Jauhiainen M

References (6)

Title : Hepatic lipase- and endothelial lipase-deficiency in mice promotes macrophage-to-feces RCT and HDL antioxidant properties - Escola-Gil_2013_Biochim.Biophys.Acta_1831_691
Author(s) : Escola-Gil JC , Chen X , Julve J , Quesada H , Santos D , Metso J , Tous M , Jauhiainen M , Blanco-Vaca F
Ref : Biochimica & Biophysica Acta , 1831 :691 , 2013
PubMedID: 23328279

Title : Phospholipid transfer protein is differentially expressed in human arterial and venous placental endothelial cells and enhances cholesterol efflux to fetal HDL - Scholler_2012_J.Clin.Endocrinol.Metab_97_2466
Author(s) : Scholler M , Wadsack C , Metso J , Chirackal Manavalan AP , Sreckovic I , Schweinzer C , Hiden U , Jauhiainen M , Desoye G , Panzenboeck U
Ref : J Clinical Endocrinology Metab , 97 :2466 , 2012
PubMedID: 22492872

Title : Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism - Lyly_2008_Hum.Mol.Genet_17_1406
Author(s) : Lyly A , Marjavaara SK , Kyttala A , Uusi-Rauva K , Luiro K , Kopra O , Martinez LO , Tanhuanpaa K , Kalkkinen N , Suomalainen A , Jauhiainen M , Jalanko A
Ref : Hum Mol Genet , 17 :1406 , 2008
PubMedID: 18245779
Gene_locus related to this paper: mouse-ppt

Title : Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1)--distinct characteristics in neurons - Lyly_2007_BMC.Cell.Biol_8_22
Author(s) : Lyly A , von Schantz C , Salonen T , Kopra O , Saarela J , Jauhiainen M , Kyttala A , Jalanko A
Ref : BMC Cell Biol , 8 :22 , 2007
PubMedID: 17565660
Gene_locus related to this paper: mouse-ppt

Title : Hypertriglyceridemia is associated with prebeta-HDL concentrations in subjects with familial low HDL - Soderlund_2005_J.Lipid.Res_46_1643
Author(s) : Soderlund S , Soro-Paavonen A , Ehnholm C , Jauhiainen M , Taskinen MR
Ref : J Lipid Res , 46 :1643 , 2005
PubMedID: 15897606

Title : Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5\% of cases with very low serum HDL cholesterol levels - Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591
Author(s) : Miettinen HE , Gylling H , Tenhunen J , Virtamo J , Jauhiainen M , Huttunen JK , Kantola I , Miettinen TA , Kontula K
Ref : Arterioscler Thromb Vasc Biol , 18 :591 , 1998
PubMedID: 9555865