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Molecular Genetics and Metabolism|May 21, 2021
Zebrafish model of human Zellweger syndrome reveals organ-specific accumulation of distinct fatty acid species and widespread gene expression changesShigeo Takashima, Shoko Takemoto, Kayoko Toyoshi, et al.The Journal of Biological Chemistry|October 17, 2003
Proteomic analysis of rat liver peroxisome: presence of peroxisome-specific isozyme of Lon proteaseMiki Kikuchi, Naoya Hatano, Sadaki Yokota, et al.Journal of Child Neurology|June 1, 2005
Molecular and neurologic findings of peroxisome biogenesis disordersNobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto, et al.American Journal of Medical Genetics. Part A|June 10, 2003
Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutationNobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto, et al.Biochimica Et Biophysica Acta|March 18, 2004
Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomesTomoko Nagase, Nobuyuki Shimozawa, Yasuhiko Takemoto, et al.Brain & Development|August 6, 2018
Characteristics of Japanese patients with X-linked adrenoleukodystrophy and concerns of their families from the 1st registry systemKen Sakurai, Toya Ohashi, Nobuyuki Shimozawa, et al.Brain & Development|September 18, 2003
Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disordersYasuhiko Takemoto, Yasuyuki Suzuki, Ryoko Horibe, et al.Journal of Lipid Research|February 21, 2020
Hexacosenoyl-CoA is the most abundant very long-chain acyl-CoA in ATP binding cassette transporter D1-deficient cellsKotaro Hama, Yuko Fujiwara, Shigeo Takashima, et al.Brain & Development|December 13, 2022
Development of a system adapted for the diagnosis and evaluation of peroxisomal disorders by measuring bile acid intermediatesHiroki Kawai, Shigeo Takashima, Akiko Ohba, et al.Journal of Biochemistry|January 24, 2006
Identification of Pex5pM, and retarded maturation of 3-ketoacyl-CoA thiolase and acyl-CoA oxidase in CHO cells expressing mutant Pex5p isoformsRitsu Ito, Masashi Morita, Norimasa Takahashi, et al.Pageof 8