BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 3989388)

  • 1. Familial lecithin:cholesterol acyltransferase deficiency. Biochemistry of the cornea.
    Winder AF; Garner A; Sheraidah GA; Barry P
    J Lipid Res; 1985 Mar; 26(3):283-7. PubMed ID: 3989388
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature].
    Weidle EG; Lisch W
    Klin Monbl Augenheilkd; 1987 Mar; 190(3):182-7. PubMed ID: 3586537
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Histopathology of corneal changes in lecithin-cholesterol acyltransferase deficiency.
    Viestenz A; Schlötzer-Schrehardt U; Hofmann-Rummelt C; Seitz B; Küchle M
    Cornea; 2002 Nov; 21(8):834-7. PubMed ID: 12410048
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144.
    Teh EM; Chisholm JW; Dolphin PJ; Pouliquen Y; Savoldelli M; de Gennes JL; Benlian P
    Atherosclerosis; 1999 Sep; 146(1):141-51. PubMed ID: 10487497
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evidence for deficiency of high density lipoprotein lecithin: cholesterol acyltransferase activity (alpha-LCAT) in fish eye disease.
    Carlson LA; Holmquist L
    Acta Med Scand; 1985; 218(2):189-96. PubMed ID: 4061122
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Corneal opacification and lecithin-cholesterol acyltransferase (LCAT) deficiency: a case report.
    Hesterberg RC; Tredici TJ
    Ann Ophthalmol; 1984 Jul; 16(7):616-21. PubMed ID: 6476690
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Corneal opacity in LCAT disease.
    Cogan DG; Kruth HS; Datilis MB; Martin N
    Cornea; 1992 Nov; 11(6):595-9. PubMed ID: 1468226
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular basis of fish-eye disease in a patient from Spain. Characterization of a novel mutation in the LCAT gene and lipid analysis of the cornea.
    Blanco-Vaca F; Qu SJ; Fiol C; Fan HZ; Pao Q; Marzal-Casacuberta A; Albers JJ; Hurtado I; Gracia V; Pintó X; Martí T; Pownall HJ
    Arterioscler Thromb Vasc Biol; 1997 Jul; 17(7):1382-91. PubMed ID: 9261271
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Renal failure in familial lecithin: cholesterol acyltransferase deficiency.
    Borysiewicz LK; Soutar AK; Evans DJ; Thompson GR; Rees AJ
    Q J Med; 1982; 51(204):411-26. PubMed ID: 7156322
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lecithin:cholesterol acyltransferase deficiency.
    Bellan L; Mikelberg F; Frohlich J
    Can J Ophthalmol; 1988 Oct; 23(6):285-7. PubMed ID: 3203243
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Ocular manifestation in LCAT deficiency--a clinicopathological correlation].
    Viestenz A; Seitz B
    Klin Monbl Augenheilkd; 2003 Jul; 220(7):499-502. PubMed ID: 12886512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met).
    Klein HG; Lohse P; Pritchard PH; Bojanovski D; Schmidt H; Brewer HB
    J Clin Invest; 1992 Feb; 89(2):499-506. PubMed ID: 1737840
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial lecithin: cholesterol acyltransferase (LCAT) deficiency. An updated review Spring 1988.
    Gjone E
    Ophthalmic Paediatr Genet; 1988 Nov; 9(3):167-9. PubMed ID: 3068599
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A first British case of fish-eye disease presenting at age 75 years: a double heterozygote for defined and new mutations affecting LCAT structure and expression.
    Winder AF; Owen JS; Pritchard PH; Lloyd-Jones D; Vallance DT; White P; Wray R
    J Clin Pathol; 1999 Mar; 52(3):228-30. PubMed ID: 10450185
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial LCAT deficiency and fish-eye disease.
    McIntyre N
    J Inherit Metab Dis; 1988; 11 Suppl 1():45-56. PubMed ID: 3141686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lipoprotein abnormalities associated with lipopolysaccharide-induced lecithin: cholesterol acyltransferase and lipase deficiency.
    Auerbach BJ; Parks JS
    J Biol Chem; 1989 Jun; 264(17):10264-70. PubMed ID: 2722868
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alpha-lecithin:cholesterol acyltransferase deficiency. Lack of both phospholipase A2 and acyltransferase activities characteristic of high density lipoprotein lecithin:cholesterol acyltransferase in fish eye disease.
    Holmquist L; Carlson LA
    Acta Med Scand; 1987; 222(1):23-6. PubMed ID: 3630775
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impaired intermediate-density lipoprotein triglyceride hydrolysis in familial lecithin:cholesterol acyltransferase (LCAT) deficiency.
    Murano S; Shirai K; Saito Y; Yoshida S; Ohta Y; Tsuchida H; Yamamoto S; Asano G; Chen CH; Albers JJ
    Scand J Clin Lab Invest; 1987 Dec; 47(8):775-83. PubMed ID: 3432999
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial LCAT deficiency].
    Idzior-Waluś B
    Przegl Lek; 2001; 58(10):919-23. PubMed ID: 11957819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.