An Integrated in Silico Approach to Analyze the Involvement of Single Amino Acid Polymorphisms in FANCD1/BRCA2-PALB2 and FANCD1/BRCA2-RAD51 Complex
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Biochemistry,General Medicine,Biophysics
Link
http://link.springer.com/content/pdf/10.1007/s12013-014-0002-9.pdf
Reference119 articles.
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2. Reid, S., Schindler, D., Hanenberg, H., Barker, K., Hanks, S., et al. (2007). Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nature Genetics, 39, 162–164.
3. Xia, B., Sheng, Q., Nakanishi, K., Ohashi, A., Wu, J., et al. (2006). Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2. Molecular Cell, 22(6), 719–729.
4. Nathanson, K. N., Wooster, R., & Weber, B. L. (2001). Breast cancer genetics: What we know and what we need. Nature Medicine, 7, 552–556.
5. Wooster, R., Bignell, G., Lancaster, J., Swift, S., Seal, S., et al. (1995). Identification of the breast cancer susceptibility gene BRCA2. Nature, 378, 789–792.
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