(+/-)-OCTANOYLCARNITINE CHLORIDE
| Title | Journal |
|---|---|
| Disruption of redox homeostasis in cerebral cortex of developing rats by acylcarnitines accumulating in medium-chain acyl-CoA dehydrogenase deficiency. | International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 20120801 |
| Increased mitochondrial substrate sensitivity in skeletal muscle of patients with type 2 diabetes. | Diabetologia 20110601 |
| Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. | Molecular genetics and metabolism 20100701 |
| Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. | The Journal of physiology 20100615 |
| Relationship of octanoylcarnitine concentrations to age at sampling in unaffected newborns screened for medium-chain acyl-CoA dehydrogenase deficiency. | Clinical chemistry 20100601 |
| Comparison of amino acids and acylcarnitines assay methods used in newborn screening assays by tandem mass spectrometry. | Clinica chimica acta; international journal of clinical chemistry 20100502 |
| Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State. | Molecular genetics and metabolism 20100301 |
| Mitochondrial fatty acid oxidation and oxidative stress: lack of reverse electron transfer-associated production of reactive oxygen species. | Biochimica et biophysica acta 20100101 |
| Dissection of biochemical borderline phenotypes in carriers and genetic variants of medium-chain acyl-CoA dehyrogenase deficiency: implications for newborn screening [corrected]. | Clinical genetics 20090801 |
| Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening. | Pediatrics 20080501 |
| Biomarker discovery, disease classification, and similarity query processing on high-throughput MS/MS data of inborn errors of metabolism. | Journal of biomolecular screening 20060201 |
| Na+, K+ ATPase activity is markedly reduced by cis-4-decenoic acid in synaptic plasma membranes from cerebral cortex of rats. | Experimental neurology 20060101 |
| Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspective. | Journal of inherited metabolic disease 20060101 |
| Crystal structure of mouse carnitine octanoyltransferase and molecular determinants of substrate selectivity. | The Journal of biological chemistry 20050107 |
| Genotypic differences of MCAD deficiency in the Asian population: novel genotype and clinical symptoms preceding newborn screening notification. | Genetics in medicine : official journal of the American College of Medical Genetics 20050101 |
| Blood acylcarnitine levels in normal newborns and heterozygotes for medium-chain acyl-CoA dehydrogenase deficiency: a relationship between genotype and biochemical phenotype? | Journal of inherited metabolic disease 20040101 |
| Molecular identification of a novel carnitine transporter specific to human testis. Insights into the mechanism of carnitine recognition. | The Journal of biological chemistry 20020927 |
| Relevance of fatty acid oxidation in regulation of the outer mitochondrial membrane permeability for ADP. | FEBS letters 20011207 |
| Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency. | Lancet (London, England) 20010929 |
| Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies. | Archives of disease in childhood. Fetal and neonatal edition 20010901 |
| A polymeric microfluidic chip for CE/MS determination of small molecules. | Analytical chemistry 20010501 |
| Errors caused by the use of D,L-octanoylcarnitine for blood-spot calibrators. | Clinical chemistry 20010401 |
| Different sensitivity of rabbit heart and skeletal muscle to endotoxin-induced impairment of mitochondrial function. | European journal of biochemistry 20010301 |