cysteine 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 | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aponte, A; Calabresi, L; Demosky, SJ; Freeman, LA; Gordon, SM; Gucek, M; Jadhav, A; Koby, RF; Konaklieva, M; Kuskovsky, R; Levine, RL; Manthei, KA; Ossoli, AF; Remaley, AT; Shamburek, RD; Shen, M; Tesmer, JJG; Vaisman, BL | 1 |
| 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 |
2 other study(ies) available for cysteine and Lecithin Cholesterol Acyltransferase Deficiency
| Article | Year |
|---|---|
Lecithin:Cholesterol Acyltransferase Activation by Sulfhydryl-Reactive Small Molecules: Role of Cysteine-31.
Topics: Cysteine; Dose-Response Relationship, Drug; Enzyme Activation; Enzyme Activators; HEK293 Cells; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Models, Molecular; Phosphatidylcholine-Sterol O-Acyltransferase; Sulfhydryl Compounds | 2017 |
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 |