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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.
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.
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