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	581.	Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I. [electronic resource] by Tamura, S Okumoto, K Toyama, R Shimozawa, N Tsukamoto, T Suzuki, Y Osumi, T Kondo, N Fujiki, Y Producer: 19980513 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)
	582.	The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein. [electronic resource] by Mosser, J Lutz, Y Stoeckel, M E Sarde, C O Kretz, C Douar, A M Lopez, J Aubourg, P Mandel, J L Producer: 19940718 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	583.	Coagulopathy in Zellweger spectrum disorders: a role for vitamin K. [electronic resource] by Zeynelabidin, Sara Klouwer, Femke C C Meijers, Joost C M Suijker, Monique H Engelen, Marc Poll-The, Bwee Tien van Ommen, C Heleen Producer: 20181226 In: Journal of inherited metabolic disease vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	584.	Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency. [electronic resource] by Faust, Phyllis L Producer: 20030731 In: The Journal of comparative neurology vol. 461 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	585.	Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders. [electronic resource] by Slawecki, M L Dodt, G Steinberg, S Moser, A B Moser, H W Gould, S J Producer: 19951002 In: Journal of cell science vol. 108 ( Pt 5) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	586.	Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly. [electronic resource] by Matsuzono, Y Kinoshita, N Tamura, S Shimozawa, N Hamasaki, M Ghaedi, K Wanders, R J Suzuki, Y Kondo, N Fujiki, Y Producer: 19990415 In: Proceedings of the National Academy of Sciences of the United States of America vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	587.	Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype. [electronic resource] by Maxwell, Megan Bjorkman, Jonas Nguyen, Tam Sharp, Peter Finnie, John Paterson, Carol Tonks, Ian Paton, Barbara C Kay, Graham F Crane, Denis I Producer: 20030829 In: Molecular and cellular biology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	588.	Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver. [electronic resource] by Krysko, Olga Hulshagen, Leen Janssen, Anneleen Schütz, Günter Klein, Rüdiger De Bruycker, Melina Espeel, Marc Gressens, Pierre Baes, Myriam Producer: 20070321 In: Journal of neuroscience research vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	589.	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)
	590.	The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder. [electronic resource] by Hiebler, Shandi Masuda, Tomohiro Hacia, Joseph G Moser, Ann B Faust, Phyllis L Liu, Anita Chowdhury, Nivedita Huang, Ning Lauer, Amanda Bennett, Jean Watkins, Paul A Zack, Donald J Braverman, Nancy E Raymond, Gerald V Steinberg, Steven J Producer: 20141128 In: Molecular genetics and metabolism vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	591.	Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders. [electronic resource] by Wiemer, E A Nuttley, W M Bertolaet, B L Li, X Francke, U Wheelock, M J Anné, U K Johnson, K R Subramani, S Producer: 19950727 In: The Journal of cell biology vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	592.	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)
	593.	A novel migration-related gene product, doublecortin, in neuronal migration disorder of fetuses and infants with Zellweger syndrome. [electronic resource] by Qin, J Mizuguchi, M Itoh, M Takashima, S Producer: 20001222 In: Acta neuropathologica vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	594.	The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells--the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family. [electronic resource] by McCollum, D Monosov, E Subramani, S Producer: 19930611 In: The Journal of cell biology vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	595.	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)
	596.	The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction. [electronic resource] by Faust, P L Su, H M Moser, A Moser, H W 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)
	597.	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)
	598.	Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. Study with a novel Pex5-impaired Chinese hamster ovary cell mutant. [electronic resource] by Matsumura, T Otera, H Fujiki, Y Producer: 20000816 In: The Journal of biological chemistry vol. 275 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	599.	Normal and abnormal neuronal migration in the developing cerebral cortex. [electronic resource] by Sun, Xue-Zhi Takahashi, Sentaro Cui, Chun Zhang, Rui Sakata-Haga, Hiromi Sawada, Kazuhiko Fukui, Yoshihiro Producer: 20021021 In: The journal of medical investigation : JMI vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	600.	Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse). [electronic resource] by Baumgart, E Vanhorebeek, I Grabenbauer, M Borgers, M Declercq, P E Fahimi, H D Baes, M Producer: 20011204 In: The American journal of pathology vol. 159 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.