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Journal of Lipid Research|December 8, 2009
Monitoring of fatty aldehyde dehydrogenase by formation of pyrenedecanoic acid from pyrenedecanalMarkus A Keller, Katrin Watschinger, Georg Golderer, et al.
Human Mutation|April 27, 2007
Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiencySacha Ferdinandusse, Simone Denis, Eveline M Hogenhout, et al.
Biochimica Et Biophysica Acta|December 14, 2005
Role of Pex19p in the targeting of PMP70 to peroxisomeYoshinori Kashiwayama, Kota Asahina, Hiroyuki Shibata, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2013
Identification and characterization of Eci3, a murine kidney-specific Δ3,Δ2-enoyl-CoA isomeraseMichel van Weeghel, Rob Ofman, Carmen A Argmann, et al.
Orphanet Journal of Rare Diseases|November 17, 2023
Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophyVincenza Gragnaniello, Daniela Gueraldi, Andrea Puma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 26, 2023
Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 geneHans R Waterham, Janet Koster, Merel S Ebberink, et al.
The European Respiratory Journal|August 2, 2006
Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failureM K H Tong, C-S Lam, T W L Mak, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 7, 2009
Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencyLap-Kay Law, Nelson L S Tang, Joannie Hui, et al.
The Journal of Cell Biology|November 13, 2008
Cardiolipin provides an essential activating platform for caspase-8 on mitochondriaFrancois Gonzalvez, Zachary T Schug, Riekelt H Houtkooper, et al.
Plos One|December 14, 2011
Alkyl-glycerol rescues plasmalogen levels and pathology of ether-phospholipid deficient micePedro Brites, Ana Sofia Ferreira, Tiago Ferreira da Silva, et al.
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