Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Stephanie Tring"'
Autor:
Barbara K Fortini, Stephanie Tring, Sarah J Plummer, Christopher K Edlund, Victor Moreno, Robert S Bresalier, Elizabeth L Barry, Timothy R Church, Jane C Figueiredo, Graham Casey
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e111914 (2014)
Genome-wide association studies (GWAS) of colorectal cancer (CRC) have led to the identification of a number of common variants associated with modest risk. Several risk variants map within the vicinity of TGFβ/BMP signaling pathway genes, including
Externí odkaz:
https://doaj.org/article/ce11f040ecc74e86b4da84901f5e86f9
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e48825 (2012)
Myotonic dystrophy (DM1) is a highly variable, multi-system disorder resulting from the expansion of an untranslated CTG tract in DMPK. In DM1 expanded CUG repeat RNAs form hairpin secondary structures that bind and aberrantly sequester the RNA splic
Externí odkaz:
https://doaj.org/article/1407f1731e7f410595a1af930d21c13a
Autor:
Katja Butterbach, Julyann Pérez-Mayoral, Douglas F. Easton, Stefanie Brezina, Ben Zhang, Frank J. Manion, Hansong Wang, Sanford D. Markowitz, Liesel M. FitzGerald, Sun Ha Jee, Michelle Cotterchio, Daniel D. Buchanan, Timothy R. Church, Wolfgang Lieb, Xiao-Ou Shu, John L. Hopper, Stephanie A. Bien, Manuela Gago-Dominguez, Jian Gong, Laurence N. Kolonel, Graham G. Giles, Leon Raskin, Yingchang Lu, Kristen Anton, Charles S. Fuchs, Fränzel J.B. van Duijnhoven, Hermann Brenner, Yi Lin, Clicerio Gonzalez-Villalpando, Yong-Bing Xiang, Aaron K. Aragaki, Daniela Seminara, Stephanie M. Gogarten, Gad Rennert, Jose E. Castelao, Rocky Fischer, Antonio J. Molina, Jarmo Virtamo, Tabitha A. Harrison, Volker Arndt, Lee Soo Chin, Michael Hoffmeister, Mark A. Jenkins, Shu Chen Huang, Chris S. Carlson, Stéphane Bézieau, Rebecca D. Jackson, Bhramar Mukherjee, Darin Taverna, Bridget M. Riggs, Christopher K. Edlund, Christopher A. Haiman, Melissa C. Southey, Anna H. Wu, Marilena Melas, Antonia Trichopoulou, Hedy S. Rennert, Gianluca Severi, Stephen B. Gruber, Noralane M. Lindor, Gerhard A. Coetzee, Richard B. Hayes, Sarah J. Plummer, Keitaro Matsuo, Mathieu Lemire, Philipp Hofer, Neil Murphy, José María Huerta, Paul D.P. Pharoah, Erin M. Siegel, Sébastien Küry, Thomas J. Hudson, Annika Lindblom, Marcia Cruz Correa, Michael O. Woods, Sophia Harlid, Tilman Kuehn, David Shibata, Christopher I. Li, Stephen N. Thibodeau, Stephen J. Chanock, Jochen Hampe, Flavio Lejbkowicz, Jeroen R. Huyghe, Suminori Kono, Jenny Chang-Claude, Aung Ko Win, Brent W. Zanke, Alicja Wolk, David V. Conti, Elena M. Gonzalez-Villalpando, Christopher I. Amos, Shuo Jiao, Domenico Palli, Vicente Martín, Jesus P. Paredes Cotoré, Stephanie J. Weinstein, Andrea Gsur, William M. Grady, Koichi Matsuda, Loic Le Marchand, Hanane Omichessan, Marc J. Gunter, Graham Casey, Li Li, Zsofia K. Stadler, Eric J. Jacobs, Kevin McDonnell, Dallas R. English, Demetrius Albanes, Amit Joshi, Wei Zheng, Mariana C. Stern, Cecelia A. Laurie, Jing Ma, Cornelia M. Ulrich, Stephanie L. Schmit, Victor Moreno, John D. Potter, Chenxu Qu, Bette J. Caan, Heinz-Josef Lenz, M. Henar Alonso, Andrea Z. LaCroix, Christoph Mancao, John F. Harju, Yun Ru Liu, Jane C. Figueiredo, Gregory Idos, Kana Wu, Duncan C. Thomas, Motoki Iwasaki, W. James Gauderman, Thomas A. Sellers, David Van Den Berg, Barbara K. Fortini, David N. Levine, James M. Church, Ya Wen Cheng, Edith J. M. Feskens, Edward Giovannucci, Manish Gala, Polly A. Newcomb, Charles Kooperberg, Iona Cheng, David J. Hunter, Martha L. Slattery, Roger L. Milne, Lars G. Fritsche, Niha Zubair, Steven Gallinger, Yi Xin Zeng, Wei Shi, Andrew T. Chan, Fotios Loupakis, Vittorio Krogh, Clemens Schafmayer, Sun-Seog Kweon, Bethany van Guelpan, Amanda Bloomer, Kenneth Offit, Stephanie Tring, Shoichiro Tsugane, David Duggan, Fredrick R. Schumacher, Joseph Vijai, Weihua Jia, Marie-Christine Boutron-Ruault, Joel K. Greenson, Frank Luh, Ulrike Peters, Keith R. Curtis, Juergen Boehm, Robert E. Schoen, Sonja I. Berndt, Elizabeth L. Barry, Sebastian Stintzing, Li Hsu, Emily White, Conghui Qu, Peter T. Campbell, Caroline McNeil, Yun Yen
