Nyström M - Search Results

1

Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.

Christensen LL, Kariola R, Korhonen MK, Wikman FP, Sunde L, Gerdes AM, Okkels H, Brandt CA, Bernstein I, Hansen TV, Hagemann-Madsen R, Andersen CL, Nyström M, Ørntoft TF. Christensen LL, et al. Among authors: nystrom m. Fam Cancer. 2009;8(4):489-500. doi: 10.1007/s10689-009-9274-4. Epub 2009 Aug 21. Fam Cancer. 2009. PMID: 19697156

2

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. Among authors: nystrom m. Fam Cancer. 2005;4(2):187-90. doi: 10.1007/s10689-004-6130-4. Fam Cancer. 2005. PMID: 15951972

3

Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.

Raevaara TE, Korhonen MK, Lohi H, Hampel H, Lynch E, Lönnqvist KE, Holinski-Feder E, Sutter C, McKinnon W, Duraisamy S, Gerdes AM, Peltomäki P, Kohonen-Ccorish M, Mangold E, Macrae F, Greenblatt M, de la Chapelle A, Nyström M. Raevaara TE, et al. Among authors: nystrom m. Gastroenterology. 2005 Aug;129(2):537-49. doi: 10.1016/j.gastro.2005.06.005. Gastroenterology. 2005. PMID: 16083711

4

The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC.

Ollila S, Fitzpatrick R, Sarantaus L, Kariola R, Ambus I, Velsher L, Hsieh E, Andersen MK, Raevaara TE, Gerdes AM, Mangold E, Peltomäki P, Lynch HT, Nyström M. Ollila S, et al. Among authors: nystrom m. Int J Oncol. 2006 Jan;28(1):149-53. Int J Oncol. 2006. PMID: 16327991

5

Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.

Ollila S, Sarantaus L, Kariola R, Chan P, Hampel H, Holinski-Feder E, Macrae F, Kohonen-Corish M, Gerdes AM, Peltomäki P, Mangold E, de la Chapelle A, Greenblatt M, Nyström M. Ollila S, et al. Among authors: nystrom m. Gastroenterology. 2006 Nov;131(5):1408-17. doi: 10.1053/j.gastro.2006.08.044. Epub 2006 Aug 22. Gastroenterology. 2006. PMID: 17101317

6

Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCC.

Korhonen MK, Raevaara TE, Lohi H, Nyström M. Korhonen MK, et al. Among authors: nystrom m. Oncol Rep. 2007 Feb;17(2):351-4. Oncol Rep. 2007. PMID: 17203173

7

The first functional study of MLH3 mutations found in cancer patients.

Korhonen MK, Vuorenmaa E, Nyström M. Korhonen MK, et al. Among authors: nystrom m. Genes Chromosomes Cancer. 2008 Sep;47(9):803-9. doi: 10.1002/gcc.20581. Genes Chromosomes Cancer. 2008. PMID: 18521850

8

Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome.

Gargiulo S, Torrini M, Ollila S, Nasti S, Pastorino L, Cusano R, Bonelli L, Battistuzzi L, Mastracci L, Bruno W, Savarino V, Sciallero S, Borgonovo G, Nyström M, Bianchi-Scarrà G, Mareni C, Ghiorzo P. Gargiulo S, et al. Among authors: nystrom m. Fam Cancer. 2009;8(4):547-53. doi: 10.1007/s10689-009-9285-1. Fam Cancer. 2009. PMID: 19728162

9

MutSbeta exceeds MutSalpha in dinucleotide loop repair.

Kantelinen J, Kansikas M, Korhonen MK, Ollila S, Heinimann K, Kariola R, Nyström M. Kantelinen J, et al. Among authors: nystrom m. Br J Cancer. 2010 Mar 16;102(6):1068-73. doi: 10.1038/sj.bjc.6605531. Epub 2010 Feb 16. Br J Cancer. 2010. PMID: 20160730 Free PMC article.

10

Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants.

Kansikas M, Kariola R, Nyström M. Kansikas M, et al. Among authors: nystrom m. Hum Mutat. 2011 Jan;32(1):107-15. doi: 10.1002/humu.21409. Hum Mutat. 2011. PMID: 21120944 Free PMC article.

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