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

S Gandrille

Showing results (11-20 of 64) with videos related to

Pageof 7
Sort By:
Thrombosis and Haemostasis|June 1, 1996
First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1)D Borgel, B Jude, M Aiach, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiencyD Borgel, S Gandrille, M Gouault-Heilmann, et al.
Pathologie-Biologie|April 5, 2015
[Clinical and biological features of patients with essential thrombocythaemia according to their mutational status JAK2 or CALR: Single-center study of 40 patients and review of the literature]M Ben Said, S Gandrille, A M Fischer, et al.
Thrombosis and Haemostasis|February 11, 2000
Thirty-three novel mutations in the protein C gene. French INSERM network on molecular abnormalities responsible for protein C and protein SM Alhenc-Gelas, S Gandrille, M L Aubry, et al.
Thrombosis and Haemostasis|December 1, 1995
Role of Fc gamma RIIA gene polymorphism in human platelet activation by monoclonal antibodiesC Bachelot, R Saffroy, S Gandrille, et al.
Journal of Thrombosis and Haemostasis : JTH|February 8, 2006
The protein S thrombin-sensitive region modulates phospholipid binding and the gamma-carboxyglutamic acid-rich (Gla) domain conformation in a non-specific mannerF Saller, T Kaabache, M Aiach, et al.
Blood|June 17, 1998
A mutation of the active protein S gene leading to an EGF1-lacking protein in a family with qualitative (type II) deficiencyC Leroy-Matheron, M Gouault-Heilmann, M Aiach, et al.
Thrombosis Research|December 1, 1995
Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor VJ S Greengard, X Xu, S Gandrille, et al.
Blood|October 15, 1994
First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletionS Gandrille, B Jude, M Alhenc-Gelas, et al.
Thrombosis and Haemostasis|November 15, 1993
Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanismS Gandrille, B Jude, M Alhenc-Gelas, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Thrombosis and Haemostasis|June 1, 1996
First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1)D Borgel, B Jude, M Aiach, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiencyD Borgel, S Gandrille, M Gouault-Heilmann, et al.
Pathologie-Biologie|April 5, 2015
[Clinical and biological features of patients with essential thrombocythaemia according to their mutational status JAK2 or CALR: Single-center study of 40 patients and review of the literature]M Ben Said, S Gandrille, A M Fischer, et al.
Thrombosis and Haemostasis|February 11, 2000
Thirty-three novel mutations in the protein C gene. French INSERM network on molecular abnormalities responsible for protein C and protein SM Alhenc-Gelas, S Gandrille, M L Aubry, et al.
Thrombosis and Haemostasis|December 1, 1995
Role of Fc gamma RIIA gene polymorphism in human platelet activation by monoclonal antibodiesC Bachelot, R Saffroy, S Gandrille, et al.
Journal of Thrombosis and Haemostasis : JTH|February 8, 2006
The protein S thrombin-sensitive region modulates phospholipid binding and the gamma-carboxyglutamic acid-rich (Gla) domain conformation in a non-specific mannerF Saller, T Kaabache, M Aiach, et al.
Blood|June 17, 1998
A mutation of the active protein S gene leading to an EGF1-lacking protein in a family with qualitative (type II) deficiencyC Leroy-Matheron, M Gouault-Heilmann, M Aiach, et al.
Thrombosis Research|December 1, 1995
Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor VJ S Greengard, X Xu, S Gandrille, et al.
Blood|October 15, 1994
First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletionS Gandrille, B Jude, M Alhenc-Gelas, et al.
Thrombosis and Haemostasis|November 15, 1993
Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanismS Gandrille, B Jude, M Alhenc-Gelas, et al.
Pageof 7