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	461.	Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes. [electronic resource] by Suzuki, Y Shimozawa, N Kawabata, I Yajima, S Inoue, K Uchida, Y Izai, K Tomatsu, S Kondo, N Orii, T Producer: 19940913 In: Brain & development vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	462.	PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease. [electronic resource] by Preuss, Natalie Brosius, Ute Biermanns, Martina Muntau, Ania C Conzelmann, Ernst Gartner, Jutta Producer: 20021029 In: Pediatric research vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	463.	Exome sequencing identifies [electronic resource] by García-García, Gema Sanchez-Navarro, Iker Aller, Elena Jaijo, Teresa Fuster-Garcia, Carla Rodríguez-Munoz, Ana Vallejo, Elena Tellería, Juan José Vázquez, Selma Beltrán, Sergi Derdak, Sophia Zurita, Olga Villaverde-Montero, Cristina Avila-Fernández, Almudena Corton, Marta Blanco-Kelly, Fiona Hakonarson, Hakon Millán, José M Ayuso, Carmen Producer: 20210204 In: Molecular vision vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	464.	[Biogenesis of peroxisomes and human peroxisomal disorders]. [electronic resource] by Fujiki, Y Producer: 19950810 In: Seikagaku. The Journal of Japanese Biochemical Society vol. 67 Availability: No items available. Save to lists Add to cart (remove)
	465.	Restoration of peroxisome biogenesis in a peroxisome-deficient mammalian cell line by expression of either the 35 kDa or the 70 kDa peroxisomal membrane proteins. [electronic resource] by Gärtner, J Obie, C Watkins, P Valle, D Producer: 19950130 In: Journal of inherited metabolic disease vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	466.	Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency. [electronic resource] by Ferdinandusse, S Overmars, H Denis, S Waterham, H R Wanders, R J Vreken, P Producer: 20010628 In: Journal of lipid research vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	467.	3-Hydroxy-3-methylglutaryl coenzyme A lyase: targeting and processing in peroxisomes and mitochondria. [electronic resource] by Ashmarina, L I Pshezhetsky, A V Branda, S S Isaya, G Mitchell, G A Producer: 19990309 In: Journal of lipid research vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	468.	Polarizing inclusions in some organs of children with congenital peroxisomal diseases (Zellweger's, Refsum's, chondrodysplasia punctata (rhizomelic form), X-linked adrenoleukodystrophy). [electronic resource] by Kerckaert, I Dingemans, K P Heymans, H S Vamecq, J Roels, F Producer: 19890606 In: Journal of inherited metabolic disease vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	469.	Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients. [electronic resource] by Shimozawa, N Suzuki, Y Tomatsu, S Tsukamoto, T Osumi, T Fujiki, Y Kamijo, K Hashimoto, T Kondo, N Orii, T Producer: 19961021 In: Pediatric research vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	470.	A newly identified mutation in the [electronic resource] by Tanaka, Akemi J Okumoto, Kanji Tamura, Shigehiko Abe, Yuichi Hirsch, Yoel Deng, Liyong Ekstein, Joseph Chung, Wendy K Fujiki, Yukio Producer: 20200330 In: Cold Spring Harbor molecular case studies vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	471.	[Intrahepatic cholestasis due to biochemical errors of bile acids. II. Clinical and therapeutic aspects]. [electronic resource] by Lovisetto, P Raviolo, P Producer: 19950310 In: Minerva medica vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	472.	Normal and defective neuronal membranes: structure and function: neuronal lesions in peroxisomal disorders. [electronic resource] by Powers, J M 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)
	473.	Approaches to studies on peroxisome biogenesis and human peroxisome-deficient disorders. [electronic resource] by Fujiki, Y Producer: 19970210 In: Annals of the New York Academy of Sciences vol. 804 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	474.	Cloning and characterization of PAS5: a gene required for peroxisome biogenesis in the methylotrophic yeast Pichia pastoris. [electronic resource] by Spong, A P Subramani, S Producer: 19931207 In: The Journal of cell biology vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	475.	An apparent decrease in cholesterol biosynthesis in peroxisomal-defective Chinese hamster ovary cells is related to impaired mitochondrial oxidation. [electronic resource] by Oettl, Karl Höfler, Gerald Ness, Gene C Sattler, Wolfgang Malle, Ernst Producer: 20030724 In: Biochemical and biophysical research communications vol. 305 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	476.	Loss of compartmentalization causes misregulation of lysine biosynthesis in peroxisome-deficient yeast cells. [electronic resource] by Breitling, Rainer Sharif, Orzala Hartman, Michelle L Krisans, Skaidrite K Producer: 20030620 In: Eukaryotic cell vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	477.	Mass spectrometric analysis of ceramide perturbations in brain and fibroblasts of mice and human patients with peroxisomal disorders. [electronic resource] by Pettus, Benjamin J Baes, Myriam Busman, Mark Hannun, Yusuf A Van Veldhoven, Paul P Producer: 20040817 In: Rapid communications in mass spectrometry : RCM vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	478.	Cholic acid therapy in Zellweger spectrum disorders. [electronic resource] by Berendse, Kevin Klouwer, Femke C C Koot, Bart G P Kemper, Elles M Ferdinandusse, Sacha Koelfat, Kiran V K Lenicek, Martin Schaap, Frank G Waterham, Hans R Vaz, Frédéric M Engelen, Marc Jansen, Peter L M Wanders, Ronald J A Poll-The, Bwee Tien Producer: 20171205 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)
	479.	Contribution of fetal MR imaging in the prenatal diagnosis of Zellweger syndrome. [electronic resource] by Mochel, F Grébille, A-G Benachi, A Martinovic, J Razavi, F Rabier, D Simon, I Boddaert, N Brunelle, F Sonigo, P Producer: 20060413 In: AJNR. American journal of neuroradiology vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	480.	Liver disease predominates in a mouse model for mild human Zellweger spectrum disorder. [electronic resource] by Berendse, Kevin Boek, Maxim Gijbels, Marion Van der Wel, Nicole N Klouwer, Femke C van den Bergh-Weerman, Marius A Shinde, Abhijit Babaji Ofman, Rob Poll-The, Bwee Tien Houten, Sander M Baes, Myriam Wanders, Ronald J A Waterham, Hans R Producer: 20200513 In: Biochimica et biophysica acta. Molecular basis of disease vol. 1865 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.