「FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients」の関連論文
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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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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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Hes1 is essential in proliferating ductal cell-mediated development of intrahepatic cholangiocarcinoma
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Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
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Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
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Fatal Dieulafoy lesion with IgG4-related disease: An autopsy case report
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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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Studies on the development of novel non-alcoholic steatohepatitis (NASH) models using rats
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Paraneoplastic isolated adrenocorticotropic hormone deficiency revealed after immune checkpoint inhibitors therapy: new insights into anti-corticotroph antibody
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Visceral Obesity and Lipid Profiles in Chinese Adults with Normal and High Body Mass Index
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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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Potential roles of gastroesophageal reflux in patients with superficial esophageal squamous cell carcinoma without major causative risk factors
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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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FGF5 and EPAS1 gene polymorphisms are associated with high-altitude adaptation in Nepalese goat breeds
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MicroRNA profiling in adults with high-functioning autism spectrum disorder
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The Natural History of Spontaneously Occurred Endometriosis in Cynomolgus Monkeys by Monthly Follow-Up Laparoscopy for Two Years.
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Minor hallucinations in isolated rapid eye movement sleep behavior disorder indicative of early phenoconversion : A preliminary study.
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Genetic and chemical inhibition of IRF5 suppresses pre-existing mouse lupus-like disease
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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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Cooperative participation of epigenomic and genomic alterations in the clinicopathological diversity of gastric adenocarcinomas : significance of cell adhesion and epithelial–mesenchymal transition-related signaling pathways (本文)
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Chemosensitivity of Patient-Derived Cancer Stem Cells Identifies Colorectal Cancer Patients with Potential Benefit from FGFR Inhibitor Therapy
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Confluent and reticulated papillomatosis with eruptions on the trunk and extremities
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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 Biomarker for Benign Adult Familial Myoclonus Epilepsy: High-Frequency Activities in Giant Somatosensory Evoked Potentials
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Exploring Hidden Atrial Fibrillation in Patients with Type 2 Diabetes Mellitus Admitted to Shinshu University Hospital
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Hyperspectral and multispectral image processing for gross-level tumor detection in skin lesions: a systematic review
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思春期早発症の9歳女児に急性発症した上腸間膜動脈症候群の1例
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Comment to our article; Effects of varicocelectomy on testis volume and semen parameters in adolescents: a randomized prospective study
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Associations between parental bonding during childhood and functional recovery in patients with schizophrenia
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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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Completely Ossified Bilateral Stylohyoid Ligaments in a Patient Undergoing Hemodialysis.
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Clinical characteristics and risk factors for mortality in patients with community-acquired staphylococcal pneumonia
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Prevalence and Prognosis of Familial Hypercholesterolemia in Patients With Acute Coronary Syndrome in Mie Prefecture, Japan ― Report From Mie ACS Registry ―
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Endoscopy-focused primary, secondary and tertiary prevention of colorectal cancer
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Studies on Peripheral Blood mMDSC Based-Biomarker Exploration and a Novel Therapeutic Agent for Cancer Immunotherapy
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Cutaneous T-cell-attracting chemokine as a novel biomarker for predicting prognosis of idiopathic pulmonary fibrosis: a prospective observational study
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Malfunctioning CD106-positive, short-term hematopoietic stem cells trigger diabetic neuropathy in mice by cell fusion.
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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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Clinical characteristics of Corynebacterium simulans
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Occurrence of cholangiocarcinoma, three years after negative seroconversion of anti-TIF1γ antibody, in a dermatomyositis patient
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Large-scale discovery of male reproductive tract-specific genes through analysis of RNA-seq datasets
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Alterations in DNA methylation rates of brain-derived neurotrophic factor in patients with schizophrenia.
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Alterations in DNA methylation rates of brain-derived neurotrophic factor in patients with schizophrenia.
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Suppression of Systemic Lupus Erythematosus in NZBWF1 mice infected with Hymenolepis microstoma
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Genetic basis of female-limited polymorphism of the damselfly Ischnura senegalensis
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Trp53 Mutation in Keratin 5 (Krt5)-Expressing Basal Cells Facilitates the Development of Basal Squamous-Like Invasive Bladder Cancer in the Chemical Carcinogenesis of Mouse Bladder
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Serum neurofilament light chain in chronic inflammatory demyelinating polyneuropathy