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C Vasseur

Showing results (61-70 of 74) with videos related to

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American Journal of Hematology|November 1, 1991
Hemoglobin Redondo [beta 92(F8) His----Asn]: an unstable hemoglobin variant associated with heme loss which occurs in two formsH Wajcman, C Vasseur, Y Blouquit, et al.
The Journal of Biological Chemistry|August 28, 1999
Additive effects of beta chain mutations in low oxygen affinity hemoglobin betaF41Y,K66TV Baudin-Creuza, C Vasseur-Godbillon, N Griffon, et al.
Protein Science : a Publication of the Protein Society|January 1, 1996
Two mutations in recombinant Hb beta F41(C7)Y, K82 (EF6)D show additive effects in decreasing oxygen affinityA Dumoulin, L Kiger, N Griffon, et al.
Annales De Genetique|January 1, 1997
PEG1 expression in maternal uniparental disomy 7L Cuisset, C Le Stunff, J M Dupont, et al.
Diabetes & Metabolism|February 14, 2007
Blood ketone monitoring: a comparison between gestational diabetes and non-diabetic pregnant womenH Gin, A Vambergue, C Vasseur, et al.
FEBS Letters|October 23, 1995
Loss of allosteric behaviour in recombinant hemoglobin alpha 2 beta 2(92)(F8) His-->Ala: restoration upon addition of strong effectorsA Dumoulin, L Kiger, R Jiang, et al.
Haematologica|November 1, 1992
Hereditary spherocytosis (HS) due to loss of anion exchange transporterA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
The Journal of Biological Chemistry|June 25, 1992
Hemoglobin Thionville. An alpha-chain variant with a substitution of a glutamate for valine at NA-1 and having an acetylated methionine NH2 terminusC Vasseur, Y Blouquit, J Kister, et al.
Proceedings. Biological Sciences|March 26, 2010
Phylogenetic isolation of host trees affects assembly of local Heteroptera communitiesA Vialatte, R I Bailey, C Vasseur, et al.
Journal of Medical Genetics|August 28, 1999
Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndromeJ M Dupont, D Le Tessier, D Rabineau, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
American Journal of Hematology|November 1, 1991
Hemoglobin Redondo [beta 92(F8) His----Asn]: an unstable hemoglobin variant associated with heme loss which occurs in two formsH Wajcman, C Vasseur, Y Blouquit, et al.
The Journal of Biological Chemistry|August 28, 1999
Additive effects of beta chain mutations in low oxygen affinity hemoglobin betaF41Y,K66TV Baudin-Creuza, C Vasseur-Godbillon, N Griffon, et al.
Protein Science : a Publication of the Protein Society|January 1, 1996
Two mutations in recombinant Hb beta F41(C7)Y, K82 (EF6)D show additive effects in decreasing oxygen affinityA Dumoulin, L Kiger, N Griffon, et al.
Annales De Genetique|January 1, 1997
PEG1 expression in maternal uniparental disomy 7L Cuisset, C Le Stunff, J M Dupont, et al.
Diabetes & Metabolism|February 14, 2007
Blood ketone monitoring: a comparison between gestational diabetes and non-diabetic pregnant womenH Gin, A Vambergue, C Vasseur, et al.
FEBS Letters|October 23, 1995
Loss of allosteric behaviour in recombinant hemoglobin alpha 2 beta 2(92)(F8) His-->Ala: restoration upon addition of strong effectorsA Dumoulin, L Kiger, R Jiang, et al.
Haematologica|November 1, 1992
Hereditary spherocytosis (HS) due to loss of anion exchange transporterA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
The Journal of Biological Chemistry|June 25, 1992
Hemoglobin Thionville. An alpha-chain variant with a substitution of a glutamate for valine at NA-1 and having an acetylated methionine NH2 terminusC Vasseur, Y Blouquit, J Kister, et al.
Proceedings. Biological Sciences|March 26, 2010
Phylogenetic isolation of host trees affects assembly of local Heteroptera communitiesA Vialatte, R I Bailey, C Vasseur, et al.
Journal of Medical Genetics|August 28, 1999
Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndromeJ M Dupont, D Le Tessier, D Rabineau, et al.
Pageof 8