| Title : Lipoprotein lipase deficiency is associated with elevated acylation stimulating protein plasma levels - Paglialunga_2009_J.Lipid.Res_50_1109 |
| Author(s) : Paglialunga S , Julien P , Tahiri Y , Cadelis F , Bergeron J , Gaudet D , Cianflone K |
| Ref : J Lipid Res , 50 :1109 , 2009 |
| Abstract : |
| PubMedSearch : Paglialunga_2009_J.Lipid.Res_50_1109 |
| PubMedID: 19237736 |
| Gene_locus related to this paper: human-LPL |
| Title : Gene polymorphisms in the Quebec population: a risk to develop hypertriglyceridemia - Garenc_2006_Biochem.Biophys.Res.Commun_344_588 |
| Author(s) : Garenc C , Aubert S , Laroche J , Bergeron J , Gagne C , Rousseau F , Julien P |
| Ref : Biochemical & Biophysical Research Communications , 344 :588 , 2006 |
| Abstract : |
| PubMedSearch : Garenc_2006_Biochem.Biophys.Res.Commun_344_588 |
| PubMedID: 16630553 |
| Title : Lipoprotein lipase and endothelial lipase expression in mouse brain: regional distribution and selective induction following kainic acid-induced lesion and focal cerebral ischemia - Paradis_2004_Neurobiol.Dis_15_312 |
| Author(s) : Paradis E , Clavel S , Julien P , Murthy MR , de Bilbao F , Arsenijevic D , Giannakopoulos P , Vallet P , Richard D |
| Ref : Neurobiol Dis , 15 :312 , 2004 |
| Abstract : |
| PubMedSearch : Paradis_2004_Neurobiol.Dis_15_312 |
| PubMedID: 15006701 |
| Title : Requirement for enzymatically active lipoprotein lipase in neuronal differentiation: a site-directed mutagenesis study - Paradis_2004_Brain.Res.Dev.Brain.Res_149_29 |
| Author(s) : Paradis E , Julien P , Ven Murthy MR |
| Ref : Brain Research Developmental Brain Research , 149 :29 , 2004 |
| Abstract : |
| PubMedSearch : Paradis_2004_Brain.Res.Dev.Brain.Res_149_29 |
| PubMedID: 15013626 |
| Title : Effect of obesity on HDL and LDL particle sizes in carriers of the null P207L or defective D9N mutation in the lipoprotein lipase gene: the Quebec LipD Study - Ruel_2003_Int.J.Obes.Relat.Metab.Disord_27_631 |
| Author(s) : Ruel IL , Gaudet D , Perron P , Bergeron J , Julien P , Lamarche B |
| Ref : Int J Obes Relat Metab Disord , 27 :631 , 2003 |
| Abstract : |
| PubMedSearch : Ruel_2003_Int.J.Obes.Relat.Metab.Disord_27_631 |
| PubMedID: 12704407 |
| Title : Effect of apolipoprotein E, peroxisome proliferator-activated receptor alpha and lipoprotein lipase gene mutations on the ability of fenofibrate to improve lipid profiles and reach clinical guideline targets among hypertriglyceridemic patients - Brisson_2002_Pharmacogenet_12_313 |
| Author(s) : Brisson D , Ledoux K , Bosse Y , St-Pierre J , Julien P , Perron P , Hudson TJ , Vohl MC , Gaudet D |
| Ref : Pharmacogenetics , 12 :313 , 2002 |
| Abstract : |
| PubMedSearch : Brisson_2002_Pharmacogenet_12_313 |
| PubMedID: 12042669 |
| Title : Molecular pathobiology of the human lipoprotein lipase gene - Murthy_1996_Pharmacol.Ther_70_101 |
| Author(s) : Murthy V , Julien P , Gagne C |
| Ref : Pharmacol Ther , 70 :101 , 1996 |
| Abstract : |
| PubMedSearch : Murthy_1996_Pharmacol.Ther_70_101 |
| PubMedID: 8843465 |
| Gene_locus related to this paper: human-LPL |
| Title : Hemolysis in primary lipoprotein lipase deficiency - Cantin_1995_Metabolism_44_652 |
| Author(s) : Cantin B , Boudriau S , Bertrand M , Brun LD , Gagne C , Rogers PA , Ven Murthy MR , Lupien PJ , Julien P |
| Ref : Metabolism , 44 :652 , 1995 |
| Abstract : |
| PubMedSearch : Cantin_1995_Metabolism_44_652 |
| PubMedID: 7752915 |