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Journal of the National Cancer Institute 111 (2019) 2
Journal of the National Cancer Institute, 111(2), 146-157
Schmit, Stephanie L; Edlund, Christopher K; Schumacher, Fredrick R; Gong, Jian; Harrison, Tabitha A; Huyghe, Jeroen R; et al.(2018). Novel Common Genetic Susceptibility Loci for Colorectal Cancer.. Journal of the National Cancer Institute. doi: 10.1093/jnci/djy099. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3bk0g2vk
Universidad de Barcelona
Journal of the National Cancer Institute 111 (2019) 2
Journal of the National Cancer Institute, 111(2), 146-157
Schmit, Stephanie L; Edlund, Christopher K; Schumacher, Fredrick R; Gong, Jian; Harrison, Tabitha A; Huyghe, Jeroen R; et al.(2018). Novel Common Genetic Susceptibility Loci for Colorectal Cancer.. Journal of the National Cancer Institute. doi: 10.1093/jnci/djy099. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3bk0g2vk
Background Previous genome-wide association studies (GWAS) have identified 42 loci (P < 5 × 10−8) associated with risk of colorectal cancer (CRC). Expanded consortium efforts facilitating the discovery of additional susceptibility loci may capture
Publikováno v:
Clinical and Translational Gastroenterology
Introduction Familial adenomatous polyposis (FAP) is a hereditary colorectal cancer (CRC) syndrome characterized by accelerated adenoma development due to inherited (or de novo) mutations in the APC regulator of WNT signaling pathway (APC) gene. The
Autor:
Sarah J. Plummer, Matthew Devall, Mourad Wagdy Ali, Stephanie Tring, Graham Casey, Barbara K. Fortini
Publikováno v:
Human Mutation
Several genome wide association studies of colorectal cancer (CRC) have identified single nucleotide polymorphisms (SNPs) on chromosome 15q13.3 associated with CRC risk. To identify functional variant(s) underlying this association, we investigated S
Autor:
Elizabeth L. Barry, Christopher K. Edlund, Robert S. Bresalier, Graham Casey, Timothy R. Church, Barbara K. Fortini, Sarah J. Plummer, Victor Moreno, Jane C. Figueiredo, Stephanie Tring
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 11, p e111914 (2014)
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS ONE, Vol 9, Iss 11, p e111914 (2014)
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Genome-wide association studies (GWAS) of colorectal cancer (CRC) have led to the identification of a number of common variants associated with modest risk. Several risk variants map within the vicinity of TGFβ/BMP signaling pathway genes, including
Autor:
Michela Biancolella, Simon G. Coetzee, David V. Conti, Judd C. Rice, Stephanie Tring, Fredrick R. Schumacher, Barbara K. Fortini, Houtan Noushmehr, Chunli Yan, Dennis J. Ahnen, Christopher K. Edlund, Elizabeth L. Barry, Michael J. Hitchler, Robert S. Bresalier, Gerhard A. Coetzee, Sarah J. Plummer, Gustavo Mendoza-Fandiño, Jaana Hartiala, Graham Casey, Benjamin P. Berman
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Genome-wide association studies of colorectal cancer (CRC) have identified a number of common variants associated with modest risk, including rs3802842 at chromosome 11q23.1. Several genes map to this region but rs3802842 does not map to any known tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b5402c173749ada30338dd40663582f
Autor:
Yukwah Kwok, Rebecca C. Fry, Paul Marjoram, Sita Reddy, Warunee Dansithong, Stephanie Tring, Robabeh Mohammadzadeh, Sharan Paul, Lucio Comai, Sonali P. Jog
We describe a new mechanism by which CTG tract expansion affects myotonic dystrophy (DM1). Changes to the levels of a panel of RNAs involved in muscle development and function that are downregulated in DM1 are due to aberrant localization of the tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d73015461c4ab371d7f79276e8a729a1
https://europepmc.org/articles/PMC3128970/
https://europepmc.org/articles/PMC3128970/
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e48825 (2012)
PLoS ONE
PLoS ONE
Myotonic dystrophy (DM1) is a highly variable, multi-system disorder resulting from the expansion of an untranslated CTG tract in DMPK. In DM1 expanded CUG repeat RNAs form hairpin secondary structures that bind and aberrantly sequester the RNA splic