Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jane S. Green"'
Autor:
Mine S. Cicek, Julie M. Cunningham, Brooke L. Fridley, Daniel J. Serie, William R. Bamlet, Brenda Diergaarde, Robert W. Haile, Loic Le Marchand, Theodore G. Krontiris, H. Banfield Younghusband, Steven Gallinger, Polly A. Newcomb, John L. Hopper, Mark A. Jenkins, Graham Casey, Fredrick Schumacher, Zhu Chen, Melissa S. DeRycke, Allyson S. Templeton, Ingrid Winship, Roger C. Green, Jane S. Green, Finlay A. Macrae, Susan Parry, Graeme P. Young, Joanne P. Young, Daniel Buchanan, Duncan C. Thomas, D. Timothy Bishop, Noralane M. Lindor, Stephen N. Thibodeau, John D. Potter, Ellen L. Goode
Publikováno v:
PLoS ONE, Vol 7, Iss 11 (2012)
Externí odkaz:
https://doaj.org/article/86ea8234b02846d48334ea268a3517e3
Autor:
Patrick S. Parfrey, Bharati V. Bapat, H. Banfield Younghusband, Steven S. Gallinger, John R. McLaughlin, Jegan Jegathesan, Jason A.W. Chaulk, Amanda Careen, Marina E. Croitoru, Roger C. Green, J. Desmond Robb, Aaron F. Pollett, Jane S. Green, Susan Stuckless, Fiona K. Curtis, Angela J. Hyde, Michael O. Woods
Purpose: Newfoundland has one of the highest rates of colorectal cancer in North America. The most common hereditary form of colorectal cancer is hereditary nonpolyposis colorectal cancer caused by mutations in genes involved in mismatch repair. Our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2278a1ecde9d8791ce3ea7a87fc7e266
https://doi.org/10.1158/1078-0432.c.6518080
https://doi.org/10.1158/1078-0432.c.6518080
Autor:
Patrick S. Parfrey, Bharati V. Bapat, H. Banfield Younghusband, Steven S. Gallinger, John R. McLaughlin, Jegan Jegathesan, Jason A.W. Chaulk, Amanda Careen, Marina E. Croitoru, Roger C. Green, J. Desmond Robb, Aaron F. Pollett, Jane S. Green, Susan Stuckless, Fiona K. Curtis, Angela J. Hyde, Michael O. Woods
Supplementary Tables 1-3 from High Frequency of Hereditary Colorectal Cancer in Newfoundland Likely Involves Novel Susceptibility Genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54f847d6be163cec8d0898f5e6b1c084
https://doi.org/10.1158/1078-0432.22440805.v1
https://doi.org/10.1158/1078-0432.22440805.v1
Autor:
Patrick S. Parfrey, Bharati V. Bapat, H. Banfield Younghusband, Steven S. Gallinger, John R. McLaughlin, Jegan Jegathesan, Jason A.W. Chaulk, Amanda Careen, Marina E. Croitoru, Roger C. Green, J. Desmond Robb, Aaron F. Pollett, Jane S. Green, Susan Stuckless, Fiona K. Curtis, Angela J. Hyde, Michael O. Woods
RLGS fragments and their corresponding chromosome loci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64d38aa64a42d45efe08a73d82db4969
https://doi.org/10.1158/1078-0432.22440808.v1
https://doi.org/10.1158/1078-0432.22440808.v1
Autor:
Daniel R. Evans, Jane S. Green, Somayyeh Fahiminiya, Jacek Majewski, Bridget A. Fernandez, Matthew A. Deardorff, Gordon J. Johnson, James H. Whelan, Dirk Hubmacher, Suneel S. Apte, Care4Rare Canada Consortium, Michael O. Woods
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Weill-Marchesani syndrome (WMS) is a rare disorder displaying short stature, brachydactyly and joint stiffness, and ocular features including microspherophakia and ectopia lentis. Brachydactyly and joint stiffness appear less commonly in patients wit
Autor:
Mine S Cicek, Julie M Cunningham, Brooke L Fridley, Daniel J Serie, William R Bamlet, Brenda Diergaarde, Robert W Haile, Loic Le Marchand, Theodore G Krontiris, H Banfield Younghusband, Steven Gallinger, Polly A Newcomb, John L Hopper, Mark A Jenkins, Graham Casey, Fredrick Schumacher, Zhu Chen, Melissa S DeRycke, Allyson S Templeton, Ingrid Winship, Roger C Green, Jane S Green, Finlay A Macrae, Susan Parry, Graeme P Young, Joanne P Young, Daniel Buchanan, Duncan C Thomas, D Timothy Bishop, Noralane M Lindor, Stephen N Thibodeau, John D Potter, Ellen L Goode, Colon CFR
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e38175 (2012)
A substantial proportion of familial colorectal cancer (CRC) is not a consequence of known susceptibility loci, such as mismatch repair (MMR) genes, supporting the existence of additional loci. To identify novel CRC loci, we conducted a genome-wide l
Externí odkaz:
https://doaj.org/article/0b08d9d435d94a02b7b255ba0dc14ced
Autor:
Shodimu‐Emmanuel Olufemi, Jane S. Green, Pachiappan Manickam, Siradanahalli C. Guru, Sunita K. Agarwal, Mary Beth Kester, Qihan Dong, A. Lee Burns, Allen M. Spiegel, Stephen J. Marx, Francis S. Collins, Settara C. Chandrasekharappa
Publikováno v:
Human Mutation. 11:264-269