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Page 1
SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients.
Swanson KD, Winter JM, Reis M, Bentires-Alj M, Greulich H, Grewal R, Hruban RH, Yeo CJ, Yassin Y, Iartchouk O, Montgomery K, Whitman SP, Caligiuri MA, Loh ML, Gilliland DG, Look AT, Kucherlapati R, Kern SE, Meyerson M, Neel BG. Swanson KD, et al. Genes Chromosomes Cancer. 2008 Mar;47(3):253-9. doi: 10.1002/gcc.20527. Genes Chromosomes Cancer. 2008. PMID: 18064648
An Msh2 point mutation uncouples DNA mismatch repair and apoptosis.
Lin DP, Wang Y, Scherer SJ, Clark AB, Yang K, Avdievich E, Jin B, Werling U, Parris T, Kurihara N, Umar A, Kucherlapati R, Lipkin M, Kunkel TA, Edelmann W. Lin DP, et al. Cancer Res. 2004 Jan 15;64(2):517-22. doi: 10.1158/0008-5472.can-03-2957. Cancer Res. 2004. PMID: 14744764
Cis lethal genetic interactions attenuate and alter p53 tumorigenesis.
Wang Y, Zhang W, Edelmann L, Kolodner RD, Kucherlapati R, Edelmann W. Wang Y, et al. Proc Natl Acad Sci U S A. 2010 Mar 23;107(12):5511-5. doi: 10.1073/pnas.1001223107. Epub 2010 Mar 8. Proc Natl Acad Sci U S A. 2010. PMID: 20212136 Free PMC article.
16 results