Zobrazeno 1 - 10 of 54 pro vyhledávání: '"M C, Garel"'
1
Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiation
Autor: C M, Rodrigue, N, Arous, D, Bachir, J, Smith-Ravin, P H, Romeo, F, Galacteros, M C, Garel
Publikováno v: British journal of haematology. 113(2)
Resveratrol, a natural dietary polyphenol, has been postulated to be implicated in the cardioprotective effect of red wine and the low incidence of breast and prostate cancers among vegetarians and Orientals respectively. This compound inhibits ribon
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::06c9da7b2f19b48cbefa5efd20ce099a
https://pubmed.ncbi.nlm.nih.gov/11380423
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3
Natural and artificial mutants of the human 2,3-bisphosphoglycerate as a tool for the evaluation of structure-function relationships
Autor: M C, Garel, V, Lemarchandel, M O, Prehu, M C, Calvin, N, Arous, R, Rosa, J, Rosa, M, Cohen-Solal
Publikováno v: Biomedica biochimica acta. 49(2-3)
2,3-bisphosphoglycerate mutase is a multifunctional enzyme which catalyses in red blood cells the synthesis and the degradation of 2,3-bisphosphoglycerate, the allosteric effector of hemoglobin. In order to study the structure-function relationships
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::77a765a533e100d629a3acb788e6508e
https://pubmed.ncbi.nlm.nih.gov/2167078
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4
Towards a mouse model for sickle cell disease: HB SAD
Autor: M, Trudel, M C, Garel, N, Saadane, P, Rouyer-Fessard, D, Vidaud, F, Costantini, Y, Beuzard
Publikováno v: Nouvelle revue francaise d'hematologie. 32(6)
Very recently a high expression of human hemoglobin S, which causes sickle cell disease, has been obtained in transgenic mice. We have constructed a modified beta S gene, beta SAD which carries two additional mutations in order to induce polymerizati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::27d14771d71702f34b8ee6fe8fcdef17
https://pubmed.ncbi.nlm.nih.gov/2101873
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5
Fate of alpha-hemoglobin chains and erythrocyte defects in beta-thalassemia
Autor: P, Rouyer-Fessard, M D, Scott, K, Leroy-Viard, M C, Garel, D, Bachir, F, Galacteros, Y, Beuzard
Publikováno v: Annals of the New York Academy of Sciences. 612
The fate of alpha-hemoglobin chains and the cause of membrane protein defects in thalassemic erythrocytes have been studied in: (1) human beta-thalassemia syndromes, (2) mouse beta-thalassemia, and (3) normal human erythrocytes loaded with purified a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e961d4c19cc2297b295bf2bb374fcdc9
https://pubmed.ncbi.nlm.nih.gov/2291540
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6
Human bisphosphoglycerate mutase. Expression in Escherichia coli and use of site-directed mutagenesis in the evaluation of the role of the carboxyl-terminal region in the enzymatic mechanism
Autor: M C, Garel, V, Joulin, P, Le Boulch, M C, Calvin, M O, Préhu, N, Arous, R, Longin, R, Rosa, J, Rosa, M, Cohen-Solal
Publikováno v: The Journal of biological chemistry. 264(32)
Bisphosphoglycerate mutase is an erythrocyte-specific enzyme whose main function is to synthesize 2,3-diphosphoglycerate, the allosteric effector of hemoglobin. In addition to its main 2,3-diphosphoglycerate synthase activity, the enzyme displays pho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1d48eb9472ec612cc3fde402bc4428b7
https://pubmed.ncbi.nlm.nih.gov/2553728
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8
[Use of a new rheometer for the study of the filtrability of a suspension of sickled red cells as a function of PO2]
Autor: J, Martin-Caburi, T, Hermann, M C, Garel, C, Domenget, F, Galacteros, J C, Healy, M, Hanss, Y, Beuzard
Publikováno v: Comptes rendus des seances de l'Academie des sciences. Serie III, Sciences de la vie. 295(5)
The filtration time of a small volume (0.1 ml) of red cell suspension from normal (AA), heterozygous (AS) and homozygous (SS) subjects for sickle cell disease was investigated as a function of PO2 The curve of filtration time of AS and SS red cell su
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1bc608eafd0fb15acdea340db4814617
https://pubmed.ncbi.nlm.nih.gov/6817872
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9
Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins
Autor: P, Basset, Y, Beuzard, M C, Garel, J, Rosa
Publikováno v: Blood. 51(5)
Isoelectric focusing on slabs of acrylamide gel was adapted for the screening of abnormal hemoglobins, the characterization of 70 human variants, and the study of minor fractions of normal hemoglobin. The screening method was as fast and inexpensive
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::24421c255b5c56ad34aaaaafab8d1501
https://pubmed.ncbi.nlm.nih.gov/638255
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10
Molecular cloning of the human 2,3-bisphosphoglycerate mutase cDNA and revised amino acid sequence
Autor: M, Cohen-Solal, V, Joulin, P H, Romeo, R, Rosa, C, Valentin, M C, Garel, J, Rosa
Publikováno v: Biomedica biochimica acta. 46(2-3)
The human erythrocyte 2,3-bisphosphoglycerate mutase (BPGM) is a multifunctional enzyme which controls the metabolism of 2,3-diphosphoglycerate (DPG), the main allosteric effector of haemoglobin. Several cDNA banks were constructed from reticulocyte
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::49555a7881b28a1301e0c66d6b674f82
https://pubmed.ncbi.nlm.nih.gov/3036106
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