「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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Annexin A10 is involved in the induction of pancreatic duodenal homeobox-1 in gastric cancer tissue, cells and organoids
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Genomic analysis for the prediction of prognosis in small-bowel cancer
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Genomic analysis for the prediction of prognosis in small-bowel cancer
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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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JNK and Yorkie drive tumor malignancy by inducing L-amino acid transporter 1 in Drosophila
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Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes
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Malfunctioning CD106-positive, short-term hematopoietic stem cells trigger diabetic neuropathy in mice by cell fusion.
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Mechanisms by which Bacterial and Viral Pathogens cause Ovarian dysfunction
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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
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Human induced pluripotent stem cells generated from a patient with idiopathic basal ganglia calcification
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Risk factors for cisplatin-induced acute kidney injury: A pilot study on the usefulness of genetic variants for predicting nephrotoxicity in clinical practice
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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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Analysis of aging-related epigenetic modifications in murine male germline cells
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Real-world application of next-generation sequencing-based test for surgically resectable colorectal cancer in clinical practice (本文)
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Remote solid cancers rewire hepatic nitrogen metabolism via host nicotinamide-N-methyltransferase
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A case of simultaneous breast cancer and ovarian cancer based on a hereditary breast and ovarian cancer syndrome
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TSC22D4/THG-1 suppresses cellular senescence in esophageal squamous cell carcinoma
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Immunohistochemical assessment of sex-determining region Y (SRY)-related high mobility group (HMG)-box 2 (Sox2) and Krüppel-like factor 4 (Klf4) in ameloblastomas
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Lack of association between seropositivity of vasculopathy-related viruses and moyamoya disease
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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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Potential roles of gastroesophageal reflux in patients with superficial esophageal squamous cell carcinoma without major causative risk factors
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Case report: Late middle-aged features of FAM111A variant, Kenny–Caffey syndrome type 2-suggestive symptoms during a long follow-up
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Comprehensive genomics in androgen receptor-dependent castration-resistant prostate cancer identifies an adaptation pathway mediated by opioid receptor kappa 1
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Utility of plasma circulating tumor DNA and tumor DNA profiles in head and neck squamous cell 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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SPC18 expression is an independent prognostic indicator of patients with esophageal squamous cell carcinoma
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SPC18 expression is an independent prognostic indicator of patients with esophageal squamous cell carcinoma
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Large-scale discovery of male reproductive tract-specific genes through analysis of RNA-seq datasets
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Identification of novel mutations and reassignment of archival xeroderma pigmentosum group C cell strains from Japanese patients
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A genome-wide association study identifying single nucleotide polymorphisms in the PPFIBP2 gene was predictive for interstitial lung disease in rheumatoid arthritis patients
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The generation and insights of an inducible diabetes mellitus mouse model based on MafA and MafB double knockout
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Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
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Prognostic impact of TP53INP1 gene expression in estrogen receptor α-positive breast cancer patients
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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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Zscan5b deficiency impairs DNA damage response and causes chromosomal aberrations during mitosis (本文)
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Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
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Pharmacogenomic study of anti-tuberculosis drugs-induced liver injury in Thais
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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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Development of an in vitro carcinogenesis model of human papillomavirus-induced cervical adenocarcinoma (本文)
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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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Studies on Cytotoxic Effects of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL) to Canine Cell Lines Derived from Hemangiosarcoma and Mammary Epithelial Tumor
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Studies on Peripheral Blood mMDSC Based-Biomarker Exploration and a Novel Therapeutic Agent for Cancer Immunotherapy
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Characterization of the Anticancer Activities of Some Natural and Synthetic Compounds: Molecular Targets and Mechanism
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Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
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Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
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ATM suppresses c-Myc overexpression in the mammary epithelium in response to estrogen
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Molecular genetic study of the FMR1 CGG repeat configurations in the Japanese population and patients with Fragile X-Associated Tremor/Ataxia Syndrome
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Genetic and Epigenetic Pathogenesis of Acromegaly
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Studies on DNA methylation changes in canine malignant melanoma [an abstract of entire text]
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UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes