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D Labie

Showing results (131-140 of 212) with videos related to

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Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1981
A case of the abnormal hemoglobin CV Balikova, H Fortová, D Labie, et al.
Hemoglobin|January 1, 1986
Sickle cell anemia in Bantu speaking AfricaJ Pagnier, V Baudin, D Labie, et al.
Human Genetics|February 1, 1986
Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern SicilyM Lombardo, A Ragusa, G Sortino, et al.
American Journal of Hematology|February 1, 1988
Beta S gene in Sicily is in linkage disequilibrium with the Benin haplotype: implications for gene flowA Ragusa, M Lombardo, G Sortino, et al.
Hemoglobin|January 1, 1980
A silent hemoglobin variant: hemoglobin necker enfants-malades alpha 20 (B1) His leads to TyrH Wajcman, J Elion, J P Boissel, et al.
Journal of Molecular Biology|March 25, 1982
Structural and functional studies of hemoglobin Barcelona (alpha 2 beta 2 94 Asp (FG1) replaced by His). Consequences of altering an important intrachain salt bridge involved in the alkaline Bohr effectH Wajcman, J L Aguilar i Bascompte, D Labie, et al.
Biochemical and Biophysical Research Communications|October 8, 1974
Isolation and partial characterization of a human prothrombin variant: prothrombin BarcelonaR Benarous, J M Lavergne, D Labie, et al.
Hemoglobin|January 1, 1991
Detection of the most frequent beta-thalassemic defect in Southeast Asia by PCRP Sebillon, T Bienvenu, R Girot, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|December 1, 1981
Minor hemoglobin components in diabetic and uremic patientsB Lantz, C Ochoa, H Wajcman, et al.
Hemoglobin|January 1, 1983
Hemoglobin Maputo: a new beta-chain variant (alpha 2 beta 2 47 (CD6) Asp replaced by Tyr) in combination with hemoglobin S, identified by high performance liquid chromatography (HPLC)M Marinucci, J P Boissel, A Massa, et al.
Pageof 22

Showing results (131-140 of 212) with videos related to

Sort By:
Pageof 22
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1981
A case of the abnormal hemoglobin CV Balikova, H Fortová, D Labie, et al.
Hemoglobin|January 1, 1986
Sickle cell anemia in Bantu speaking AfricaJ Pagnier, V Baudin, D Labie, et al.
Human Genetics|February 1, 1986
Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern SicilyM Lombardo, A Ragusa, G Sortino, et al.
American Journal of Hematology|February 1, 1988
Beta S gene in Sicily is in linkage disequilibrium with the Benin haplotype: implications for gene flowA Ragusa, M Lombardo, G Sortino, et al.
Hemoglobin|January 1, 1980
A silent hemoglobin variant: hemoglobin necker enfants-malades alpha 20 (B1) His leads to TyrH Wajcman, J Elion, J P Boissel, et al.
Journal of Molecular Biology|March 25, 1982
Structural and functional studies of hemoglobin Barcelona (alpha 2 beta 2 94 Asp (FG1) replaced by His). Consequences of altering an important intrachain salt bridge involved in the alkaline Bohr effectH Wajcman, J L Aguilar i Bascompte, D Labie, et al.
Biochemical and Biophysical Research Communications|October 8, 1974
Isolation and partial characterization of a human prothrombin variant: prothrombin BarcelonaR Benarous, J M Lavergne, D Labie, et al.
Hemoglobin|January 1, 1991
Detection of the most frequent beta-thalassemic defect in Southeast Asia by PCRP Sebillon, T Bienvenu, R Girot, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|December 1, 1981
Minor hemoglobin components in diabetic and uremic patientsB Lantz, C Ochoa, H Wajcman, et al.
Hemoglobin|January 1, 1983
Hemoglobin Maputo: a new beta-chain variant (alpha 2 beta 2 47 (CD6) Asp replaced by Tyr) in combination with hemoglobin S, identified by high performance liquid chromatography (HPLC)M Marinucci, J P Boissel, A Massa, et al.
Pageof 22