| 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 |
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| Zammit VA | The effect of glucagon treatment and starvation of virgin and lactating rats on the rates of oxidation of octanoyl-L-carnitine and octanoate by isolated liver mitochondria. | 1980 | Biochem. J. | pmid:7470052 |
| Jones CT | Is there a gloxylate cycle in the liver of the fetal guinea pig? | 1980 | Biochem. Biophys. Res. Commun. | pmid:7417292 |
| Parameswaran M and Arinze IJ | Phosphoenolpyruvate synthesis by fetal guinea-pig liver mitochondria. | 1981 | Biochim. Biophys. Acta | pmid:7225415 |
| Davis-van Thienen W and Davis EJ | The effects of energetic steady state, pyruvate concentration, and octanoyl-(--)-carnitine on the relative rates of carboxylation and decarboxylation of pyruvate by rat liver mitochondria. | 1981 | J. Biol. Chem. | pmid:7263658 |
| Nakatani T et al. | Effects of (+)-octanoylcarnitine on deoxyribonucleic acid synthesis in regenerating rabbit liver. | 1982 | Clin. Sci. | pmid:7060336 |
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| Roe CR et al. | Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death. | 1987 | Lancet | pmid:2881073 |
| Brass EP | Metabolism of octanoyl- and palmitoylcarnitine by intact rat hepatocytes. | 1989 | Biochim. Biophys. Acta | pmid:2730893 |
| Millington DS and Roe CR | Medium-chain acyl-CoA dehydrogenase deficiency. | 1989 | N. Engl. J. Med. | pmid:2710197 |
| Squire RS | Synthesis and purification of radioactive fatty acylcarnitines of high specific activity. | 1991 | Anal. Biochem. | pmid:1952050 |
| Bhuiyan AK and Pande SV | One-step facile synthesis of radioactive acyl-CoA and acylcarnitines using rat liver outer mitochondrial membrane as the enzyme source. | 1991 | Biochem. Soc. Trans. | pmid:1889559 |
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| 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 |
| 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 |
| Clayton PT et al. | Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry. | 1998 | Arch. Dis. Child. | pmid:9797589 |
| 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 |
| Pourfarzam M et al. | Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency. | 2001 | Lancet | pmid:11589939 |
| Carpenter K et al. | Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies. | 2001 | Arch. Dis. Child. Fetal Neonatal Ed. | pmid:11517203 |
| Chace DH et al. | Errors caused by the use of D,L-octanoylcarnitine for blood-spot calibrators. | 2001 | Clin. Chem. | pmid:11274033 |
| 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 |
| Toleikis A et al. | Relevance of fatty acid oxidation in regulation of the outer mitochondrial membrane permeability for ADP. | 2001 | FEBS Lett. | pmid:11741597 |
| Lehotay DC et al. | Blood acylcarnitine levels in normal newborns and heterozygotes for medium-chain acyl-CoA dehydrogenase deficiency: a relationship between genotype and biochemical phenotype? | 2004 | J. Inherit. Metab. Dis. | pmid:14970748 |
| Jogl G et al. | Crystal structure of mouse carnitine octanoyltransferase and molecular determinants of substrate selectivity. | 2005 | J. Biol. Chem. | pmid:15492013 |
| Ensenauer R et al. | Genotypic differences of MCAD deficiency in the Asian population: novel genotype and clinical symptoms preceding newborn screening notification. | 2005 May-Jun | Genet. Med. | pmid:15915086 |
| de Assis DR et al. | Na+, K+ ATPase activity is markedly reduced by cis-4-decenoic acid in synaptic plasma membranes from cerebral cortex of rats. | 2006 | Exp. Neurol. | pmid:16203000 |
| Baumgartner C and Baumgartner D | Biomarker discovery, disease classification, and similarity query processing on high-throughput MS/MS data of inborn errors of metabolism. | 2006 | J Biomol Screen | pmid:16314408 |
| Rhead WJ | Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspective. | 2006 Apr-Jun | J. Inherit. Metab. Dis. | pmid:16763904 |
| Hsu HW et al. | Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening. | 2008 | Pediatrics | pmid:18450854 |
| 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 |
| 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 |
| 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 |
| 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 |