Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mireille Delay"'
Autor:
Mathilde Di Filippo, Christophe Marçais, Sybil Charrière, Oriane Marmontel, Martine Broyer, Mireille Delay, Micheline Merlin, Axel Nollace, René Valéro, Michel Lagarde, Valérie Pruneta-Deloche, Philippe Moulin, Agnès Sassolas
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e96482 (2014)
BACKGROUND: Determination of lipoprotein lipase (LPL) activity is important for hyperchylomicronemia diagnosis, but remains both unreliable and cumbersome with current methods. Consequently by using human VLDL as substrate we developed a new LPL assa
Externí odkaz:
https://doaj.org/article/52db34c3708f4327920442435ee41040
Autor:
Vanessa Euthine, Charlotte Cuerq, Cyrielle Caussy, Mireille Delay, Etienne Lefai, Aline Meirhaeghe, Sophie Rome, Sybil Charrière, Philippe Moulin, Mathilde Di Filippo, C. Marcais, Jean Dallongeville, Oriane Marmontel, Michel Lagarde
Publikováno v:
Atherosclerosis
Atherosclerosis, 2016, 246, pp.280-286. ⟨10.1016/j.atherosclerosis.2016.01.010⟩
Atherosclerosis, Elsevier, 2016, 246, pp.280-286. ⟨10.1016/j.atherosclerosis.2016.01.010⟩
Atherosclerosis, 2016, 246, pp.280-286. ⟨10.1016/j.atherosclerosis.2016.01.010⟩
Atherosclerosis, Elsevier, 2016, 246, pp.280-286. ⟨10.1016/j.atherosclerosis.2016.01.010⟩
Background Lipoprotein lipase (LPL) is a key enzyme in triglyceride (TG) metabolism. LPL gene single nucleotide polymorphisms (SNPs) are associated with TG concentrations however the functionality of many of these SNPs remains poorly understood. Micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87d9bcabbf4c24adf043d4f631d1bcba
https://univ-lyon1.hal.science/hal-01986056
https://univ-lyon1.hal.science/hal-01986056
Autor:
Philippe Moulin, Sophie Rome, J. Dallongeville, Etienne Lefai, Aline Meirhaeghe, Mireille Delay, C. Marcais, Vanessa Euthine, C. Caussy, Sybil Charrière, M. Di Filippo
Publikováno v:
Atherosclerosis
Atherosclerosis, Elsevier, 2015, 241 (1), pp.e12. ⟨10.1016/j.atherosclerosis.2015.04.059⟩
Atherosclerosis, Elsevier, 2015, 241 (1), pp.e12. ⟨10.1016/j.atherosclerosis.2015.04.059⟩
International audience; Aim: Identification and functional study of Lipoprotein Lipase (LPL) 3'UTR polymorphisms associated with triglyceridemia and predicted to modulate miRNA binding.Methods: We sequenced LPL 3'UTR in 271 type 2 diabetic patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6f3b6075005b32506e4620169920150
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02049002
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02049002
Autor:
Christophe Marçais, Michel Lagarde, Laurence Perrot, Mireille Delay, Philippe Moulin, Bruno Estour, Valérie Pruneta-Deloche, Agnès Sassolas
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 90:3995-3998
Sporadic hyperchylomicronemia (type V hyperlipoproteinemia) results from complex interactions between genetic and environmental factors that often remain unknown.Upon investigation of a patient suffering from recurrent hypertriglyceridemic pancreatit
Autor:
Michel Lagarde, Micheline Merlin, Mireille Delay, Philippe Moulin, Agnès Sassolas, Oriane Marmontel, Mathilde Di Filippo, Axel Nollace, Christophe Marçais, Valérie Pruneta-Deloche, René Valéro, Sybil Charrière, Martine Broyer
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99721 (2014)
Plos One 5 (9), . (2014)
PLoS ONE
PLoS ONE, Vol 9, Iss 5, p e96482 (2014)
PLoS ONE, Public Library of Science, 2014, 9 (5), pp.e96482. ⟨10.1371/journal.pone.0096482⟩
Plos One 5 (9), . (2014)
PLoS ONE
PLoS ONE, Vol 9, Iss 5, p e96482 (2014)
PLoS ONE, Public Library of Science, 2014, 9 (5), pp.e96482. ⟨10.1371/journal.pone.0096482⟩
International audience; BACKGROUND: Determination of lipoprotein lipase (LPL) activity is important for hyperchylomicronemia diagnosis, but remains both unreliable and cumbersome with current methods. Consequently by using human VLDL as substrate we
Autor:
Sophie Rome, Cyrielle Caussy, Vanessa Euthine, Mathilde Di Filippo, Sybil Charrière, Etienne Lefai, Agnès Sassolas, Philippe Moulin, C. Marcais, Mireille Delay, Audrey Jalabert
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 94 (1), pp.129-34. ⟨10.1016/j.ajhg.2013.12.001⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 94 (1), pp.129-34. ⟨10.1016/j.ajhg.2013.12.001⟩
International audience; APOA5 c.*158C\textgreaterT (rs2266788), located in the 3' UTR, belongs to APOA5 haplotype 2 (APOA5*2), which is strongly associated with plasma triglyceride levels and modulates the occurrence of both moderate and severe hyper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ed6b2535703e11bb7a6f7aa5618ae81
https://hal.archives-ouvertes.fr/hal-01859007
https://hal.archives-ouvertes.fr/hal-01859007
Autor:
Cyrille Debard, Philippe Moulin, Micheline Merlin, Noël Peretti, Etienne Lefai, Sophie Bernard, C. Marcais, Sybil Charrière, Agnès Sassolas, Mathilde Di Filippo, Mireille Delay, Alain Lachaux
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2011, 96 (10), ⟨10.1210/jc.2011-1444⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2011, 96 (10), ⟨10.1210/jc.2011-1444⟩
Context: GPIHBP1 is a new endothelial binding site for lipoprotein lipase (LPL), the key enzyme for intravascular lipolysis of triglyceride-rich lipoproteins (TGRL). We have identified two new missense mutations of the GPIHBP1 gene, C89F and G175R, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54df06b26864046ada7081c0b9820d4c
https://hal.inrae.fr/hal-02652262
https://hal.inrae.fr/hal-02652262
Autor:
Mathilde Charcosset, M. Guitard, Mireille Delay, Philippe Moulin, Sybil Charrière, Valérie Pruneta-Deloche, C. Marcais, S. Billon, Agnès Sassolas, L. Groisne, M. Merlin, C. Cugnet, Sophie Bernard
Publikováno v:
Atherosclerosis. 207(1)
Objective: To provide phenotypic and functional data in new patients with APOA5 mutations and to identify genetic and metabolic factors influencing their phenotypic expression. Methods and results: By sequencing APOA5 gene in a cohort of 286 hyperchy
Autor:
Sophie Rome, Sybil Charrière, Etienne Lefai, P. Moulin, Mireille Delay, Christophe Marçais, Vanessa Euthine, M. Di Filippo, Cyrielle Caussy
Publikováno v:
Annales d'Endocrinologie. 75:268
Objectif Etudier les polymorphismes en 3′UTR du gene de la LPL associes a la triglyceridemie et determiner leurs implications dans la regulation de l’expression du gene LPL par la modification de sites de liaison de miRNA. Materiels Genotypage de