Germline copy number variations in BRCA1-associated ovarian cancer patients. - Wikidata - wikimedia - TriplyDB

Germline copy number variations in BRCA1-associated ovarian cancer patients.

Germline copy number variations in BRCA1-associated ovarian cancer patients.

http://www.wikidata.org/entity/Q45909891

about

A computational framework to infer human disease-associated long noncoding RNAs Genomic-Wide Analysis with Microarrays in Human Oncology A survey of copy-number variation detection tools based on high-throughput sequencing data.Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.Prediction of potential cancer-risk regions based on transcriptome data: towards a comprehensive view Expanding the genetic basis of copy number variation in familial breast cancer.Up-regulation of 91H promotes tumor metastasis and predicts poor prognosis for patients with colorectal cancer.Germline DNA copy number aberrations identified as potential prognostic factors for breast cancer recurrence.Molecular characterization of an intact p53 pathway subtype in high-grade serous ovarian cancer.Optimizing molecular-targeted therapies in ovarian cancer: the renewed surge of interest in ovarian cancer biomarkers and cell signaling pathways.Copy number polymorphism in plant genomes Germline DNA copy number variation in familial and early-onset breast cancer Identification of large-scale genomic variation in cancer genomes using in silico reference models Germline copy number variations associated with breast cancer susceptibility in a Japanese population.Identification of germline genomic copy number variation in familial pancreatic cancer.Germline copy number variations and cancer predisposition.Germline DNA copy number variations as potential prognostic markers for non-muscle invasive bladder cancer progression.ABCC4 copy number variation is associated with susceptibility to esophageal squamous cell carcinoma.Germline copy number variations are associated with breast cancer risk and prognosis.DNA copy number profiling in microsatellite-stable and microsatellite-unstable hereditary non-polyposis colorectal cancers by targeted CNV array.Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.

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P2860

Germline copy number variations in BRCA1-associated ovarian cancer patients.

http://www.wikidata.org/entity/Q45909891

description

2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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2010年學術文章

@zh-hant

name

Germline copy number variations in BRCA1-associated ovarian cancer patients.

@en

Germline copy number variations in BRCA1-associated ovarian cancer patients.

@nl

type

label

Germline copy number variations in BRCA1-associated ovarian cancer patients.

@en

Germline copy number variations in BRCA1-associated ovarian cancer patients.

@nl

prefLabel

Germline copy number variations in BRCA1-associated ovarian cancer patients.

@en

Germline copy number variations in BRCA1-associated ovarian cancer patients.

@nl

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Genes, Chromosomes and Cancer

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Germline copy number variations in BRCA1-associated ovarian cancer patients.

@en

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Hiroaki Kase

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Ituro Inoue

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Jinhua Quan

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Kenichi Tanaka

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Kosuke Yoshihara

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Masayuki Sekine

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Sosuke Adachi

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Tetsuro Yahata

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P2860

BRCA1 haploinsufficiency, but not heterozygosity for a BRCA1-truncating mutation, deregulates homologous recombination.

Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinoma.

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167-177

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scholarly article

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10.1002/GCC.20841

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3

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50

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21213370

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