Zobrazeno 1 - 10
of 310
pro vyhledávání: '"J. L. De Gennes"'
Autor:
P Benlian, J Etienne, J L de Gennes, L Noé, D Brault, A Raisonnier, F Arnault, J Hamelin, L Foubert, J C Chuat
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 2, Pp 356-366 (1995)
We studied a homozygous deletion in the lipoprotein lipase gene at the molecular level. Comprising the end of intron 8, the whole of exon 9, and about two-thirds of intron 9, this 2.136-kb deletion caused complete lipoprotein lipase deficiency and se
Externí odkaz:
https://doaj.org/article/249cfca83ba14529b09bf38b29089e04
Autor:
Evelyn M. Teh, Michelle Savoldelli, J.-L. de Gennes, Yves Pouliquen, Peter J. Dolphin, Pascale Benlian, Jeffrey W. Chisholm
Publikováno v:
Atherosclerosis. 146:141-151
Lecithin: cholesterolacyltransferase (LCAT) transacylates the fatty acid at the sn-2 position of lecithin to the 3β-OH group of cholesterol forming lysolecithin and the majority of cholesteryl ester found in plasma. LCAT participates in the reverse
Publikováno v:
Journal of Lipid Research, Vol 17, Iss 3, Pp 203-210 (1976)
Postheparin plasma lipolytic activity consists of two hydrolytic activities, hepatic triglyceride lipase and lipoprotein lipase. These two enzymes were separated and partially purified by means of ammonium sulfate precipitation and affinity chromatog
Externí odkaz:
https://doaj.org/article/559f1a39aa014bc2a9bc15875a13a168
Autor:
Michael R. Hayden, J. L. De Gennes, Pascale Benlian, J.P. Lagarde, J.P. Girardet, L. Foubert, A. Raisonnier, Ewa Ehrenborg
Publikováno v:
Karolinska Institutet
Mutations in the LPL gene show high levels of allelic heterogeneity between and within different populations. Complete LPL deficiency has a very high prevalence in French Canadians, where only three missense mutations account for > 97% of cases, most
Publikováno v:
Clinical Cardiology. 18:621-629
Five multicenter, randomized, double-blind, placebo-controlled studies were conducted in France to compare the efficacy and safety of once-daily simvastatin treatment (10-40 mg/day) with conventional therapy with gemfibrozil 900 mg/day, ciprofibrate
Autor:
J L de Gennes, F. Arnault, A. Raisonnier, L. Foubert, J Hamelin, J. Etienne, Jean-Claude Chuat, D. Brault, Lydie Noé, Pascale Benlian
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 2, Pp 356-366 (1995)
We studied a homozygous deletion in the lipoprotein lipase gene at the molecular level. Comprising the end of intron 8, the whole of exon 9, and about two-thirds of intron 9, this 2.136-kb deletion caused complete lipoprotein lipase deficiency and se
Autor:
J.-L. De Gennes, M. Thomas, P Richard, G Béréziat, A. Cassaigne, M P de Zulueta, A. Iron, G Thomas
Publikováno v:
Clinical Chemistry. 40:24-29
The three common isoforms of human apolipoprotein E (apo E) differ at positions 112 and 158 and are named E3, E4, and E2 according to phenotyping by isoelectric focusing (IEF). The polymerase chain reaction (PCR) method allows the detection of common
Publikováno v:
Clinical Chemistry. 38:1698-1705
The aim of our study was to estimate the potential relationship between smoking behavior and other coronary heart disease risk factors in 250 hyperlipidemic patients. We present data obtained through self-reporting of the number of cigarettes smoked
Autor:
Catherine Boileau, N. Loux, B. Saint-Jore, F. Dairou, Truffert J, J. L. de Gennes, Claudine Junien, P. Douste-Blazy, B. Dastugue, Benlian P, G. Collod
Publikováno v:
Hum Mutat
Hum Mutat, 1992, 1 (4), pp.325-32. ⟨10.1002/humu.1380010411⟩
Hum Mutat, 1992, 1 (4), pp.325-32. ⟨10.1002/humu.1380010411⟩
To investigate the molecular basis of familial hypercholesterolemia (FH) in France, we applied the single strand conformation polymorphism (SSCP) method to the promoter region and the 18 exons of the low density lipoprotein receptor (LDLR) gene. Seve