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	401.	[Symptomatic calcification in the newborn. Phenocopies of chondrodysplasia punctata]. [electronic resource] by Leicher-Düber, A Schumacher, R Spranger, J Producer: 19900615 In: RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin vol. 152 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	402.	Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy. [electronic resource] by Small, G M Santos, M J Imanaka, T Poulos, A Danks, D M Moser, H W Lazarow, P B 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)
	403.	[Clinical and molecular aspects of peroxisome-deficient disorders]. [electronic resource] by Suzuki, Y Shimozawa, N Orii, T Producer: 19931122 In: Nihon rinsho. Japanese journal of clinical medicine vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	404.	Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex. [electronic resource] by Furuki, Satomi Tamura, Shigehiko Matsumoto, Naomi Miyata, Non Moser, Ann Moser, Hugo W Fujiki, Yukio Producer: 20060317 In: The Journal of biological chemistry vol. 281 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	405.	Analysis of a Chinese pedigree with Zellweger syndrome reveals a novel PEX1 mutation by next-generation sequencing. [electronic resource] by Sun, Yan Wang, Lixia Wei, Xiaoming Zhu, Qian Yang, Yun Lan, Zhangzhang Qu, Ning Chu, Yuxing Wang, Yuhui Yang, Shuang Liang, Yu Wang, Wei Yi, Xin Producer: 20130827 In: Clinica chimica acta; international journal of clinical chemistry vol. 417 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	406.	Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome. [electronic resource] by van Roermund, C W Brul, S Tager, J M Schutgens, R B Wanders, R J Producer: 19911004 In: Journal of inherited metabolic disease vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	407.	Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model. [electronic resource] by Kovacs, Werner J Shackelford, Janis E Tape, Khanichi N Richards, Michael J Faust, Phyllis L Fliesler, Steven J Krisans, Skaidrite K Producer: 20040121 In: Molecular and cellular biology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	408.	Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders. [electronic resource] by Shimozawa, N Imamura, A Zhang, Z Suzuki, Y Orii, T Tsukamoto, T Osumi, T Fujiki, Y Wanders, R J Besley, G Kondo, N Producer: 19991119 In: Journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	409.	13-(S)-hydroxyoctadecadienoic acid (13-HODE) incorporation and conversion to novel products by endothelial cells. [electronic resource] by Fang, X Kaduce, T L Spector, A A Producer: 19990503 In: Journal of lipid research vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	410.	Bile acid analysis in human disorders of bile acid biosynthesis. [electronic resource] by Vaz, Frédéric M Ferdinandusse, Sacha Producer: 20180409 In: Molecular aspects of medicine vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	411.	Bile acid synthetic defects and liver disease. [electronic resource] by Bove, K E Daugherty, C C Tyson, W Mierau, G Heubi, J E Balistreri, W F Setchell, K D Producer: 20000118 In: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	412.	Identification of a novel PEX14 mutation in Zellweger syndrome. [electronic resource] by Huybrechts, S J Van Veldhoven, P P Hoffman, I Zeevaert, R de Vos, R Demaerel, P Brams, M Jaeken, J Fransen, M Cassiman, D Producer: 20080811 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	413.	Liver disease in infancy: a 20 year perspective. [electronic resource] by Mieli-Vergani, G Howard, E R Mowat, A P Producer: 19911120 In: Gut vol. Suppl Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	414.	Adrenoleukodystrophy and other peroxisomal diseases. [electronic resource] by Aubourg, P Producer: 19941118 In: Current opinion in genetics & development vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	415.	[PMP70, the 70-kDa peroxisomal membrane protein: a member of the ATP-binding cassette transporters]. [electronic resource] by Kamijo, K Osumi, T Hashimoto, T Producer: 19931122 In: Nihon rinsho. Japanese journal of clinical medicine vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	416.	Pathogenesis of peroxisomal deficiency disorders (Zellweger syndrome) may be mediated by misregulation of the GABAergic system via the diazepam binding inhibitor. [electronic resource] by Breitling, Rainer Producer: 20040601 In: BMC pediatrics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	417.	Diagnostic and prognostic value of in vivo proton MR spectroscopy for Zellweger syndrome spectrum patients. [electronic resource] by Rosewich, H Dechent, P Krause, C Ohlenbusch, A Brockmann, K Gärtner, J 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)
	418.	Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome. [electronic resource] by Gärtner, J Moser, H Valle, D Producer: 19930610 In: Nature genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	419.	Docosahexaenoic acid deficit is not a major pathogenic factor in peroxisome-deficient mice. [electronic resource] by Janssen, A Baes, M Gressens, P Mannaerts, G P Declercq, P Van Veldhoven, P P Producer: 20000217 In: Laboratory investigation; a journal of technical methods and pathology vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	420.	Induction of peroxisomal changes in oligodendrocytes treated with 7-ketocholesterol: Attenuation by α-tocopherol. [electronic resource] by Nury, Thomas Sghaier, Randa Zarrouk, Amira Ménétrier, Franck Uzun, Tugba Leoni, Valerio Caccia, Claudio Meddeb, Wiem Namsi, Amira Sassi, Khouloud Mihoubi, Wafa Riedinger, Jean-Marc Cherkaoui-Malki, Mustapha Moreau, Thibault Vejux, Anne Lizard, Gérard Producer: 20181211 In: Biochimie vol. 153 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.