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kynurenine and Autosomal Dominant Cerebellar Ataxia, Type II

kynurenine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 1 studies

Kynurenine: A metabolite of the essential amino acid tryptophan metabolized via the tryptophan-kynurenine pathway.
kynurenine : A ketone that is alanine in which one of the methyl hydrogens is substituted by a 2-aminobenzoyl group.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ward, JM1
Stoyas, CA1
Switonski, PM1
Ichou, F1
Fan, W1
Collins, B1
Wall, CE1
Adanyeguh, I1
Niu, C1
Sopher, BL1
Kinoshita, C1
Morrison, RS1
Durr, A1
Muotri, AR1
Evans, RM1
Mochel, F1
La Spada, AR1

Other Studies

1 other study available for kynurenine and Autosomal Dominant Cerebellar Ataxia, Type II

ArticleYear
Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease.
    Cell reports, 2019, 01-29, Volume: 26, Issue:5

    Topics: Adipose Tissue; Animals; Ataxin-7; Blood Glucose; Energy Metabolism; Humans; Kynurenine; Metabolomic

2019