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American Journal of Human Genetics|December 18, 1997
Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patientM Huizing, V Iacobazzi, L Ijlst, et al.
The Journal of Biological Chemistry|July 28, 2010
The Arabidopsis peroxisomal ABC transporter, comatose, complements the Saccharomyces cerevisiae pxa1 pxa2Delta mutant for metabolism of long-chain fatty acids and exhibits fatty acyl-CoA-stimulated ATPase activityYvonne Nyathi, Carine De Marcos Lousa, Carlo W van Roermund, et al.
The Prostate|December 16, 2004
Peroxisomal branched chain fatty acid beta-oxidation pathway is upregulated in prostate cancerShan Zha, Sacha Ferdinandusse, Jessica L Hicks, et al.
Journal of Medicinal Chemistry|February 18, 2005
Fully 2'-modified oligonucleotide duplexes with improved in vitro potency and stability compared to unmodified small interfering RNACharles R Allerson, Namir Sioufi, Russell Jarres, et al.
JAMA|August 24, 2006
Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiencyBianca T van Maldegem, Marinus Duran, Ronald J A Wanders, et al.
American Journal of Human Genetics|May 11, 2006
Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.
Biochemical and Biophysical Research Communications|August 27, 1999
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patientsN Shimozawa, Z Zhang, Y Suzuki, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 31, 2017
A novel case of ACOX2 deficiency leads to recognition of a third human peroxisomal acyl-CoA oxidaseSacha Ferdinandusse, Simone Denis, Carlo W T van Roermund, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
Molecular and Cellular Biology|June 8, 2001
Identification of a peroxisomal ATP carrier required for medium-chain fatty acid beta-oxidation and normal peroxisome proliferation in Saccharomyces cerevisiaeC W van Roermund, R Drissen, M van Den Berg, et al.
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