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Publications 2010 2017

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2010

MutSbeta exceeds MutSalpha in dinucleotide loop repair

Kantelinen, J., Kansikas, M., Korhonen, M., Ollila, S., Heinimann, K., Kariola, R. & Nyström, M., 2010, In : British Journal of Cancer. 102, 6, p. 1068–1073 6 p.

Research output: Contribution to journalArticleScientificpeer-review

2011

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

Kantelinen, J., Hansen, T. V. O., Kansikas, M., Krogh, L. N., Korhonen, M. K., Ollila, S., Nystrom, M., Gerdes, A-M. & Kariola, R., 2011, In : Familial Cancer. 2011, 10, p. 515-520 6 p.

Research output: Contribution to journalArticleScientificpeer-review

2012

Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients.

Kantelinen, J., Kansikas, M., Candelin, S., Hampel, H., Smith, B., Holm, L., Kariola, R. & Nyström, M., 2012, In : Human Mutation. 33, 8, p. 1294-1301 8 p.

Research output: Contribution to journalArticleScientificpeer-review

2014

Assessing How Reduced Expression Levels of the Mismatch Repair Genes MLH1, MSH2, and MSH6 Affect Repair Efficiency

Kansikas, M., Kasela, M., Kantelinen, J. & Nystrom, M., Sep 2014, In : Human Mutation. 35, 9, p. 1123-1127 5 p.

Research output: Contribution to journalArticleScientificpeer-review

2016

Human DNA polymerase α interacts with mismatch repair proteins MSH2 and MSH6

Itkonen, H. M., Kantelinen, J., Vaara, M., Parkkinen, S., Schlott, B., Grosse, F., Nystrom, M., Syvaoja, J. E. & Pospiech, H., Dec 2016, In : FEBS Letters. 590, 23, p. 4233-4241 9 p.

Research output: Contribution to journalArticleScientificpeer-review

2017

Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants

Tricarico, R., Kasela, M., Mareni, C., Thompson, B. A., Drouet, A., Staderini, L., Gorelli, G., Crucianelli, F., Ingrosso, V., Kantelinen, J., Papi, L., De Angioletti, M., Berardi, M., Gaildrat, P., Soukarieh, O., Turchetti, D., Martins, A., Spurdle, A. B., Nyström, M., Genuardi, M. & 1 othersInSiGHT Variant Interpretation, Jan 2017, In : Human Mutation. 38, 1, p. 64-77 14 p.

Research output: Contribution to journalArticleScientificpeer-review

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