Moulin P - Search Results

1

Modulation of phenotypic expression of APOA5 Q97X and L242P mutations.

Charrière S, Cugnet C, Guitard M, Bernard S, Groisne L, Charcosset M, Pruneta-Deloche V, Merlin M, Billon S, Delay M, Sassolas A, Moulin P, Marçais C. Charrière S, et al. Among authors: moulin p. Atherosclerosis. 2009 Nov;207(1):150-6. doi: 10.1016/j.atherosclerosis.2009.04.021. Epub 2009 Apr 24. Atherosclerosis. 2009. PMID: 19447388

2

Severe hypertriglyceridaemia in Type II diabetes: involvement of apoC-III Sst-I polymorphism, LPL mutations and apo E3 deficiency.

Marçais C, Bernard S, Merlin M, Ulhmann M, Mestre B, Rochet-Mingret L, Revol A, Berthezene F, Moulin P. Marçais C, et al. Among authors: moulin p. Diabetologia. 2000 Nov;43(11):1346-52. doi: 10.1007/s001250051537. Diabetologia. 2000. PMID: 11126401

3

Lack of association between carotid intima-media thickness and paraoxonase gene polymorphism in non-insulin dependent diabetes mellitus.

Cao H, Girard-Globa A, Serusclat A, Bernard S, Bondon P, Picard S, Berthezene F, Moulin P. Cao H, et al. Among authors: moulin p. Atherosclerosis. 1998 Jun;138(2):361-6. doi: 10.1016/s0021-9150(98)00031-8. Atherosclerosis. 1998. PMID: 9690920

4

Ex vivo measurement of lipoprotein lipase-dependent very low density lipoprotein (VLDL)-triglyceride hydrolysis in human VLDL: an alternative to the postheparin assay of lipoprotein lipase activity?

Pruneta V, Autran D, Ponsin G, Marcais C, Duvillard L, Verges B, Berthezene F, Moulin P. Pruneta V, et al. Among authors: moulin p. J Clin Endocrinol Metab. 2001 Feb;86(2):797-803. doi: 10.1210/jcem.86.2.7261. J Clin Endocrinol Metab. 2001. PMID: 11158049

5

The first results demonstrating efficiency and safety of a double-column whole blood method of LDL-apheresis.

Hequet O, Le QH, Rigal D, Mekhloufi F, Jaeger S, Sassolas A, Groisne L, Moulin P. Hequet O, et al. Among authors: moulin p. Transfus Apher Sci. 2010 Feb;42(1):3-10. doi: 10.1016/j.transci.2009.10.001. Epub 2009 Nov 20. Transfus Apher Sci. 2010. PMID: 19932056

6

Single, short in-del, and copy number variations detection in monogenic dyslipidemia using a next-generation sequencing strategy.

Marmontel O, Charrière S, Simonet T, Bonnet V, Dumont S, Mahl M, Jacobs C, Nony S, Chabane K, Bozon D, Janin A, Peretti N, Lachaux A, Bardel C, Millat G, Moulin P, Marçais C, Di Filippo M. Marmontel O, et al. Among authors: moulin p. Clin Genet. 2018 Jul;94(1):132-140. doi: 10.1111/cge.13250. Epub 2018 Apr 25. Clin Genet. 2018. PMID: 29572815

7

VLDL-bound lipoprotein lipase facilitates the cholesteryl ester transfer protein-mediated transfer of cholesteryl esters from HDL to VLDL.

Pruneta V, Pulcini T, Lalanne F, Marçais C, Berthezène F, Ponsin G, Moulin P. Pruneta V, et al. Among authors: moulin p. J Lipid Res. 1999 Dec;40(12):2333-9. J Lipid Res. 1999. PMID: 10588959 Free article.

8

LDL from obese patients with the metabolic syndrome show increased lipid peroxidation and activate platelets.

Colas R, Sassolas A, Guichardant M, Cugnet-Anceau C, Moret M, Moulin P, Lagarde M, Calzada C. Colas R, et al. Among authors: moulin p. Diabetologia. 2011 Nov;54(11):2931-40. doi: 10.1007/s00125-011-2272-8. Epub 2011 Aug 17. Diabetologia. 2011. PMID: 21847583 Free PMC article. Clinical Trial.

9

Moderate oral supplementation with docosahexaenoic acid improves platelet function and oxidative stress in type 2 diabetic patients.

Véricel E, Colas R, Calzada C, Lê QH, Feugier N, Cugnet C, Vidal H, Laville M, Moulin P, Lagarde M. Véricel E, et al. Among authors: moulin p. Thromb Haemost. 2015 Aug;114(2):289-96. doi: 10.1160/TH14-12-1003. Epub 2015 Apr 2. Thromb Haemost. 2015. PMID: 25832443 Free article. Clinical Trial.

10

Association between plasma HDL-cholesterol concentration and Taq1B CETP gene polymorphism in non-insulin-dependent diabetes mellitus.

Bernard S, Moulin P, Lagrost L, Picard S, Elchebly M, Ponsin G, Chapuis F, Berthezène F. Bernard S, et al. Among authors: moulin p. J Lipid Res. 1998 Jan;39(1):59-65. J Lipid Res. 1998. PMID: 9469586 Free article.

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