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There are 6365 results for: content related to: The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome

  1. Genetic Testing for Hereditary Nonpolyposis Colorectal Cancer (HNPCC)

    Unit

    Current Protocols in Human Genetics

    10:10.12.1–10.12.28

    Madhuri R. Hegde and Benjamin B. Roa

    Published Online : 1 APR 2009, DOI: 10.1002/0471142905.hg1012s61

  2. Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining

    The Journal of Pathology

    Volume 207, Issue 4, December 2005, Pages: 385–395, Elisabeth Mangold, Constanze Pagenstecher, Waltraut Friedl, Hans-Peter Fischer, Sabine Merkelbach-Bruse, Maike Ohlendorf, Nicolaus Friedrichs, Stefan Aretz, Reinhard Buettner, Peter Propping and Micaela Mathiak

    Version of Record online : 10 OCT 2005, DOI: 10.1002/path.1858

  3. Germ line MLH1 and MSH2 mutations in Taiwanese Lynch syndrome families: characterization of a founder genomic mutation in the MLH1 gene

    Clinical Genetics

    Volume 75, Issue 4, April 2009, Pages: 334–345, R Tang, C Hsiung, J-Y Wang, C-H Lai, H-T Chien, L-L Chiu, C-T Liu, H-H Chen, H-M Wang, S-X Chen, L-L Hsieh and the TCOG HNPCC Consortium

    Version of Record online : 15 APR 2009, DOI: 10.1111/j.1399-0004.2009.01162.x

  4. You have free access to this content
    Analysis of telomere dynamics in peripheral blood cells from patients with Lynch syndrome

    Cancer

    Volume 117, Issue 18, 15 September 2011, Pages: 4325–4335, Cristina Bozzao, Patrizia Lastella, Maurizio Ponz de Leon, Monica Pedroni, Carmela Di Gregorio, Francesco D. D'Ovidio, Nicoletta Resta, Fernando Prete, Ginevra Guanti and Alessandro Stella

    Version of Record online : 8 MAR 2011, DOI: 10.1002/cncr.26022

  5. You have free access to this content
    Evidence for the role of aberrant DNA methylation in the pathogenesis of Lynch syndrome adenomas

    International Journal of Cancer

    Volume 120, Issue 9, 1 May 2007, Pages: 1922–1929, Andrew Kaz, Young-Ho Kim, Slavomir Dzieciatkowski, Henry Lynch, Patrice Watson, Mary Kay Washington, Li Lin and William M. Grady

    Version of Record online : 2 FEB 2007, DOI: 10.1002/ijc.22544

  6. You have free access to this content
    Characterization of components of the mismatch repair machinery in Trypanosoma brucei

    Molecular Microbiology

    Volume 51, Issue 1, January 2004, Pages: 159–173, Joanna S. Bell, Timothy I. Harvey, Anne-Marie Sims and Richard McCulloch

    Version of Record online : 11 NOV 2003, DOI: 10.1046/j.1365-2958.2003.03804.x

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

    Human Mutation

    Volume 38, Issue 1, January 2017, Pages: 64–77, Rossella Tricarico, Mariann Kasela, Cristina Mareni, Bryony A. Thompson, Aurélie Drouet, Lucia Staderini, Greta Gorelli, Francesca Crucianelli, Valentina Ingrosso, Jukka Kantelinen, Laura Papi, Maria De Angioletti, Margherita Berardi, Pascaline Gaildrat, Omar Soukarieh, Daniela Turchetti, Alexandra Martins, Amanda B. Spurdle, Minna Nyström, Maurizio Genuardi and InSiGHT Variant Interpretation Committee

    Version of Record online : 17 OCT 2016, DOI: 10.1002/humu.23117

  8. Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome

    Genes, Chromosomes and Cancer

    Volume 48, Issue 8, August 2009, Pages: 737–744, Renée C. Niessen, Robert M. W. Hofstra, Helga Westers, Marjolijn J. L. Ligtenberg, Krista Kooi, Paul O. J. Jager, Marloes L. de Groote, Trijnie Dijkhuizen, Maran J. W. Olderode-Berends, Harry Hollema, Jan H. Kleibeuker and Rolf H. Sijmons

    Version of Record online : 19 MAY 2009, DOI: 10.1002/gcc.20678

  9. Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility

    Human Mutation

    Volume 33, Issue 1, January 2012, Pages: 180–188, Michel Crépin, Marie-Claire Dieu, Sophie Lejeune, Fabienne Escande, Denis Boidin, Nicole Porchet, Gilles Morin, Sylvie Manouvrier, Michèle Mathieu and Marie-Pierre Buisine

    Version of Record online : 31 OCT 2011, DOI: 10.1002/humu.21617

  10. Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome

    The Journal of Pathology

    Volume 214, Issue 1, January 2008, Pages: 10–16, N Rahner, N Friedrichs, V Steinke, S Aretz, W Friedl, R Buettner, E Mangold, P Propping and C Walldorf

    Version of Record online : 31 OCT 2007, DOI: 10.1002/path.2263

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    Diethylstilbestrol effects and lymphomagenesis in Mlh1-deficient mice

    International Journal of Cancer

    Volume 115, Issue 4, 1 July 2005, Pages: 666–669, Omar Kabbarah, Andrea K. Sotelo, Mary Ann Mallon, Erin L. Winkeler, Ming-Yu Fan, John D. Pfeifer, Darryl Shibata, David H. Gutmann and Paul J. Goodfellow

