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	541.	Unique multifunctional HSD17B4 gene product: 17beta-hydroxysteroid dehydrogenase 4 and D-3-hydroxyacyl-coenzyme A dehydrogenase/hydratase involved in Zellweger syndrome. [electronic resource] by de Launoit, Y Adamski, J Producer: 19990802 In: Journal of molecular endocrinology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	542.	Drug delivery to peroxisomes: employing unique trafficking mechanisms to target protein therapeutics. [electronic resource] by Terlecky, Stanley R Koepke, Jay I Producer: 20071220 In: Advanced drug delivery reviews vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	543.	Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain. [electronic resource] by Sharp, P Johnson, D Poulos, A Producer: 19910215 In: Journal of neurochemistry vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	544.	[Pathogenic gene in an inherited peroxisome disorder and its cellular dysfunction]. [electronic resource] by Tamura, Shigehiko Producer: 20070719 In: Seikagaku. The Journal of Japanese Biochemical Society vol. 79 Availability: No items available. Save to lists Add to cart (remove)
	545.	Oral bile acid treatment and the patient with Zellweger syndrome. [electronic resource] by Setchell, K D Bragetti, P Zimmer-Nechemias, L Daugherty, C Pelli, M A Vaccaro, R Gentili, G Distrutti, E Dozzini, G Morelli, A Producer: 19920311 In: Hepatology (Baltimore, Md.) vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	546.	Peroxisomal disorders. Neurodevelopmental and biochemical aspects. [electronic resource] by Brown, F R Voigt, R Singh, A K Singh, I Producer: 19930707 In: American journal of diseases of children (1960) vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	547.	Plasmalogens, phospholipase A2, and docosahexaenoic acid turnover in brain tissue. [electronic resource] by Farooqui, A A Horrocks, L A Producer: 20020214 In: Journal of molecular neuroscience : MN vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	548.	Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels. [electronic resource] by Walter, C Gootjes, J Mooijer, P A Portsteffen, H Klein, C Waterham, H R Barth, P G Epplen, J T Kunau, W H Wanders, R J Dodt, G Producer: 20010802 In: American journal of human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	549.	Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals. [electronic resource] by Tateishi, K Okumoto, K Shimozawa, N Tsukamoto, T Osumi, T Suzuki, Y Kondo, N Okano, I Fujiki, Y Producer: 19971001 In: European journal of cell biology vol. 73 Availability: No items available. Save to lists Add to cart (remove)
	550.	Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. [electronic resource] by Honsho, M Tamura, S Shimozawa, N Suzuki, Y Kondo, N Fujiki, Y Producer: 19990201 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	551.	Differential deficiency of mevalonate kinase and phosphomevalonate kinase in patients with distinct defects in peroxisome biogenesis: evidence for a major role of peroxisomes in cholesterol biosynthesis. [electronic resource] by Wanders, R J Romeijn, G J Producer: 19980731 In: Biochemical and biophysical research communications vol. 247 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	552.	Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders. [electronic resource] by Yik, Wing Yan Steinberg, Steven J Moser, Ann B Moser, Hugo W Hacia, Joseph G Producer: 20090528 In: Human mutation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	553.	Evidence that the bradykinin-induced activation of phospholipase D and of the mitogen-activated protein kinase cascade involve different protein kinase C isoforms. [electronic resource] by Clark, K J Murray, A W Producer: 19950510 In: The Journal of biological chemistry vol. 270 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	554.	Lipoprotein[a] is not present in the plasma of patients with some peroxisomal disorders. [electronic resource] by van der Hoek, Y Y Wanders, R J van den Ende, A E Kraft, H G Gabel, B R Kastelein, J J Koschinsky, M L Producer: 19971029 In: Journal of lipid research vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	555.	Histopathologic approach to metabolic liver disease: Part 1. [electronic resource] by Jevon, G P Dimmick, J E Producer: 19990928 In: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	556.	Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation. [electronic resource] by Havali, Cengiz Dorum, Sevil Akbaş, Yılmaz Görükmez, Orhan Hirfanoglu, Tugba Producer: 20201207 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	557.	Evidence that photodynamic stress kills Zellweger fibroblasts by a nonapoptotic mechanism. [electronic resource] by Spisni, E Cavazzoni, M Griffoni, C Calzolari, E Tomasi, V Producer: 19980508 In: Biochimica et biophysica acta vol. 1402 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	558.	Abnormality in catalase import into peroxisomes leads to severe neurological disorder. [electronic resource] by Sheikh, F G Pahan, K Khan, M Barbosa, E Singh, I Producer: 19980410 In: Proceedings of the National Academy of Sciences of the United States of America vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	559.	Zellweger spectrum disorder patient-derived fibroblasts with the PEX1-Gly843Asp allele recover peroxisome functions in response to flavonoids. [electronic resource] by MacLean, Gillian E Argyriou, Catherine Di Pietro, Erminia Sun, Xuting Birjandian, Sara Saberian, Panteha Hacia, Joseph G Braverman, Nancy E Producer: 20200226 In: Journal of cellular biochemistry vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	560.	Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects. [electronic resource] by Paton, B C Sharp, P C Crane, D I Poulos, A Producer: 19960529 In: The Journal of clinical investigation vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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