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

D Labie

Showing results (151-160 of 212) with videos related to

Pageof 22
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Structural analysis of the 5' flanking region of the beta-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle cell mutation in AfricaY Chebloune, J Pagnier, G Trabuchet, et al.
Nucleic Acids Research|June 10, 1988
A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2C Beldjord, C Lapoumeroulie, J Pagnier, et al.
Nouvelle Revue Francaise D'Hematologie|November 1, 1973
[Hemolytic anaemia due to unstable hemoglobin with deletion, study of two new cases: Hb Tours (Thr beta87 (F3) deleted) and Hb St.-Antoine (Gly-Leu beta74-75 (E18-19) deleted) (author's transl)]A Najman, G Duhamel, R André, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Multiple molecular bases for thalassemia intermedia in east SicilyC Troungos, R Krishnamoorthy, J Elion, et al.
Blood|December 1, 1985
The -158 site 5' to the G gamma gene and G gamma expressionD Labie, O Dunda-Belkhodja, F Rouabhi, et al.
Sangre|January 1, 1975
[Congenital non-spherocytic haemoloytic anaemia due to haemoglobin köln. clinical aspects and structural study (author's transl)]J L Vives-corrons, E Vela, D Labie, et al.
Nature|March 20, 1975
Appearance of beta globin synthesis in erythroid cells of Ferrara beta -o-thalassaemic patients following blood transfusionF Conconi, L Del Senno, P Ferrarese, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1984
[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site]J Rochette, J P Boissel, D Labie, et al.
The Journal of Clinical Investigation|July 1, 1981
Impairment of the growth of Plasmodium falciparum in HbEE erythrocytesR L Nagel, C Raventos-Suarez, M E Fabry, et al.
Molecular Biology & Medicine|August 1, 1984
Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemiaC Beldjord, M Arbane, C Lapoumeroulie, et al.
Pageof 22

Showing results (151-160 of 212) with videos related to

Sort By:
Pageof 22
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Structural analysis of the 5' flanking region of the beta-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle cell mutation in AfricaY Chebloune, J Pagnier, G Trabuchet, et al.
Nucleic Acids Research|June 10, 1988
A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2C Beldjord, C Lapoumeroulie, J Pagnier, et al.
Nouvelle Revue Francaise D'Hematologie|November 1, 1973
[Hemolytic anaemia due to unstable hemoglobin with deletion, study of two new cases: Hb Tours (Thr beta87 (F3) deleted) and Hb St.-Antoine (Gly-Leu beta74-75 (E18-19) deleted) (author's transl)]A Najman, G Duhamel, R André, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Multiple molecular bases for thalassemia intermedia in east SicilyC Troungos, R Krishnamoorthy, J Elion, et al.
Blood|December 1, 1985
The -158 site 5' to the G gamma gene and G gamma expressionD Labie, O Dunda-Belkhodja, F Rouabhi, et al.
Sangre|January 1, 1975
[Congenital non-spherocytic haemoloytic anaemia due to haemoglobin köln. clinical aspects and structural study (author's transl)]J L Vives-corrons, E Vela, D Labie, et al.
Nature|March 20, 1975
Appearance of beta globin synthesis in erythroid cells of Ferrara beta -o-thalassaemic patients following blood transfusionF Conconi, L Del Senno, P Ferrarese, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1984
[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site]J Rochette, J P Boissel, D Labie, et al.
The Journal of Clinical Investigation|July 1, 1981
Impairment of the growth of Plasmodium falciparum in HbEE erythrocytesR L Nagel, C Raventos-Suarez, M E Fabry, et al.
Molecular Biology & Medicine|August 1, 1984
Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemiaC Beldjord, M Arbane, C Lapoumeroulie, et al.
Pageof 22