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of 10
pro vyhledávání: '"Gary Dawson"'
Autor:
Stephen C. L. Gough, Angie P Green, Jayne A. Franklyn, Delilah Zabaneh, Bryan M. Dechairo, Thomas Heiberg Brix, Anthony P. Weetman, J. E. Collins, Gary Dawson, Laszlo Hegedüs, Oliver J. Brand, Ian Mackay, Wilmar M. Wiersinga, John Wass, Bruce G. Robinson, John M. C. Connell, Penny J. Hunt, Alisoun H. Carey
Publikováno v:
European journal of human genetics, 13(11), 1223-1230. Nature Publishing Group
The development of autoimmune thyroid disease (AITD) is associated with autoantibodies directed against the thyroid stimulating hormone receptor (TSHR). Previous studies have failed to demonstrate a consistent association between the TSHR and AITD, o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44a74c1a0cde5268104e6a9df9acab9e
https://ora.ox.ac.uk/objects/uuid:c4a66c91-6442-4de9-85c3-78d18f3828af
https://ora.ox.ac.uk/objects/uuid:c4a66c91-6442-4de9-85c3-78d18f3828af
Autor:
Nicholas Lench, Dermot P.B. McGovern, Bryan M. Dechairo, David A. van Heel, Ian Mackay, Alisoun H. Carey, Kenichi Negoro, Derek P. Jewell, Gary Dawson, Lon R. Cardon
Genetic studies in inflammatory bowel disease have identified multiple susceptibility loci, whose relevance depends critically on verification in independent cohorts. Genetic variants associated with Crohn's disease have now been identified on chromo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f51a47683667deb167289d726207b11f
https://doi.org/10.1093/hmg/ddg281
https://doi.org/10.1093/hmg/ddg281
Publikováno v:
Radiography. 16:238-243
The developing nature of nuclear medicine practice highlights the need for an evaluation of the fundamental qualities of a Radiographer working within this discipline. Existing guidelines appear to be in place for clinical technologists working withi
Autor:
Gary Dawson, Prema P Thirunavukarasu, Keneth Waldron, David Robertson, Euan M. Wallace, Anna Dole
Publikováno v:
Placenta. 24:370-377
Previous studies have identified the presence of unidentified small molecular weight (mol wt) forms of inhibin and the pro-alphaC region of the inhibin alpha subunit in serum from women during late pregnancy. The aim of this study was to investigate
Autor:
M. Ashwin Reddy, Shomi S. Bhattacharya, Eranga N. Vithana, Vanita Berry, Roy A. Quinlan, Peter J. Francis, Gary Dawson, Ian Mackay, Alisoun H. Carey, Dean Collyer, Anthony T. Moore
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
American journal of human genetics, 2001, Vol.69(5), pp.1141-1145 [Peer Reviewed Journal]
instname
American journal of human genetics, 2001, Vol.69(5), pp.1141-1145 [Peer Reviewed Journal]
5 páginas, 4 figuras.-- et al.
Congenital cataracts are an important cause of bilateral visual impairment in infants. In a four-generation family of English descent, we mapped dominant congenital posterior polar cataract to chromosome 11q22-q22
Congenital cataracts are an important cause of bilateral visual impairment in infants. In a four-generation family of English descent, we mapped dominant congenital posterior polar cataract to chromosome 11q22-q22
Autor:
Gary Dawson, Nicholas G. Martin, David H. Barlow, Jacqueline Wicks, Stephen Kennedy, Kelly R. Ewen-White, Vicki Smith, Susan A. Treloar, Grant W. Montgomery, David L. Duffy, Daniel T. O'Connor, Melanie Bahlo, Simon T. Bennett, Dale R. Nyholt, Ian Mackay, Daniel E. Weeks, Alisoun H. Carey
Publikováno v:
ResearcherID
Endometriosis is a common gynecological disease that affects up to 10% of women in their reproductive years. It causes pelvic pain, severe dysmenorrhea, and subfertility. The disease is defined as the presence of tissue resembling endometrium in site
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a96f918a351cffd3d7bdebd77ba71887
https://europepmc.org/articles/PMC1226203/
https://europepmc.org/articles/PMC1226203/
Autor:
Nicola Boxall, Roger M. Harbord, Gary Dawson, Richard M. Sibly, John C. Whittaker, Ian Mackay
Publikováno v:
Genetics. 164(2)
Microsatellites are widely used in genetic analyses, many of which require reliable estimates of microsatellite mutation rates, yet the factors determining mutation rates are uncertain. The most straightforward and conclusive method by which to study
Autor:
Ian Mackay, Eranga N. Vithana, Vanita Berry, Anthony T. Moore, Roy A. Quinlan, Dean Collyer, Alisoun H. Carey, M. Ashwin Reddy, Shomi S. Bhattacharya, Peter J. Francis, Gary Dawson
To the Editor:We thank Dr. Siiri Veromann (Veromann 2002xTheoretical considerations regarding the study “Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.”. Veromann, S. Am J Hum Genet. 2002;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6be5048237cb61ef4ffea245d701e04a
https://europepmc.org/articles/PMC379207/
https://europepmc.org/articles/PMC379207/
Autor:
Thomas S. Whitecloud, Robert L. Barrack, Rodrek E. Williams, Paul Michas, Treg D. Brown, Gary Dawson
Publikováno v:
Journal of orthopaedic trauma. 11(3)
To determine the prevalence of gunshot wound related orthopaedic injuries in an urban trauma center and outline the socioeconomic background of this patient population.Retrospective study conducted from January 1, 1994, through December 30, 1994.Univ
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