cystine and alpha-LCAT Deficiency

cystine has been researched along with alpha-LCAT Deficiency in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hill, JS; O, K; Pritchard, PH; Wang, X1
BĂ©rard, AM; Brewer, B; Clerc, M; Santamarina-Fojo, S1

Other Studies

2 other study(ies) available for cystine and alpha-LCAT Deficiency

ArticleYear
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
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