crotonyl-coenzyme a has been researched along with tiglyl-coenzyme a in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Diez, TA; Nikolau, BJ; Wurtele, ES | 1 |
| Bedoyan, JK; Bennett, MJ; Bloom, K; Burlina, A; Chatfield, K; Coughlin, CR; Dishop, MK; Elpeleg, O; Ferdinandusse, S; Friederich, MW; Gallagher, RC; Gowan, K; Ruiter, JP; Van Hove, JL; Vaz, FM; Wanders, RJ; Waterham, HR | 1 |
| Aiba, K; Fukushi, D; Kitaura, Y; Kondo, Y; Murayama, K; Nakamura, Y; Nomura, N; Pitt, J; Shimomura, Y; Wakamatsu, N; Yamada, K; Yamaguchi, S; Yokochi, K | 1 |
3 other study(ies) available for crotonyl-coenzyme a and tiglyl-coenzyme a
| Article | Year |
|---|---|
Purification and characterization of 3-methylcrotonyl-coenzyme-A carboxylase from leaves of Zea mays.
Topics: Acyl Coenzyme A; Adenosine Triphosphate; Bicarbonates; Biotin; Carbon-Carbon Ligases; Cations, Divalent; Hydrogen-Ion Concentration; Kinetics; Ligases; Magnesium; Molecular Weight; Protein Conformation; Zea mays | 1994 |
Clinical and biochemical characterization of four patients with mutations in ECHS1.
Topics: Acyl Coenzyme A; Child; Enoyl-CoA Hydratase; Female; Heterozygote; Humans; Infant; Infant, Newborn; Leigh Disease; Male; Mutation | 2015 |
Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion.
Topics: Acetylcysteine; Acyl Coenzyme A; Child; Child, Preschool; Enoyl-CoA Hydratase; Female; Humans; Japan; Male; Metabolic Networks and Pathways; Metabolism, Inborn Errors; Mutation; Valine | 2015 |