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J Bardakdjian-Michau

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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|February 20, 2003
[Neonatal detection of sickle cell disease]J Bardakdjian-Michau
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2008
[Neonatal screening of sickle cell disease in France]J Bardakdjian-Michau
Biochimica Et Biophysica Acta|December 5, 1990
Functional and NMR studies of Hb Sassari (Asp-126 alpha----His); role of the inter-subunit contacts in the affinity control of human hemoglobinJ Bardakdjian-Michau, F Galactéros, C T Craescu
Hemoglobin|December 22, 1998
Gamma chain heterogeneity: determination of Hb F composition by perfusion chromatographyI Papassotiriou, R Ducrocq, C Préhu, et al.
Hemoglobin|January 1, 1989
Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stabilityJ Bardakdjian-Michau, J Rosa, F Galactéros, et al.
Hemoglobin|January 1, 1994
Hemoglobin variants in North AfricaB Chami, Y Blouquit, J Bardakdjian-Michau, et al.
Journal of Medical Screening|May 12, 1998
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell diseaseR Ducrocq, A Bévier, A Leneveu, et al.
Hemoglobin|January 17, 2002
A new Ggamma chain variant: Hb F-Coignieres [gamma75(E19)Ile-->Val]H Wajcman, A P Yapo, J Riou, et al.
Biochimica Et Biophysica Acta|January 29, 1988
Mouse alpha chains inhibit polymerization of hemoglobin induced by human beta S or beta S Antilles chainsM D Rhoda, C Domenget, M Vidaud, et al.
Hemoglobin|January 1, 1989
Hb N-Timone [alpha 2 beta 2(8)(A5)Lys----Glu]: a new fast-moving variant with normal stability and oxygen affinityD Léna-Russo, A Orsini, L Vovan, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|February 20, 2003
[Neonatal detection of sickle cell disease]J Bardakdjian-Michau
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2008
[Neonatal screening of sickle cell disease in France]J Bardakdjian-Michau
Biochimica Et Biophysica Acta|December 5, 1990
Functional and NMR studies of Hb Sassari (Asp-126 alpha----His); role of the inter-subunit contacts in the affinity control of human hemoglobinJ Bardakdjian-Michau, F Galactéros, C T Craescu
Hemoglobin|December 22, 1998
Gamma chain heterogeneity: determination of Hb F composition by perfusion chromatographyI Papassotiriou, R Ducrocq, C Préhu, et al.
Hemoglobin|January 1, 1989
Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stabilityJ Bardakdjian-Michau, J Rosa, F Galactéros, et al.
Hemoglobin|January 1, 1994
Hemoglobin variants in North AfricaB Chami, Y Blouquit, J Bardakdjian-Michau, et al.
Journal of Medical Screening|May 12, 1998
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell diseaseR Ducrocq, A Bévier, A Leneveu, et al.
Hemoglobin|January 17, 2002
A new Ggamma chain variant: Hb F-Coignieres [gamma75(E19)Ile-->Val]H Wajcman, A P Yapo, J Riou, et al.
Biochimica Et Biophysica Acta|January 29, 1988
Mouse alpha chains inhibit polymerization of hemoglobin induced by human beta S or beta S Antilles chainsM D Rhoda, C Domenget, M Vidaud, et al.
Hemoglobin|January 1, 1989
Hb N-Timone [alpha 2 beta 2(8)(A5)Lys----Glu]: a new fast-moving variant with normal stability and oxygen affinityD Léna-Russo, A Orsini, L Vovan, et al.
Pageof 3