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

N Lanir

Showing results (31-40 of 43) with videos related to

Pageof 5
Sort By:
Blood|December 9, 1998
A missense mutation in gamma-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factorsB Brenner, B Sánchez-Vega, S M Wu, et al.
The New England Journal of Medicine|March 21, 1996
Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosisH Mandel, B Brenner, M Berant, et al.
Arthritis and Rheumatism|January 1, 1995
Transfer of experimental antiphospholipid syndrome by bone marrow cell transplantation. The importance of the T cellM Blank, I Krause, N Lanir, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 1, 1995
Application of a bedside whole blood D-dimer assay in the diagnosis of deep vein thrombosisB Brenner, M Pery, N Lanir, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 1, 1988
Macrophage migration in fibrin gel matrices. II. Effects of clotting factor XIII, fibronectin, and glycosaminoglycan content on cell migrationN Lanir, P S Ciano, L Van de Water, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutationZ Hochberg, A Van Lieburg, L Even, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 16, 2001
Prophylactic therapy with enoxaparin during L-asparaginase treatment in children with acute lymphoblastic leukemiaR Elhasid, N Lanir, R Sharon, et al.
Biochimica Et Biophysica Acta|February 1, 1989
Pathogenesis of tumor stroma generation: a critical role for leaky blood vessels and fibrin depositionJ A Nagy, L F Brown, D R Senger, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular characterization of four novel mutations causing factor VII deficiencyH Tamary, Y Fromovich-Amit, L Shalmon, et al.
Acta Biomaterialia|January 7, 2014
The formation of an anti-restenotic/anti-thrombotic surface by immobilization of nitric oxide synthase on a metallic carrierM Alagem-Shafir, E Kivovich, I Tzchori, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Blood|December 9, 1998
A missense mutation in gamma-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factorsB Brenner, B Sánchez-Vega, S M Wu, et al.
The New England Journal of Medicine|March 21, 1996
Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosisH Mandel, B Brenner, M Berant, et al.
Arthritis and Rheumatism|January 1, 1995
Transfer of experimental antiphospholipid syndrome by bone marrow cell transplantation. The importance of the T cellM Blank, I Krause, N Lanir, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 1, 1995
Application of a bedside whole blood D-dimer assay in the diagnosis of deep vein thrombosisB Brenner, M Pery, N Lanir, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 1, 1988
Macrophage migration in fibrin gel matrices. II. Effects of clotting factor XIII, fibronectin, and glycosaminoglycan content on cell migrationN Lanir, P S Ciano, L Van de Water, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutationZ Hochberg, A Van Lieburg, L Even, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 16, 2001
Prophylactic therapy with enoxaparin during L-asparaginase treatment in children with acute lymphoblastic leukemiaR Elhasid, N Lanir, R Sharon, et al.
Biochimica Et Biophysica Acta|February 1, 1989
Pathogenesis of tumor stroma generation: a critical role for leaky blood vessels and fibrin depositionJ A Nagy, L F Brown, D R Senger, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular characterization of four novel mutations causing factor VII deficiencyH Tamary, Y Fromovich-Amit, L Shalmon, et al.
Acta Biomaterialia|January 7, 2014
The formation of an anti-restenotic/anti-thrombotic surface by immobilization of nitric oxide synthase on a metallic carrierM Alagem-Shafir, E Kivovich, I Tzchori, et al.
Pageof 5