    Version of Record online : 7 FEB 2005, DOI: 10.1002/ijc.20918

  12. Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)

    Genes, Chromosomes and Cancer

    Volume 44, Issue 2, October 2005, Pages: 123–138, Heleen van der Klift, Juul Wijnen, Anja Wagner, Paul Verkuilen, Carli Tops, Robyn Otway, Maija Kohonen-Corish, Hans Vasen, Cristina Oliani, Daniela Barana, Pal Moller, Celia DeLozier-Blanchet, Pierre Hutter, William Foulkes, Henry Lynch, John Burn, Gabriela Möslein and Riccardo Fodde

    Version of Record online : 7 JUN 2005, DOI: 10.1002/gcc.20219

  13. Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

    Clinical Genetics

    Volume 69, Issue 1, January 2006, Pages: 40–47, G Kurzawski, J Suchy, M Lener, E Kłujszo-Grabowska, J Kładny, K Safranow, K Jakubowska, A Jakubowska, T Huzarski, T Byrski, T Dębniak, C Cybulski, J Gronwald, O Oszurek, D Oszutowska, E Kowalska, S Góźdź, S Niepsuj, R Słomski, A Pławski, A Łącka-Wojciechowska, A Rozmiarek, Ł Fiszer-Maliszewska, M Bębenek, D Sorokin, MM Sąsiadek, A Stembalska, Z Grzebieniak, E Kilar, M Stawicka, D Godlewski, P Richter, I Brożek, B Wysocka, J Limon, A Jawień, Z Banaszkiewicz, H Janiszewska, J Kowalczyk, D Czudowska, RJ Scott and J Lubiński

    Version of Record online : 13 DEC 2005, DOI: 10.1111/j.1399-0004.2006.00550.x

  14. Semiquantitative assessment of immunohistochemistry for mismatch repair proteins in Lynch syndrome

    Histopathology

    Volume 56, Issue 3, February 2010, Pages: 331–344, Emma Barrow, Emma Jagger, Judith Brierley, Andrew Wallace, Gareth Evans, James Hill and Ray McMahon

    Version of Record online : 22 FEB 2010, DOI: 10.1111/j.1365-2559.2010.03485.x

  15. Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts

    Journal of Gastroenterology and Hepatology

    Volume 32, Issue 2, February 2017, Pages: 427–438, Daniel D Buchanan, Mark Clendenning, Christophe Rosty, Stine V Eriksen, Michael D Walsh, Rhiannon J Walters, Stephen N Thibodeau, Jenna Stewart, Susan Preston, Aung Ko Win, Louisa Flander, Driss Ait Ouakrim, Finlay A Macrae, Alex Boussioutas, Ingrid M Winship, Graham G Giles, John L Hopper, Melissa C Southey, Dallas English, Mark A Jenkins and on behalf of the Melbourne Collaborative Cohort Study and the Australasian Colorectal Cancer Family Registry Cohort investigators

    Version of Record online : 21 FEB 2017, DOI: 10.1111/jgh.13468

  16. You have full text access to this OnlineOpen article
    Lynch Syndrome Associated with Two MLH1 Promoter Variants and Allelic Imbalance of MLH1 Expression

    Human Mutation

    Volume 36, Issue 6, June 2015, Pages: 622–630, Luke B. Hesson, Deborah Packham, Chau-To Kwok, Andrea C. Nunez, Benedict Ng, Christa Schmidt, Michael Fields, Jason W.H. Wong, Mathew A. Sloane and Robyn L. Ward

    Version of Record online : 17 APR 2015, DOI: 10.1002/humu.22785

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    Large genomic rearrangements and germline epimutations in Lynch syndrome

    International Journal of Cancer

    Volume 124, Issue 10, 15 May 2009, Pages: 2333–2340, Annette Gylling, Maaret Ridanpää, Outi Vierimaa, Kristiina Aittomäki, Kristiina Avela, Helena Kääriäinen, Hannele Laivuori, Minna Pöyhönen, Satu-Leena Sallinen, Carina Wallgren-Pettersson, Heikki J. Järvinen, Jukka-Pekka Mecklin and Paivi Peltomäki

    Version of Record online : 18 DEC 2008, DOI: 10.1002/ijc.24230

  18. You have full text access to this OnlineOpen article
    Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants

    Human Mutation

    Volume 32, Issue 1, January 2011, Pages: 107–115, Minttu Kansikas, Reetta Kariola and Minna Nyström

    Version of Record online : 22 DEC 2010, DOI: 10.1002/humu.21409

  19. You have free access to this content
    Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

    International Journal of Cancer

    Volume 103, Issue 5, 20 February 2003, Pages: 636–641, Yaping Wang, Waltraut Friedl, Christof Lamberti, Matthias Jungck, Micaela Mathiak, Constanze Pagenstecher, Peter Propping and Elisabeth Mangold

    Version of Record online : 6 DEC 2002, DOI: 10.1002/ijc.10869

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    Evidence for breast cancer as an integral part of lynch syndrome

    Genes, Chromosomes and Cancer

    Volume 51, Issue 1, January 2012, Pages: 83–91, Nicole Buerki, Lucienne Gautier, Michal Kovac, Giancarlo Marra, Mauro Buser, Hansjakob Mueller and Karl Heinimann

    Version of Record online : 27 OCT 2011, DOI: 10.1002/gcc.20935