Report for Marcais C

General

Full name :

First name :

Mail :

Zip Code :

City :

Country :

Email :

Phone :

Fax :

Website :

Directory :

References (5)

Title : Multiple microRNA regulation of lipoprotein lipase gene abolished by 3'UTR polymorphisms in a triglyceride-lowering haplotype harboring p.Ser474Ter - Caussy_2016_Atherosclerosis_246_280
Author(s) : Caussy C , Charriere S , Meirhaeghe A , Dallongeville J , Lefai E , Rome S , Cuerq C , Euthine V , Delay M , Marmontel O , Di Filippo M , Lagarde M , Moulin P , Marcais C
Ref : Atherosclerosis , 246 :280 , 2016
Abstract : Caussy_2016_Atherosclerosis_246_280
ESTHER : Caussy_2016_Atherosclerosis_246_280
PubMedSearch : Caussy_2016_Atherosclerosis_246_280
PubMedID: 26820803

Title : Prevalence and function of anti-lipoprotein lipase auto-antibodies in type V hyperchylomicronemia - Moret_2010_Atherosclerosis_208_324
Author(s) : Moret M , Pruneta-Deloche V , Sassolas A , Marcais C , Moulin P
Ref : Atherosclerosis , 208 :324 , 2010
Abstract : Moret_2010_Atherosclerosis_208_324
ESTHER : Moret_2010_Atherosclerosis_208_324
PubMedSearch : Moret_2010_Atherosclerosis_208_324
PubMedID: 19695572

Title : Combination of circulating antilipoprotein lipase (Anti-LPL) antibody and heterozygous S172 fsX179 mutation of LPL gene leading to chronic hyperchylomicronemia - Pruneta-Deloche_2005_J.Clin.Endocrinol.Metab_90_3995
Author(s) : Pruneta-Deloche V , Marcais C , Perrot L , Sassolas A , Delay M , Estour B , Lagarde M , Moulin P
Ref : J Clinical Endocrinology Metab , 90 :3995 , 2005
Abstract : Pruneta-Deloche_2005_J.Clin.Endocrinol.Metab_90_3995
ESTHER : Pruneta-Deloche_2005_J.Clin.Endocrinol.Metab_90_3995
PubMedSearch : Pruneta-Deloche_2005_J.Clin.Endocrinol.Metab_90_3995
PubMedID: 15840743

Title : Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment - Marcais_2005_J.Clin.Invest_115_2862
Author(s) : Marcais C , Verges B , Charriere S , Pruneta V , Merlin M , Billon S , Perrot L , Drai J , Sassolas A , Pennacchio LA , Fruchart-Najib J , Fruchart JC , Durlach V , Moulin P
Ref : J Clinical Investigation , 115 :2862 , 2005
Abstract : Marcais_2005_J.Clin.Invest_115_2862
ESTHER : Marcais_2005_J.Clin.Invest_115_2862
PubMedSearch : Marcais_2005_J.Clin.Invest_115_2862
PubMedID: 16200213

Title : [Familial hyperchylomicronemia with a new mutation of the lipoprotein lipase gene] - Causeret_2001_Ann.Dermatol.Venereol_128_1343
Author(s) : Causeret AS , Souillet AL , Marcais C , Prunetta V , Lachaux A , Faure M , Claudy A
Ref : Ann Dermatol Venereol , 128 :1343 , 2001
Abstract : Causeret_2001_Ann.Dermatol.Venereol_128_1343
ESTHER : Causeret_2001_Ann.Dermatol.Venereol_128_1343
PubMedSearch : Causeret_2001_Ann.Dermatol.Venereol_128_1343
PubMedID: 11908140