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Biochimica Et Biophysica Acta
|
January 29, 1988
Mouse alpha chains inhibit polymerization of hemoglobin induced by human beta S or beta S Antilles chains
M D Rhoda, C Domenget, M Vidaud, et al.
Biochimica Et Biophysica Acta
|
April 27, 1984
Effects of the alpha 20 mutation on the polymerization of Hb S
M D Rhoda, Y Blouquit, J Caburi-Martin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1986
Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes
N Monplaisir, G Merault, C Poyart, et al.
Hemoglobin
|
January 1, 1986
Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndrome
M D Rhoda, N Arous, M C Garel, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1985
[Abnormal hemoglobins identified in Martinique]
N Monplaisir, F Galacteros, N Arous, et al.
The Journal of Biological Chemistry
|
May 25, 1986
Glycerated hemoglobin, alpha 2A beta 2(82) (EF6) N epsilon-glyceryllysine. A new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency
Y Blouquit, M D Rhoda, J Delanoe-Garin, et al.
Biomedica Biochimica Acta
|
January 1, 1987
Glycerated hemoglobin alpha 2 beta 2(82) (EF6) N-epsilon-glyceryllysine: a new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency
Y Blouquit, M D Rhoda, J Delanoe-Garin, et al.
Hemoglobin
|
January 1, 1988
Hb J-Cordoba [alpha 2A beta 2(95)(FG2)Lys----Met]. A new Hb variant found in Argentina
J Bardakdjian, J Kister, M D Rhoda, et al.
Hemoglobin
|
January 1, 1986
Hemoglobin J Iran alpha 2 beta 2 77 (EF1) his----Asp in a Russian-Armenian family
J Delanoe-Garin, M D Rhoda, C T Craescu, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
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You have reached the last page of results.
This site can display upto 19 results.
Biochimica Et Biophysica Acta
|
January 29, 1988
Mouse alpha chains inhibit polymerization of hemoglobin induced by human beta S or beta S Antilles chains
M D Rhoda, C Domenget, M Vidaud, et al.
Biochimica Et Biophysica Acta
|
April 27, 1984
Effects of the alpha 20 mutation on the polymerization of Hb S
M D Rhoda, Y Blouquit, J Caburi-Martin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1986
Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes
N Monplaisir, G Merault, C Poyart, et al.
Hemoglobin
|
January 1, 1986
Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndrome
M D Rhoda, N Arous, M C Garel, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1985
[Abnormal hemoglobins identified in Martinique]
N Monplaisir, F Galacteros, N Arous, et al.
The Journal of Biological Chemistry
|
May 25, 1986
Glycerated hemoglobin, alpha 2A beta 2(82) (EF6) N epsilon-glyceryllysine. A new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency
Y Blouquit, M D Rhoda, J Delanoe-Garin, et al.
Biomedica Biochimica Acta
|
January 1, 1987
Glycerated hemoglobin alpha 2 beta 2(82) (EF6) N-epsilon-glyceryllysine: a new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency
Y Blouquit, M D Rhoda, J Delanoe-Garin, et al.
Hemoglobin
|
January 1, 1988
Hb J-Cordoba [alpha 2A beta 2(95)(FG2)Lys----Met]. A new Hb variant found in Argentina
J Bardakdjian, J Kister, M D Rhoda, et al.
Hemoglobin
|
January 1, 1986
Hemoglobin J Iran alpha 2 beta 2 77 (EF1) his----Asp in a Russian-Armenian family
J Delanoe-Garin, M D Rhoda, C T Craescu, et al.
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of 2