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Updated: Aug 13, 2026

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Measurement of Fatty Acid β-Oxidation in a Suspension of Freshly Isolated Mouse Hepatocytes
Published on: September 9, 2021
Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfall
R J Soorani-Lunsing1, F J van Spronsen, I Stolte-Dijkstra
1Department of Child Neurology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands. r.j.soorani@neuro.umcg.nl
Journal of Inherited Metabolic Disease
|January 26, 2006
Abstract:
We present a relatively mild case of peroxisomal D-bifunctional protein deficiency with inconsistent screening results in plasma for peroxisomal disorders.
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Peroxisomes lack the genetic machinery required to code for their own proteins. Hence, most peroxisomal membrane, lumenal and transmembrane proteins are synthesized in the cytoplasm or ER and transported to the peroxisome...
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Fatty acids are catabolized in a process called beta-oxidation, which takes place in the matrix of the mitochondria and converts their fatty acid chains into two-carbon units of acetyl groups. The acetyl...
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