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

M Garbarz

Showing results (51-60 of 56) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 56 results.
British Journal of Haematology|February 1, 1992
Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chainM C Lecomte, H Gautero, O Bournier, et al.
European Journal of Haematology|May 1, 1987
Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemiaL Morlé, B Pothier, N Alloisio, et al.
The Journal of Clinical Investigation|March 1, 1992
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrinP G Gallagher, W T Tse, T Coetzer, et al.
The Journal of Clinical Investigation|January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosisP B Jenkins, G K Abou-Alfa, D Dhermy, et al.
British Journal of Haematology|October 1, 1996
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in BeninC Glele-Kakai, M Garbarz, M C Lecomte, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPID Moatti, P Seknadji, C Galand, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
British Journal of Haematology|February 1, 1992
Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chainM C Lecomte, H Gautero, O Bournier, et al.
European Journal of Haematology|May 1, 1987
Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemiaL Morlé, B Pothier, N Alloisio, et al.
The Journal of Clinical Investigation|March 1, 1992
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrinP G Gallagher, W T Tse, T Coetzer, et al.
The Journal of Clinical Investigation|January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosisP B Jenkins, G K Abou-Alfa, D Dhermy, et al.
British Journal of Haematology|October 1, 1996
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in BeninC Glele-Kakai, M Garbarz, M C Lecomte, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPID Moatti, P Seknadji, C Galand, et al.
Pageof 6