Abdel-Rahman WM - Search Results

1

Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancer.

Renkonen E, Zhang Y, Lohi H, Salovaara R, Abdel-Rahman WM, Nilbert M, Aittomaki K, Jarvinen HJ, Mecklin JP, Lindblom A, Peltomaki P. Renkonen E, et al. J Clin Oncol. 2003 Oct 1;21(19):3629-37. doi: 10.1200/JCO.2003.03.181. J Clin Oncol. 2003. PMID: 14512394

2

Differential cancer predisposition in Lynch syndrome: insights from molecular analysis of brain and urinary tract tumors.

Gylling AH, Nieminen TT, Abdel-Rahman WM, Nuorva K, Juhola M, Joensuu EI, Järvinen HJ, Mecklin JP, Aarnio M, Peltomäki PT. Gylling AH, et al. Carcinogenesis. 2008 Jul;29(7):1351-9. doi: 10.1093/carcin/bgn133. Epub 2008 Jun 12. Carcinogenesis. 2008. PMID: 18550572

3

Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number.

Abdel-Rahman WM, Lohi H, Knuutila S, Peltomäki P. Abdel-Rahman WM, et al. Oncogene. 2005 Jan 20;24(4):706-13. doi: 10.1038/sj.onc.1208129. Oncogene. 2005. PMID: 15580308

4

Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations.

Abdel-Rahman WM, Ollikainen M, Kariola R, Järvinen HJ, Mecklin JP, Nyström-Lahti M, Knuutila S, Peltomäki P. Abdel-Rahman WM, et al. Oncogene. 2005 Feb 24;24(9):1542-51. doi: 10.1038/sj.onc.1208387. Oncogene. 2005. PMID: 15674332

5

Molecular analysis of familial endometrial carcinoma: a manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome?

Ollikainen M, Abdel-Rahman WM, Moisio AL, Lindroos A, Kariola R, Järvelä I, Pöyhönen M, Butzow R, Peltomäki P. Ollikainen M, et al. J Clin Oncol. 2005 Jul 20;23(21):4609-16. doi: 10.1200/JCO.2005.06.055. Epub 2005 Apr 18. J Clin Oncol. 2005. PMID: 15837969

6

Adenomatous polyposis families that screen APC mutation-negative by conventional methods are genetically heterogeneous.

Renkonen ET, Nieminen P, Abdel-Rahman WM, Moisio AL, Järvelä I, Arte S, Järvinen HJ, Peltomäki P. Renkonen ET, et al. J Clin Oncol. 2005 Aug 20;23(24):5651-9. doi: 10.1200/JCO.2005.14.712. J Clin Oncol. 2005. PMID: 16110024

7

The genetics of HNPCC: application to diagnosis and screening.

Abdel-Rahman WM, Mecklin JP, Peltomäki P. Abdel-Rahman WM, et al. Crit Rev Oncol Hematol. 2006 Jun;58(3):208-20. doi: 10.1016/j.critrevonc.2005.11.001. Epub 2006 Jan 23. Crit Rev Oncol Hematol. 2006. PMID: 16434208 Review.

8

Molecular analysis of endometrial tumorigenesis: importance of complex hyperplasia regardless of atypia.

Nieminen TT, Gylling A, Abdel-Rahman WM, Nuorva K, Aarnio M, Renkonen-Sinisalo L, Järvinen HJ, Mecklin JP, Bützow R, Peltomäki P. Nieminen TT, et al. Clin Cancer Res. 2009 Sep 15;15(18):5772-83. doi: 10.1158/1078-0432.CCR-09-0506. Epub 2009 Sep 1. Clin Cancer Res. 2009. PMID: 19723644

9

Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases.

Lotsari JE, Gylling A, Abdel-Rahman WM, Nieminen TT, Aittomäki K, Friman M, Pitkänen R, Aarnio M, Järvinen HJ, Mecklin JP, Kuopio T, Peltomäki P. Lotsari JE, et al. Breast Cancer Res. 2012 Jun 12;14(3):R90. doi: 10.1186/bcr3205. Breast Cancer Res. 2012. PMID: 22691310 Free PMC article.

10

Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency.

Nieminen TT, O'Donohue MF, Wu Y, Lohi H, Scherer SW, Paterson AD, Ellonen P, Abdel-Rahman WM, Valo S, Mecklin JP, Järvinen HJ, Gleizes PE, Peltomäki P. Nieminen TT, et al. Gastroenterology. 2014 Sep;147(3):595-598.e5. doi: 10.1053/j.gastro.2014.06.009. Epub 2014 Jun 15. Gastroenterology. 2014. PMID: 24941021 Free PMC article.

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