「Genotype-specific cortisol production associated with Cushing's syndrome adenoma with PRKACA mutations」の関連論文
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Isolation of tumor endothelial cells from murine cancer
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Features of Duration Mismatch Negativity Around the Onset of Overt Psychotic Disorders: A Longitudinal Study
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Brief HIV stigma scale for Japanese people living with HIV: validation and restructuring using questionnaire survey data
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Brief HIV stigma scale for Japanese people living with HIV: validation and restructuring using questionnaire survey data
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Study on the Function of α-Defensin, Paneth cell-secreted Antimicrobial Peptide, as a Regulator of Intestinal Ecological System under Psychological Stress
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Zscan5b deficiency impairs DNA damage response and causes chromosomal aberrations during mitosis (本文)
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Steroid profiling for assessing adrenal hepatic syndrome in canine hepatocellular carcinoma
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Investigation of the mechanism for emergence of spatial heterogeneity of invading glioblastoma cells in the presence of perivascular factors (本文)
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UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
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Genetic and chemical inhibition of IRF5 suppresses pre-existing mouse lupus-like disease
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SAK3 Administration Improves Spine Abnormalities and Cognitive Deficits in AppNL-G-F/NL-G-F Knock-in Mice by Increasing Proteasome Activity through CaMKII/Rpt6 Signaling
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Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
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Impact of sleep-disordered breathing on glucose metabolism among individuals with a family history of diabetes: the Nagahama study
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Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation
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Incontinentia pigmenti in a female infant with somatic mosaicism due to the IKBKG variant
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Beneficial screening of Fabry disease in patients with hypohidrosis
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Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease
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Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing
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Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing
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Biochemical properties Scardovia wiggsiae, a novel caries-associated bacterium-Sugar metabolism and growth-promoting factors-
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Unique morpho-functional characteristics of folliculogenesis found in the ovary of cotton rat (Sigmodon hispidus)
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Hes1 is essential in proliferating ductal cell-mediated development of intrahepatic cholangiocarcinoma
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Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
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Dilated cardiomyopathy-linked heat shock protein family D member 1 mutations cause up-regulation of reactive oxygen species and autophagy through mitochondrial dysfunction (本文)
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Potential role of administration of menaquinone-4 and its chemically related compound for neuroinflammatory modulation
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コーヒー成分に含まれるクロロゲン酸とカフェインは膵β細胞のインスリンシグナルを改善する
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Occurrence of cholangiocarcinoma, three years after negative seroconversion of anti-TIF1γ antibody, in a dermatomyositis patient
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Combined Hypophysitis and Type 1 Diabetes Mellitus Related to Immune Checkpoint Inhibitors
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The effect of acute social defeat stress on sleep in mice
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Alpha-Arbutin Promotes Wound Healing by Lowering ROS and Upregulating Insulin/IGF-1 Pathway in Human Dermal Fibroblast
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The role of inflammatory biomarkers in predicting primary acquired nasolacrimal duct obstruction and postoperative recurrence
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Studies on astragaloside IV metabolism in lactic acid bacteria and bifidobacteria
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Prenatal diagnosis of severe mitochondrial disease caused by nuclear gene defects: a study in Japan
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MicroRNA profiling in adults with high-functioning autism spectrum disorder
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Systemic Supplementation of Collagen VI by Neonatal Transplantation of iPSC-Derived MSCs Improves Histological Phenotype and Function of Col6-Deficient Model Mice
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Loss of Arid1a and Pten in Pancreatic Ductal Cells Induces Intraductal Tubulopapillary Neoplasm via the YAP/TAZ Pathway
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Hippo-TAZ signaling is the master regulator of the onset of triple-negative basal-like breast cancers
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The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
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A case of eosinophilic polyangiitis with granulomatosis that evolved to cardiac arrest due to advanced atrioventricular block
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Increased Matrix Metalloproteinases in Cerebrospinal Fluids of Patients With Major Depressive Disorder and Schizophrenia
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Increased Matrix Metalloproteinases in Cerebrospinal Fluids of Patients With Major Depressive Disorder and Schizophrenia
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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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Intracrine activity involving NAD-dependent circadian steroidogenic activity governs age-associated meibomian gland dysfunction
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Structural brain changes in severe and enduring anorexia nervosa: A multimodal magnetic resonance imaging study of gray matter volume, cortical thickness, and white matter integrity
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Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers
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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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尿管癌を契機にリンチ症候群と診断された1例
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Expansion of gastric intestinal metaplasia with copy number aberrations contributes to field cancerization
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Safety comparisons among monoamine oxidase inhibitors against Parkinson’s disease using FDA adverse event reporting system
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Clinical efficacy of the combined treatment of anti-PD-L1 rat-bovine chimeric antibody with a COX-2 inhibitor in calves infected with Mycoplasma bovis