Zobrazeno 1 - 10
of 118
pro vyhledávání: '"M. M. Galteau"'
Autor:
Alain Colvez, Marie-Laure Laroche, Bienvenu Bongue, Nabil Maarouf, Claire Guy, Jean-Pierre Convers, René Gueguen, Florence Naudin, M. M. Galteau
Publikováno v:
Pharmacoepidemiology and Drug Safety. 18:1125-1133
Purpose To describe the trends of potentially inappropriate medication (PIM) use in older adults from 1995 to 2004 in the East of France, by using the 1997 Beers criteria and its French update, and to assess risk factors for this PIM use. Methods We
Autor:
M. M. Galteau, Sophia Visvikis, Gérard Siest, Josiane Steinmetz, Eric Boerwinkle, René Gueguen
Publikováno v:
Scopus-Elsevier
Web of Science
Web of Science
Plasma from 158 presumed healthy nuclear families has been analyzed by high-resolution, two-dimensional electrophoresis to study the frequency and effects of the genetic polymorphism in human apolipoprotein A-IV. Two common alleles, apo A-IV 1 and ap
Autor:
G. Plomteux, P. Laleigerie, C. Dorche, J. P. Bretaudiere, F. Schiele, M. Vancraeynest, J. Guidollet, M. M. Galteau, M. Mathieu, P. Louisot, M. Bailly, J. C. Leunis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::762886a108b0b83f4dbce7e80c4d06e7
https://doi.org/10.1159/000401722
https://doi.org/10.1159/000401722
Publikováno v:
Clinical Biochemistry. 28:31-38
Objective : To assess lipid and lipoprotein genetic variability in the French Population. Methods : Many health examination centers are covering a great part of France (700,000 individuals are examined in 54 centers every year). Each citizen has the
Autor:
M. M. Galteau, Zelia Braz Vieira da Silva Pontes, Gérard Siest, René Gueguen, Monique Vincent-Viry
Publikováno v:
Genetic Epidemiology. 11:115-129
Human acetylation phenotypes were determined with caffeine (137X) as the test substance, improved by measuring urinary caffeine metabolites with a previously described HPLC method. Caffeine, 5-acetylamino-6-formylamino-3-methyluracil (AFMU), 1-methyl
Autor:
M. Vincent-Viry, M. M. Galteau, C. Mura, R. Krishnamoorthy, Evelyne Jacqz-Aigrain, Stéphane Panserat
Publikováno v:
Human Genetics. 92:367-372
Deficient debrisoquine/sparteine type oxidation is inherited as an autosomal recessive trait. Of all Caucasians, 5-10% are poor metabolisers, due to the absence of cytochrome P4502D6. Extensive metabolisers (EMs) exhibit highly variable metabolic act
Publikováno v:
British Journal of Clinical Pharmacology. 35:161-165
1. Cytochrome P450 debrisoquine (CYP2D6) activity is polymorphic and under genetic control. Most Caucasians are extensive metabolizers, but 5%-10% are poor metabolizers. 2. Restriction fragment length polymorphism analysis of the CYP2D6 locus identif
Autor:
René Gueguen, S. Visvikis, Yves Artur, Joseph Henny, Françoise Schiele, Gérard Siest, J. P. Deschamps, Josiane Steinmetz, M. Jaid, M. M. Galteau, A. Regis, Mohamed Zaiou, Bernard Herbeth
Publikováno v:
Scopus-Elsevier
Since its establishment, the Center for Preventive Medicine in Vandoeuvre-les-Nancy, France, performed specific studies on healthy humans, and its approach was very useful for defining reference values. Prevention should extend its interest to chroni
Publikováno v:
Clinica Chimica Acta. 209:109-121
Enzyme induction by drugs mostly concerns those enzymes involved in drug metabolism: cytochromes P-450, UDP-glucuronosyltransferases, glutathione S-transferases, gamma-glutamyltransferases and epoxide hydrolases. A large variety of molecular forms ex