Germline DNA copy number variation in familial and early-onset breast cancer - Wikidata - awgldk - TriplyDB

Germline DNA copy number variation in familial and early-onset breast cancer

Germline DNA copy number variation in familial and early-onset breast cancer

http://www.wikidata.org/entity/Q36393187

about

Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma nbCNV: a multi-constrained optimization model for discovering copy number variants in single-cell sequencing data Hereditary breast cancer: ever more pieces to the polygenic puzzle.The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations.Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.Expanding the genetic basis of copy number variation in familial breast cancer.Clinical and genetic characterization of basal cell carcinoma and breast cancer in a single patient Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion.Rare copy number variants observed in hereditary breast cancer cases disrupt genes in estrogen signaling and TP53 tumor suppression network Structural architecture of SNP effects on complex traits.Germline DNA copy number aberrations identified as potential prognostic factors for breast cancer recurrence.Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil.Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer.copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.Identification of rare germline copy number variations over-represented in five human cancer types.Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example The association of copy number variation and percent mammographic density Identification of genes involved in breast cancer and breast cancer stem cells.miR-548d-3p/TP53BP2 axis regulates the proliferation and apoptosis of breast cancer cells.Number of rare germline CNVs and TP53 mutation types.Germline copy number variations associated with breast cancer susceptibility in a Japanese population.Tracking Cancer Genetic Evolution using OncoTrack.The Role of Constitutional Copy Number Variants in Breast Cancer.Copy number variation in hereditary non-polyposis colorectal cancer.Germline large genomic alterations on 7q in patients with multiple primary cancers.Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.BCIP: a gene-centered platform for identifying potential regulatory genes in breast cancer.Germline copy number variations and cancer predisposition.Integration of genomics in cancer care.Role of rare germline copy number variation in melanoma-prone patients.C21orf57 is a human homologue of bacterial YbeY proteins.Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients Genome-wide copy number analysis in pediatric glioblastoma multiforme.Germline copy number variation analysis in Finnish families with hereditary prostate cancer.Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development.Application of Machine Learning to Development of Copy Number Variation-based Prediction of Cancer Risk Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas.Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis.The 30 kb deletion in the APOBEC3 cluster decreases APOBEC3A and APOBEC3B expression and creates a transcriptionally active hybrid gene but does not associate with breast cancer in the European population.Germline copy number variations are associated with breast cancer risk and prognosis.

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Germline DNA copy number variation in familial and early-onset breast cancer

http://www.wikidata.org/entity/Q36393187

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2012 nî lūn-bûn

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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Germline DNA copy number variation in familial and early-onset breast cancer

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Germline DNA copy number variation in familial and early-onset breast cancer

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type

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Germline DNA copy number variation in familial and early-onset breast cancer

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Germline DNA copy number variation in familial and early-onset breast cancer

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Germline DNA copy number variation in familial and early-onset breast cancer

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Germline DNA copy number variation in familial and early-onset breast cancer

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Breast Cancer Research

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Germline DNA copy number variation in familial and early-onset breast cancer

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Amanda F Nóbrega

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Amanda Gonçalves

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Ana Cv Krepischi

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Angela M Vianna-Morgante

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Bianca Cg Lisboa

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Erika Mm Santos

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Peter L Pearson

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Ricardo R Brentani

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Silvia S Costa

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Tiago M Santos

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Genetic variation in an individual human exome

Structural variation in the human genome

Human Cancer Syndromes: Clues to the Origin and Nature of Cancer

Copy number variation at 1q21.1 associated with neuroblastoma

Genes that mediate breast cancer metastasis to the brain

Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification

GOTree Machine (GOTM): a web-based platform for interpreting sets of interesting genes using Gene Ontology hierarchies

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Detection of large-scale variation in the human genome

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

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1

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14

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Maria Isabel Achatz

Helena Brentani

Carla Rosenberg

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2012-02-07T00:00:00Z

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