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Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact

Nature communications, 2018-05, Vol.9 (1), p.1761-13, Article 1761

2018

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Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

Reviews in endocrine & metabolic disorders, 2018-03, Vol.19 (1), p.93-106

2018

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The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives

Orphanet journal of rare diseases, 2012-10, Vol.7 (1), p.83-83

2012

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N-lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids

Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (21), p.6601-6606

2015

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A role for the human peroxisomal half-transporter ABCD3 in the oxidation of dicarboxylic acids

Biochimica et biophysica acta, 2014-04, Vol.1841 (4), p.563-568

2014

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The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters

The FASEB journal, 2008-12, Vol.22 (12), p.4201-4208

2008

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Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae

The Journal of biological chemistry, 2012-06, Vol.287 (24), p.20144-20153

2012

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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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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates

International journal of molecular sciences, 2020-04, Vol.21 (7), p.2589

2020

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enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results

Journal of inherited metabolic disease, 2010-10, Vol.33 (5), p.479-494

2010

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Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III

Molecular genetics and metabolism, 2012-12, Vol.107 (4), p.705-710

2012

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Carnitine palmitoyltransferase 2 and carnitine/acylcarnitine translocase are involved in the mitochondrial synthesis and export of acylcarnitines

The FASEB journal, 2013-05, Vol.27 (5), p.2039-2044

2013

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Peroxisomal Metabolite and Cofactor Transport in Humans

Frontiers in cell and developmental biology, 2021-01, Vol.8, p.613892-613892

2021

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New insights on the mechanisms of valproate-induced hyperammonemia: Inhibition of hepatic N -acetylglutamate synthase activity by valproyl-CoA

Journal of hepatology, 2011-08, Vol.55 (2), p.426-434

2011

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Mutagenesis separates ATPase and thioesterase activities of the peroxisomal ABC transporter, Comatose

Scientific reports, 2019-07, Vol.9 (1), p.10502-13, Article 10502

2019

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Peroxisomal NAD(H) Homeostasis in the Yeast Debaryomyces hansenii Depends on Two Redox Shuttles and the NAD + Carrier, Pmp47

Biomolecules (Basel, Switzerland), 2023-08, Vol.13 (9), p.1294

2023

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Metabolite transport across the peroxisomal membrane

Biochemical journal, 2007-01, Vol.401 (2), p.365-375

2007

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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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Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis

Biochemical pharmacology, 2010-03, Vol.79 (5), p.792-799

2010

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Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD Transporters

Frontiers in cell and developmental biology, 2022-01, Vol.9, p.788921-788921

2022

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An UPLC-MS/MS Assay to Measure Glutathione as Marker for Oxidative Stress in Cultured Cells

Metabolites, 2019-03, Vol.9 (3), p.45

2019

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Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency

Human mutation, 2007-09, Vol.28 (9), p.904-912

2007

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An algorithm to predict phenotypic severity in mucopolysaccharidosis type I in the first month of life

Orphanet journal of rare diseases, 2013-07, Vol.8 (1), p.99-99, Article 99

2013

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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients

Pediatrics (Evanston), 2002-01, Vol.109 (1), p.99-104

2002

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Subcellular localization and physiological role of alpha-methylacyl-CoA racemase

Journal of lipid research, 2000-11, Vol.41 (11), p.1890-1896

2000

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Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives

N-lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids

A role for the human peroxisomal half-transporter ABCD3 in the oxidation of dicarboxylic acids

The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters

Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae

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

Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates

enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results

Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III

Carnitine palmitoyltransferase 2 and carnitine/acylcarnitine translocase are involved in the mitochondrial synthesis and export of acylcarnitines

Peroxisomal Metabolite and Cofactor Transport in Humans

New insights on the mechanisms of valproate-induced hyperammonemia: Inhibition of hepatic N -acetylglutamate synthase activity by valproyl-CoA

Mutagenesis separates ATPase and thioesterase activities of the peroxisomal ABC transporter, Comatose

Peroxisomal NAD(H) Homeostasis in the Yeast Debaryomyces hansenii Depends on Two Redox Shuttles and the NAD + Carrier, Pmp47

Metabolite transport across the peroxisomal membrane

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

Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis

Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD Transporters

An UPLC-MS/MS Assay to Measure Glutathione as Marker for Oxidative Stress in Cultured Cells

Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency

An algorithm to predict phenotypic severity in mucopolysaccharidosis type I in the first month of life

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients

Subcellular localization and physiological role of alpha-methylacyl-CoA racemase

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