MeSH term | MeSH ID | Detail |
---|---|---|
Parkinsonian Disorders | D020734 | 20 associated lipids |
Dihydrolipoamide is a lipid of Fatty Acyls (FA) class. Dihydrolipoamide is associated with abnormalities such as Wiskott-Aldrich Syndrome. The involved functions are known as Citric Acid Cycle, Electron Transport, NADH oxidation, Oxidation and Oxidants. Dihydrolipoamide often locates in Mitochondria, Mitochondrial matrix and Chloroplasts. The associated genes with Dihydrolipoamide are Mutant Proteins, Recombinant Proteins, mycothione reductase, Genes, Mitochondrial and alanylproline.
To understand associated biological information of Dihydrolipoamide, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.
Dihydrolipoamide is suspected in and other diseases in descending order of the highest number of associated sentences.
Disease | Cross reference | Weighted score | Related literature |
---|
We collected disease MeSH terms mapped to the references associated with Dihydrolipoamide
MeSH term | MeSH ID | Detail |
---|---|---|
Parkinsonian Disorders | D020734 | 20 associated lipids |
There are no associated biomedical information in the current reference collection.
Associated locations are in red color. Not associated locations are in black.
Location | Cross reference | Weighted score | Related literatures |
---|
Function | Cross reference | Weighted score | Related literatures |
---|
There are no associated biomedical information in the current reference collection.
Gene | Cross reference | Weighted score | Related literatures |
---|
There are no associated biomedical information in the current reference collection.
Authors | Title | Published | Journal | PubMed Link |
---|---|---|---|---|
Trofimova L et al. | Behavioral impact of the regulation of the brain 2-oxoglutarate dehydrogenase complex by synthetic phosphonate analog of 2-oxoglutarate: implications into the role of the complex in neurodegenerative diseases. | 2010 | Int J Alzheimers Dis | pmid:21049004 |
Ninomiya M et al. | PBC: Animal Models of Cholangiopathies and Possible Endogenous Viral Infections. | 2012 | Int J Hepatol | pmid:22007316 |
Sasaki M and Nakanuma Y | Novel approach to bile duct damage in primary biliary cirrhosis: participation of cellular senescence and autophagy. | 2012 | Int J Hepatol | pmid:21994884 |
Golas A et al. | Sperm mitochondria diaphorase activity--a gene mapping study of recombinant inbred strains of mice. | 2010 | Int. J. Dev. Biol. | pmid:20209439 |
Jeffery CJ | Proteins with neomorphic moonlighting functions in disease. | 2011 | IUBMB Life | pmid:21698752 |
Barbieri E et al. | Morphofunctional and Biochemical Approaches for Studying Mitochondrial Changes during Myoblasts Differentiation. | 2011 | J Aging Res | pmid:21629710 |
Vernon SD and Reeves WC | Evaluation of autoantibodies to common and neuronal cell antigens in Chronic Fatigue Syndrome. | 2005 | J Autoimmune Dis | pmid:15916704 |
Packer L and Cadenas E | Lipoic acid: energy metabolism and redox regulation of transcription and cell signaling. | 2011 | J Clin Biochem Nutr | pmid:21297908 |
Jiang Y and Wang X | Comparative mitochondrial proteomics: perspective in human diseases. | 2012 | J Hematol Oncol | pmid:22424240 |
Moraes N et al. | NADPH-diaphorase activity and nitric oxide synthase isoforms in the trophoblast of Calomys callosus. | 2001 | J. Anat. | pmid:11327206 |