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	521.	Requirement for microtubules and dynein motors in the earliest stages of peroxisome biogenesis. [electronic resource] by Brocard, Cécile B Boucher, Krissy K Jedeszko, Christopher Kim, Peter K Walton, Paul A Producer: 20050808 In: Traffic (Copenhagen, Denmark) vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	522.	Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients. [electronic resource] by Krause, Cindy Rosewich, Hendrik Thanos, Melissa Gärtner, Jutta Producer: 20061207 In: Human mutation vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	523.	PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress. [electronic resource] by Müller, C Catharina Nguyen, Tam H Ahlemeyer, Barbara Meshram, Mallika Santrampurwala, Nishreen Cao, Siyu Sharp, Peter Fietz, Pamela B Baumgart-Vogt, Eveline Crane, Denis I Producer: 20110406 In: Disease models & mechanisms vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	524.	The Pichia pastoris PER6 gene product is a peroxisomal integral membrane protein essential for peroxisome biogenesis and has sequence similarity to the Zellweger syndrome protein PAF-1. [electronic resource] by Waterham, H R de Vries, Y Russel, K A Xie, W Veenhuis, M Cregg, J M Producer: 19960621 In: Molecular and cellular biology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	525.	Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids. [electronic resource] by Aubourg, P Kremser, K Roland, M O Rocchiccioli, F Singh, I Producer: 19940418 In: Pediatric research vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	526.	The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation. [electronic resource] by Baes, M Gressens, P Huyghe, S De, Nys K Qi, C Jia, Y Mannaerts, G P Evrard, P Van, Veldhoven P P Declercq, P E Reddy, J K Producer: 20020430 In: Journal of neuropathology and experimental neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	527.	Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein. [electronic resource] by Ferdinandusse, S van Grunsven, E G Oostheim, W Denis, S Hogenhout, E M IJlst, L van Roermund, C W T Waterham, H R Goldfischer, S Wanders, R J A 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)
	528.	Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis. [electronic resource] by Krause, Cindy Rosewich, Hendrik Woehler, Andrew Gärtner, Jutta Producer: 20140318 In: Human molecular genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	529.	PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p. [electronic resource] by Okumoto, K Shimozawa, N Kawai, A Tamura, S Tsukamoto, T Osumi, T Moser, H Wanders, R J Suzuki, Y Kondo, N Fujiki, Y Producer: 19980716 In: Molecular and cellular biology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	530.	Proton magnetic resonance spectroscopy (1H-MRS) of the cerebrum in two young infants with Zellweger syndrome. [electronic resource] by Groenendaal, F Bianchi, M C Battini, R Tosetti, M Boldrini, A de Vries, L S Cioni, G Producer: 20010920 In: Neuropediatrics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	531.	[Peroxisomal disorders--DNA analysis]. [electronic resource] by Orii, T Suzuki, Y Shimozawa, N Yajima, S Asano, J Producer: 19930423 In: Nihon rinsho. Japanese journal of clinical medicine vol. 51 Suppl Availability: No items available. Save to lists Add to cart (remove)
	532.	Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B. [electronic resource] by Okumoto, K Itoh, R Shimozawa, N Suzuki, Y Tamura, S Kondo, N Fujiki, Y Producer: 19981016 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	533.	Peroxisomal bifunctional enzyme deficiency with associated retinal findings. [electronic resource] by Al-Hazzaa, S A Ozand, P T Producer: 19970916 In: Ophthalmic genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	534.	[Peroxisomal disorders--clinical and biochemical studies]. [electronic resource] by Shimozawa, N Suzuki, Y Yamaguchi, S Shimizu, N Orii, T Producer: 19890526 In: No to hattatsu = Brain and development vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	535.	Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder. [electronic resource] by Faust, P L Hatten, M E Producer: 19971230 In: The Journal of cell biology vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	536.	Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G. [electronic resource] by Muntau, A C Mayerhofer, P U Paton, B C Kammerer, S Roscher, A A Producer: 20001031 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	537.	Quantitative analysis of peroxisomal protein import in vitro. [electronic resource] by Terlecky, S R Legakis, J E Hueni, S E Subramani, S Producer: 20010329 In: Experimental cell research vol. 263 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	538.	Low bone mineral density is a common feature of Zellweger spectrum disorders. [electronic resource] by Rush, Eric T Goodwin, Jennifer L Braverman, Nancy E Rizzo, William B Producer: 20161024 In: Molecular genetics and metabolism vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	539.	Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures. [electronic resource] by Shimozawa, N Suzuki, Y Zhang, Z Imamura, A Ghaedi, K Fujiki, Y Kondo, N Producer: 20001012 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	540.	Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid. [electronic resource] by Ferdinandusse, S Denis, S Mooijer, P A Zhang, Z Reddy, J K Spector, A A Wanders, R J Producer: 20020305 In: Journal of lipid research vol. 42 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 604 results.