Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Anne Marie Sims"'
Autor:
B. Paul Wordsworth, Gordon W. Duff, Andrei Calin, Owen Beynon, Aaron Abbott, Anne Marie Sims, A. M. Crane, Linda A. Bradbury, Ibi Herzberg, Heather J. Cordell, Andrew E. Timms, Lon R. Cardon, Matthew A. Brown, Mark R.E. Coyne
Ankylosing spondylitis (AS) is a common and highly heritable inflammatory arthropathy. Although the gene HLA-B27 is almost essential for the inheritance of the condition, it alone is not sufficient to explain the pattern of familial recurrence of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ea5a91180a015f6cc2d73742819a86
https://doi.org/10.1086/424695
https://doi.org/10.1086/424695
Autor:
William C. Bailey, Sarah R. Bujac, Ubaldo J. Martin, Eugene R. Bleecker, Deborah A. Meyers, Anne-Marie Sims, M. Goldman
Publikováno v:
Chest. 142(2)
Background Effects of β 2 -adrenergic receptor gene ( ADRB2 ) polymorphism on therapeutic responses to long-acting β 2 -adrenergic agonists have not been evaluated in long-term COPD trials. We aimed to investigate the effects of the ADRB2 Gly16Arg
Autor:
Anne-Marie Sims, Eugene R. Bleecker, Mitchell Goldman, Sarah R. Bujac, Deborah A. Meyers, William C. Bailey, Ubaldo J. Martin
Publikováno v:
C22. PATHOBIOLOGY OF COPD: LESSONS FROM INFLAMMATORY MECHANISMS AND GENOMIC STUDIES.
Autor:
Lars-Goran Carlsson, Marie Carlholm, D. S. Postma, Anne-Marie Sims, Mikael Knutsson, Claes-Göran Löfdahl, Kristina F. Semb, Anders Damholt
Publikováno v:
D46. CHRONIC OBSTRUCTIVE PULMONARY DISEASE: DIAGNOSIS AND EVALUATION.
Autor:
Panos Deloukas, Michael M. Ward, Linda A. Bradbury, Johanna Hadler, Jacqueline Taylor, Walter P. Maksymowych, L H Appleton, Xiaodong Zhou, R Mogg, Vasudev Kumanduri, Emma Pomeroy, Patrick Danoy, Tugce Karaderi, Karena Pryce, J J Pointon, John D. Reveille, Matthew A. Brown, Gethin P. Thomas, Evgeny A. Glazov, Susan M. Ring, Tracey Doan, John C. Davis, B. Paul Wordsworth, Pamela Whittaker, Ran Duan, David M. Evans, Robert D. Inman, Millicent A. Stone, Alison Dowling, C Farrar, David Harvey, Anne Marie Sims, Laura Diekman, Rui Jin, L. Savage, Leena Peltonen, Michael H. Weisman, Emma L. Duncan, Paul Leo
Publikováno v:
Nature genetics. 42(2)
To identify susceptibility loci for ankylosing spondylitis, we undertook a genome-wide association study in 2,053 unrelated ankylosing spondylitis cases among people of European descent and 5,140 ethnically matched controls, with replication in an in
Autor:
Jennifer J, Pointon, Kay, Chapman, David, Harvey, Anne-Marie, Sims, Linda, Bradbury, Kari, Laiho, Markku, Kauppi, Kalevi, Kaarela, Jaakko, Tuomilehto, Matthew A, Brown, B Paul, Wordsworth
Publikováno v:
The Journal of rheumatology. 35(8)
To investigate the association of CD14 and Toll-like receptor (TLR4) with ankylosing spondylitis (AS).A promoter variant in CD14 and 2 coding polymorphisms in TLR4 were investigated in UK and Finnish families with AS and in a UK case-control study. A
Autor:
C. T. Chou, Matthew A. Brown, Markku J Kauppi, Alison Dowling, Jácome Bruges-Armas, Andrew E. Timms, Anne Marie Sims, Kalevi Kaarela, K. Laiho, John D. Reveille, Raquel Nunes Fialho, Rosa Sorrentino, Tracy Doan, P. Gergely, Jaakko Tuomilehto, Gilberto Vargas-Alarcón, Walter P. Maksymowych, J J Pointon, Huji Xu, Rubén Burgos-Vargas, Dafna D. Gladman, Proton Rahman, Robert D. Inman, B. P. Wordsworth
OBJECTIVES: The aim of the current study was to determine the contribution of interleukin (IL)1 gene cluster polymorphisms previously implicated in susceptibility for ankylosing spondylitis (AS) to AS susceptibility in different populations worldwide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62766828fe4b4d384e376b8652ccdc9c
http://hdl.handle.net/11573/83947
http://hdl.handle.net/11573/83947
Autor:
Kirk A. Rockett, Andrew E. Timms, Anne Marie Sims, C. Darke, B. Paul Wordsworth, J Newton, Dominic P. Kwiatkowski, Sinead Harney, Matthew A. Brown
Publikováno v:
Arthritis and rheumatism. 50(7)
Objective. We have previously identified a single-nucleotide polymorphism (SNP) haplotype involving the lymphotoxin alpha (LTA) and tumor necrosis factor (TNF) loci (termed haplotype LTA-TNF2) on chromosome 6 that shows differential association with
Publikováno v:
Molecular microbiology. 51(1)
Mismatch repair is one of a number of DNA repair pathways that cells possess to deal with damage to their genome. Mismatch repair is concerned with the recognition and correction of incorrectly paired bases, which can be base-base mismatches or inser
Autor:
Julia L. Newton, Sinéad M. J. Harney, Andrew E. Timms, Anne‐Marie Sims, Kirk Rockett, Chris Darke, B. Paul Wordsworth, Dominic Kwiatkowski, Matthew A. Brown
Publikováno v:
Arthritis & Rheumatism; Jul2004, Vol. 50 Issue 7, p2122-2129, 8p