Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Bruce Ponder"'
Hormonal carcinogenesis is an important and controversial area of current research. In addition to accelerating existing cancers, can hormones play the role of primary carcinogens? How do genetic factors influence hormone-related cancer risk? Hormone
Autor:
Edwards, Stephen M., Kote-Jarai, Zsofia, Meitz, Julia, Hamoudi, Rifat, Hope, Questa, Osin, Peter, Jackson, Rachel, Southgate, Christine, Singh, Rashmi, Falconer, Alison, Dearnaley, David P., Ardern-Jones, Audrey, Murkin, Annette, Dowe, Anna, Kelly, Jo, Williams, Sue, Oram, Richard, Stevens, Margaret, Teare, Dawn M., Bruce Ponder, A.J., Gayther, Simon A., Easton, Doug F., Eeles, Rosalind A.
Publikováno v:
In The American Journal of Human Genetics 2003 72(1):1-12
Autor:
Bruce Ponder, Hyoungshick Kim, Martin O'Reilly, Federico M. Giorgi, Kerstin B. Meyer, Zvi Livneh, Barak Markus, Y. Evgy, Robert C. Rintoul, Tamar Paz-Elizur, Yael Leitner-Dagan
Publikováno v:
Journal of Thoracic Oncology. 14:S447-S448
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37375a21893c55277e32638e1b66ad76
https://doi.org/10.1016/j.jtho.2019.08.925
https://doi.org/10.1016/j.jtho.2019.08.925
Autor:
L. Freedman, Tamar Paz-Elizur, R. Fluss, Yael Leitner-Dagan, Robert C. Rintoul, Martin O'Reilly, Kerstin B. Meyer, Bruce Ponder, Hyunjin Kim, Barak Markus, Zvi Livneh, Federico M. Giorgi, Y. Evgy
Publikováno v:
Journal of Thoracic Oncology. 14:S516
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc27941b11a305ce636333d7a94bf405
https://doi.org/10.1016/j.jtho.2019.08.1077
https://doi.org/10.1016/j.jtho.2019.08.1077
Autor:
Douglas F. Easton, Donald M Conroy, Craig Luccarini, Fabienne Lesueur, Mitul Shah, Paul D.P. Pharoah, Nicholas E. Day, Bruce Ponder, Alison M. Dunning, Patrick R. Benusiglio
Publikováno v:
Breast Cancer Research
INTRODUCTION: About two-thirds of the excess familial risk associated with breast cancer is still unaccounted for and may be explained by multiple weakly predisposing alleles. A gene thought to be involved in low-level predisposition to the disease i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::467fdb8a40738bf3ac75437e00377ee9
http://europepmc.org/articles/PMC1064135
http://europepmc.org/articles/PMC1064135
Autor:
W. Martin Howell, Alison M. Dunning, Bruce Ponder, Caroline Baynes, Philip R. Evans, Roz Gibbs, Elizabeth A. Bulpitt, Douglas F. Easton
Publikováno v:
Genes & Immunity. 5:S52-S55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a816bdccf78d52cc5365982cf9b96cb
https://doi.org/10.1038/sj.gene.6364085
https://doi.org/10.1038/sj.gene.6364085
Publikováno v:
Journal of Applied Social Psychology. 30:2610-2621
Hispanic jurors' verdicts and whether these decisions were related to jurors' judgments of the credibility of the witness were the focus of this experiment. A prosecution witness testified in English or in Spanish with interpretation in English. Witn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be37a3bdb9043e662db4cda1bb518f8d
https://doi.org/10.1111/j.1559-1816.2000.tb02452.x
https://doi.org/10.1111/j.1559-1816.2000.tb02452.x
Publikováno v:
Oncogene. 15:1213-1217
Germline mutations in the RET proto-oncogene are seen in the majority of patients with the dominantly inherited cancer syndromes multiple endocrine neoplasia type 2 (MEN 2). The clinical subtypes of MEN 2 (MEN 2A, MEN 2B and familial MTC) all have me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5270ec43af22bfca1f2d23ffa8ddff6
https://doi.org/10.1038/sj.onc.1201481
https://doi.org/10.1038/sj.onc.1201481
Autor:
Timothy J. Stonehouse, Tony Pawson, Bruce Ponder, Gerald D. Gish, Darrin P. Smith, Carol Houghton, M. J. Lorenzo
Publikováno v:
Oncogene. 14:763-771
Activating germline mutations of the RET receptor tyrosine kinase are found in the majority of cases of inherited cancer syndrome MEN 2, and inactivating mutations in some cases of dominantly inherited Hirschsprung disease. Using RET activated by a M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb1ef89daaa65a6efad3e2fd30d0a30f
https://doi.org/10.1038/sj.onc.1200894
https://doi.org/10.1038/sj.onc.1200894