M. Korhonen

发表

Functional characterization of MutL homologue mismatch repair proteins and their variants

M. Korhonen, 2009 .

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

T. Ørntoft, C. Andersen, I. Bernstein, 2009, Familial Cancer.

A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance—functional analysis reveals the pathogenic one

S. Ollila, M. Nyström, A. Gerdes, 2011, Familial Cancer.

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

A. de la Chapelle, C. Sutter, P. Peltomäki, 2005, Gastroenterology.

The first functional study of MLH3 mutations found in cancer patients

M. Nyström, M. Korhonen, Elina Vuorenmaa, 2008, Genes, chromosomes & cancer.

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

T. Raevaara, M. Nyström, H. Lohi, 2007, Oncology reports.

BRAF mutation in sporadic colorectal cancer and Lynch syndrome

A. Ristimäki, P. Peltomäki, J. Mecklin, 2013, Virchows Archiv.

MutSβ exceeds MutSα in dinucleotide loop repair

S. Ollila, M. Nyström, M. Kansikas, 2010, British Journal of Cancer.

Enzyme immunoassay of estriol in pregnancy urine.

U. Stenman, M. Korhonen, K. Juntunen, 1980, Clinical Chemistry.