Mailly F - Search Results

1

A common variant in the gene for lipoprotein lipase (Asp9-->Asn). Functional implications and prevalence in normal and hyperlipidemic subjects.

Mailly F, Tugrul Y, Reymer PW, Bruin T, Seed M, Groenemeyer BF, Asplund-Carlson A, Vallance D, Winder AF, Miller GJ, et al. Mailly F, et al. Arterioscler Thromb Vasc Biol. 1995 Apr;15(4):468-78. doi: 10.1161/01.atv.15.4.468. Arterioscler Thromb Vasc Biol. 1995. PMID: 7749858

2

Lipoprotein lipase activity in patients with combined hyperlipidaemia.

Seed M, Mailly F, Vallance D, Doherty E, Winder A, Talmud P, Humphries SE. Seed M, et al. Among authors: mailly f. Clin Investig. 1994 Jan;72(2):100-6. doi: 10.1007/BF00184584. Clin Investig. 1994. PMID: 8186654

3

Apolipoprotein E phenotype and lipoprotein(a) in familial hypercholesterolaemia: implication for lipoprotein(a) metabolism.

Lindahl G, Mailly F, Humphries S, Seed M. Lindahl G, et al. Among authors: mailly f. Clin Investig. 1994 Aug;72(8):631-8. doi: 10.1007/BF00227457. Clin Investig. 1994. PMID: 7819721

4

Interaction of the lipoprotein lipase asparagine 291-->serine mutation with body mass index determines elevated plasma triacylglycerol concentrations: a study in hyperlipidemic subjects, myocardial infarction survivors, and healthy adults.

Fisher RM, Mailly F, Peacock RE, Hamsten A, Seed M, Yudkin JS, Beisiegel U, Feussner G, Miller G, Humphries SE, et al. Fisher RM, et al. Among authors: mailly f. J Lipid Res. 1995 Oct;36(10):2104-12. J Lipid Res. 1995. PMID: 8576637 Free article.

5

Association between the LPL-D9N mutation in the lipoprotein lipase gene and plasma lipid traits in myocardial infarction survivors from the ECTIM Study.

Mailly F, Fisher RM, Nicaud V, Luong LA, Evans AE, Marques-Vidal P, Luc G, Arveiler D, Bard JM, Poirier O, Talmud PJ, Humphries SE. Mailly F, et al. Atherosclerosis. 1996 Apr 26;122(1):21-8. doi: 10.1016/0021-9150(95)05736-6. Atherosclerosis. 1996. PMID: 8724108

6

Familial lipoprotein lipase (LPL) deficiency: a catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy.

Mailly F, Palmen J, Muller DP, Gibbs T, Lloyd J, Brunzell J, Durrington P, Mitropoulos K, Betteridge J, Watts G, Lithell H, Angelico F, Humphries SE, Talmud PJ. Mailly F, et al. Hum Mutat. 1997;10(6):465-73. doi: 10.1002/(SICI)1098-1004(1997)10:6<465::AID-HUMU8>3.0.CO;2-C. Hum Mutat. 1997. PMID: 9401010

7

Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia.

de Bruin TW, Mailly F, van Barlingen HH, Fisher R, Castro Cabezas M, Talmud P, Dallinga-Thie GM, Humphries SE. de Bruin TW, et al. Among authors: mailly f. Eur J Clin Invest. 1996 Aug;26(8):631-9. doi: 10.1111/j.1365-2362.1996.tb02146.x. Eur J Clin Invest. 1996. PMID: 8872057

8

The molecular genetics of pediatric lipid disorders: recent progress and future research directions.

Humphries SE, Mailly F, Gudnason V, Talmud P. Humphries SE, et al. Among authors: mailly f. Pediatr Res. 1993 Oct;34(4):403-15. doi: 10.1203/00006450-199310000-00005. Pediatr Res. 1993. PMID: 8255668 Review.

9

Characterization of a new apolipoprotein E5 variant detected in two French-Canadian subjects.

Mailly F, Xu CF, Xhignesse M, Lussier-Cacan S, Talmud PJ, Davignon J, Humphries SE, Nestruck AC. Mailly F, et al. J Lipid Res. 1991 Apr;32(4):613-20. J Lipid Res. 1991. PMID: 1713245 Free article.

10

Reduced cholesteryl ester transfer in plasma of patients with lipoprotein lipase deficiency.

Bagdade JD, Ritter MC, Lithell H, Bassett D, Mailly F, Talmud P, Hayden MR. Bagdade JD, et al. Among authors: mailly f. J Lipid Res. 1996 Aug;37(8):1696-703. J Lipid Res. 1996. PMID: 8864953 Free article.

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