「Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population」の関連論文
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Clinical and genetic features of cystic fibrosis in Japan
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Combination of tumor necrosis factor-α and epidermal growth factor induces the adrenergic-to-mesenchymal transdifferentiation in SH-SY5Y neuroblastoma cells
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Identifying Potentially Beneficial Genetic Mutations Associated with Monophyletic Selective Sweep and a Proof-of-Concept Study with Viral Genetic Data
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Inventory and Evolution of Mitochondrion-localized Family A DNA Polymerases in Euglenozoa
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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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De Novo T790M Mutation in an L858R Epidermal Growth Factor Receptor Mutant-Associated Lung Adenocarcinoma
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Elucidation of cause and natural feature of cheating rhizobia, and host defense mechanism against them
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Relationship between gene mutations and clinicopathological features in nonampullary duodenal epithelial tumors
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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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A novel urinary microRNA biomarker panel for detecting gastric cancer
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Biosynthetic study of miuraenamide A, an antifungal antibiotic of a slightly halophilic myxobacterium
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Next Generation Sequencing-Based Transcriptome Predicts Bevacizumab Efficacy in Combination with Temozolomide in Glioblastoma
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Thiopurine Use During Pregnancy Has Deleterious Effects on Offspring in Nudt15 R138C Knock-In Mice.
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Regional spread of three distinct genotypes of Mycoplasma pneumoniae and different timing of macrolide-resistant strain appearance among genotypes between 2011 and 2013 in Yamagata, Japan
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Functional and genomic characterization of patient-derived xenograft model to study adaptation to mTORC1 inhibitor in clear cell renal cell carcinoma
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Improvement of mouse genome editing protocol and the application:investigation of the physiological roles of glycine receptor alpha 4 subunit.
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Genetic and Physiological Characterization of Tomato F-box Gene HAWAIIAN SKIRT Mutants
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Genetic and chemical inhibition of IRF5 suppresses pre-existing mouse lupus-like disease
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Screening method for congenital dysfibrinogenemia using clot waveform analysis with the Clauss method
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A model for estimating the brainstem volume in normal healthy individuals and its application to diffuse axonal injury patients
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T2-FLAIR mismatch sign in dysembryoplastic neuroepithelial tumor
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T2-FLAIR mismatch sign in dysembryoplastic neuroepithelial tumor
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Large-scale discovery of male reproductive tract-specific genes through analysis of RNA-seq datasets
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6. Life Science and Medical Science
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A novel structural maintenance of chromosomes (SMC)-related protein family specific to Archaea
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Molecular epidemiology of Enterobacter cloacae complex isolates with reduced carbapenem susceptibility recovered by blood culture
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Studies on epidemiology, development of chemotherapy and genetic modification of piroplasmosis
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Comprehensive analysis of full-length transcripts reveals novel splicing abnormalities and oncogenic transcripts in liver cancer
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A pipeline for complete characterization of complex germline rearrangements from long DNA reads
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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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Single-cell transcriptomics of human cholesteatoma identifies an activin A-producing osteoclastogenic fibroblast subset inducing bone destruction
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Immunohistochemically Detected Expression of ATRX, TSC2, and PTEN Predicts Clinical Outcomes in Patients With Grade 1 and 2 Pancreatic Neuroendocrine Tumors
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Tsga8 is required for spermatid morphogenesis and male fertility in mice
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The transcription factor ZFP64 facilitates climbing-fiber synapse elimination along signaling pathway mediated by P/Q-type voltage-dependent Ca2+ channel in the developing cerebellum
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Clinicopathological and molecular features of responders to nivolumab for patients with advanced gastric cancer
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Networking and Specificity-Changing DNA Methyltransferases in Helicobacter pylori.
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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Clinical Significance of Serum Galectin-9 and Soluble CD155 Levels in Patients with Systemic Sclerosis
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Population genetics of variants in infectious diseases and its application to the prediction of variant replacement
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Characterization of an active LINE-1 in the naked mole-rat genome.
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Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma
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Inherent genomic properties underlie the epigenomic heterogeneity of human induced pluripotent stem cells
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Paraneoplastic Pemphigus Mimicking Toxic Epidermal Necrolysis Associated with Follicular Lymphoma: Possible Pathological Role of CD8 T Cells.
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The role of GPNMB ectodomain in breast cancer development
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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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Genetic and Epigenetic Pathogenesis of Acromegaly
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Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells
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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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CEBPγ facilitates lamellipodia formation and cancer cell migration through CERS6 upregulation