Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Gary D Sinclair

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|October 5, 2012
Interpreting results from Factor V Leiden mutation analysis: a cautionary noteGary D Sinclair, Man-Chiu Poon
Blood|December 9, 2008
The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutationShannon C Jackson, Gary D Sinclair, Stephanie Cloutier, et al.
Blood|July 1, 2004
A novel type 2A von Willebrand factor mutation located at the last nucleotide of exon 26 (3538G>A) causes skipping of 2 nonadjacent exonsPaula D James, Lee A O'Brien, Carol A Hegadorn, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|July 27, 2010
Nasal epithelial cells of donor origin after allogeneic hematopoietic cell transplantation are generated at a faster rate in the first 3 months compared with later posttransplantationFaisal M Khan, Sarah Sy, Polly Louie, et al.
Blood|June 16, 2010
Genomic instability after allogeneic hematopoietic cell transplantation is frequent in oral mucosa, particularly in patients with a history of chronic graft-versus-host disease, and rare in nasal mucosaFaisal M Khan, Sarah Sy, Polly Louie, et al.
Nature Medicine|March 27, 2007
Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic bloodStephen R Clark, Adrienne C Ma, Samantha A Tavener, et al.
Blood|August 30, 2008
Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancyCarolyn J Owen, Cynthia L Toze, Anna Koochin, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|October 5, 2012
Interpreting results from Factor V Leiden mutation analysis: a cautionary noteGary D Sinclair, Man-Chiu Poon
Blood|December 9, 2008
The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutationShannon C Jackson, Gary D Sinclair, Stephanie Cloutier, et al.
Blood|July 1, 2004
A novel type 2A von Willebrand factor mutation located at the last nucleotide of exon 26 (3538G>A) causes skipping of 2 nonadjacent exonsPaula D James, Lee A O'Brien, Carol A Hegadorn, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|July 27, 2010
Nasal epithelial cells of donor origin after allogeneic hematopoietic cell transplantation are generated at a faster rate in the first 3 months compared with later posttransplantationFaisal M Khan, Sarah Sy, Polly Louie, et al.
Blood|June 16, 2010
Genomic instability after allogeneic hematopoietic cell transplantation is frequent in oral mucosa, particularly in patients with a history of chronic graft-versus-host disease, and rare in nasal mucosaFaisal M Khan, Sarah Sy, Polly Louie, et al.
Nature Medicine|March 27, 2007
Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic bloodStephen R Clark, Adrienne C Ma, Samantha A Tavener, et al.
Blood|August 30, 2008
Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancyCarolyn J Owen, Cynthia L Toze, Anna Koochin, et al.
Pageof 1