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Hydroxylated long-chain acylcarnitines are biomarkers of mitochondrial myopathy

https://doi.org/10.1210/jc.2019-00721

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1 of the 43 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.2337/db13-0264 (notice 2021-07-08).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Muscle Phenotype and Mutation Load in 51 Persons With the 3243A>G Mitochondrial DNA Mutation

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Fat Metabolism During Exercise in Patients With Mitochondrial Disease

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PRENATAL DIAGNOSIS OF MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS

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Exercise fuel mobilization in mitochondrial myopathy: A metabolic dilemma

inferredcites →https://doi.org/10.1002/mus.21541openalex-snapshot

Limited diagnostic value of enzyme analysis in patients with mitochondrial tRNA mutations

inferredcites →https://doi.org/10.1007/8904_2015_459openalex-snapshot

Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation

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Carnitine and Acylcarnitines

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Mitochondrial DNA Medicine

inferredcites →https://doi.org/10.1007/s11010-014-2106-3openalex-snapshot

Long-chain acylcarnitine content determines the pattern of energy metabolism in cardiac mitochondria

inferredcites →https://doi.org/10.1016/0003-9861(68)90450-5openalex-snapshot

The effect of carnitine, fatty acyl carnitine, and fatty acyl coenzyme A on mitochondrial contraction

inferredcites →https://doi.org/10.1016/j.bbalip.2014.04.001openalex-snapshot

Plasma acylcarnitines inadequately reflect tissue acylcarnitine metabolism

inferredcites →https://doi.org/10.1016/j.cmet.2007.10.013openalex-snapshot

Mitochondrial Overload and Incomplete Fatty Acid Oxidation Contribute to Skeletal Muscle Insulin Resistance

inferredcites →https://doi.org/10.1016/j.ejpn.2014.10.006openalex-snapshot

A mitochondrial tRNAMet mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood

inferredcites →https://doi.org/10.1016/j.mam.2011.10.008openalex-snapshot

The mitochondrial carnitine/acylcarnitine carrier: Function, structure and physiopathology

inferredcites →https://doi.org/10.1023/a:1005673828469openalex-snapshot

Acylcarnitines in plasma and blood spots of patients with long‐chain 3‐hydroxyacyl‐coenzyme A dehydrogenase defiency

inferredcites →https://doi.org/10.1038/s41431-018-0286-0openalex-snapshot

Mitochondrial complex IV deficiency caused by a novel frameshift variant in MT-CO2 associated with myopathy and perturbed acylcarnitine profile

inferredcites →https://doi.org/10.1038/tp.2012.143openalex-snapshot

Unique acyl-carnitine profiles are potential biomarkers for acquired mitochondrial disease in autism spectrum disorder

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The effect of respiratory chain impairment of β-oxidation in rat heart mitochondria

inferredcites →https://doi.org/10.1053/meta.2002.30521openalex-snapshot

Acylcarnitine profiles in fibroblasts from patients with respiratory chain defects can resemble those from patients with mitochondrial fatty acid [beta ]-oxidation disorders

inferredcites →https://doi.org/10.1056/nejmoa020350openalex-snapshot

Paternal Inheritance of Mitochondrial DNA

inferredcites →https://doi.org/10.1056/nejmoa025225openalex-snapshot

Screening Newborns for Inborn Errors of Metabolism by Tandem Mass Spectrometry

inferredcites →https://doi.org/10.1093/brain/awg028openalex-snapshot

The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients

inferredcites →https://doi.org/10.1093/clinchem/43.11.2106openalex-snapshot

Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry

inferredcites →https://doi.org/10.1093/nar/gnf067openalex-snapshot

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR

inferredcites →https://doi.org/10.1096/fj.14-255901openalex-snapshot

Acylcarnitines: potential implications for skeletal muscle insulin resistance

inferredcites →https://doi.org/10.1097/gim.0b013e3181614289openalex-snapshot

Acylcarnitine profile analysis

inferredcites →https://doi.org/10.1113/jphysiol.2008.166033openalex-snapshot

Examination of ‘lipotoxicity’ in skeletal muscle of high‐fat fed and ob / ob mice

inferredcites →https://doi.org/10.1136/jmedgenet-2014-102914openalex-snapshot

Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature

inferredcites →https://doi.org/10.1172/jci114409openalex-snapshot

Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.

inferredcites →https://doi.org/10.1186/s12891-017-1781-0openalex-snapshot

Pure exercise intolerance and ophthalmoplegia associated with the m.12,294G > A mutation in the MT-TL2 gene: a case report

inferredcites →https://doi.org/10.1196/annals.1320.003openalex-snapshot

Kinetics, Pharmacokinetics, and Regulation of l‐Carnitine and Acetyl‐l‐carnitine Metabolism

inferredcites →https://doi.org/10.1203/00006450-199910000-00013openalex-snapshot

Dynamic Changes of Plasma Acylcarnitine Levels Induced by Fasting and Sunflower Oil Challenge Test in Children

inferredcites →https://doi.org/10.1210/jc.2014-1831openalex-snapshot

Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy

inferredcites →https://doi.org/10.1210/jc.2019-00721openalex-snapshot

Hydroxylated long-chain acylcarnitines are biomarkers of mitochondrial myopathy

inferredcites →https://doi.org/10.1212/wnl.0b013e3182929fb2openalex-snapshot

Recurrent myoglobinuria and deranged acylcarnitines due to a mutation in the mtDNA MT-CO2 gene

inferredcites →https://doi.org/10.1212/wnl.50.6.1875openalex-snapshot

A new mitochondrial tRNA Met gene mutation in a patient with dystrophic muscle and exercise intolerance

inferredcites →https://doi.org/10.1371/journal.pone.0200817openalex-snapshot

Prolonged fasting-induced metabolic signatures in human skeletal muscle of lean and obese men

inferredcites →https://doi.org/10.1385/0-89603-518-2:233openalex-snapshot

Quantitative Analysis of Human DNA Sequences by PCR and Solid-Phase Minisequencing

inferredcites →https://doi.org/10.1385/mb:15:2:123openalex-snapshot

Quantitative Analysis of Human DNA Sequences by PCR and Solid-Phase Minisequencing

inferredcites →https://doi.org/10.2174/138955751505150408142032openalex-snapshot

Mitochondrial Carnitine/Acylcarnitine Translocase: Insights in Structure/ Function Relationships. Basis for Drug Therapy and Side Effects Prediction

inferredcites →https://doi.org/10.2337/db12-0466openalex-snapshot

Acylcarnitines

inferredcites →https://doi.org/10.2337/db13-0264openalex-snapshot

Mitochondrial Substrate Availability and Its Role in Lipid-Induced Insulin Resistance and Proinflammatory Signaling in Skeletal Muscle

inferredcites →https://doi.org/10.3945/jn.108.103754openalex-snapshot

Plasma Acylcarnitine Profiles Suggest Incomplete Long-Chain Fatty Acid β-Oxidation and Altered Tricarboxylic Acid Cycle Activity in Type 2 Diabetic African-American Women

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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