Published September 20, 2015
| Version 1.0
Conference paper
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Absence of NBS1 657Del5 and TP53 exon 8 mutations in Serbian BRCA1/2 negative hereditary breast /ovarian cancer
Creators
- 1. Institute for Oncology and Radiology of Serbia IORS
- 2. Institute for Oncology and Radiology of Serbia IORS
Description
lntroduction: Although hereditary breast cancer usualy arises as the consequence of BRCA /2 deleterious mutations, a large portion of hereditary suspectibility still remains unexplained. Under the polygenic model of inheritance, TP53 and NBS1 where shown to contribute to hereditary breast cancer. NBS1 657Del5 mutation increases the risk for breast cancer three times while mutations in TP53 exon 8 increase the risk for early-onset breast cancer. Since mutations in BRCA1/2 can't explain the whole range of hereditary predisposition, we aimed to investigate the presence of NBS1657del5 and TP53 exon 8 mutations in hereditary breast cancer in Serbia.
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11th Balkan cogress_Ana Krivokuća.pdf
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Additional details
Identifiers
- Other
- COBISS ID 32213721
- URL
- https://plus.cobiss.net/cobiss/si/sl/bib/COBIB/32213721#full
Related works
- Is part of
- 32213721 (Other)
Funding
- Pharmacodynamic and pharmacogenomic research of new drugs in the treatment of solid tumors 41026
- Ministry of Education, Science and Technological Development
Dates
- Available
-
2015