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Minna Nyström

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Chemicals & Drugs

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Physiology

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Publications

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Jukka Kantelinen; Reetta Kariola; Betsy Smith; Satu Candelin; Heather Hampel; Liisa Holm; Minttu Kansikas; Minna Nyström
Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients.
Jukka Kantelinen; Anne-Marie Gerdes; Thomas V O Hansen; Minttu Kansikas; Mari K Korhonen; Lotte Nylandsted Krogh; Minna Nyström; Saara Ollila; Reetta Kariola
A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one.
Minttu Kansikas; Reetta Kariola; Minna Nyström
Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants.

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All Publications

2012: Jukka Kantelinen; Reetta Kariola; Betsy Smith; Satu Candelin; Heather Hampel; Liisa Holm; Minttu Kansikas; Minna Nyström
Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients.
Human mutation 2012;33(8):1294-301.
2011: Jukka Kantelinen; Anne-Marie Gerdes; Thomas V O Hansen; Minttu Kansikas; Mari K Korhonen; Lotte Nylandsted Krogh; Minna Nyström; Saara Ollila; Reetta Kariola
A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one.
Familial cancer 2011;10(3):515-20.
2011: Minttu Kansikas; Reetta Kariola; Minna Nyström
Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants.
Human mutation 2011;32(1):107-15.
2010: J Kantelinen; M Kansikas; M K Korhonen; Saara Ollila; K Heinimann; Reetta Kariola; Minna Nyström
MutSbeta exceeds MutSalpha in dinucleotide loop repair.
British journal of cancer 2010;102(6):1068-73.
2009: Lise Lotte Christensen; Reetta Kariola; Mari K Korhonen; Friedrik P Wikman; Lone Sunde; Anne-Marie Gerdes; Henrik Okkels; Carsten A Brandt; Inge Bernstein; Thomas V O Hansen; Rikke Hagemann-Madsen; Claus L Andersen; Minna Nyström; Torben F Ørntoft
Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.
Familial cancer 2009;8(4):489-500.
2008: Saara Ollila; Denis Dermadi Bebek; Josef Jiricny; Minna Nyström
Mechanisms of pathogenicity in human MSH2 missense mutants.
Human mutation 2008;29(11):1355-63.
2008: Mari K Korhonen; Elina Vuorenmaa; Minna Nyström
The first functional study of MLH3 mutations found in cancer patients.
Genes, chromosomes & cancer 2008;47(9):803-9.
2008: Saara Ollila; Denis Dermadi Bebek; Marc S Greenblatt; Minna Nyström
Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification.
International journal of cancer. Journal international du cancer 2008;123(3):720-4.
2007: Philip A Chan; Sekhar Duraisamy; Peter J Miller; Joan A Newell; Carole McBride; Jeffrey P Bond; Tiina E Raevaara; Saara Ollila; Minna Nyström; Andrew J Grimm; John Christodoulou; William S Oetting; Marc S Greenblatt
Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR).
Human mutation 2007;28(7):683-93.
2007: Mari K Korhonen; Tiina E Raevaara; Hannes Lohi; Minna Nyström
Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCC.
Oncology reports 2007;17(2):351-4.
2006: Saara Ollila; Laura Sarantaus; Reetta Kariola; Philip Chan; Heather Hampel; Elke Holinski-Feder; Finlay Macrae; M R J Kohonen-Corish; Anne-Marie Gerdes; Päivi Peltomäki; Elisabeth Mangold; Albert de La Chapelle; Marc S Greenblatt; Minna Nyström
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.
Gastroenterology 2006;131(5):1408-17.
2006: Saara Ollila; Roslyn Fitzpatrick; Laura Sarantaus; Reetta Kariola; Ingrid Ambus; Lea Velsher; Eugene Hsieh; Mette K Andersen; Tiina E Raevaara; Anne-Marie Gerdes; Elisabeth Mangold; Päivi Peltomäki; Henry T Lynch; Minna Nyström
The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC.
International journal of oncology 2006;28(1):149-53.
2005: Tiina E Raevaara; Mari K Korhonen; Hannes Lohi; Heather Hampel; Elly Lynch; Karin E Lönnqvist; Elke Holinski-Feder; Christian Sutter; Wendy McKinnon; Sekhar Duraisamy; Anne-Marie Gerdes; Päivi Peltomäki; Maija Kohonen-Ccorish; Elisabeth Mangold; Finlay Macrae; Marc S Greenblatt; Albert de La Chapelle; Minna Nyström
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.
Gastroenterology 2005;129(2):537-49.
2005: Reetta Kariola; Wael M Abdel-Rahman; Miina Ollikainen; Ralf Butzow; Päivi Peltomäki; Minna Nyström
APC and beta-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers.
Familial cancer 2005;4(2):187-90.