Abdel-Rahman WM - Search Results

1

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

2

Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach.

Ollikainen M, Hannelius U, Lindgren CM, Abdel-Rahman WM, Kere J, Peltomäki P. Ollikainen M, et al. Oncogene. 2007 Jul 5;26(31):4541-9. doi: 10.1038/sj.onc.1210236. Epub 2007 Jan 29. Oncogene. 2007. PMID: 17260015

3

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

4

HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1.

Raevaara TE, Gerdes AM, Lönnqvist KE, Tybjaerg-Hansen A, Abdel-Rahman WM, Kariola R, Peltomäki P, Nyström-Lahti M. Raevaara TE, et al. Genes Chromosomes Cancer. 2004 Jul;40(3):261-5. doi: 10.1002/gcc.20040. Genes Chromosomes Cancer. 2004. PMID: 15139004

5

Molecular basis and diagnostics of hereditary colorectal cancers.

Abdel-Rahman WM, Peltomäki P. Abdel-Rahman WM, et al. Ann Med. 2004;36(5):379-88. doi: 10.1080/07853890410018222. Ann Med. 2004. PMID: 15478312 Free article. Review.

6

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

7

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

8

APC and beta-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers.

Kariola R, Abdel-Rahman WM, Ollikainen M, Butzow R, Peltomäki P, Nyström M. Kariola R, et al. Fam Cancer. 2005;4(2):187-90. doi: 10.1007/s10689-004-6130-4. Fam Cancer. 2005. PMID: 15951972

9

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.

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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