132 related articles for article (PubMed ID: 35598637)
1. Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans.
Pavanello C; Ossoli A; Strazzella A; Risè P; Veglia F; Lhomme M; Parini P; Calabresi L
J Lipid Res; 2022 Jul; 63(7):100232. PubMed ID: 35598637
[TBL] [Abstract][Full Text] [Related]
2. Plasma cholesteryl esters provided by lecithin:cholesterol acyltransferase and acyl-coenzyme a:cholesterol acyltransferase 2 have opposite atherosclerotic potential.
Lee RG; Kelley KL; Sawyer JK; Farese RV; Parks JS; Rudel LL
Circ Res; 2004 Nov; 95(10):998-1004. PubMed ID: 15486318
[TBL] [Abstract][Full Text] [Related]
3. In vivo contribution of LCAT to apolipoprotein B lipoprotein cholesteryl esters in LDL receptor and apolipoprotein E knockout mice.
Furbee JW; Francone O; Parks JS
J Lipid Res; 2002 Mar; 43(3):428-37. PubMed ID: 11893779
[TBL] [Abstract][Full Text] [Related]
4. Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia.
Conca P; Pileggi S; Simonelli S; Boer E; Boscutti G; Magnolo L; Tarugi P; Penco S; Franceschini G; Calabresi L; Gomaraschi M
J Clin Lipidol; 2012; 6(3):244-50. PubMed ID: 22658148
[TBL] [Abstract][Full Text] [Related]
5. Formation of pregnenolone- and dehydroepiandrosterone-fatty acid esters by lecithin-cholesterol acyltransferase in human plasma high density lipoproteins.
Lavallée B; Provost PR; Belanger A
Biochim Biophys Acta; 1996 Feb; 1299(3):306-12. PubMed ID: 8597585
[TBL] [Abstract][Full Text] [Related]
6. ACAT2 contributes cholesteryl esters to newly secreted VLDL, whereas LCAT adds cholesteryl ester to LDL in mice.
Lee RG; Shah R; Sawyer JK; Hamilton RL; Parks JS; Rudel LL
J Lipid Res; 2005 Jun; 46(6):1205-12. PubMed ID: 15805543
[TBL] [Abstract][Full Text] [Related]
7. Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis.
Klein HG; Santamarina-Fojo S; Duverger N; Clerc M; Dumon MF; Albers JJ; Marcovina S; Brewer HB
J Clin Invest; 1993 Jul; 92(1):479-85. PubMed ID: 8326012
[TBL] [Abstract][Full Text] [Related]
8. Recombinant human LCAT normalizes plasma lipoprotein profile in LCAT deficiency.
Simonelli S; Tinti C; Salvini L; Tinti L; Ossoli A; Vitali C; Sousa V; Orsini G; Nolli ML; Franceschini G; Calabresi L
Biologicals; 2013 Nov; 41(6):446-9. PubMed ID: 24140107
[TBL] [Abstract][Full Text] [Related]
9. Regulation of plasma lecithin:cholesterol acyltransferase in man. III. Role of high density lipoprotein cholesteryl esters in the activating effect of a high-fat test meal.
Rose HG; Juliano J
J Lipid Res; 1979 Mar; 20(3):399-407. PubMed ID: 221605
[TBL] [Abstract][Full Text] [Related]
10. Familial lecithin-cholesterol acyltransferase deficiency: biochemical characteristics and molecular analysis of a new LCAT mutation in a Polish family.
Idzior-Waluś B; Sieradzki J; Kostner G; Małecki MT; Klupa T; Wesołowska T; Rostworowski W; Hartwich J; Waluś M; Kieć AD; Naruszewicz M
Atherosclerosis; 2006 Apr; 185(2):413-20. PubMed ID: 16051254
[TBL] [Abstract][Full Text] [Related]
11. Compound heterozygosity (G71R/R140H) in the lecithin:cholesterol acyltransferase (LCAT) gene results in an intermediate phenotype between LCAT-deficiency and fish-eye disease.
