| MeSH term | MeSH ID | Detail |
|---|---|---|
| Starvation | D013217 | 47 associated lipids |
| Ventricular Dysfunction, Left | D018487 | 33 associated lipids |
| Heart Failure, Systolic | D054143 | 3 associated lipids |
Total
3
O-octanoylcarnitine
O-octanoylcarnitine is a lipid of Fatty Acyls (FA) class.
Cross Reference
There are no associated biomedical information in the current reference collection.
Current reference collection contains 212 references associated with O-octanoylcarnitine in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.
Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.
Here are additional resources we collected from PubChem and MeSH for O-octanoylcarnitine
Possible diseases from mapped MeSH terms on references
We collected disease MeSH terms mapped to the references associated with O-octanoylcarnitine
NCBI Entrez Crosslinks
All references with O-octanoylcarnitine
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Trumbeckaite S et al. | Different sensitivity of rabbit heart and skeletal muscle to endotoxin-induced impairment of mitochondrial function. | 2001 | Eur. J. Biochem. | pmid:11231295 |
| Mroczkowska JE et al. | Blood-brain barrier controls carnitine level in the brain: a study on a model system with RBE4 cells. | 2000 | Biochem. Biophys. Res. Commun. | pmid:10623637 |
| Clayton PT et al. | Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry. | 1998 | Arch. Dis. Child. | pmid:9797589 |
| Zangar RC and Novak RF | Effects of fatty acids and ketone bodies on cytochromes P450 2B, 4A, and 2E1 expression in primary cultured rat hepatocytes. | 1997 | Arch. Biochem. Biophys. | pmid:9016816 |
| Chace DH et al. | Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry. | 1997 | Clin. Chem. | pmid:9365395 |
| Ziadeh R et al. | Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies. | 1995 | Pediatr. Res. | pmid:7603790 |
| Van Hove JL et al. | Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood. | 1993 | Am. J. Hum. Genet. | pmid:8488845 |
| Minkler PE and Hoppel CL | Quantification of free carnitine, individual short- and medium-chain acylcarnitines, and total carnitine in plasma by high-performance liquid chromatography. | 1993 | Anal. Biochem. | pmid:8214594 |
| Schmidt-Sommerfeld E et al. | Urinary medium-chain acylcarnitines in medium-chain acyl-CoA dehydrogenase deficiency, medium-chain triglyceride feeding and valproic acid therapy: sensitivity and specificity of the radioisotopic exchange/high performance liquid chromatography method. | 1992 | Pediatr. Res. | pmid:1635814 |
| Farquharson J et al. | Direct gas chromatographic assay of urinary medium-chain fatty acylcarnitines by their thermal decomposition. | 1992 | Clin. Chim. Acta | pmid:1576748 |