「Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2‐mutation carriers」の関連論文
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Antioxidants and Therapeutic Targets in Ovarian Clear Cell Carcinoma.
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Brg1 is required to maintain colorectal cancer stem cells
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大腸癌におけるアポトーシス、ネクロトーシス、オートファジー:腫瘍の病理学的悪性度とp53タンパク発現状態との関連性について
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Immunohistochemically Detected Expression of ATRX, TSC2, and PTEN Predicts Clinical Outcomes in Patients With Grade 1 and 2 Pancreatic Neuroendocrine Tumors
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Overexpression of aldolase, fructose-bisphosphate C and its association with spheroid formation in colorectal cancer
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Overexpression of aldolase, fructose-bisphosphate C and its association with spheroid formation in colorectal cancer
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Expression of urokinase-type plasminogen activator system in non-metastatic prostate cancer
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Amino acid catabolite markers for early prognostication of pneumonia in patients with COVID-19
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2-nitroimidazoles induce mitochondrial stress and ferroptosis in glioma stem cells residing in a hypoxic niche (本文)
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4q25 Microdeletion with Axenfeld-Rieger Syndrome and Developmental Delay
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Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
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Genomic stability of mouse spermatogonial stem cells in vitro
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A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia
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Analysis of Anti-metabolic Syndrome Effect of Kaempferol in TSOD Mice
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Colorectal cancer-derived CAT1-positive extracellular vesicles alter nitric oxide metabolism in endothelial cells and promote angiogenesis
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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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DDIT4 Facilitates Lymph Node Metastasis via the Activation of NF-κB Pathway and Epithelial-Mesenchymal Transition
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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Constitutively active signaling of MDA5 in Treg cells causes apoptosis of Treg cells and results in autoimmune diseases
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Two effects of GATA2 enhancer repositioning by 3q chromosomal rearrangements.
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Development of genetic management methods for rice varieties and prediction of spontaneous mutation frequencies using next-generation sequencing technology [an abstract of entire text]
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Identification of T cell receptors targeting a neoantigen derived from recurrently mutated FGFR3
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Significance of PD-L1 expression in carbon-ion radiotherapy for uterine cervical adeno/adenosquamous carcinoma (本文)
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Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2 (本文)
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Analyses of genetic and retinal lesions in Ccdc85c knockout rats: a rat model of genetic hydrocephalus
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Studies on the development of novel non-alcoholic steatohepatitis (NASH) models using rats
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Cryptotanshinone is a candidate therapeutic agent for interstitial lung disease associated with a BRICHOS-domain mutation of SFTPC
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Regulation of Cell Motility by La-Related Protein 4 in Ovarian Cancer Cell
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Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia
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Risk factors and diagnostic biomarkers for nonalcoholic fatty liver disease-associated hepatocellular carcinoma: Current evidence and future perspectives
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A clinical and genetic study of SPG31 in Japan
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Genetic and chemical inhibition of IRF5 suppresses pre-existing mouse lupus-like disease
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Lusutrombopag effectively promotes the growth and differentiation of megakaryocytic cells from patients with myelodysplastic syndrome
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EYS is a major gene involved in retinitis pigmentosa in Japan: Genetic landscapes revealed by stepwise genetic screening.
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In vivo induction of activin A-producing alveolar macrophages supports the progression of lung cell carcinoma
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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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Inhibition of autophagy in theca cells induces CYP17A1 and PAI-1 expression via ROS/p38 and JNK signalling during the development of polycystic ovary syndrome
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The landscape of genetic aberrations in myxofibrosarcoma
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Combined Hypophysitis and Type 1 Diabetes Mellitus Related to Immune Checkpoint Inhibitors
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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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Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia
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Cell migration is impaired in XPA-deficient cells
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Conserved Double Translation Initiation Site for Δ160p53 Protein Hints at Isoform’s Key Role in Mammalian Physiology
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Glucose transporter Glut1 controls diffuse invasion phenotype with perineuronal satellitosis in diffuse glioma microenvironment
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Next Generation Sequencing-Based Transcriptome Predicts Bevacizumab Efficacy in Combination with Temozolomide in Glioblastoma
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Combination of RERG and ZNF671 methylation rates in circulating cell-free DNA: A novel biomarker for screening of nasopharyngeal carcinoma
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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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Study on the role of CtBP2 in pancreatic β cell
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The ACTN3 577XX Null Genotype Is Associated with Low Left Ventricular Dilation-Free Survival Rate in Patients with Duchenne Muscular Dystrophy
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Identification and characterization of slow‑cycling cells in Ewing sarcoma