Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Microsatellite Instability and MUTYH[original query] |
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Contribution of common monoallelic MUTYH gene variants in German patients with familial colorectal cancer. Cancer biomarkers : section A of Disease markers 2008 4 (2): 55-61. Grünhage Frank, Jungck Matthias, Lamberti Christof, Schulte-Witte Hildegard, Plassmann Dominik, Becker Ursula, Rahner Nils, Aretz Stefan, Friedrichs Nicolaus, Buettner Reinhard, Sauerbruch Tilman, Lammert Fra |
The value of MUTYH testing in patients with early onset microsatellite stable colorectal cancer referred for hereditary nonpolyposis colon cancer syndrome testing. Genetic testing 2007 11 (4): 361-5. Riegert-Johnson Douglas L, Johnson Ruth A, Rabe Kari G, Wang Liang, Thomas Brittany, Baudhuin Linnea M, Thibodeau Stephen N, Boardman Lisa |
Implications of familial colorectal cancer risk profiles and microsatellite instability status. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2009 Mar . Lubbe SJ, Webb EL, Chandler IP, Houlston RS |
Increased cancer predisposition in family members of colorectal cancer patients harboring the p.V600E BRAF mutation: a population-based study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010 Jul 19 (7): 1831-9. Wish Tyler A, Hyde Angela J, Parfrey Patrick S, Green Jane S, Younghusband H Banfield, Simms Michelle I, Fontaine Dan G, Dicks Elizabeth L, Stuckless Susan N, Gallinger Steven, McLaughlin John R, Woods Michael O, Green Roger |
Molecular genetic analysis of 103 sporadic colorectal tumours in Czech patients. PloS one 2011 6 (8): e24114. Vasovcak Peter, Pavlikova Kristyna, Sedlacek Zdenek, Skapa Petr, Kouda Martin, Hoch Jiri, Krepelova An |
Clinical and molecular detection of inherited colorectal cancers in northeast Italy: a first prospective study of incidence of Lynch syndrome and MUTYH-related colorectal cancer in Italy. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2012 Jun 33 (3): 857-64. Urso E, Agostini M, Pucciarelli S, Rugge M, Bertorelle R, Maretto I, Bedin C, D'Angelo E, Mescoli C, Zorzi M, Viel A, Bruttocao G, Ferraro B, Erroi F, Contin P, De Salvo G L, Nitti |
Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients. Scandinavian journal of gastroenterology 2013 Jun 48 (6): 672-8. Tanskanen Tomas, Gylfe Alexandra E, Katainen Riku, Taipale Minna, Renkonen-Sinisalo Laura, Mecklin Jukka-Pekka, Järvinen Heikki, Tuupanen Sari, Kilpivaara Outi, Vahteristo Pia, Aaltonen Lauri |
Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms. PloS one 2013 8 (11): e81194. De Lellis Laura, Aceto Gitana Maria, Curia Maria Cristina, Catalano Teresa, Mammarella Sandra, Veschi Serena, Fantini Fabiana, Battista Pasquale, Stigliano Vittoria, Messerini Luca, Mareni Cristina, Sala Paola, Bertario Lucio, Radice Paolo, Cama Alessand |
Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis. American journal of human genetics 2016 Aug 99 (2): 337-51. Adam Ronja, Spier Isabel, Zhao Bixiao, Kloth Michael, Marquez Jonathan, Hinrichsen Inga, Kirfel Jutta, Tafazzoli Aylar, Horpaopan Sukanya, Uhlhaas Siegfried, Stienen Dietlinde, Friedrichs Nicolaus, Altmüller Janine, Laner Andreas, Holzapfel Stefanie, Peters Sophia, Kayser Katrin, Thiele Holger, Holinski-Feder Elke, Marra Giancarlo, Kristiansen Glen, Nöthen Markus M, Büttner Reinhard, Möslein Gabriela, Betz Regina C, Brieger Angela, Lifton Richard P, Aretz Stef |
Efficacy of immune checkpoint blockade in MUTYH-associated hereditary colorectal cancer. Investigational new drugs 2019 Aug . Volkov Nikita M, Yanus Grigoriy A, Ivantsov Alexandr O, Moiseenko Fedor V, Matorina Olga G, Bizin Ilya V, Moiseyenko Vladimir M, Imyanitov Evgeny |
Genomic Analysis Reveals Novel Specific Metastatic Mutations in Chinese Clear Cell Renal Cell Carcinoma. BioMed research international 2020 2020 2495157. Meng Hui, Jiang Xuewen, Cui Jianfeng, Yin Gang, Shi Benkang, Liu Qi, Xuan He, Wang |
Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome. Cancers 2022 9 14 (17): . Dos Santos Wellington, de Andrade Edilene Santos, Garcia Felipe Antonio de Oliveira, Campacci Natália, Sábato Cristina da Silva, Melendez Matias Eliseo, Reis Rui Manuel, Galvão Henrique de Campos Reis, Palmero Edenir In |
Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral center. ESMO open 2022 11 7 (6): 100607. Poliani L, Greco L, Barile M, Dal Buono A, Bianchi P, Basso G, Giatti V, Genuardi M, Malesci A, Laghi L, |
Germline pathogenic variants in patients with early onset neuroendocrine neoplasms. Endocrine-related cancer 2023 3 . Riechelmann Rachel Pimenta, Donadio Mauro D, Jesus Victor Hugo F de, de Carvalho Nathalia de Angelis, Santiago Karina Miranda, Barros Milton J, Lopes Laura, Santos Gabriel Oliveira Dos, Formiga Maria Nirvana, Carraro Dirce Maria, Torrezan Giovana Tard |
Actionable genomic landscapes from a real-world cohort of urothelial carcinoma patients. Urologic oncology 2023 1 41 (3): 148.e17-148.e24. Gerald Thomas, Margulis Vitaly, Meng Xiaosong, Bagrodia Aditya, Cole Suzanne, Qin Qian, Call S Greg, Mauer Elizabeth, Lotan Yair, Woldu Solomon |
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- Page last updated:Apr 29, 2024
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