Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations von ABDEL-RAHMAN, Wael M, OLLIKAINEN, Miina, KARIOLA, Reetta, JÄRVINEN, Heikki J, MECKLIN, Jukka-Pekka, NYSTRÖM-LAHTI, Minna, KNUUTILA, Sakari, PELTOMÄKI, Päivi

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Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndrome von Kariola, Reetta, Raevaara, Tiina E., Lönnqvist, Karin E., Nyström-Lahti, Minna

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Novel MLH1 and MSH2 germline mutations in the first HNPCC families identified in Slovakia von Bartosova, Zdena, Fridrichova, Ivana, Bujalkova, Maria, Wolf, Brigitte, Ilencikova, Denisa, Krizan, Peter, Hlavcak, Peter, Palaj, Julius, Lukac, Ludovit, Lukacova, Margita, Böör, Andrej, Haider, Ritva, Jiricny, Josef, Nyström-Lahti, Minna, Marra, Giancarlo

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Life‐time risk of different cancers in hereditary non‐polyposis colorectal cancer (hnpcc) syndrome von Aarnio, Markku, Mecklin, Jukka‐Pekka, Aaltonen, Lauri A., Nyström‐Lahti, Minna, Järvinen, Heikki J.

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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer von Leach, Fredrick S., Nicolaides, Nicholas C., Papadopoulos, Nickolas, Liu, Bo, Jen, Jin, Parsons, Ramon, Peltomäki, Päivi, Sistonen, Pertti, Aaltonen, Lauri A., Nyström-Lahti, Minna, Guan, X.-Y., Zhang, Ji, Meltzer, Paul S., Yu, Jing-Wei, Kao, Fa-Ten, Chen, David J., Cerosaletti, Karen M., Fournier, R.E.Keith, Todd, Sean, Lewis, Tracey, Leach, Robin J., Naylor, Susan L., Weissenbach, Jean, Mecklin, Jukka-Pekka, Järvinen, Heikki, Petersen, Gloria M., Hamilton, Stanley R., Green, Jane, Jass, Jeremy, Watson, Patrice, Lynch, Henry T., Trent, Jeffrey M., de la Chapelle, Albert, Kinzler, Kenneth W., Vogelstein, Bert

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Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer von Peltomäki, Päivi, Hemminki, Akseli, Nyström-Lahti, Minna, Aaltonen, Lauri A, Mecklin, Jukka-Pekka, Salovaara, Reijo, Järvinen, Heikki, de la Chapelle, Albert

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MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis von Wu, Ying, Nyström-Lahti, Minna, Osinga, Jan, Looman, Maaike W. G., Peltomäki, Päivi, Aaltonen, Lauri A., de la Chapelle, Albert, Hofstra, Robert M. W., Buys, Charles H. C. M.

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Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer von Nyström-Lahti, Minna, Perrera, Claudia, Räschle, Markus, Panyushkina-Seiler, Elena, Marra, Giancarlo, Curci, Anna, Quaresima, Barbara, Costanzo, Francesco, D'Urso, Michele, Venuta, Salvatore, Jiricny, Josef

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Predictive genetic testing for hereditary non‐polyposis colorectal cancer: Uptake and long‐term satisfaction von Aktan‐Collan, Katja, Mecklin, Jukka‐Pekka, Järvinen, Heikki, Nyström‐Lahti, Minna, Peltomäki, Päivi, Söderling, Ismo, Uutela, Antti, de la Chapelle, Albert, Kääriäinen, Helena

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Epigenetic Phenotypes Distinguish Microsatellite-Stable and -Unstable Colorectal Cancers von Kuismanen, Shannon A., Holmberg, Mari T., Salovaara, Reijo, Schweizer, Pascal, Aaltonen, Lauri A., de la Chapelle, Albert, Nyström-Lahti, Minna, Peltomäki, Päivi

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PTEN Mutational Spectra, Expression Levels, and Subcellular Localization in Microsatellite Stable and Unstable Colorectal Cancers von Zhou, Xiao-Ping, Loukola, Anu, Salovaara, Reijo, Nystrom-Lahti, Minna, Peltomäki, Päivi, de la Chapelle, Albert, Aaltonen, Lauri A., Eng, Charis

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Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein von Raevaara, Tiina E, Vaccaro, Carlos, Abdel-Rahman, Wael M, Mocetti, Esteban, Bala, Shashi, Lönnqvist, Karin E, Kariola, Reetta, Lynch, Henry T, Peltomäki, Päivi, Nyström-Lahti, Minna

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Mismatch repair defects in cancer von Jiricny, Josef, Nyström-Lahti, Minna

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Tolerance of Human MSH2+/-Lymphoblastoid Cells to the Methylating Agent Temozolomide von Marra, Giancarlo, D'Atri, Stefania, Corti, Chantal, Bonmassar, Laura, Cattaruzza, Maria Sofia, Schweizer, Pascal, Heinimann, Karl, Bartosova, Zdena, Nyström-Lahti, Minna, Jiricny, Josef

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HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1 von Raevaara, Tiina E., Gerdes, Anne-Marie, Lönnqvist, Karin E., Tybjærg-Hansen, Anne, Abdel-Rahman, Wael M., Kariola, Reetta, Peltomäki, Päivi, Nyström-Lahti, Minna

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Endometrial and Colorectal Tumors from Patients with Hereditary Nonpolyposis Colon Cancer Display Different Patterns of Microsatellite Instability von Kuismanen, Shannon A., Moisio, Anu-Liisa, Schweizer, Pascal, Truninger, Kaspar, Salovaara, Reijo, Arola, Johanna, Butzow, Ralf, Jiricny, Josef, Nyström-Lahti, Minna, Peltomäki, Päivi

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Low frequency of hMSH2 mutations in Swedish HNPCC families von Wahlberg, Siobhan S., Nyström‐Lahti, Minna, Kane, Michael F., Kolodner, Richard D., Peltomäki, Päivi, Lindblom, Annika

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Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds von Nyström-Lahti, Minna, Holmberg, Mari, Fidalgo, Paulo, Salovaara, Reijo, de la Chapelle, Albert, Jiricny, Josef, Peltomäki, Päivi

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Founding mutations and Alu-mediated recombination in hereditary colon cancer von Nyström-Lahti, Minna, Kristo, Paula, Nicolaides, Nicholas C, Chang, Sheng-Yung, Aaltonen, Lauri A, Moisio, Anu-Liisa, Järvinen, Heikki J, Mecklin, Jukka-Pekka, Kinzler, Kenneth W, Vogelstein, Bert, De La Chapelle, Albert, Peltomäki, Päivi

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Identification of hMutLβ, a Heterodimer of hMLH1 and hPMS1 von Räschle, Markus, Marra, Giancarlo, Nyström-Lahti, Minna, Schär, Primo, Jiricny, Josef

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