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Heart-Type Fatty Acid Binding Protein Binds Long-Chain Acylcarnitines and Protects against Lipotoxicity

International journal of molecular sciences, 2023-03, Vol.24 (6), p.5528

2023

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Quantitation and evaluation of perinatal medium-chain and long-chain acylcarnitine blood concentrations in 12,000 full-term breastfed newborns

Journal of Pediatric Endocrinology and Metabolism, 2021-08, Vol.34 (8), p.1023-1030

2021

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Characterization of plasma acylcarnitines in patients under valproate monotherapy using ESI-MS/MS

Clinical biochemistry, 2001-11, Vol.34 (8), p.635-638

2001

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Valproate Induces in Vitro Accumulation of Long-Chain Fatty Acylcarnitines

Molecular genetics and metabolism, 2001-08, Vol.73 (4), p.358-361

2001

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L-Carnitine treatment for congestive heart failure―experimental and clinical study

Japanese circulation journal, 1992, Vol.56 (1), p.86-94

1992

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Effects of L-carnitine on mechanical recovery of isolated rat hearts in relation to the perfusion with glucose and palmitate

Molecular and cellular biochemistry, 1998-08, Vol.185 (1-2), p.65-75

1998

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Release of ischemia in paced rat Langendorff hearts by supply of L-carnitine: role of endogenous long-chain acylcarnitine

Molecular and cellular biochemistry, 1996-03, Vol.156 (1), p.87-91

1996

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Tissue lipid accumulation by l-aminocarnitine, an inhibitor of carnitine-palmitoyltransferase-2. Studies in intact rats and isolated mitochondria

Biochimica et biophysica acta, 1992-07, Vol.1127 (1), p.81-86

1992

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Delineation of the influence of propionylcarnitine on the accumulation of long-chain acylcarnitines and electrophysiologic derangements evoked by hypoxia in canine myocardium

Cardiovascular drugs and therapy, 1991-02, Vol.5 Suppl 1 (1), p.67-76

1991

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MYOCARDIAL FREE CARNITINE AND FATTY ACYLCARNITINE LEVELS IN PATIENTS WITH CHRONIC HEART FAILURE

JAPANESE CIRCULATION JOURNAL, 1990/12/20, Vol.54(12), pp.1471-1476

1990

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Tutorial: Triheptanoin and Nutrition Management for Treatment of Long‐Chain Fatty Acid Oxidation Disorders

JPEN. Journal of parenteral and enteral nutrition, 2021-02, Vol.45 (2), p.230-238

2021

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Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient

Biochimica et biophysica acta, 2013-09, Vol.1831 (9), p.1467-1474

2013

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Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan

International journal of neonatal screening, 2024-02, Vol.10 (1), p.15

2024

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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation

Frontiers in pharmacology, 2021-01, Vol.11, p.616834

2021

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Diagnosis, Treatment, and Clinical Outcome of Patients with Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxy Acyl-CoA Dehydrogenase Deficiency

JIMD Reports, Volume 31, 2017-01, Vol.31, p.63-71

2017

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Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress

European journal of clinical investigation, 2004-03, Vol.34 (3), p.191-196

2004

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Evidence for Intermediate Channeling in Mitochondrial β-Oxidation (∗)

The Journal of biological chemistry, 1995-01, Vol.270 (2), p.530-535

1995

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Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia

The American journal of clinical nutrition, 1998-03, Vol.67 (3), p.386-390

1998

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Acylcarnitine formation and fatty acid oxidation in hepatocytes from rats treated with tetradecylthioacetic acid (a 3-thia fatty acid)

Biochimica et biophysica acta, 1993-04, Vol.1167 (2), p.189-196

1993

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Incomplete fatty acid oxidation by heart mitochondria: β-Hydroxy fatty acid production

Journal of molecular and cellular cardiology, 1982-08, Vol.14 (8), p.451-459

1982

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Heart-Type Fatty Acid Binding Protein Binds Long-Chain Acylcarnitines and Protects against Lipotoxicity

Quantitation and evaluation of perinatal medium-chain and long-chain acylcarnitine blood concentrations in 12,000 full-term breastfed newborns

Characterization of plasma acylcarnitines in patients under valproate monotherapy using ESI-MS/MS

Valproate Induces in Vitro Accumulation of Long-Chain Fatty Acylcarnitines

L-Carnitine treatment for congestive heart failure―experimental and clinical study

Effects of L-carnitine on mechanical recovery of isolated rat hearts in relation to the perfusion with glucose and palmitate

Release of ischemia in paced rat Langendorff hearts by supply of L-carnitine: role of endogenous long-chain acylcarnitine

Tissue lipid accumulation by l-aminocarnitine, an inhibitor of carnitine-palmitoyltransferase-2. Studies in intact rats and isolated mitochondria

Delineation of the influence of propionylcarnitine on the accumulation of long-chain acylcarnitines and electrophysiologic derangements evoked by hypoxia in canine myocardium

MYOCARDIAL FREE CARNITINE AND FATTY ACYLCARNITINE LEVELS IN PATIENTS WITH CHRONIC HEART FAILURE

Tutorial: Triheptanoin and Nutrition Management for Treatment of Long‐Chain Fatty Acid Oxidation Disorders

Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient

Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan

Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation

Diagnosis, Treatment, and Clinical Outcome of Patients with Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxy Acyl-CoA Dehydrogenase Deficiency

Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress

Evidence for Intermediate Channeling in Mitochondrial β-Oxidation (∗)

Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia

Acylcarnitine formation and fatty acid oxidation in hepatocytes from rats treated with tetradecylthioacetic acid (a 3-thia fatty acid)

Incomplete fatty acid oxidation by heart mitochondria: β-Hydroxy fatty acid production

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