Page last updated: 2024-09-05

beta-methylcrotonylglycine and tiglyl-coenzyme a

beta-methylcrotonylglycine has been researched along with tiglyl-coenzyme a in 1 studies

Compound Research Comparison

Studies (beta-methylcrotonylglycine)	Trials (beta-methylcrotonylglycine)	Recent Studies (post-2010) (beta-methylcrotonylglycine)	Studies (tiglyl-coenzyme a)	Trials (tiglyl-coenzyme a)	Recent Studies (post-2010) (tiglyl-coenzyme a)
27	0	4	18	0	7

Research

Studies (1)

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	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baumgartner, MR; Burda, P; Bürer, C; Fowler, B; Grünert, SC; Morscher, RJ; Suormala, T	1

Other Studies

1 other study(ies) available for beta-methylcrotonylglycine and tiglyl-coenzyme a

Article	Year
A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency. Molecular genetics and metabolism, 2012, Volume: 105, Issue:4 Topics: Acyl Coenzyme A; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child; Child, Preschool; DNA Mutational Analysis; Female; Fibroblasts; Glycine; Heterozygote; Humans; Infant; Infant, Newborn; Male; Mutation; Neonatal Screening; Real-Time Polymerase Chain Reaction; Skin; Urea Cycle Disorders, Inborn	2012

Article

Year

A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency.

Molecular genetics and metabolism, 2012, Volume: 105, Issue:4

Topics: Acyl Coenzyme A; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child; Child, Preschool; DNA Mutational Analysis; Female; Fibroblasts; Glycine; Heterozygote; Humans; Infant; Infant, Newborn; Male; Mutation; Neonatal Screening; Real-Time Polymerase Chain Reaction; Skin; Urea Cycle Disorders, Inborn

2012