Report for Julien P

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References (17)

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 : Paglialunga_2009_J.Lipid.Res_50_1109
ESTHER : Paglialunga_2009_J.Lipid.Res_50_1109
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 : Garenc_2006_Biochem.Biophys.Res.Commun_344_588
ESTHER : Garenc_2006_Biochem.Biophys.Res.Commun_344_588
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 : Paradis_2004_Neurobiol.Dis_15_312
ESTHER : Paradis_2004_Neurobiol.Dis_15_312
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 : Paradis_2004_Brain.Res.Dev.Brain.Res_149_29
ESTHER : Paradis_2004_Brain.Res.Dev.Brain.Res_149_29
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 : Ruel_2003_Int.J.Obes.Relat.Metab.Disord_27_631
ESTHER : Ruel_2003_Int.J.Obes.Relat.Metab.Disord_27_631
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 : Brisson_2002_Pharmacogenet_12_313
ESTHER : Brisson_2002_Pharmacogenet_12_313
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 : Murthy_1996_Pharmacol.Ther_70_101
ESTHER : Murthy_1996_Pharmacol.Ther_70_101
PubMedSearch : Murthy_1996_Pharmacol.Ther_70_101
PubMedID: 8843465

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 : Cantin_1995_Metabolism_44_652
ESTHER : Cantin_1995_Metabolism_44_652
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 : Bergeron_1992_Clin.Genet_41_206
ESTHER : Bergeron_1992_Clin.Genet_41_206
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 : Ma_1992_Genomics_13_649
ESTHER : Ma_1992_Genomics_13_649
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 : Normand_1992_Hum.Genet_89_671
ESTHER : Normand_1992_Hum.Genet_89_671
PubMedSearch : Normand_1992_Hum.Genet_89_671
PubMedID: 1511985

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 : Ma_1991_N.Engl.J.Med_324_1761
ESTHER : Ma_1991_N.Engl.J.Med_324_1761
PubMedSearch : Ma_1991_N.Engl.J.Med_324_1761
PubMedID: 2038366
Gene_locus related to this paper: human-LPL

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 : De Braekeleer_1991_Hum.Hered_41_168
ESTHER : De Braekeleer_1991_Hum.Hered_41_168
PubMedSearch : De Braekeleer_1991_Hum.Hered_41_168
PubMedID: 1937490
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 : Monsalve_1990_J.Clin.Invest_86_728
ESTHER : Monsalve_1990_J.Clin.Invest_86_728
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. -
Author(s) : Gagne C , Brun LD , Julien P , Moorjani S , Lupien PJ
Ref : Can Med Assoc J , 140 :405 , 1989
PubMedID:

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 : Gagne_1989_Cmaj_140_405
ESTHER : Gagne_1989_Cmaj_140_405
PubMedSearch : Gagne_1989_Cmaj_140_405
PubMedID: 2914262