Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Muhydine El-Jamil"'
Autor:
Muhydine El-Jamil, Claire S. Philipp, Anne Dilley, Anne Patterson-Barnett, Hugh Randall, Harland Austin, Patrick S. Sullivan, Dorothy Ellingsen, Elizabeth R. Barnhart, Bruce L. Evatt, Daniel P. Eller, W. Craig Hooper
Publikováno v:
American Journal of Obstetrics and Gynecology. 183:1271-1277
Objective: Polymorphisms in the genes for factor V (factor V Leiden), prothrombin, methylenetetrahydrofolate reductase, and angiotensin-converting enzyme have been associated with the occurrence of venous thrombosis. The objective of this study was t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10386b2d6fb437f65e5476d72ac09956
https://doi.org/10.1067/mob.2000.106820
https://doi.org/10.1067/mob.2000.106820
Autor:
Jane M. Benson, Bruce L. Evatt, Nanette K. Wenger, Anne Dilley, Carolyn Whitsett, W. Craig Hooper, Muhydine El-Jamil, Harland Austin
Publikováno v:
Journal of Laboratory and Clinical Medicine. 132:452-455
A genetic variation in the prothrombin gene is located in the 3-untranslated region at position 20210 where a G-->A transition occurs. The prevalence of the mutation is 1% to 2% in white populations, and the mutation is associated with an increased r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5945d4d4fe1f5a7aa56b2cdbbba8eab5
https://doi.org/10.1016/s0022-2143(98)90121-4
https://doi.org/10.1016/s0022-2143(98)90121-4
Autor:
Claire S. Philipp, Donald L. Phillips, W. Craig Hooper, Muhydine El-Jamil, Dorothy Ellingsen, Bruce L. Evatt, Anne Dilley
Publikováno v:
Thrombosis research. 102(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dcc17845b602c34f95de9deb9fb303d
https://pubmed.ncbi.nlm.nih.gov/11323012
https://pubmed.ncbi.nlm.nih.gov/11323012
Autor:
Dorothy Ellingsen, W. Craig Hooper, Muhydine El-Jamil, Meredith Jenkins, Anne Dilley, Jane M. Benson, Connie H. Miller, Bruce L. Evatt
Publikováno v:
Scopus-Elsevier
SummaryThrombophilia is a multigenic disease in which the combination of genetic polymorphisms increases the risk of deep vein thrombosis (DVT). The rapid identification of these genetic combinations requires high-throughput analysis of single nucleo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3874996a17dbcbb07f5ffd0d8b075af
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035169840&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035169840&partnerID=MN8TOARS
