Leren TP

References (7)

Title : Molecular genetic testing and measurement of levels of GPIHBP1 autoantibodies in patients with severe hypertriglyceridemia: The importance of identifying the underlying cause of hypertriglyceridemia - Strom_2023_J.Clin.Lipidol__
Author(s) : Strom TB , Tveita AA , Bogsrud MP , Leren TP
Ref : J Clin Lipidol , : , 2023
PubMedID: 37981531

Title : Lysosomal acid lipase does not have a propeptide and should not be considered being a proprotein - Strom_2020_Proteins_88_440
Author(s) : Strom TB , Vinje T , Bjune K , da Costa LT , Laerdahl JK , Leren TP
Ref : Proteins , 88 :440 , 2020
PubMedID: 31587363
Gene_locus related to this paper: human-LIPA

Title : Characterization of the mechanisms by which missense mutations in the lysosomal acid lipase gene disrupt enzymatic activity - Vinje_2019_Hum.Mol.Genet_28_3043
Author(s) : Vinje T , Laerdahl JK , Bjune K , Leren TP , Strom TB
Ref : Hum Mol Genet , 28 :3043 , 2019
PubMedID: 31131398
Gene_locus related to this paper: human-LIPA

Title : Prevalence of cholesteryl ester storage disease among hypercholesterolemic subjects and functional characterization of mutations in the lysosomal acid lipase gene - Vinje_2018_Mol.Genet.Metab_123_169
Author(s) : Vinje T , Wierod L , Leren TP , Strom TB
Ref : Mol Genet Metab , 123 :169 , 2018
PubMedID: 29196158
Gene_locus related to this paper: human-LIPA

Title : Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia - Pingitore_2016_J.Clin.Lipidol_10_816
Author(s) : Pingitore P , Lepore SM , Pirazzi C , Mancina RM , Motta BM , Valenti L , Berge KE , Retterstol K , Leren TP , Wiklund O , Romeo S
Ref : J Clin Lipidol , 10 :816 , 2016
PubMedID: 27578112
Gene_locus related to this paper: human-LPL

Title : Lecithin: Cholesterol Acyltransferase (LCAT) Deficiency: renal lesions with early graft recurrence - Strom_2011_Ultrastruct.Pathol_35_139
Author(s) : Strom EH , Sund S , Reier-Nilsen M , Dorje C , Leren TP
Ref : Ultrastruct Pathol , 35 :139 , 2011
PubMedID: 21323422
Gene_locus related to this paper: human-LCAT

Title : Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia - Pasalic_2004_Clin.Chim.Acta_343_179
Author(s) : Pasalic D , Jurcic Z , Stipancic G , Ferencak G , Leren TP , Djurovic S , Stavljenic-Rukavina A
Ref : Clinica Chimica Acta , 343 :179 , 2004
PubMedID: 15115692