Compounds > arginine

arginine and alpha-LCAT Deficiency

arginine has been researched along with alpha-LCAT Deficiency in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (75.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Assmann, G; Collins, D; Cullen, P; Funke, H; Owen, JS; Sharp, PS; Wiebusch, H1
Hill, JS; O, K; Pritchard, PH; Wang, X1
Chapman, MJ; Chevet, D; Dachet, C; Dolphin, PJ; Goulinet, S; Guerin, M; Rouis, M1
Bérard, AM; Brewer, B; Clerc, M; Santamarina-Fojo, S1

Other Studies

4 other study(ies) available for arginine and alpha-LCAT Deficiency

ArticleYear
Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene.
    Human molecular genetics, 1995, Volume: 4, Issue:1

    Topics: Adolescent; Aged; Amino Acid Sequence; Arginine; Base Sequence; Female; Glycine; Heterozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Middle Aged; Molecular Sequence Data; Mutagenesis, Insertional; Mutation; Oligodeoxyribonucleotides; Phosphatidylcholine-Sterol O-Acyltransferase

1995
Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.
    Biochimica et biophysica acta, 1993, Jun-19, Volume: 1181, Issue:3

    Topics: Alanine; Amino Acid Sequence; Arginine; Base Sequence; Cystine; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins; Molecular Sequence Data; Mutation; Phosphatidylcholine-Sterol O-Acyltransferase; Polymorphism, Genetic; Threonine

1993
Familial lecithin:cholesterol acyltransferase deficiency: molecular analysis of a compound heterozygote: LCAT (Arg147 --> Trp) and LCAT (Tyr171 --> Stop).
    Atherosclerosis, 1997, Volume: 131, Issue:1

    Topics: Apolipoprotein A-I; Arginine; Cholesterol; Cholesterol Esters; Cholesterol, HDL; DNA; Female; Heterozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Middle Aged; Pedigree; Phosphatidylcholine-Sterol O-Acyltransferase; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Sequence Analysis, DNA; Tyrosine

1997
A normal rate of cellular cholesterol removal can be mediated by plasma from a patient with familial lecithin-cholesterol acyltransferase (LCAT) deficiency.
    Clinica chimica acta; international journal of clinical chemistry, 2001, Volume: 314, Issue:1-2

    Topics: Adult; Apolipoproteins; Arginine; Cells, Cultured; Cholesterol; Cystine; DNA, Complementary; Fibroblasts; Humans; Kinetics; Lecithin Cholesterol Acyltransferase Deficiency; Lipids; Lipoproteins; Male; Phenotype; Point Mutation; Reverse Transcriptase Polymerase Chain Reaction

2001