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M C Garel

Showing results (31-40 of 58) with videos related to

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FEBS Letters|October 15, 1975
Hemoglobin C Ziguinchor alphaA2 beta62 (A3) Glu leads to Val beta58 (E2) Pro leads to Arg: the second sickling variant with amino acid substitutions in 2 residues of the beta polypeptide chainM Goossens, M C Garel, J Auvinet, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1990
Towards a mouse model for sickle cell disease: HB SADM Trudel, M C Garel, N Saadane, et al.
The Journal of Biological Chemistry|November 15, 1989
A study of membrane protein defects and alpha hemoglobin chains of red blood cells in human beta thalassemiaP Rouyer-Fessard, M C Garel, C Domenget, et al.
Circulation Research|April 14, 2000
Enhanced cardiac function in transgenic mice expressing a Ca(2+)-stimulated adenylyl cyclaseL Lipskaia, N Defer, G Esposito, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1975
[A new case of hemoglobin G Georgia (author's transl)]M L North, M C Garel, J Thillet, et al.
Biomedica Biochimica Acta|January 1, 1987
Molecular cloning of the human 2,3-bisphosphoglycerate mutase cDNA and revised amino acid sequenceM Cohen-Solal, V Joulin, P H Romeo, et al.
The Journal of Biological Chemistry|October 25, 1988
Isolation and characterization of the human 2,3-bisphosphoglycerate mutase geneV Joulin, M C Garel, P Le Boulch, et al.
Biorheology|January 1, 1989
Filterability of sickle cells as a function of pO2: role of physico-chemical factorsA Kraiem, C T Craescu, F Galacteros, et al.
Biochimica Et Biophysica Acta|April 27, 1984
Effects of the alpha 20 mutation on the polymerization of Hb SM D Rhoda, Y Blouquit, J Caburi-Martin, et al.
FEBS Letters|October 1, 1974
Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effectJ Thillet, J Caburi, B Brun, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
FEBS Letters|October 15, 1975
Hemoglobin C Ziguinchor alphaA2 beta62 (A3) Glu leads to Val beta58 (E2) Pro leads to Arg: the second sickling variant with amino acid substitutions in 2 residues of the beta polypeptide chainM Goossens, M C Garel, J Auvinet, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1990
Towards a mouse model for sickle cell disease: HB SADM Trudel, M C Garel, N Saadane, et al.
The Journal of Biological Chemistry|November 15, 1989
A study of membrane protein defects and alpha hemoglobin chains of red blood cells in human beta thalassemiaP Rouyer-Fessard, M C Garel, C Domenget, et al.
Circulation Research|April 14, 2000
Enhanced cardiac function in transgenic mice expressing a Ca(2+)-stimulated adenylyl cyclaseL Lipskaia, N Defer, G Esposito, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1975
[A new case of hemoglobin G Georgia (author's transl)]M L North, M C Garel, J Thillet, et al.
Biomedica Biochimica Acta|January 1, 1987
Molecular cloning of the human 2,3-bisphosphoglycerate mutase cDNA and revised amino acid sequenceM Cohen-Solal, V Joulin, P H Romeo, et al.
The Journal of Biological Chemistry|October 25, 1988
Isolation and characterization of the human 2,3-bisphosphoglycerate mutase geneV Joulin, M C Garel, P Le Boulch, et al.
Biorheology|January 1, 1989
Filterability of sickle cells as a function of pO2: role of physico-chemical factorsA Kraiem, C T Craescu, F Galacteros, et al.
Biochimica Et Biophysica Acta|April 27, 1984
Effects of the alpha 20 mutation on the polymerization of Hb SM D Rhoda, Y Blouquit, J Caburi-Martin, et al.
FEBS Letters|October 1, 1974
Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effectJ Thillet, J Caburi, B Brun, et al.
Pageof 6