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Detection of unusual very-long-chain fatty acid and ether lipid derivatives in the fibroblasts and plasma of patients with peroxisomal diseases using liquid chromatography-mass spectrometry.
Takashima S, Toyoshi K, Itoh T, Kajiwara N, Honda A, Ohba A, Takemoto S, Yoshida S, Shimozawa N. Takashima S, et al. Among authors: shimozawa n. Mol Genet Metab. 2017 Mar;120(3):255-268. doi: 10.1016/j.ymgme.2016.12.013. Epub 2017 Jan 7. Mol Genet Metab. 2017. PMID: 28089346
Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype.
Yamashita T, Mitsui J, Shimozawa N, Takashima S, Umemura H, Sato K, Takemoto M, Hishikawa N, Ohta Y, Matsukawa T, Ishiura H, Yoshimura J, Doi K, Morishita S, Tsuji S, Abe K. Yamashita T, et al. Among authors: shimozawa n. J Neurol Sci. 2017 Apr 15;375:424-429. doi: 10.1016/j.jns.2017.02.058. Epub 2017 Feb 27. J Neurol Sci. 2017. PMID: 28320181
Profiling and Imaging of Phospholipids in Brains of Abcd1-Deficient Mice.
Hama K, Fujiwara Y, Morita M, Yamazaki F, Nakashima Y, Takei S, Takashima S, Setou M, Shimozawa N, Imanaka T, Yokoyama K. Hama K, et al. Among authors: shimozawa n. Lipids. 2018 Jan;53(1):85-102. doi: 10.1002/lipd.12022. Epub 2018 Feb 22. Lipids. 2018. PMID: 29469952
302 results