Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Stephen M, Edwards"'
Autor:
Jo Fen Liu, Timothy R. Rebbeck, Brian E. Henderson, Vincent Khoo, Lynne T. O'Brien, Anna M. Ray, Klara Stefflova, Ethan M. Lange, Joanne L. Dickinson, Shannon K. McDonnell, Sarah J Lewis, Amit Joshi, Thilo Dörk, Jyotsna Batra, Yong-Jie Lu, Manuel Luedeke, Rosemary A. Wilkinson, Michelle Guy, C. R. J. Woodhouse, David E. Neal, Christopher A. Haiman, Gianluca Severi, Liesel M. FitzGerald, Audrey Ardern-Jones, Douglas F. Easton, Erika M. Kwon, Colin Cooper, Dallas R. English, Kathleen A. Cooney, Daniel Leongamornlert, Graham G. Giles, Loic Le Marchand, Laurence N. Kolonel, C. Slavov, Daniel J. Schaid, Ahva Shahabi, Suzanne K. Chambers, Teuvo L.J. Tammela, Jong Y. Park, Johanna Schleutker, Robert Huddart, Melissa C. Southey, Sue A. Ingles, Tim Christmas, Judith A. Clements, Mary-Anne Kedda, Malgorzata Tymrakiewicz, David P. Dearnaley, Radka Kaneva, Edward J. Saunders, Thomas A. Sellers, Janet L. Stanford, Anssi Auvinen, Alan Thompson, Jonathan J. Morrison, Guangwen Cao, Amanda L. Hall, Humera Khan, Pierre Hutter, Stephen M. Edwards, Esther M. John, Emma J. Sawyer, Angela Cox, Lisa A. Cannon-Albright, Tiina Wahlfors, Pierre O. Chappuis, Stephen N. Thibodeau, Freddie C. Hamdy, Elaine A. Ostrander, Hong Wei Zhang, Nicholas Van As, John L. Hopper, Walther Vogel, Amanda B. Spurdle, Jürgen Serth, Joanne F. Aitken, Chris Ogden, Atanaska Mitkova, Felicity Lose, Zsofia Kote-Jarai, Elizabeth Page, Christiane Maier, Joseph S. Koopmeiners, William D. Foulkes, Kenneth Muir, Alan Horwich, Danielle M. Karyadi, Chris Parker, Briony Patterson, Julio M. Pow-Sang, Robert A. Gardiner, Ali Amin Al Olama, Mariana C. Stern, Roman Corral, Maurice P. Zeegers, Andrea M. Polanowski, Artitaya Lophatananon, Rosalind A. Eeles, Andreas Meyer, J. M. Farnham, Jenny L Donovan
Publikováno v:
Nature Genetics, 41(10), 1116-21. Nature Publishing Group
Prostate cancer (PrCa) is the most frequently diagnosed cancer in males in developed countries. To identify common PrCa susceptibility alleles, we previously conducted a genome-wide association study in which 541,129 SNPs were genotyped in 1,854 PrCa
Autor:
Douglas F. Easton, Ali A min Al Olama, Bo Johanneson, Malgorzata Tymrakiewicz, Daniel J. Schaid, Artitaya Lophatananon, Zsofia Kote-Jarai, Mary-Anne Kedda, Graham G. Giles, William D. Foulkes, Danielle M. Karyadi, Tiina Wahlfors, Rosalind A. Eeles, Janet L. Stanford, Rainer Kuefer, Peter Schürmann, Michelle Guy, Shannon K. McDonnell, Robert A. Gardiner, Andreas Meyer, Joseph S. Koopmeiners, Joanne F. Aitken, Stephen N. Thibodeau, Nancy Hamel, Amit Joshi, Jo Fen Liu, Suzanne K. Steginga, David E. Neal, Sue A. Ingles, Teuvo L.J. Tammela, W. Vogel, Gianluca Severi, Amanda B. Spurdle, Stephen M. Edwards, Thilo Dörk, Daniel Leongamornlert, Roman Corral, Mariana C. Stern, Esther M. John, Claudia A. Salinas, Pierre Hutter, Kenneth Muir, Elaine A. Ostrander, John L. Hopper, Christiane Maier, Tracy A. O'Mara, Johanna Schleutker, Melissa C. Southey, Dallas R. English, Angela Cox, Pierre O. Chappuis
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 17:2052-2061
A recent genome-wide association study found that genetic variants on chromosomes 3, 6, 7, 10, 11, 19 and X were associated with prostate cancer risk. We evaluated the most significant single-nucleotide polymorphisms (SNP) in these loci using a world
Autor:
Douglas F. Easton, Kenneth Muir, Gianluca Severi, Sarah Bullock, Ketil Heimdal, Richard S. Houlston, William D. Foulkes, Questa Hope, David P. Dearnaley, Lovise Maehle, Stephen M. Edwards, Sameer Jhavar, David Roquis, James C. Engert, Christine Southgate, Daniel Sinnett, Nancy Hamel, Michael D. Badzioch, Jacques Simard, Melissa C. Southey, Alison Falconer, A Dowe, Graham G. Giles, John L. Hopper, Christopher H. Evans, Pål Møller, Rosalind A. Eeles, Dallas R. English, Julia C. Meitz
