cystine has been researched along with alpha-LCAT Deficiency in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hill, JS; O, K; Pritchard, PH; Wang, X | 1 |
BĂ©rard, AM; Brewer, B; Clerc, M; Santamarina-Fojo, S | 1 |
2 other study(ies) available for cystine and alpha-LCAT Deficiency
Article | Year |
---|---|
Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.
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.
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 |