Lipoamide is a lipid of Fatty Acyls (FA) class. Lipoamide is associated with abnormalities such as Wiskott-Aldrich Syndrome. The involved functions are known as Phosphorylation, Protonation, Mutagenesis, Site-Directed, Oxidants and Acetylation. Lipoamide often locates in Mitochondria, Mitochondrial matrix, nucleocapsid location and Chloroplasts. The associated genes with lipoamide are Mutant Proteins, Recombinant Proteins, mycothione reductase, alanylproline and Genes, Mitochondrial.
To understand associated biological information of lipoamide, 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.
lipoamide 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 lipoamide
| MeSH term | MeSH ID | Detail |
|---|---|---|
| Hyperglycinemia, Nonketotic | D020158 | 2 associated lipids |
| Liver Cirrhosis, Biliary | D008105 | 12 associated lipids |
| Nerve Degeneration | D009410 | 53 associated lipids |
| Prostatic Neoplasms | D011471 | 126 associated lipids |
| Body Weight | D001835 | 333 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 |
|---|---|---|---|---|
| Chen Z et al. | Myocardial overexpression of Mecr, a gene of mitochondrial FAS II leads to cardiac dysfunction in mouse. | 2009 | PLoS ONE | pmid:19440339 |
| Günther S et al. | Knockout studies reveal an important role of Plasmodium lipoic acid protein ligase A1 for asexual blood stage parasite survival. | 2009 | PLoS ONE | pmid:19434237 |
| Fang F and Liu GT | Protective effects of compound FLZ, a novel synthetic analogue of squamosamide, on beta-amyloid-induced rat brain mitochondrial dysfunction in vitro. | 2009 | Acta Pharmacol. Sin. | pmid:19417731 |
| Chelh I et al. | Molecular profiles of Quadriceps muscle in myostatin-null mice reveal PI3K and apoptotic pathways as myostatin targets. | 2009 | BMC Genomics | pmid:19397818 |
| Ludlam A et al. | Chaperones of F1-ATPase. | 2009 | J. Biol. Chem. | pmid:19383603 |
| Shcherbo D et al. | Practical and reliable FRET/FLIM pair of fluorescent proteins. | 2009 | BMC Biotechnol. | pmid:19321010 |
| Chi F et al. | Identification of IbeR as a stationary-phase regulator in meningitic Escherichia coli K1 that carries a loss-of-function mutation in rpoS. | 2009 | J. Biomed. Biotechnol. | pmid:19300523 |
| Skvorak KJ et al. | Hepatocyte transplantation improves phenotype and extends survival in a murine model of intermediate maple syrup urine disease. | 2009 | Mol. Ther. | pmid:19436271 |
| Lu G et al. | Protein phosphatase 2Cm is a critical regulator of branched-chain amino acid catabolism in mice and cultured cells. | 2009 | J. Clin. Invest. | pmid:19411760 |
| Fujimura Y et al. | Modified method for purifying rat liver branched-chain alpha-ketoacid dehydrogenase complex. | 2009 | Biosci. Biotechnol. Biochem. | pmid:19270407 |