Zobrazeno 1 - 10 of 373 pro vyhledávání: '"J. L. De Gennes"'
1
Akademický článek
Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombination.
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
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4
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf7a642e46450b2f53b5eb741e4013c
https://doi.org/10.1016/s0021-9150(99)00112-4
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5
Akademický článek
Measurement of two plasma triglyceride lipases by an immunochemical method: studies in patients with hypertriglyceridemia
Autor: H Greten, R DeGrella, G Klose, W Rascher, J L de Gennes, E Gjone
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
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6
Assessment of French patients with LPL deficiency for French Canadian mutations
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8d064170f11372bee1676ea98457c34
https://doi.org/10.1136/jmg.34.8.672
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7
Comparison of the efficacy of simvastatin and standard fibrate therapy in the treatment of primary hypercholesterolemia and combined hyperlipidemia
Autor: Eric Bruckert, W. Malbecq, J. L. De Gennes, F. Baigts
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c26c06b205bf88b7f08870d7554db39
https://doi.org/10.1002/clc.4960181107
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8
Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombination
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae70538e0e1a618ef8c6837039724e6c
https://doi.org/10.1016/s0022-2275(20)39913-2
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9
Common and rare genotypes of human apolipoprotein E determined by specific restriction profiles of polymerase chain reaction-amplified DNA
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::27ab58102740218e0ec61c37bef675d5
https://doi.org/10.1093/clinchem/40.1.24
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10
Relationship Between Smoking Status and Serum Lipids in a Hyperlipidemic Population and Analysis of Possible Confounding Factors
Autor: Truffert J, N Jacob, Eric Bruckert, L Lamaire, J.-L. De Gennes, F Percheron
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bdfdd84bc6b192af0e4a3481e33b2b67
https://doi.org/10.1093/clinchem/38.9.1698
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