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Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1993
[Polymerization and solubility of recombinant hemoglobins alpha 2 beta 2 6 Glu-->Ala (Hb Makassar) and alpha 2 beta 2 6 Glu-->Ala, 23 Val-->Ile]
J Pagnier, M T Bihoreau, V Baudin, et al.
Hemoglobin
|
January 1, 1986
Sickle cell anemia in Bantu speaking Africa
J Pagnier, V Baudin, D Labie, et al.
Hemoglobin
|
February 1, 1996
The role of proline beta 5(A2) in the functional properties of human adult hemoglobin
V Baudin, J Kister, G Caron, et al.
Artificial Cells, Blood Substitutes, and Immobilization Biotechnology
|
January 1, 1994
Functional properties of beta(NA1)Val-deleted,(NA2)His-->Met hemoglobin synthesized in Escherichia coli
V Baudin, M T Bihoreau, J Kister, et al.
The Journal of Biological Chemistry
|
July 19, 1996
Functional studies and polymerization of recombinant hemoglobin Glu-alpha2beta26(A3) --> Val/Glu-7(A4) --> Ala
S Lesecq, V Baudin, J Kister, et al.
British Journal of Haematology
|
October 1, 1988
Occurrence of hereditary spherocytosis and beta thalassaemia in the same family: globin chain synthesis and visco diffractometric studies
B Pautard, C Feo, D Dhermy, et al.
Artificial Cells, Blood Substitutes, and Immobilization Biotechnology
|
January 1, 1994
Chimeric hemoglobin subunits: functional properties of a recombinant beta/alpha hemoglobin
A Dumoulin, V Baudin, L Kiger, et al.
Protein Science : a Publication of the Protein Society
|
April 16, 1998
Tetramer-dimer equilibrium of oxyhemoglobin mutants determined from auto-oxidation rates
N Griffon, V Baudin, W Dieryck, et al.
Hemoglobin
|
January 1, 1988
Hemoglobin Brest [beta 127 (H5)Gln----Lys] a new unstable human hemoglobin variant located at the alpha 1 beta 1 interface with specific electrophoretic behavior
V Baudin-Chich, H Wajcman, G Gombaud-Saintonge, et al.
The New England Journal of Medicine
|
April 4, 1985
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type
R L Nagel, M E Fabry, J Pagnier, et al.
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of 5
Search research articles
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Showing results (21-30 of 50) with videos related to
Sort By:
Page
of 5
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1993
[Polymerization and solubility of recombinant hemoglobins alpha 2 beta 2 6 Glu-->Ala (Hb Makassar) and alpha 2 beta 2 6 Glu-->Ala, 23 Val-->Ile]
J Pagnier, M T Bihoreau, V Baudin, et al.
Hemoglobin
|
January 1, 1986
Sickle cell anemia in Bantu speaking Africa
J Pagnier, V Baudin, D Labie, et al.
Hemoglobin
|
February 1, 1996
The role of proline beta 5(A2) in the functional properties of human adult hemoglobin
V Baudin, J Kister, G Caron, et al.
Artificial Cells, Blood Substitutes, and Immobilization Biotechnology
|
January 1, 1994
Functional properties of beta(NA1)Val-deleted,(NA2)His-->Met hemoglobin synthesized in Escherichia coli
V Baudin, M T Bihoreau, J Kister, et al.
The Journal of Biological Chemistry
|
July 19, 1996
Functional studies and polymerization of recombinant hemoglobin Glu-alpha2beta26(A3) --> Val/Glu-7(A4) --> Ala
S Lesecq, V Baudin, J Kister, et al.
British Journal of Haematology
|
October 1, 1988
Occurrence of hereditary spherocytosis and beta thalassaemia in the same family: globin chain synthesis and visco diffractometric studies
B Pautard, C Feo, D Dhermy, et al.
Artificial Cells, Blood Substitutes, and Immobilization Biotechnology
|
January 1, 1994
Chimeric hemoglobin subunits: functional properties of a recombinant beta/alpha hemoglobin
A Dumoulin, V Baudin, L Kiger, et al.
Protein Science : a Publication of the Protein Society
|
April 16, 1998
Tetramer-dimer equilibrium of oxyhemoglobin mutants determined from auto-oxidation rates
N Griffon, V Baudin, W Dieryck, et al.
Hemoglobin
|
January 1, 1988
Hemoglobin Brest [beta 127 (H5)Gln----Lys] a new unstable human hemoglobin variant located at the alpha 1 beta 1 interface with specific electrophoretic behavior
V Baudin-Chich, H Wajcman, G Gombaud-Saintonge, et al.
The New England Journal of Medicine
|
April 4, 1985
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type
R L Nagel, M E Fabry, J Pagnier, et al.
Page
of 5