Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Catherine Leiendecker-Foster"'
Autor:
Paul C Adams, James C Barton, Gordon D McLaren, Ronald T Acton, Mark Speechley, Christine E McLaren, David M Reboussin, Catherine Leiendecker-Foster, Emily L Harris, Beverly M Snively, Thomas Vogt, Phyliss Sholinsky, Elizabeth Thomson, Fitzroy W Dawkins, Victor R Gordeuk, John H Eckfeldt
Publikováno v:
Canadian Journal of Gastroenterology, Vol 23, Iss 11, Pp 769-772 (2009)
BACKGROUND: The HEmochromatosis and IRon Overload Screening (HEIRS) Study provided data on a racially, ethnically and geographically diverse cohort of participants in North America screened from primary care populations.
Externí odkaz:
https://doaj.org/article/6e53e75d0a134cf2a8ea25d468034d8f
Autor:
Rachel R Huxley, Faye L Lopez, Richard F MacLehose, John H Eckfeldt, David Couper, Catherine Leiendecker-Foster, Ron C Hoogeveen, Lin Yee Chen, Elsayed Z Soliman, Sunil K Agarwal, Alvaro Alonso
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59052 (2013)
Previous cross-sectional studies have suggested that biomarkers of extracellular matrix remodelling are associated with atrial fibrillation (AF), but no prospective data have yet been published. Hence, we examine whether plasma matrix metalloproteina
Externí odkaz:
https://doaj.org/article/ab948cf7661d4bdb8dc834d33efa2b33
Autor:
Xue Zhang, Amy I Lynch, Barry R Davis, Charles E Ford, Eric Boerwinkle, John H Eckfeldt, Catherine Leiendecker-Foster, Donna K Arnett
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e34217 (2012)
Nitric oxide synthase 3 (NOS3) catalyzes production of NO in the endothelium and may play a role in cardiovascular disease (CVD). We assessed the pharmacogenetic associations of three NOS3 polymorphisms and three antihypertensive drugs with CVD outco
Externí odkaz:
https://doaj.org/article/5268a3b38da14e3d8926eed2ddfdcbbe
Autor:
Christine E McLaren, Stela McLachlan, Chad P Garner, Chris D Vulpe, Victor R Gordeuk, John H Eckfeldt, Paul C Adams, Ronald T Acton, Joseph A Murray, Catherine Leiendecker-Foster, Beverly M Snively, Lisa F Barcellos, James D Cook, Gordon D McLaren
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e38339 (2012)
The existence of multiple inherited disorders of iron metabolism suggests genetic contributions to iron deficiency. We previously performed a genome-wide association study of iron-related single nucleotide polymorphisms (SNPs) using DNA from white me
Externí odkaz:
https://doaj.org/article/d5755e27d1bf4d418711620200f170ca
Autor:
Christine E McLaren, Chad P Garner, Clare C Constantine, Stela McLachlan, Chris D Vulpe, Beverly M Snively, Victor R Gordeuk, Debbie A Nickerson, James D Cook, Catherine Leiendecker-Foster, Kenneth B Beckman, John H Eckfeldt, Lisa F Barcellos, Joseph A Murray, Paul C Adams, Ronald T Acton, Anthony A Killeen, Gordon D McLaren
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e17390 (2011)
The existence of multiple inherited disorders of iron metabolism in man, rodents and other vertebrates suggests genetic contributions to iron deficiency. To identify new genomic locations associated with iron deficiency, a genome-wide association stu
Externí odkaz:
https://doaj.org/article/b65e48c2eebe475e8db2cd147aec2f3d
Autor:
James C. Barton, Catherine Leiendecker-Foster, Honggui Li, Susie DelRio-LaFreniere, Ronald T. Acton, John H. Eckfeldt
Publikováno v:
Haematologica, Vol 94, Iss 10 (2009)
Externí odkaz:
https://doaj.org/article/1a4de0d40f13435684aeda73b0bffeba
Autor:
Donna K. Arnett, John H. Eckfeldt, Eric Boerwinkle, Amy I. Lynch, Catherine Leiendecker-Foster, Barry R. Davis, Charles E. Ford
Publikováno v:
Pharmacogenetics and Genomics. 22:355-366
To identify panels of genetic variants that predict treatment-related coronary heart disease (CHD) outcomes in hypertensive patients on one of four different classes of initial antihypertensive treatment. The goal was to identify subgroups of individ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3179958e70505a390cc42cd263533c8
https://doi.org/10.1097/fpc.0b013e3283516ff8
https://doi.org/10.1097/fpc.0b013e3283516ff8
Autor:
James C. Barton, Ronald T. Acton, Christopher Zaun, John H. Eckfeldt, Catherine Leiendecker-Foster, Christine E. McLaren
Publikováno v:
Blood Cells, Molecules, and Diseases. 44:252-256
We sought to determine if TNF promoter variants could explain iron phenotype heterogeneity in adults with previous HFE genotyping. HEIRS Study participants genotyped for C282Y and H63D were designated as high transferrin saturation (TS) and/or serum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9328e986c8c5c665aa93f2bf8de66e7
https://doi.org/10.1016/j.bcmd.2010.01.007
https://doi.org/10.1016/j.bcmd.2010.01.007
Autor:
Catherine Leiendecker-Foster, Honggui Li, Susie A. LaFreniere, Richard D. Press, Ronald T. Acton, James C. Barton, John H. Eckfeldt
Publikováno v:
American Journal of Hematology. 84:710-714
We sought to identify mutations that could explain iron phenotype heterogeneity in adults with previous HFE genotyping to detect C282Y and H63D. HEIRS Study participants genotyped for C282Y and H63D were designated as high transferrin saturation (TS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49e19d6020e182c3c55151a7dca12dbd
https://doi.org/10.1002/ajh.21524
https://doi.org/10.1002/ajh.21524
Autor:
Barry R. Davis, Charles E. Ford, Donna K. Arnett, Catherine Leiendecker-Foster, John H. Eckfeldt, Amy I. Lynch, Eric Boerwinkle
Publikováno v:
Pharmacogenetics and Genomics. 19:415-421
The FGB gene codes for fibrinogen-beta, a polypeptide of the coagulation factor fibrinogen, which is positively associated with cardiovascular diseases. Studies show that angiotensin-converting enzyme (ACE) inhibitors lower plasma fibrinogen concentr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b25f6f8e21be7344b965c2ca28504fd
https://doi.org/10.1097/fpc.0b013e32832a8e81
https://doi.org/10.1097/fpc.0b013e32832a8e81