「Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing」の関連論文
-
Lack of association between seropositivity of vasculopathy-related viruses and moyamoya disease
-
BMP and activin membrane-bound inhibitor (BAMBI) regulates mesothelioma cell proliferation and clinical outcome
-
BMP and activin membrane-bound inhibitor (BAMBI) regulates mesothelioma cell proliferation and clinical outcome
-
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)
-
Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
-
Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
-
EYS is a major gene involved in retinitis pigmentosa in Japan: Genetic landscapes revealed by stepwise genetic screening.
-
Development of DNA markers for improvement of meat quality in a Japanese Black cattle population in Hyogo Prefecture
-
Comparative study of mammalian evolution by genomic analyses and pluripotent stem cell technology
-
Development of genetic management methods for rice varieties and prediction of spontaneous mutation frequencies using next-generation sequencing technology [an abstract of entire text]
-
An autopsy case of primary gliosarcoma with multiple extracranial metastases: pathology after administration of bevacizumab and genetic profile
-
Differentiation of Hypertrophic Chondrocytes from Human iPSCs for the In Vitro Modeling of Chondrodysplasias
-
Circulating microRNA/isomiRs as novel biomarkers of esophageal squamous cell carcinoma
-
Circulating microRNA/isomiRs as novel biomarkers of esophageal squamous cell carcinoma
-
Studies on Cytotoxic Effects of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL) to Canine Cell Lines Derived from Hemangiosarcoma and Mammary Epithelial Tumor
-
Genome-wide association study of IgA nephropathy using 23 465 microsatellite markers in a Japanese population
-
Studies on Circadian Clock RNA Methylation and Micturition Rhythm
-
The Natural History of Spontaneously Occurred Endometriosis in Cynomolgus Monkeys by Monthly Follow-Up Laparoscopy for Two Years.
-
Sarcomatoid mesothelioma diagnosed in a patient with mesothelioma in situ: a case report on morphologic differences after 9-month interval with details analysis of cytology in early-stage mesothelioma
-
Horizontally Transferred DNA in the Genome of the Fungus Pyricularia oryzae is Associated With Repressive Histone Modifications
-
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
-
A drug repurposing study based on clinical big data for the protective role of vitamin D in olanzapine-induced dyslipidemia
-
Temporal arteritis with focal pachymeningitis: a deceptive association
-
A digital twin reproducing gene regulatory network dynamics of early Ciona embryos indicates robust buffers in the network
-
Improvement of mouse genome editing protocol and the application:investigation of the physiological roles of glycine receptor alpha 4 subunit.
-
A proof-of-concept study to construct Bayesian network decision models for supporting the categorization of sudden unexpected infant death
-
The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
-
Pharmacogenomic study of anti-tuberculosis drugs-induced liver injury in Thais
-
Efficacious Combination Drug Treatment for Colorectal Cancer that Overcomes Resistance to KRAS G12C Inhibitors
-
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)
-
Risk factors and diagnostic biomarkers for nonalcoholic fatty liver disease-associated hepatocellular carcinoma: Current evidence and future perspectives
-
Circulatory C-type natriuretic peptide reduces mucopolysaccharidosis-associated craniofacial hypoplasia in vivo
-
Identification and analysis of mechanisms that bypass the essentiality of Polo, a mitotic regulator
-
A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia
-
Clinical impact of detecting low-frequency variants in cell-free DNA on treatment of castration-resistant prostate cancer
-
Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
-
Colorectal cancer-derived CAT1-positive extracellular vesicles alter nitric oxide metabolism in endothelial cells and promote angiogenesis
-
Gut bacteria identified in colorectal cancer patients promote tumourigenesis via butyrate secretion
-
Investigation of the current situation regarding diagnosis and treatment of Alport syndrome in Asian countries: results of survey of the Asian Paediatric Nephrology association (AsPNA) tubular and inherited working group
-
Study on Accessory Gene Regulator(AGR)Variants in Staphylococcus aureus
-
Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2 (本文)
-
Detection of genetic changes involved in adaptive evolution by comparing the genomes of Cuban Anolis lizards
-
Antioxidants and Therapeutic Targets in Ovarian Clear Cell Carcinoma.
-
Frequent PIK3CA mutations in eutopic endometrium of patients with ovarian clear cell carcinoma
-
Current status of genome‐wide epigenetic profiling of mammalian preimplantation embryos
-
Development of highly efficient methods for comprehensive pathogen detection using next generation sequencing
-
Sessile serrated lesions with dysplasia: is it possible to nip them in the bud?
-
Editorial: Crop breeding involving epigenetic inheritance
-
FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
-
Alterations in DNA methylation rates of brain-derived neurotrophic factor in patients with schizophrenia.