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 14:397-402
Background: Variants in the gene encoding the macrophage scavenger receptor 1 (MSR14) protein have been identified in men with prostate cancer, and several small studies have suggested that the 999C>T (R293X) protein-truncating mutation may be associ
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 2, Iss 3, Pp 111-121 (2004)
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice
Prostate cancer is the most common cancer in men and the second highest cause of cancer-related mortality in the U.K. A genetic component in predisposition to prostate cancer has been recognized for decades. One of the strongest epidemiological risk
Autor:
Brigitte Chapot, Norman Moullan, Audrey Ardern-Jones, Sandra Angèle, A. R. Norman, Richard S. Houlston, David P. Dearnaley, Christine Southgate, Michael Bremer, S Bullock, Stephen M. Edwards, Julia C. Meitz, Q Hope, A Dowe, Janet Hall, Thilo Dörk, Kenneth Muir, Rosalind A. Eeles, Doug Easton, A Falconer
Publikováno v:
British Journal of Cancer
Europe PubMed Central
Scopus-Elsevier
Europe PubMed Central
Scopus-Elsevier
The risk of prostate cancer is known to be elevated in carriers of germline mutations in BRCA2, and possibly also in carriers of BRCA1 and CHEK2 mutations. These genes are components of the ATM-dependent DNA damage signalling pathways. To evaluate th
Autor:
Rosalind A. Eeles, Stephen M. Edwards
Publikováno v:
American Journal of Medical Genetics. :65-73
This review describes what is currently known about the genetics of prostate cancer. Traditionally, the genetics of a suspected inherited cancer predisposition have generally been thought of in terms of a single, high-risk gene with a dominant mode o
Autor:
Stephen M. Edwards, S Williams, R A Jackson, Audrey Ardern-Jones, Michael R. Stratton, Julia C. Meitz, A Murkin, Doug Easton, Richard S. Houlston, David P. Dearnaley, Rosalind A. Eeles
Publikováno v:
British Journal of Cancer
The candidate prostate cancer susceptibility gene HPC2/ELAC2 has two common coding polymorphisms: (Ser→Leu 217) and (Ala→Thr 541). The Thr541 variant in the HPC2/ELAC2 gene has previously been reported to be at an increased frequency in prostate
Androgen receptor polymorphisms: Association with prostate cancer risk, relapse and overall survival
Autor:
Stephen M. Edwards, Rosalind A. Eeles, A Dowe, Simon Osborne, J. Kelly, R. J. Shearer, Doug Easton, Audrey Ardern-Jones, Ralph Minter, N. Collins, Mike Badzioch, Rifat Hamoudi, David P. Dearnaley, Grady F. Saunders
Publikováno v:
International Journal of Cancer. 84:458-465
Several reports have suggested that one or both of the trinucleotide repeat polymorphisms in the human androgen receptor (hAR) gene, (CAG)n coding for polyglutamine and (GGC)ncoding for polyglycine, may be associated with prostate cancer risk; but no
Autor:
J Broni, Peter Osin, Gyula Kovacs, S Gill, Martin J. S. Dyer, Rosalind A. Eeles, Tony G. Willis, Norman J. Maitland, Stephen M. Edwards, S Jefferies, Colin Cooper
Publikováno v:
British Journal of Cancer. 80:1565-1568
We have used single-strand conformation polymorphism (SSCP) analysis to screen for mutations in the BCL10 gene in 81 primary prostate carcinomas, 20 squamous cell cancers of the head and neck, 15 small-cell lung cancer cell lines, 24 renal carcinoma
Autor:
W. D. Dunsmuir, Audrey Ardern-Jones, M.P.A. Young, Roger Kirby, Rosalind A. Eeles, Sunil R. Lakhani, A Dowe, David P. Dearnaley, Stephen M. Edwards, Cathy Corbishley, J. Kelly
Publikováno v:
British Journal of Cancer. 78:1430-1433
A recent report has provided strong evidence for a major prostate cancer susceptibility locus (HPC1) on chromosome 1q24-25 (Smith et al, 1996). Most inherited cancer susceptibility genes function as tumour-suppressor genes (TSGs). Allelic loss or imb