Works matching DE "MSH2 gene"

Results: 86
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    Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells.

    Published in:
    Nature Medicine, 2011, v. 17, n. 10, p. 1298, doi. 10.1038/nm.2430
    By:
    • Diouf, Barthelemy;
    • Cheng, Qing;
    • Krynetskaia, Natalia F;
    • Yang, Wenjian;
    • Cheok, Meyling;
    • Pei, Deqing;
    • Fan, Yiping;
    • Cheng, Cheng;
    • Krynetskiy, Evgeny Y;
    • Geng, Hui;
    • Chen, Siying;
    • Thierfelder, William E;
    • Mullighan, Charles G;
    • Downing, James R;
    • Hsieh, Peggy;
    • Pui, Ching-Hon;
    • Relling, Mary V;
    • Evans, William E
    Publication type:
    Article
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    Randomized phase III clinical trial comparing the combination of capecitabine and oxaliplatin (CAPOX) with the combination of 5-fluorouracil, leucovorin and oxaliplatin (modified FOLFOX6) as adjuvant therapy in patients with operated high-risk stage II or stage III colorectal cancer

    Published in:
    BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1406-7
    By:
    • Pectasides, Dimitrios;
    • Karavasilis, Vasilios;
    • Papaxoinis, George;
    • Gourgioti, Georgia;
    • Makatsoris, Thomas;
    • Raptou, Georgia;
    • Vrettou, Eleni;
    • Sgouros, Joseph;
    • Samantas, Epaminontas;
    • Basdanis, George;
    • Papakostas, Pavlos;
    • Bafaloukos, Dimitrios;
    • Kotoula, Vassiliki;
    • Kalofonos, Haralambos P.;
    • Scopa, Chrisoula D.;
    • Pentheroudakis, George;
    • Fountzilas, George
    Publication type:
    Article
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    BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma.

    Published in:
    Cancer (0008543X), 2013, v. 119, n. 2, p. 332, doi. 10.1002/cncr.27720
    By:
    • Pennington, Kathryn P.;
    • Walsh, Tom;
    • Lee, Ming;
    • Pennil, Christopher;
    • Novetsky, Akiva P.;
    • Agnew, Kathy J.;
    • Thornton, Anne;
    • Garcia, Rochelle;
    • Mutch, David;
    • King, Mary‐Claire;
    • Goodfellow, Paul;
    • Swisher, Elizabeth M.
    Publication type:
    Article
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    Azathioprine-Induced Carcinogenesis in Mice According to Msh2 Genotype.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2010, v. 102, n. 22, p. 1731, doi. 10.1093/jnci/djq389
    By:
    • Chalastanis, Alexandra;
    • Penard-Lacronique, Virginie;
    • Svrcek, Magali;
    • Defaweux, Valérie;
    • Antoine, Nadine;
    • Buhard, Olivier;
    • Dumont, Sylvie;
    • Fabiani, Bettina;
    • Renault, Isabelle;
    • Tubacher, Emmanuel;
    • Fléjou, Jean-François;
    • Riele, Hein te;
    • Duval, Alex;
    • Muleris, Martine
    Publication type:
    Article
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    Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study).

    Published in:
    Clinical Genetics, 2006, v. 69, n. 1, p. 40, doi. 10.1111/j.1399-0004.2006.00550.x
    By:
    • Kurzawski, G.;
    • Suchy, J.;
    • Lener, M.;
    • Kłujszo-Grabowska, E.;
    • Kładny, J.;
    • Safranow, K.;
    • Jakubowska, K.;
    • Jakubowska, A.;
    • Huzarski, T.;
    • Byrski, T.;
    • Dȩbniak, T.;
    • Cybulski, C.;
    • Gronwald, J.;
    • Oszurek, O.;
    • Oszutowska, D.;
    • Kowalska, E.;
    • Góźdź, S.;
    • Niepsuj, S;
    • Słomski, R;
    • Pławski, A.
    Publication type:
    Article
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    Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 1, p. 55, doi. 10.1038/ejhg.2012.117
    By:
    • Baas, Annette F;
    • Gabbett, Michael;
    • Rimac, Milan;
    • Kansikas, Minttu;
    • Raphael, Martine;
    • Nievelstein, Rutger AJ;
    • Nicholls, Wayne;
    • Offerhaus, Johan;
    • Bodmer, Danielle;
    • Wernstedt, Annekatrin;
    • Krabichler, Birgit;
    • Strasser, Ulrich;
    • Nyström, Minna;
    • Zschocke, Johannes;
    • Robertson, Stephen P;
    • van Haelst, Mieke M;
    • Wimmer, Katharina
    Publication type:
    Article