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| Title : The Endothelium Is Both a Target and a Barrier of HDL's Protective Functions - Robert_2021_Cells_10_ |
| Author(s) : Robert J , Osto E , von Eckardstein A |
| Ref : Cells , 10 : , 2021 |
| Abstract : Robert_2021_Cells_10_ |
| ESTHER : Robert_2021_Cells_10_ |
| PubMedSearch : Robert_2021_Cells_10_ |
| PubMedID: 33924941 |
| Title : High density lipoproteins in the intersection of diabetes mellitus, inflammation and cardiovascular disease - Rohrer_2004_Curr.Opin.Lipidol_15_269 |
| Author(s) : Rohrer L , Hersberger M , von Eckardstein A |
| Ref : Curr Opin Lipidol , 15 :269 , 2004 |
| Abstract : Rohrer_2004_Curr.Opin.Lipidol_15_269 |
| ESTHER : Rohrer_2004_Curr.Opin.Lipidol_15_269 |
| PubMedSearch : Rohrer_2004_Curr.Opin.Lipidol_15_269 |
| PubMedID: 15166782 |
| Title : Modulated serum activities and concentrations of paraoxonase in high density lipoprotein deficiency states - James_1998_Atherosclerosis_139_77 |
| Author(s) : James RW , Blatter Garin MC , Calabresi L , Miccoli R , von Eckardstein A , Tilly-Kiesi M , Taskinen MR , Assmann G , Franceschini G |
| Ref : Atherosclerosis , 139 :77 , 1998 |
| Abstract : James_1998_Atherosclerosis_139_77 |
| ESTHER : James_1998_Atherosclerosis_139_77 |
| PubMedSearch : James_1998_Atherosclerosis_139_77 |
| PubMedID: 9699894 |
| Title : Compound heterozygosity for a known (D250N) and a novel (E410K) missense mutation in the C-terminal domain of lipoprotein lipase causes familial chylomicronemia - |
| Author(s) : Wiebusch H , Funke H , Bruin T , Bucher H , von Eckardstein A , Kastelein JJ , Assmann G |
| Ref : Hum Mutat , 8 :381 , 1996 |
| PubMedID: 8956048 |
| Gene_locus related to this paper: human-LPL |
| Title : Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease - Funke_1993_J.Clin.Invest_91_677 |
| Author(s) : Funke H , von Eckardstein A , Pritchard PH , Hornby AE , Wiebusch H , Motti C , Hayden MR , Dachet C , Jacotot B , Gerdes U , Faergeman O , Albers JJ , Colleoni N , Catapano A , Frohlich J , Assmann G |
| Ref : J Clinical Investigation , 91 :677 , 1993 |
| Abstract : Funke_1993_J.Clin.Invest_91_677 |
| ESTHER : Funke_1993_J.Clin.Invest_91_677 |
| PubMedSearch : Funke_1993_J.Clin.Invest_91_677 |
| PubMedID: 8432868 |
| Gene_locus related to this paper: human-LCAT |
| Title : A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity - Funke_1991_Proc.Natl.Acad.Sci.U.S.A_88_4855 |
| Author(s) : Funke H , von Eckardstein A , Pritchard PH , Albers JJ , Kastelein JJ , Droste C , Assmann G |
| Ref : Proc Natl Acad Sci U S A , 88 :4855 , 1991 |
| Abstract : Funke_1991_Proc.Natl.Acad.Sci.U.S.A_88_4855 |
| ESTHER : Funke_1991_Proc.Natl.Acad.Sci.U.S.A_88_4855 |
| PubMedSearch : Funke_1991_Proc.Natl.Acad.Sci.U.S.A_88_4855 |
| PubMedID: 2052566 |
| Title : Lecithin:cholesterol acyltransferase deficiency and fish eye disease. - Assmann_1991_Curr.Opin.Lipidol_2_110 |
| Author(s) : Assmann G , von Eckardstein A , Funke H |
| Ref : Curr Opin Lipidol , 2 :110 , 1991 |
| Abstract : Assmann_1991_Curr.Opin.Lipidol_2_110 |
| ESTHER : Assmann_1991_Curr.Opin.Lipidol_2_110 |
| PubMedSearch : Assmann_1991_Curr.Opin.Lipidol_2_110 |
| PubMedID: |