Frequent mutation of the p53 gene in human esophageal cancer - Wikidata - awgldk - TriplyDB

Frequent mutation of the p53 gene in human esophageal cancer

Frequent mutation of the p53 gene in human esophageal cancer

http://www.wikidata.org/entity/Q33927516

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Esophageal Cancer: Insights From Mouse Models The tumor microenvironment in esophageal cancer From molecular classification to targeted therapeutics: the changing face of systemic therapy in metastatic gastroesophageal cancer An LOH and mutational investigation of the ST7 gene locus in human esophageal carcinoma Ral GTPase down-regulation stabilizes and reactivates p53 to inhibit malignant transformation The roles of post-translational modifications in the context of protein interaction networks Identification of New Candidate Genes and Chemicals Related to Esophageal Cancer Using a Hybrid Interaction Network of Chemicals and Proteins Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers Multigene analysis of Rb pathway and apoptosis control in esophageal squamous cell carcinoma identifies patients with good prognosis.Demystified ... p53.None-endoscopic Screening for Esophageal Squamous Cell Carcinoma- A Review.DNA repair gene status in oesophageal cancer Prediction of CCND1 amplification using plasma DNA as a prognostic marker in oesophageal squamous cell carcinoma Circulating microRNAs: novel biomarkers for esophageal cancer CD44 and p53 immunoexpression patterns in NF1 neoplasms - indicators of malignancy and infiltration.Plasma microRNA profiles: identification of miR-25 as a novel diagnostic and monitoring biomarker in oesophageal squamous cell carcinoma.A role for sunlight in skin cancer: UV-induced p53 mutations in squamous cell carcinoma.Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma.Loss of transcription factor KLF5 in the context of p53 ablation drives invasive progression of human squamous cell cancer Correlation between cathepsin D expression and p53 protein nuclear accumulation in oesophageal squamous cell carcinoma.Overexpression and localization of cyclin D1 mRNA and antigen in esophageal cancer.High prevalence of mutations of the p53 gene in poorly differentiated human thyroid carcinomas.Overexpression of human cyclin D1 reduces the transforming growth factor beta (TGF-beta) type II receptor and growth inhibition by TGF-beta 1 in an immortalized human esophageal epithelial cell line Frequent mutations of p53 gene in oesophageal squamous cell carcinomas with and without human papillomavirus (HPV) involvement suggest the dominant role of environmental carcinogens in oesophageal carcinogenesis.Frequent loss of heterozygosity on chromosome 17 at 17q11.2-q12 in Barrett's adenocarcinoma Benzo[a]pyrene-induced murine skin tumors exhibit frequent and characteristic G to T mutations in the p53 gene.Somatic alteration and depleted nuclear expression of BAP1 in human esophageal squamous cell carcinoma.A constitutional de novo mutation in exon 8 of the p53 gene in a patient with multiple primary malignancies.Comparative genomic analysis of esophageal adenocarcinoma and squamous cell carcinoma.Altered expression of the cyclin D1 and retinoblastoma genes in human esophageal cancer.Study of p53 gene alteration as a biomarker to evaluate the malignant risk of Lugol-unstained lesion with non-dysplasia in the oesophagus.Overexpression of metastasis-associated MTA1 mRNA in invasive oesophageal carcinomas Metallothionein expression correlates with metastatic and proliferative potential in squamous cell carcinoma of the oesophagus.Overexpression of P53 and its risk factors in esophageal cancer in urban areas of Xi'an.Genomic Characterization of Esophageal Squamous Cell Carcinoma Reveals Critical Genes Underlying Tumorigenesis and Poor Prognosis Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers.Rat p53 gene mutations in primary Zymbal gland tumors induced by 2-amino-3-methylimidazo[4,5-f]quinoline, a food mutagen.Genomic alterations in advanced esophageal cancer may lead to subtype-specific therapies.An infrequent point mutation of the p53 gene in human nasopharyngeal carcinoma.p53 protein accumulation in oesophageal squamous cell carcinomas and precancerous lesions

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P2860

Frequent mutation of the p53 gene in human esophageal cancer

http://www.wikidata.org/entity/Q33927516

description

1990 nî lūn-bûn

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1990 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1990 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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1990年の論文

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1990年論文

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1990年論文

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1990年論文

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1990年論文

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1990年論文

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1990年论文

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name

Frequent mutation of the p53 gene in human esophageal cancer

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Frequent mutation of the p53 gene in human esophageal cancer

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Frequent mutation of the p53 gene in human esophageal cancer

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Frequent mutation of the p53 gene in human esophageal cancer

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Frequent mutation of the p53 gene in human esophageal cancer

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Frequent mutation of the p53 gene in human esophageal cancer

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Harris CC

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Hollstein MC

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DNA sequencing with chain-terminating inhibitors

Detection of carcinogens as mutagens in the Salmonella/microsome test: assay of 300 chemicals

A genetic model for colorectal tumorigenesis

Mutations in the p53 gene occur in diverse human tumour types

DNA repair enzymes

Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas

[21] Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction

ras oncogenes in human cancer: a review

INDUCTION OF SPECIFIC MUTATIONS WITH 5-BROMOURACIL.

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