Murine deficiency of peroxisomal l-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis
Pablo Ranea‐Robles, Sara Violante, Carmen Argmann, Tetyana Dodatko, D. Bhattacharya, Hongjie Chen, Chunli Yu, Scott L. Friedman, Michelle A. Puchowicz, Sander M. Houten
Topics & Concepts
PeroxisomeBiochemistryMetabolismBeta oxidationPhosphofructokinase 2BiologyBiosynthesisMitochondrionEnzymeLipid metabolismFlux (metallurgy)ChemistryGeneOrganic chemistryPeroxisome Proliferator-Activated ReceptorsAdipose Tissue and MetabolismMetabolism and Genetic Disorders