Residential College | false |
Status | 已發表Published |
Epigenetic changes in BRCA1-mutated familial breast cancer | |
Wang, S. M. | |
2015-02-04 | |
Source Publication | Cancer Genetics |
ISSN | 2210-7762 |
Pages | 237-240 |
Abstract | Familial breast cancer occurs in about 10% of breast cancer cases. Germline mutation in BRCA1 is the most penetrant predisposition for the disease. Mutated BRCA1 leads to disease by causing genome instability via multiple mechanisms including epigenetic changes. This review summarizes recent progress in studying the correlation between BRCA1 predisposition and epigenetic alterations in BRCA1-type familial breast cancer. |
Keyword | Brca1 Familial Breast Cancer Gremlin Mutation Epigenetic Alteration Autosomal Dominant |
DOI | 10.1016/j.cancergen.2015.02.001 |
Language | 英語English |
The Source to Article | PB_Publication |
Fulltext Access | |
Citation statistics | |
Document Type | Journal article |
Collection | DEPARTMENT OF PUBLIC HEALTH AND MEDICINAL ADMINISTRATION Faculty of Health Sciences |
Corresponding Author | Wang, S. M. |
Recommended Citation GB/T 7714 | Wang, S. M.. Epigenetic changes in BRCA1-mutated familial breast cancer[J]. Cancer Genetics, 2015, 237-240. |
APA | Wang, S. M..(2015). Epigenetic changes in BRCA1-mutated familial breast cancer. Cancer Genetics, 237-240. |
MLA | Wang, S. M.."Epigenetic changes in BRCA1-mutated familial breast cancer".Cancer Genetics (2015):237-240. |
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