「Eighteen-years follow-up of congenital hypothyroidism by TSHR gene p.Arg109Gln and p.Arg450His variants」の関連論文
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Manganese transport in mammals by zinc transporter family proteins, ZNT and ZIP
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Malfunctioning CD106-positive, short-term hematopoietic stem cells trigger diabetic neuropathy in mice by cell fusion.
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Antioxidants and Therapeutic Targets in Ovarian Clear Cell Carcinoma.
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Identification and analysis of mechanisms that bypass the essentiality of Polo, a mitotic regulator
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Identification of anti-citrullinated osteopontin antibodies and increased inflammatory response by enhancement of osteopontin binding to fibroblast-like synoviocytes in rheumatoid arthritis
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Functional properties of iminosugar 1-deoxynojirimycin: main focus on its insulin-sensitizing effect for maintenance of healthy metabolic and brain functions
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Primary functional brain connections associated with melancholic major depressive disorder and modulation by antidepressants
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Primary functional brain connections associated with melancholic major depressive disorder and modulation by antidepressants
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Combination of target site mutation and associated CYPs confers high-level resistance to pyridaben in Tetranychus urticae
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Molecular characterization of Mycobacterium avium clinical isolates from Japan and development of diagnostic tools [an abstract of entire text]
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Case report : Vascular graft infection due to Aspergillus species presenting with recurrent vascular occlusion
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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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Survival Analyses Based on Tumor Microenvironment Profile in Endometrial Carcinoma
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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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Population genetics of variants in infectious diseases and its application to the prediction of variant replacement
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TNFRSF11A-Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum
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Clinical characteristics of Corynebacterium simulans
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In silico study of RNA-seq and H3 Trimethylation ChIP-seq analysis in combination with laser-microdissection on human lung cancer cells
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Gut bacteria identified in colorectal cancer patients promote tumourigenesis via butyrate secretion
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Association Between Tooth Loss and Longitudinal Changes in B-Type Natriuretic Peptide Over 5 Years in Postmenopausal Women: The Nagahama Study
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Suppression of malignant rhabdoid tumors through Chb-M′-mediated RUNX1 inhibition
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PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan
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Successful diagnosis and treatment of pheochromocytoma during severe coronavirus disease 2019 (COVID-19): a case report
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Current Overview of Osteogenesis Imperfecta.
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Natural genetic transformation mediates MRSA emergence
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GSK3 inhibitor enhances gemtuzumab ozogamicin-induced apoptosis in primary human leukemia cells by overcoming multiple mechanisms of resistance
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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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Mitochondrial Dysfunction in Pulmonary Hypertension
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De Novo T790M Mutation in an L858R Epidermal Growth Factor Receptor Mutant-Associated Lung Adenocarcinoma
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Chronic Active Epstein–Barr Virus Infection Indistinguishable from Autoimmune Hepatitis: A Case Report
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HER2 G776S mutation promotes oncogenic potential in colorectal cancer cells when accompanied by loss of APC function
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Zscan5b deficiency impairs DNA damage response and causes chromosomal aberrations during mitosis (本文)
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Prognostic implications of preoperative versus postoperative circulating tumor DNA in surgically resected lung cancer patients: a pilot study
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Tumor Shrinkage by Metyrapone in Cushing Disease Exhibiting Glucocorticoid-Induced Positive Feedback
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Analysis of aging-related epigenetic modifications in murine male germline cells
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Improvement in semen parameters by switching steroids in a male congenital adrenal hyperplasia patient with severe oligozoospermia
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Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
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Real-life progression of the use of a genetic panel in to diagnose neonatal cholestasis
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Myh9 R702C is associated with erythroid abnormality with splenomegaly in mice
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Development of Remote Inflammation through Interneuron Network in the Spinal Cord
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Nicotinamide Phosphoribosyltransferase (Nampt)/Nicotinamide Adenine Dinucleotide (NAD)Axis Suppresses Atrial Fibrillation by Modulating the Calcium Handling Pathway
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Suppression of Systemic Lupus Erythematosus in NZBWF1 mice infected with Hymenolepis microstoma
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Study on biological clocks that underly various diseases
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Fish bone migration after pancreaticoduodenectomy: Incidence and treatment options
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Editorial: Advances in Human Immune System Mouse Models for Studying Human Hematopoiesis and Cancer Immunotherapy
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Identification and characterization of substrates crosslinked by transglutaminases in liver and kidney fibrosis
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Case report of a ventricular fibrillation storm with a cardiac conduction disorder and HCN4 variant 18 years after ablation of atrial flutter
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Elderly patient with 5q spinal muscular atrophy type 4 markedly improved by Nusinersen
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Studies on Peripheral Blood mMDSC Based-Biomarker Exploration and a Novel Therapeutic Agent for Cancer Immunotherapy
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Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia