tyrosine has been researched along with Lecithin Cholesterol Acyltransferase 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 | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Defesche, JC; Hollak, CE; Holleboom, AG; Hovingh, GK; Kastelein, JJ; Kuivenhoven, JA; Levels, JH; Peter, J; Schimmel, AW; Stroes, ES; Valentijn, RM; van Olden, CC; Vos, P | 1 |
| Chapman, MJ; Chevet, D; Dachet, C; Dolphin, PJ; Goulinet, S; Guerin, M; Rouis, M | 1 |
2 other study(ies) available for tyrosine and Lecithin Cholesterol Acyltransferase Deficiency
| Article | Year |
|---|---|
Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase.
Topics: Adolescent; Anemia, Hemolytic; Angiotensin-Converting Enzyme Inhibitors; Animals; Child; Child, Preschool; Chlorocebus aethiops; Cholesterol, HDL; Corneal Opacity; COS Cells; Cysteine; Disulfides; Diuretics; Female; Genetic Predisposition to Disease; Homozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Male; Mutation; Phosphatidylcholine-Sterol O-Acyltransferase; Proteinuria; Transfection; Treatment Outcome; Tyrosine | 2011 |
Familial lecithin:cholesterol acyltransferase deficiency: molecular analysis of a compound heterozygote: LCAT (Arg147 --> Trp) and LCAT (Tyr171 --> Stop).
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 |