「Genotype-specific cortisol production associated with Cushing's syndrome adenoma with PRKACA mutations」の関連論文
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Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes
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Time‐resolved 3D cine phase‐contrast magnetic resonance imaging (4D‐flow MRI) can quantitatively assess portosystemic shunt severity and confirm normalization of portal flow after embolization of large portosystemic shunts
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Biclonal Gammopathy as a Misleading Indicator to Diagnose POEMS Syndrome: An Autopsy Case Report and a Review of the Literature
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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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Studies on Age-related Changes of Lipid Metabolisms
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Systemic therapy for salivary gland malignancy: current status and future perspectives
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Prognostic stratification for IDH-wild-type lower-grade astrocytoma by Sanger sequencing and copy-number alteration analysis with MLPA
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Regulation of interstitial cell behaviors during branching morphogenesis of medusa tentacles in the jellyfish, Cladonema pacificum
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Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia
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Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice
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Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report
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Lusutrombopag effectively promotes the growth and differentiation of megakaryocytic cells from patients with myelodysplastic syndrome
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A systemic form chronic active Epstein-Barr virus infection diagnosed from erythema nodosum-like skin lesions
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Chronic Active Epstein–Barr Virus Infection Indistinguishable from Autoimmune Hepatitis: A Case Report
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Gestational psittacosis: A case report and literature review.
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Adaptive radiation of invasive asexual Daphnia pulex in Japan: ecological implications of clonal variations in phenotypic traits and plasticity
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Individual differences of neuronal groups in the basal forebrain
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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Elderly patient with 5q spinal muscular atrophy type 4 markedly improved by Nusinersen
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Labyrinthine calcification in ears with otitis media and antineutrophil cytoplasmic antibody-associated vasculitis (OMAAV): A report of two cases
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Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
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A Case with Iron Deficiency Anemia Developed Aplastic Crisis
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Expression of urokinase-type plasminogen activator system in non-metastatic prostate cancer
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Mutation spectrum and health status in skeletal muscle channelopathies in Japan
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Analyses of genetic and retinal lesions in Ccdc85c knockout rats: a rat model of genetic hydrocephalus
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Expression dynamics of HAND1/2 in in vitro human cardiomyocyte differentiation
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Genome-wide association study of IgA nephropathy using 23 465 microsatellite markers in a Japanese population
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Circulatory C-type natriuretic peptide reduces mucopolysaccharidosis-associated craniofacial hypoplasia in vivo
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Surgical revascularization for quasi-moyamoya disease associated with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome: a case report and literature review
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Reverse Genetic Studies on Mitochondrial tRNA-related Disorders
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Diagnostic ability of artificial intelligence using deep learning analysis of cyst fluid in differentiating malignant from benign pancreatic cystic lesions
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Networking and Specificity-Changing DNA Methyltransferases in Helicobacter pylori.
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Glucose transporter Glut1 controls diffuse invasion phenotype with perineuronal satellitosis in diffuse glioma microenvironment
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Acute Coronary Syndrome Due to Intraplaque Hemorrhage in a Post-gastrectomy Patient with a Latent Severe Glycemic Disorder
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Progression of Recurrent Pancreatitis to Chronic Pancreatitis within 3 Years due to SPINK1 Mutation IVS3+2T>C
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Identification of sur2 mutation affecting the lifespan of fission yeast
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An autopsy case of primary gliosarcoma with multiple extracranial metastases: pathology after administration of bevacizumab and genetic profile
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Effects of long-term childhood exercise and detraining on lipid accumulation in metabolic-related organs
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Genetic analysis of neurons involved in sleep-wake regulation
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Gut bacteria identified in colorectal cancer patients promote tumourigenesis via butyrate secretion
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Study of Mitochonic Acid 5 to improve neuromuscular dysfunction associated with aging and diseases using C. elegans
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Increased blood group 2 innate lymphoid cells are associated with the clinical severity of Kimura disease.
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Studies on Peripheral Blood mMDSC Based-Biomarker Exploration and a Novel Therapeutic Agent for Cancer Immunotherapy
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Patient-derived ovarian cancer organoids capture the genomic profiles of primary tumours applicable for drug sensitivity and resistance testing (本文)
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Concepts of Regeneration for Spinal Diseases in 2021
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TNFRSF11A-Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum
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Frequent PIK3CA mutations in eutopic endometrium of patients with ovarian clear cell carcinoma
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Examination of the body composition of patients with Werner syndrome using bioelectrical impedance analysis
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Multidisciplinary diagnostic approach for fulminant myocarditis related to coronavirus disease 2019 messenger RNA vaccines: a case report
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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