Hörl G; Kroisel PM; Wagner E; Tiran B; Petek E; Steyrer E
Atherosclerosis; 2006 Jul; 187(1):101-9. PubMed ID: 16216249
[TBL] [Abstract][Full Text] [Related]
12. Familial lecithin:cholesterol acyltransferase deficiency: molecular analysis of a compound heterozygote: LCAT (Arg147 --> Trp) and LCAT (Tyr171 --> Stop).
Guerin M; Dachet C; Goulinet S; Chevet D; Dolphin PJ; Chapman MJ; Rouis M
Atherosclerosis; 1997 May; 131(1):85-95. PubMed ID: 9180249
[TBL] [Abstract][Full Text] [Related]
13. LIPA gene mutations affect the composition of lipoproteins: Enrichment in ACAT-derived cholesteryl esters.
Arnaboldi L; Ossoli A; Giorgio E; Pisciotta L; Lucchi T; Grigore L; Pavanello C; Granata A; Pasta A; Arosio B; Azzolino D; Baragetti A; Castelnuovo S; Corsini A; Catapano AL; Calabresi L; Gomaraschi M
Atherosclerosis; 2020 Mar; 297():8-15. PubMed ID: 32058863
[TBL] [Abstract][Full Text] [Related]
14. Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: effects of incubation with lecithin: cholesterol acyltransferase in vitro.
Norum KR; Glomset JA; Nichols AV; Forte T; Albers JJ; King WC; Mitchell CD; Applegate KR; Gong EL; Cabana V
Scand J Clin Lab Invest Suppl; 1975; 142():31-55. PubMed ID: 169567
[TBL] [Abstract][Full Text] [Related]
15. Advances in understanding of the role of lecithin cholesterol acyltransferase (LCAT) in cholesterol transport.
Dobiásová M; Frohlich JJ
Clin Chim Acta; 1999 Aug; 286(1-2):257-71. PubMed ID: 10511297
[TBL] [Abstract][Full Text] [Related]
16. Recombinant lecithin:cholesterol acyltransferase containing a Thr123-->Ile mutation esterifies cholesterol in low density lipoprotein but not in high density lipoprotein.
O K; Hill JS; Wang X; Pritchard PH
J Lipid Res; 1993 Jan; 34(1):81-8. PubMed ID: 8445345
[TBL] [Abstract][Full Text] [Related]
17. Complete and Partial Lecithin:Cholesterol Acyltransferase Deficiency Is Differentially Associated With Atherosclerosis.
Oldoni F; Baldassarre D; Castelnuovo S; Ossoli A; Amato M; van Capelleveen J; Hovingh GK; De Groot E; Bochem A; Simonelli S; Barbieri S; Veglia F; Franceschini G; Kuivenhoven JA; Holleboom AG; Calabresi L
Circulation; 2018 Sep; 138(10):1000-1007. PubMed ID: 29748187
[TBL] [Abstract][Full Text] [Related]
18. The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families.
Calabresi L; Pisciotta L; Costantin A; Frigerio I; Eberini I; Alessandrini P; Arca M; Bon GB; Boscutti G; Busnach G; Frascà G; Gesualdo L; Gigante M; Lupattelli G; Montali A; Pizzolitto S; Rabbone I; Rolleri M; Ruotolo G; Sampietro T; Sessa A; Vaudo G; Cantafora A; Veglia F; Calandra S; Bertolini S; Franceschini G
Arterioscler Thromb Vasc Biol; 2005 Sep; 25(9):1972-8. PubMed ID: 15994445
[TBL] [Abstract][Full Text] [Related]
19. Disruption of the murine lecithin:cholesterol acyltransferase gene causes impairment of adrenal lipid delivery and up-regulation of scavenger receptor class B type I.
Ng DS; Francone OL; Forte TM; Zhang J; Haghpassand M; Rubin EM
J Biol Chem; 1997 Jun; 272(25):15777-81. PubMed ID: 9188474
[TBL] [Abstract][Full Text] [Related]
20. In vitro effects of lecithin:cholesterol acyltransferase on apolipoprotein distribution in familial lecithin:cholesterol acyltransferase deficiency.
Glomset JA; Mitchell CD; King WC; Applegate KA; Forte T; Norum KR; Gjone E
Ann N Y Acad Sci; 1980; 348():224-43. PubMed ID: 6930928
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]