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phosphorylethanolamine and Mitochondrial Diseases

phosphorylethanolamine has been researched along with Mitochondrial Diseases in 1 studies

phosphorylethanolamine: RN given refers to parent cpd; structure
O-phosphoethanolamine : The ethanolamine mono-ester of phosphoric acid, and a metabolite of phospholipid metabolism. This phosphomonoester shows strong structural similarity to the inhibitory neurotransmitter GABA, and is decreased in post-mortem Alzheimer's disease brain.

Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.

Research

Studies (1)

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

Authors

AuthorsStudies
Modica-Napolitano, JS1
Renshaw, PF1

Other Studies

1 other study available for phosphorylethanolamine and Mitochondrial Diseases

ArticleYear
Ethanolamine and phosphoethanolamine inhibit mitochondrial function in vitro: implications for mitochondrial dysfunction hypothesis in depression and bipolar disorder.
    Biological psychiatry, 2004, Feb-01, Volume: 55, Issue:3

    Topics: Animals; Bipolar Disorder; Choline; Depressive Disorder; Dose-Response Relationship, Drug; Ethanolam

2004