These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 9555865)

  • 1. 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 HE; Gylling H; Tenhunen J; Virtamo J; Jauhiainen M; Huttunen JK; Kantola I; Miettinen TA; Kontula K
    Arterioscler Thromb Vasc Biol; 1998 Apr; 18(4):591-8. PubMed ID: 9555865
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia.
    Tobar HE; Cataldo LR; González T; Rodríguez R; Serrano V; Arteaga A; Álvarez-Mercado A; Lagos CF; Vicuña L; Miranda JP; Pereira A; Bravo C; Aguilera CM; Eyheramendy S; Uauy R; Martínez Á; Gil Á; Francone O; Rigotti A; Santos JL
    Lipids Health Dis; 2019 Jun; 18(1):132. PubMed ID: 31164121
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency.
    Miettinen H; Gylling H; Ulmanen I; Miettinen TA; Kontula K
    Arterioscler Thromb Vasc Biol; 1995 Apr; 15(4):460-7. PubMed ID: 7749857
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes.
    Pisciotta L; Calabresi L; Lupattelli G; Siepi D; Mannarino MR; Moleri E; Bellocchio A; Cantafora A; Tarugi P; Calandra S; Bertolini S
    Atherosclerosis; 2005 Sep; 182(1):153-9. PubMed ID: 16115486
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia.
    Koizumi J; Mabuchi H; Yoshimura A; Michishita I; Takeda M; Itoh H; Sakai Y; Sakai T; Ueda K; Takeda R
    Atherosclerosis; 1985 Dec; 58(1-3):175-86. PubMed ID: 3937535
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Determinants of plasma HDL-cholesterol in hypertriglyceridemic patients. Role of cholesterol-ester transfer protein and lecithin cholesteryl acyl transferase.
    Tato F; Vega GL; Grundy SM
    Arterioscler Thromb Vasc Biol; 1997 Jan; 17(1):56-63. PubMed ID: 9012638
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cholesteryl ester transfer protein expressed in lecithin cholesterol acyltransferase-deficient mice.
    Wu CA; Tsujita M; Okumura-Noji K; Usui S; Kakuuchi H; Okazaki M; Yokoyama S
    Arterioscler Thromb Vasc Biol; 2002 Aug; 22(8):1347-53. PubMed ID: 12171799
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new molecular defect in the lecithin: cholesterol acyltransferase (LCAT) gene associated with fish eye disease.
    Contacos C; Sullivan DR; Rye KA; Funke H; Assmann G
    J Lipid Res; 1996 Jan; 37(1):35-44. PubMed ID: 8820100
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband.
    Argyropoulos G; Jenkins A; Klein RL; Lyons T; Wagenhorst B; St Armand J; Marcovina SM; Albers JJ; Pritchard PH; Garvey WT
    J Lipid Res; 1998 Sep; 39(9):1870-6. PubMed ID: 9741700
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Elevated plasma cholesteryl ester transfer in NIDDM: relationships with apolipoprotein B-containing lipoproteins and phospholipid transfer protein.
    Riemens S; van Tol A; Sluiter W; Dullaart R
    Atherosclerosis; 1998 Sep; 140(1):71-9. PubMed ID: 9733217
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic and environmental determinants of plasma high density lipoprotein cholesterol and apolipoprotein AI concentrations in healthy middle-aged men.
    Talmud PJ; Hawe E; Robertson K; Miller GJ; Miller NE; Humphries SE
    Ann Hum Genet; 2002 Mar; 66(Pt 2):111-24. PubMed ID: 12174215
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Inherited disorders of HDL metabolism and atherosclerosis.
    Hovingh GK; de Groot E; van der Steeg W; Boekholdt SM; Hutten BA; Kuivenhoven JA; Kastelein JJ
    Curr Opin Lipidol; 2005 Apr; 16(2):139-45. PubMed ID: 15767853
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lecithin:cholesterol acyltransferase overexpression generates hyperalpha-lipoproteinemia and a nonatherogenic lipoprotein pattern in transgenic rabbits.
    Hoeg JM; Vaisman BL; Demosky SJ; Meyn SM; Talley GD; Hoyt RF; Feldman S; Bérard AM; Sakai N; Wood D; Brousseau ME; Marcovina S; Brewer HB; Santamarina-Fojo S
    J Biol Chem; 1996 Feb; 271(8):4396-402. PubMed ID: 8626790
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Potential gene therapy for lecithin-cholesterol acyltransferase (LCAT)-deficient and hypoalphalipoproteinemic patients with adenovirus-mediated transfer of human LCAT gene.
    Séguret-Macé S; Latta-Mahieu M; Castro G; Luc G; Fruchart JC; Rubin E; Denèfle P; Duverger N
    Circulation; 1996 Nov; 94(9):2177-84. PubMed ID: 8901669
    [TBL] [Abstract][Full Text] [Related]  

  • 18. In vitro production of beta-very low density lipoproteins and small, dense low density lipoproteins in mildly hypertriglyceridemic plasma: role of activities of lecithin:cholester acyltransferase, cholesterylester transfer proteins and lipoprotein lipase.
    Chung BH; Segrest JP; Franklin F
    Atherosclerosis; 1998 Dec; 141(2):209-25. PubMed ID: 9862170
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of elevated lecithin: cholesterol acyltransferase and cholesteryl ester transfer protein activities in abnormal lipoproteins from proteinuric patients.
    Dullaart RP; Gansevoort RT; Dikkeschei BD; de Zeeuw D; de Jong PE; Van Tol A
    Kidney Int; 1993 Jul; 44(1):91-7. PubMed ID: 8355471
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mechanisms of hypo and hyper alphalipoproteinemia in Chilean adults].
    Cuevas A; Alvarez V; Acosta AM; Altayó M; Montero J; Rigotti A
    Rev Med Chil; 2004 Apr; 132(4):421-8. PubMed ID: 15382513
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.