholestasis
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PML-RARαはMED1との結合を介して全トランス型レチノイン酸依存性の転写活性化を誘導する
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A RUNX-targeted gene switch-off approach modulates the BIRC5/PIF1-p21 pathway and reduces glioblastoma growth in mice
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FGF5 and EPAS1 gene polymorphisms are associated with high-altitude adaptation in Nepalese goat breeds
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Generalized Pustular Psoriasis: Clinical Management and Update on Autoinflammatory Aspects
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Risk factors for cisplatin-induced acute kidney injury: A pilot study on the usefulness of genetic variants for predicting nephrotoxicity in clinical practice
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Genetic and chemical inhibition of IRF5 suppresses pre-existing mouse lupus-like disease
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Discovery and biological significance of the sialate:O-sulfotransferases in vertebrates
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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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Tumour-immune microenvironment in duodenal-type follicular lymphoma
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Analysis of immunologic comorbidities in ulcerative colitis patients: a tool to prevent exacerbations in ulcerative colitis cases
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Malfunctioning CD106-positive, short-term hematopoietic stem cells trigger diabetic neuropathy in mice by cell fusion.
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Differentiation of hypertrophic chondrocytes from human iPSCs for the in vitro modeling of chondrodysplasias
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Continued growth of locally aggressive fibrous dysplasia of 22 years duration after reaching adulthood: a case report
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Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia
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Real-world application of next-generation sequencing-based test for surgically resectable colorectal cancer in clinical practice (本文)
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Networking and Specificity-Changing DNA Methyltransferases in Helicobacter pylori.
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Horizontally Transferred DNA in the Genome of the Fungus Pyricularia oryzae is Associated With Repressive Histone Modifications
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Significance of PD-L1 expression in carbon-ion radiotherapy for uterine cervical adeno/adenosquamous carcinoma (本文)
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Study of the Effects of Inhibition of Epigenetic Regulators on the Proliferation of Hematological Malignant Tumor Cells
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Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers
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The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage Behcet’s disease
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Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants
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Temporal arteritis with focal pachymeningitis: a deceptive association
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Clinical characteristics of Corynebacterium simulans
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Hes1 is essential in proliferating ductal cell-mediated development of intrahepatic cholangiocarcinoma
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iPSC-derived type IV collagen α5-expressing kidney organoids model Alport syndrome
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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