| 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 |
|---|---|---|---|---|
| Larsen S et al. | Increased mitochondrial substrate sensitivity in skeletal muscle of patients with type 2 diabetes. | 2011 | Diabetologia | pmid:21424396 |
| Schönfeld P et al. | Mitochondrial fatty acid oxidation and oxidative stress: lack of reverse electron transfer-associated production of reactive oxygen species. | 2010 Jun-Jul | Biochim. Biophys. Acta | pmid:20085746 |
| Smith EH et al. | Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. | 2010 | Mol. Genet. Metab. | pmid:20434380 |
| Khalid JM et al. | Relationship of octanoylcarnitine concentrations to age at sampling in unaffected newborns screened for medium-chain acyl-CoA dehydrogenase deficiency. | 2010 | Clin. Chem. | pmid:20413428 |
| De Jesús VR et al. | Comparison of amino acids and acylcarnitines assay methods used in newborn screening assays by tandem mass spectrometry. | 2010 | Clin. Chim. Acta | pmid:20122909 |
| Arnold GL et al. | Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State. | 2010 | Mol. Genet. Metab. | pmid:20036593 |
| Kraunsøe R et al. | Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. | 2010 | J. Physiol. (Lond.) | pmid:20421291 |
| Tsuchida H et al. | Identification of a novel organic anion transporter mediating carnitine transport in mouse liver and kidney. | 2010 | Cell. Physiol. Biochem. | pmid:20332632 |
| Maier EM et al. | Dissection of biochemical borderline phenotypes in carriers and genetic variants of medium-chain acyl-CoA dehyrogenase deficiency: implications for newborn screening [corrected]. | 2009 | Clin. Genet. | pmid:19780764 |
| Hsu HW et al. | Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening. | 2008 | Pediatrics | pmid:18450854 |