Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk. - Wikidata - awgldk - TriplyDB

Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk.

Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk.

http://www.wikidata.org/entity/Q54550455

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Comparing methods for mapping cis acting polymorphisms using allelic expression ratios SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr Extent of differential allelic expression of candidate breast cancer genes is similar in blood and breast Allele-specific CDH1 downregulation and hereditary diffuse gastric cancer.SIBLING family genes and bone mineral density: association and allele-specific expression in humans Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2.Cis-acting genetic variation at an E2F1/YY1 response site and putative p53 site is associated with altered allele-specific expression of ERCC5 (XPG) transcript in normal human bronchial epithelium.Allelic imbalance (AI) identifies novel tissue-specific cis-regulatory variation for human UGT2B15 Allele-specific expression of TGFBR1 in colon cancer patients.Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study.Identifying breast cancer risk loci by global differential allele-specific expression (DASE) analysis in mammary epithelial transcriptome.No association between germline allele-specific expression of TGFBR1 and colorectal cancer risk in Caucasian and Ashkenazi populations.Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management.Stress alters rates and types of loss of heterozygosity in Candida albicans.A comprehensively molecular haplotype-resolved genome of a European individual Increased variance in germline allele-specific expression of APC associates with colorectal cancer.SNP55, a new functional polymorphism of MDM2-P2 promoter, contributes to allele-specific expression of MDM2 in endometrial cancers.Functional single-nucleotide polymorphisms in the BRCA1 gene and risk of salivary gland carcinoma Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers.Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex.Allele-specific DNA methylation: beyond imprinting.Debate about TGFBR1 and the susceptibility to colorectal cancer Recognition of and recent issues in hereditary diffuse gastric cancer.Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site.Allelic expression imbalance polymorphisms in susceptibility chromosome regions and the risk and survival of breast cancer.The Protein Encoded by the CCDC170 Breast Cancer Gene Functions to Organize the Golgi-Microtubule Network Allele-specific expression of APC in adenomatous polyposis families.Allelic imbalance in human breast cancer.Identification of common variants in BRCA2 and MAP2K4 for susceptibility to sporadic pancreatic cancer.Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease.Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer.BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer.Cervical cancer-associated promoter polymorphism affects akna expression levels.Imprinting in the schizophrenia candidate gene GABRB2 encoding GABAA receptor β2 subunit

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P2860

Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk.

http://www.wikidata.org/entity/Q54550455

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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2008年學術文章

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name

Allelic imbalance in BRCA1 and ...... increased breast cancer risk.

@en

Allelic imbalance in BRCA1 and ...... increased breast cancer risk.

@nl

type

label

Allelic imbalance in BRCA1 and ...... increased breast cancer risk.

@en

Allelic imbalance in BRCA1 and ...... increased breast cancer risk.

@nl

prefLabel

Allelic imbalance in BRCA1 and ...... increased breast cancer risk.

@en

Allelic imbalance in BRCA1 and ...... increased breast cancer risk.

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Human Molecular Genetics

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Allelic imbalance in BRCA1 and ...... increased breast cancer risk.

@en

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Alexander Miron

http://www.w3.org/2001/XMLSchema#string

Andrew K Godwin

http://www.w3.org/2001/XMLSchema#string

Betsy A Bove

http://www.w3.org/2001/XMLSchema#string

Joellen Weaver

http://www.w3.org/2001/XMLSchema#string

Lisa A Vanderveer

http://www.w3.org/2001/XMLSchema#string

Mary B Daly

http://www.w3.org/2001/XMLSchema#string

Susan C Weil

http://www.w3.org/2001/XMLSchema#string

Xiaowei Chen

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P2860

Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway

Deficiency of human BRCA2 leads to impaired homologous recombination but maintains normal nonhomologous end joining

MicroInspector: a web tool for detection of miRNA binding sites in an RNA sequence.

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

Oncomirs - microRNAs with a role in cancer

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

Cancer statistics, 2007

MicroRNAs direct rapid deadenylation of mRNA

Real time quantitative PCR

Micro RNAs are complementary to 3' UTR sequence motifs that mediate negative post-transcriptional regulation

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1336-1348

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10.1093/HMG/DDN022

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9

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17

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18204050

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