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	541.	Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome. [electronic resource] by Itoh, M Suzuki, Y Akaboshi, S Zhang, Z Miyabara, S Takashima, S Producer: 20000425 In: Brain research vol. 858 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	542.	Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders. [electronic resource] by Shimozawa, N Suzuki, Y Zhang, Z Imamura, A Toyama, R Mukai, S Fujiki, Y Tsukamoto, T Osumi, T Orii, T Wanders, R J Kondo, N Producer: 19990708 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	543.	Clinical consequences of defects in peroxisomal beta-oxidation. [electronic resource] by Clayton, P T Producer: 20010906 In: Biochemical Society transactions vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	544.	Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation. [electronic resource] by Shimozawa, Nobuyuki Nagase, Tomoko Takemoto, Yasuhiko Ohura, Toshihiro Suzuki, Yasuyuki Kondo, Naomi Producer: 20040210 In: American journal of medical genetics. Part A vol. 120A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	545.	A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype. [electronic resource] by Maxwell, M A Nelson, P V Chin, S J Paton, B C Carey, W F Crane, D I Producer: 19990923 In: Human genetics vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	546.	Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteins. [electronic resource] by Ito, M Ito, R Huang, Y Miura, S Imamura, A Suzuki, Y Shimozawa, N Producer: 20000629 In: Biochimica et biophysica acta vol. 1496 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	547.	Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiency. [electronic resource] by Thompson, S A Calvin, J Hogg, S Ferdinandusse, S Wanders, R J A Barker, R A Producer: 20080407 In: Journal of neurology, neurosurgery, and psychiatry vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	548.	Phospholipase D activity is altered in X-linked adrenoleukodystrophy heterozygous carriers, but not in hemizygous patients. [electronic resource] by Logan, H E Byers, D M Ridgway, N D Cook, H W Producer: 19980812 In: Biochimica et biophysica acta vol. 1407 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	549.	Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance. [electronic resource] by Nguyen, Tam Bjorkman, Jonas Paton, Barbara C Crane, Denis I Producer: 20060612 In: Journal of cell science vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	550.	The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes. [electronic resource] by Muntau, A C Holzinger, A Mayerhofer, P U Gärtner, J Roscher, A A Kammerer, S Producer: 20000322 In: Biochemical and biophysical research communications vol. 268 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	551.	Localization of a portion of extranuclear ATM to peroxisomes. [electronic resource] by Watters, D Kedar, P Spring, K Bjorkman, J Chen, P Gatei, M Birrell, G Garrone, B Srinivasa, P Crane, D I Lavin, M F Producer: 19991229 In: The Journal of biological chemistry vol. 274 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	552.	Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency. [electronic resource] by Schröder, J M Hackel, V Wanders, R J A Göhlich-Ratmann, G Voit, T Producer: 20040920 In: Acta neuropathologica vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	553.	Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction. [electronic resource] by Tamura, S Matsumoto, N Imamura, A Shimozawa, N Suzuki, Y Kondo, N Fujiki, Y Producer: 20010823 In: The Biochemical journal vol. 357 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	554.	Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant. [electronic resource] by Tsukamoto, T Miura, S Nakai, T Yokota, S Shimozawa, N Suzuki, Y Orii, T Fujiki, Y Sakai, F Bogaki, A Yasumo, H Osumi, T Producer: 19960111 In: Nature genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	555.	Identification and characterization of the human peroxin PEX3. [electronic resource] by Soukupova, M Sprenger, C Gorgas, K Kunau, W H Dodt, G Producer: 19990928 In: European journal of cell biology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	556.	Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients. [electronic resource] by Shimozawa, N Zhang, Z Suzuki, Y Imamura, A Tsukamoto, T Osumi, T Fujiki, Y Orii, T Barth, P G Wanders, R J Kondo, N Producer: 19991001 In: Biochemical and biophysical research communications vol. 262 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	557.	Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. [electronic resource] by Matsumoto, Naomi Tamura, Shigehiko Furuki, Satomi Miyata, Non Moser, Ann Shimozawa, Nobuyuki Moser, Hugo W Suzuki, Yasuyuki Kondo, Naomi Fujiki, Yukio Producer: 20030924 In: American journal of human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	558.	Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders. [electronic resource] by Corzo, Deyanira Gibson, William Johnson, Kisha Mitchell, Grant LePage, Guy Cox, Gerald F Casey, Robin Zeiss, Carolyn Tyson, Heidi Cutting, Garry R Raymond, Gerald V Smith, Kirby D Watkins, Paul A Moser, Ann B Moser, Hugo W Steinberg, Steven J Producer: 20020627 In: American journal of human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	559.	Selective receptor-mediated impairment of growth factor activity in neonatal- and X-linked adrenoleukodystrophy patients. [electronic resource] by Al-Essa, Mazen Dhaunsi, Gursev S Producer: 20191227 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	560.	PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import. [electronic resource] by Chang, C C Warren, D S Sacksteder, K A Gould, S J Producer: 19991217 In: The Journal of cell biology vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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