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Biochimica Et Biophysica Acta|December 3, 2014
Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferationAnnelies Peeters, Abhijit Babaji Shinde, Ruud Dirkx, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 13, 2018
Peroxisomes can oxidize medium- and long-chain fatty acids through a pathway involving ABCD3 and HSD17B4Sara Violante, Nihad Achetib, Carlo W T van Roermund, et al.
The Biochemical Journal|April 17, 2014
Role of AMACR (α-methylacyl-CoA racemase) and MFE-1 (peroxisomal multifunctional enzyme-1) in bile acid synthesis in miceKaija J Autio, Werner Schmitz, Remya R Nair, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 31, 2003
Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissuesAnneleen Janssen, Pierre Gressens, Markus Grabenbauer, et al.
Human Molecular Genetics|August 14, 2003
Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctataPedro Brites, Alison M Motley, Pierre Gressens, et al.
Mitochondrion|September 4, 2017
Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolitesAbhijit Babaji Shinde, Ritesh Kumar Baboota, Simone Denis, et al.
The Journal of Cell Biology|October 10, 2025
PEX14 acts as a molecular link between optineurin and the autophagic machinery to induce pexophagyHongli Li, Suyuan Chen, Celien Lismont, et al.
Plos Genetics|June 23, 2017
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouseMichael F Wangler, Yu-Hsin Chao, Vafa Bayat, et al.
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