Search Results - "Roberts, Stacy C"

  • Showing 1 - 4 results of 4
Refine Results
  1. 1

    Thrombomodulin Ala455Val Polymorphism and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study by Cole, John W, Roberts, Stacy C, Gallagher, Margaret, Giles, Wayne H, Mitchell, Braxton D, Steinberg, Karen K, Wozniak, Marcella A, Macko, Richard F, Reinhart, Laurie J, Kittner, Steven J

    Published in BMC neurology (01-12-2004)
    “…The genes encoding proteins in the thrombomodulin-protein C pathway are promising candidate genes for stroke susceptibility because of their importance in…”
    Get full text
    Journal Article
  2. 2

    Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection by O'Donovan, Michael C., Oefner, Peter J., Roberts, Stacy C., Austin, Jehannine, Hoogendoorn, Bastiaan, Guy, Carol, Speight, Graham, Upadhyaya, Meena, Sommer, Steve S., McGuffin, Peter

    Published in Genomics (San Diego, Calif.) (15-08-1998)
    “…Denaturing high-performance liquid chromatography (DHPLC) is a novel high-capacity technique for detecting new mutations. We have evaluated the sensitivity and…”
    Get full text
    Journal Article
  3. 3

    Hemostatic gene polymorphisms and the prevalence of thrombotic complications in polycythemia vera and essential thrombocythemia by Afshar-Kharghan, Vahid, López, José A, Gray, Leigh A, Padilla, Arnoldo, Borthakur, Gautam, Roberts, Stacy C, Pruthi, Rajiv K, Tefferi, Ayalew

    Published in Blood coagulation & fibrinolysis (01-01-2004)
    “…Patients with polycythemia vera and essential thrombocythemia are at risk for thrombotic and bleeding complications. Currently, no diagnostic test can predict…”
    Get full text
    Journal Article
  4. 4

    Sensitivity and specificity of denaturing high-pressure liquid chromatography for unknown protein C gene mutations by Taliani, M R, Roberts, S C, Dukek, B A, Pruthi, R K, Nichols, W L, Heit, J A

    Published in Genetic testing (2001)
    “…Screening methods for unknown DNA sequence variations are laborious, expensive, and relatively insensitive. To evaluate the sensitivity and specificity of…”
    Get more information
    Journal Article