| Title : Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Quebec - Bergeron_1992_Clin.Genet_41_206 |
| Author(s) : Bergeron J , Normand T , Bharucha A , Ven Murthy MR , Julien P , Gagne C , Dionne C , De Braekeleer M , Brun D , Hayden MR , Luplen PJ |
| Ref : Clin Genet , 41 :206 , 1992 |
| Abstract : |
| PubMedSearch : Bergeron_1992_Clin.Genet_41_206 |
| PubMedID: 1576758 |
| Gene_locus related to this paper: human-LPL |
| Title : A missense mutation (Asp250----Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries - Ma_1992_Genomics_13_649 |
| Author(s) : Ma Y , Wilson BI , Bijvoet S , Henderson HE , Cramb E , Roederer G , Ven Murthy MR , Julien P , Bakker HD , Kastelein JJ , Brunzel JD , Hayden MR |
| Ref : Genomics , 13 :649 , 1992 |
| Abstract : |
| PubMedSearch : Ma_1992_Genomics_13_649 |
| PubMedID: 1639392 |
| Gene_locus related to this paper: human-LPL |
| Title : Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Quebec - Normand_1992_Hum.Genet_89_671 |
| Author(s) : Normand T , Bergeron J , Fernandez-Margallo T , Bharucha A , Ven Murthy MR , Julien P , Gagne C , Dionne C , De Braekeleer M , Ma R , Hayden MR , Lupien PJ |
| Ref : Hum Genet , 89 :671 , 1992 |
| Abstract : |
| PubMedSearch : Normand_1992_Hum.Genet_89_671 |
| PubMedID: 1511985 |
| Title : Identification of the molecular defects underlying chylomicronemia in the majority of 75 separate probands with LPL deficiency. (Abstract) - |
| Author(s) : Henderson H , Ma Y , Kastelein J , Roederer G , Julien P , Brunzell J , Hayden MR |
| Ref : Clin Res , 39 :336A , 1991 |
| PubMedID: |
| Title : Founder effect in familial hyperchylomicronemia among French Canadians of Quebec - De Braekeleer_1991_Hum.Hered_41_168 |
| Author(s) : De Braekeleer M , Dionne C , Gagne C , Julien P , Brun D , Ven Murthy MR , Lupien PJ |
| Ref : Hum Hered , 41 :168 , 1991 |
| Abstract : |
| PubMedSearch : De Braekeleer_1991_Hum.Hered_41_168 |
| PubMedID: 1937490 |
| Gene_locus related to this paper: human-LPL |
| Title : A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians - Ma_1991_N.Engl.J.Med_324_1761 |
| Author(s) : Ma Y , Henderson HE , Murthy V , Roederer G , Monsalve MV , Clarke LA , Normand T , Julien P , Gagne C , Lambert M , et al. |
| Ref : N Engl J Med , 324 :1761 , 1991 |
| Abstract : |
| PubMedSearch : Ma_1991_N.Engl.J.Med_324_1761 |
| PubMedID: 2038366 |
| Gene_locus related to this paper: human-LPL |
| Title : A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries - Monsalve_1990_J.Clin.Invest_86_728 |
| Author(s) : Monsalve MV , Henderson H , Roederer G , Julien P , Deeb S , Kastelein JJ , Peritz L , Devlin R , Bruin T , Murthy MR , et al. |
| Ref : J Clinical Investigation , 86 :728 , 1990 |
| Abstract : |
| PubMedSearch : Monsalve_1990_J.Clin.Invest_86_728 |
| PubMedID: 1975597 |
| Gene_locus related to this paper: human-LPL |
| Title : Primary lipoprotein-lipase-activity deficiency: clinical investigation of a French Canadian population - Gagne_1989_Cmaj_140_405 |
| Author(s) : Gagne C , Brun LD , Julien P , Moorjani S , Lupien PJ |
| Ref : Cmaj , 140 :405 , 1989 |
| Abstract : |
| PubMedSearch : Gagne_1989_Cmaj_140_405 |
| PubMedID: 2914262 |
| Title : Primary lipoprotein lipase activity deficiency: clinical investigation of a French Canadian population. - |
| Author(s) : Gagne C , Brun LD , Julien P , Moorjani S , Lupien PJ |
| Ref : Can Med Assoc J , 140 :405 , 1989 |
| PubMedID: |