Germline DNA copy number variation in familial and early-onset breast cancer
about
Rare Germline Copy Number Variations and Disease Susceptibility in Familial MelanomanbCNV: a multi-constrained optimization model for discovering copy number variants in single-cell sequencing dataHereditary 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 patientLi-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 networkStructural 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 exampleThe association of copy number variation and percent mammographic densityIdentification 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 patientsGenome-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 RiskMutations 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.
P2860
Q28394958-4DB943AB-F72B-4694-B429-2DEBC9552EC5Q31131418-5E9437D8-D348-40A5-A45D-48842B2F398CQ33356511-453EF228-C305-48C1-BF60-A2A836675D01Q33615771-6F72BD38-B59C-4E0B-BA1E-5ACC60ACDDF9Q33684029-4E3C3076-0F92-4B3B-A9DA-0475EDF37FA3Q33780936-A72D45D4-903C-41DB-B820-6B82A6D84E39Q34110933-3DF0920A-B15E-4080-B63A-B6A336C7F053Q34301309-9EA06230-B168-484B-AACF-DA86B0140B44Q34318239-60C3786C-7059-4038-AFA7-D4858DFF4CF3Q34478069-1C614D5E-AE24-4925-8D6E-C60E3A3C0D72Q34558816-6AE4253A-DE16-4797-BA8A-D9EE66FF3CB8Q34613122-D4CFA773-4B86-4B3D-8361-EA7E61917FA6Q34695260-E1C3CC47-2C1B-4F25-A9FD-AE64F6D3F3ECQ34964524-E87AB7A1-BFA5-4370-BFB8-2F533C17B655Q35238058-DC4B1DE1-0CB2-46F9-8A58-3B311A325552Q35631708-F51C18DB-C38D-4558-AC56-4E132A7AFA76Q35685546-DE1E912D-F724-4541-9832-653AB77CF9CCQ35866409-5F79F66A-DE66-4321-A300-79F8C0B371BEQ36528396-4937E049-2691-4312-9F34-F7AED8D87EECQ36572009-7F2C3EF7-421F-43F6-B260-76D9A6F37371Q36683904-7F461AC7-3F22-482E-9D53-05F1D3CB3CDFQ37093114-DEB39AD9-C87D-4CCA-B941-1E73A774F131Q37200793-EDD09A97-7D0A-4EBE-B87C-7EFE9BE691C0Q37590426-A70E759F-B8FF-4F07-905C-49BE806F16F0Q37615396-0926BE11-7671-41ED-9D70-9FF469753AD4Q37708268-7C68A865-2D17-4127-A068-46703A5CF5DCQ37714913-D0B29251-1B76-488A-9960-E00289B75EB4Q38003668-70EC32EF-691F-4043-A1CE-FDBD2F4A888CQ38072148-C6070EF3-1CDB-4E2A-BB60-1C2318B9D37EQ38889379-B7B2D637-F95C-4CCF-92ED-A8925A5C3FDEQ38983260-792C47C6-9CB2-4F4C-B90B-AAA8BF9D19D6Q39973575-218FD30E-9FBA-4299-8EFC-52305E1D99F5Q40950711-587FA877-CC6B-4130-B3A3-B4D7689C5D8AQ41137258-FD12589B-C6F3-4C2D-AC39-D836A0977AD7Q41356138-61A705CB-ACB2-4239-BA1E-60DA84BE9308Q41715498-4C2AFB5C-9A2E-4FA3-8551-FCCA33B2CA0BQ42514400-FF64D817-3FBB-42D3-BA96-7D0E1FFCB218Q44577314-404D95F1-96A8-476F-B63E-6AC767B746C9Q47127499-79618A9A-670E-4420-B2FE-7BD436722375Q47425936-5146B27F-C61B-42F3-9EC7-9E8C5E490D6D
P2860
Germline DNA copy number variation in familial and early-onset breast cancer
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Germline DNA copy number variation in familial and early-onset breast cancer
@ast
Germline DNA copy number variation in familial and early-onset breast cancer
@en
type
label
Germline DNA copy number variation in familial and early-onset breast cancer
@ast
Germline DNA copy number variation in familial and early-onset breast cancer
@en
prefLabel
Germline DNA copy number variation in familial and early-onset breast cancer
@ast
Germline DNA copy number variation in familial and early-onset breast cancer
@en
P2093
P2860
P50
P356
P1476
Germline DNA copy number variation in familial and early-onset breast cancer
@en
P2093
Amanda F Nóbrega
Amanda Gonçalves
Ana Cv Krepischi
Angela M Vianna-Morgante
Bianca Cg Lisboa
Erika Mm Santos
Peter L Pearson
Ricardo R Brentani
Silvia S Costa
Tiago M Santos
P2860
P2888
P356
10.1186/BCR3109
P577
2012-02-07T00:00:00Z
P5875
P6179
1050236947