Compounds > asparagine

asparagine and BCKD Deficiency

asparagine has been researched along with BCKD Deficiency in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chuang, DT; Cox, RP; Fisher, CR; Fisher, CW1
Crabb, DW; Edenberg, HJ; Goodwin, GW; Harris, RA; Kuntz, MJ; Zhang, B1

Other Studies

2 other study(ies) available for asparagine and BCKD Deficiency

ArticleYear
Occurrence of a Tyr393----Asn (Y393N) mutation in the E1 alpha gene of the branched-chain alpha-keto acid dehydrogenase complex in maple syrup urine disease patients from a Mennonite population.
    American journal of human genetics, 1991, Volume: 49, Issue:2

    Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Alleles; Asparagine; Base Sequence; Blotting, Southern; DNA; Ethnicity; Genes; Humans; Ketone Oxidoreductases; Maple Syrup Urine Disease; Molecular Sequence Data; Multienzyme Complexes; Mutation; Oligonucleotide Probes; Philadelphia; Polymerase Chain Reaction; Tyrosine

1991
cDNA cloning of the E1 alpha subunit of the branched-chain alpha-keto acid dehydrogenase and elucidation of a molecular basis for maple syrup urine disease.
    Annals of the New York Academy of Sciences, 1989, Volume: 573

    Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Alleles; Animals; Asparagine; Cloning, Molecular; DNA; Fibroblasts; Gene Library; Humans; Immunoblotting; Ketone Oxidoreductases; Liver; Maple Syrup Urine Disease; Multienzyme Complexes; Mutation; Rats; Tyrosine

1989