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	281.	Synthesis of mevalonate pathway lipids in fibroblasts from Zellweger and X-linked ALD patients. [electronic resource] by Appelkvist, E L Venizelos, N Zhang, Y Parmryd, I Hagenfeldt, L Dallner, G Producer: 19991027 In: Pediatric research vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	282.	Zellweger syndrome and associated brain malformations: report of a novel Peroxin1 (PEX1) mutation in a Native American infant. [electronic resource] by Mohebbi, Mohammad R Rush, Eric T Rizzo, William B Banagale, Raul C Producer: 20130509 In: Journal of child neurology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	283.	Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood. [electronic resource] by Berendse, Kevin Engelen, Marc Ferdinandusse, Sacha Majoie, Charles B L M Waterham, Hans R Vaz, Frédéric M Koelman, Johannes H T M Barth, Peter G Wanders, Ronald J A Poll-The, Bwee Tien Producer: 20161017 In: Journal of inherited metabolic disease vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	284.	A longitudinal study of retinopathy in the PEX1-Gly844Asp mouse model for mild Zellweger Spectrum Disorder. [electronic resource] by Argyriou, Catherine Polosa, Anna Cecyre, Bruno Hsieh, Monica Di Pietro, Erminia Cui, Wei Bouchard, Jean-François Lachapelle, Pierre Braverman, Nancy Producer: 20200220 In: Experimental eye research vol. 186 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	285.	Increased urinary excretion of LTB4 and omega-carboxy-LTB4 in patients with Zellweger syndrome. [electronic resource] by Mayatepek, E Flock, B Producer: 19990708 In: Clinica chimica acta; international journal of clinical chemistry vol. 282 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	286.	Study of mutant proteins with folding defects in cultured patient cells. [electronic resource] by Dodt, Gabriele Walter, Claudia Producer: 20040302 In: Methods in molecular biology (Clifton, N.J.) vol. 232 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	287.	Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders. [electronic resource] by Poll-The, B T Skjeldal, O H Stokke, O Poulos, A Demaugre, F Saudubray, J M Producer: 19890306 In: Human genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	288.	Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts. [electronic resource] by Heikoop, J C Van den Berg, M Strijland, A Weijers, P J Schutgens, R B Just, W W Wanders, R J Tager, J M Producer: 19910904 In: Biochimica et biophysica acta vol. 1097 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	289.	Late-onset generalized disorder of peroxisomes. [electronic resource] by Burdette, D E Kremser, K Fink, J K Pahan, K Stanley, W Singh, I Producer: 19960613 In: Neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	290.	Disorders of peroxisome biogenesis: complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency). [electronic resource] by Wanders, R J Mooijer, P A Dekker, C Suzuki, Y Shimozawa, N Producer: 19990910 In: Journal of inherited metabolic disease vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	291.	Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes. [electronic resource] by Nakayama, Minoru Sato, Hiroyasu Okuda, Takayuki Fujisawa, Nao Kono, Nozomu Arai, Hiroyuki Suzuki, Emiko Umeda, Masato Ishikawa, Hiroyuki O Matsuno, Kenji Producer: 20111214 In: PloS one vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	292.	A novel mutation in the PEX12 gene causing a peroxisomal biogenesis disorder. [electronic resource] by Konkoľová, Jana Petrovič, Robert Chandoga, Ján Halasová, Edita Jungová, Petra Böhmer, Daniel Producer: 20160607 In: Molecular biology reports vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	293.	Peroxisomal disorders: clinical commentary and future prospects. [electronic resource] by Wilson, G N Holmes, R D Hajra, A K Producer: 19881207 In: American journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	294.	Complementation analysis of peroxisomal disorders and classical Refsum. [electronic resource] by Poll-The, B T Skjeldal, O H Stokke, O Demaugre, F Saudubray, J M Producer: 19900517 In: Progress in clinical and biological research vol. 321 Availability: No items available. Save to lists Add to cart (remove)
	295.	Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage. [electronic resource] by Hoefler, G Paschke, E Hoefler, S Moser, A B Moser, H W Producer: 19920129 In: The Journal of clinical investigation vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	296.	Complementation analysis of patients with intact peroxisomes and impaired peroxisomal beta-oxidation. [electronic resource] by McGuinness, M C Moser, A B Poll-The, B T Watkins, P A Producer: 19930610 In: Biochemical medicine and metabolic biology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	297.	Lack of requirement for sterol carrier protein-2 in the intracellular trafficking of lysosomal cholesterol. [electronic resource] by Johnson, W J Reinhart, M P Producer: 19940720 In: Journal of lipid research vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	298.	Phosphatidyl ethanolamine with increased polyunsaturated fatty acids in compensation for plasmalogen defect in the Zellweger syndrome brain. [electronic resource] by Saitoh, Makiko Itoh, Masayuki Takashima, Sachio Mizuguchi, Masashi Iwamori, Masao Producer: 20090427 In: Neuroscience letters vol. 449 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	299.	Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations. [electronic resource] by Al-Dirbashi, O Y Shaheen, R Al-Sayed, M Al-Dosari, M Makhseed, N Abu Safieh, L Santa, T Meyer, B F Shimozawa, N Alkuraya, F S Producer: 20090730 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	300.	Formation of a novel arachidonic acid metabolite in peroxisomes. [electronic resource] by Gordon, J A Heller, S K Rhead, W J Watkins, P A Spector, A A Producer: 19950718 In: Prostaglandins, leukotrienes, and essential fatty acids vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 604 results.