Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer. - Wikidata - wikimedia - TriplyDB

Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer.

Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer.

http://www.wikidata.org/entity/Q34809698

about

Application of on-line nanoLC-IT-TOF in the identification of serum β-catenin complex in mice scald model No association between a candidate TCF7L2 variant and risk of breast or ovarian cancer.Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers Transcriptomic effects of di-(2-ethylhexyl)-phthalate in Syrian hamster embryo cells: an important role of early cytoskeleton disturbances in carcinogenesis?Centrosome-related genes, genetic variation, and risk of breast cancer.Wnt signaling pathway pharmacogenetics in non-small cell lung cancer Key signaling nodes in mammary gland development and cancer: β-catenin.Association of single nucleotide polymorphisms in Wnt signaling pathway genes with breast cancer in Saudi patients.The role of chalcones in suppression of NF-κB-mediated inflammation and cancer.Concurrent gene signatures for han chinese breast cancers Differential activation of Wnt-β-catenin pathway in triple negative breast cancer increases MMP7 in a PTEN dependent manner.Association of genetic variants in Wnt signaling pathway with tuberculosis in Chinese Han population.Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice.Dense and nondense mammographic area and risk of breast cancer by age and tumor characteristics.Quantitative assessment of the association between AXIN2 rs2240308 polymorphism and cancer risk.Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk.AXIN2 rs2240308 polymorphism contributes to increased cancer risk: evidence based on a meta-analysis.The contribution of protein intrinsic disorder to understand the role of genetic variants uncovered by autism spectrum disorders exome studies.The PDZ protein TIP-1 facilitates cell migration and pulmonary metastasis of human invasive breast cancer cells in athymic mice.Clinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian population No evidence for association of inherited variation in genes involved in mitosis and percent mammographic density.A novel automated mammographic density measure and breast cancer risk.Interaction between APC and Fen1 during breast carcinogenesis.Genetic variation in the chromosome 17q23 amplicon and breast cancer risk.Transposon mutagenesis identifies genes that cooperate with mutant Pten in breast cancer progression.Association of genetic variation in mitotic kinases with breast cancer risk.An analysis of polymorphisms within the Wnt signaling pathway in relation to ovarian cancer risk in a Polish population.Mammographic density and risk of breast cancer by age and tumor characteristics.Genetic polymorphisms of Wnt/β-catenin pathway genes are associated with the efficacy and toxicities of radiotherapy in patients with nasopharyngeal carcinoma.AXIN1 and AXIN2 variants in gastrointestinal cancers.Development of an eight gene expression profile implicating human breast tumours of all grade.Association of Wnt signaling pathway genetic variants in gallbladder cancer susceptibility and survival.The genomic signature of breast cancer prevention Diagnostic value of HMGAs, p53 and β-catenin in discriminating adenocarcinoma from adenoma or reactive atypia in ampulla and common bile duct biopsies.Association of common gene variants in the WNT/β-catenin pathway with colon cancer recurrence.Epigenetic and genetic analysis of WNT signaling pathway in sporadic colorectal cancer patients from Iran.AXIN2 polymorphism and its association with prostate cancer in a Turkish population.

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P2860

Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer.

http://www.wikidata.org/entity/Q34809698

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2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2008 թվականի օգոստոսին հրատարակված գիտական հոդված

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Association of genetic variati ...... ex with risk of breast cancer.

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Association of genetic variati ...... ex with risk of breast cancer.

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Association of genetic variati ...... ex with risk of breast cancer.

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Association of genetic variati ...... ex with risk of breast cancer.

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Association of genetic variati ...... ex with risk of breast cancer.

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Association of genetic variati ...... ex with risk of breast cancer.

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Association of genetic variati ...... ex with risk of breast cancer.

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Cancer Epidemiology, Biomarkers & Prevention

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Association of genetic variati ...... ex with risk of breast cancer.

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P2093

David N Rider

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Ellen L Goode

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James R Cerhan

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V Shane Pankratz

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Wen Liu-Mares

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Zachary S Fredericksen

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P2860

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling

Pin1 regulates turnover and subcellular localization of beta-catenin by inhibiting its interaction with APC

Increased Wnt signaling triggers oncogenic conversion of human breast epithelial cells by a Notch-dependent mechanism

A Wnt-Axin2-GSK3beta cascade regulates Snail1 activity in breast cancer cells

Downregulation of beta-catenin by human Axin and its association with the APC tumor suppressor, beta-catenin and GSK3 beta

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

Casein kinase I phosphorylates and destabilizes the beta-catenin degradation complex

The SCFbeta-TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in IkappaBalpha and beta-catenin and stimulates IkappaBalpha ubiquitination in vitro

Casein kinase iepsilon in the wnt pathway: regulation of beta-catenin function

A haplotype map of the human genome

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Robert Vierkant

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18708403

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