Zobrazeno 1 - 10 of 23 pro vyhledávání: '"Jennifer Rhees"'
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Akademický článek
Novel Mutations in MLH1 and MSH2 Genes in Mexican Patients with Lynch Syndrome
Autor: Jose Miguel Moreno-Ortiz, María de la Luz Ayala-Madrigal, Jorge Román Corona-Rivera, Manuel Centeno-Flores, Víctor Maciel-Gutiérrez, Ramón Antonio Franco-Topete, Juan Armendáriz-Borunda, Erin Hotchkiss, Lucia Pérez-Carbonell, Jennifer Rhees, Clement Richard Boland, Melva Gutiérrez-Angulo
Publikováno v: Gastroenterology Research and Practice, Vol 2016 (2016)
Background. Lynch Syndrome (LS) is characterized by germline mutations in the DNA mismatch repair (MMR) genes MLH1, MSH2, MSH6, and PMS2. This syndrome is inherited in an autosomal dominant pattern and is characterized by early onset colorectal cance
Externí odkaz: https://doaj.org/article/3bb6b119d0cd4cbdb3ffef732c690b3d
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5
Data from Prohibitin Attenuates Colitis-Associated Tumorigenesis in Mice by Modulating p53 and STAT3 Apoptotic Responses
Autor: Arianne L. Theiss, Rhonda F. Souza, Stephen J. Meltzer, Robert M. Genta, Yulan Cheng, Erin Hotchkiss, Jennifer Rhees, William L. Neumann, Arwa S. Kathiria
Although inflammatory bowel disease is associated with higher risk of colorectal cancer, the precise pathogenic mechanisms underlying this association are not completely understood. Prohibitin 1 (PHB), a protein implicated in the regulation of prolif
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a0268b1c5b25303135419ef5a7eb3c28
https://doi.org/10.1158/0008-5472.c.6503316.v1
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9
Novel Mutations inMLH1andMSH2Genes in Mexican Patients with Lynch Syndrome
Autor: Víctor Maciel-Gutiérrez, Melva Gutiérrez-Angulo, Jose Miguel Moreno-Ortiz, Lucía Pérez-Carbonell, Jorge Román Corona-Rivera, Jennifer Rhees, Erin Hotchkiss, Juan Armendáriz-Borunda, María de la Luz Ayala-Madrigal, Clement Richard Boland, M. Centeno-Flores, Ramón Franco-Topete
Publikováno v: Gastroenterology Research and Practice
Gastroenterology Research and Practice, Vol 2016 (2016)
Background. Lynch Syndrome (LS) is characterized by germline mutations in the DNA mismatch repair (MMR) genesMLH1,MSH2,MSH6,andPMS2. This syndrome is inherited in an autosomal dominant pattern and is characterized by early onset colorectal cancer (CR
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b83a2fd5a5557f1a5fac16e1ca271d
https://doi.org/10.1155/2016/5278024
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10
De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one
Autor: Erin Hotchkiss, Pia Banerji, Lara Lipton, Mildred Arnold, Deborah Packham, Hon Chiu Eastwood Leung, Thuy Nguyen, Takeshi Nagasaka, C. Richard Boland, Minoru Koi, Megan P. Hitchins, Robyn L. Ward, Chau To Kwok, Ajay Goel, Jennifer Rhees
Publikováno v: International Journal of Cancer. 128:869-878
Lynch syndrome is an autosomal dominant cancer predisposition syndrome classically caused by germline mutations of the mismatch repair genes, MLH1, MSH2, MSH6 and PMS2. Constitutional epimutations of the MLH1 gene, characterized by soma-wide methylat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd1137a6367d27ae3ced1bacbddf04b8
https://doi.org/10.1002/ijc.25422
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