Kayoko Toyoshi

Hypomorphic mutation of PEX3 with peroxisomal mosaicism reveals the oscillating nature of peroxisome biogenesis coupled with differential metabolic activities.

N. Shimozawa, Y. Hirata, S. Takashima, 2022, Molecular genetics and metabolism.

Positional determination of the carbon–carbon double bonds in unsaturated fatty acids mediated by solvent plasmatization using LC–MS

N. Shimozawa, Takuhei Yamamoto, S. Takashima, 2020, Scientific Reports.

A method to determine the double bond position in unsaturated fatty acids by solvent plasmatization using liquid chromatography-mass spectrometry

N. Shimozawa, Takuhei Yamamoto, S. Takashima, 2019, bioRxiv.

Zebrafish model of human Zellweger syndrome reveals organ specific accumulation of distinct fatty acid species and widespread gene expression changes

N. Shimozawa, S. Takashima, Kayoko Toyoshi, 2021, bioRxiv.

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.

N. Shimozawa, S. Takashima, Ayako Honda, 2017, Molecular genetics and metabolism.

Development of a system adapted for the diagnosis and evaluation of peroxisomal disorders by measuring bile acid intermediates

N. Shimozawa, H. Ohnishi, Hiroki Kawai, 2022, Brain and Development.

Zebrafish model of human Zellweger syndrome reveals organ-specific accumulation of distinct fatty acid species and widespread gene expression changes.

N. Shimozawa, S. Takashima, Kayoko Toyoshi, 2021, Molecular genetics and metabolism.

Positional determination of the carbon–carbon double bonds in unsaturated fatty acids mediated by solvent plasmatization using LC–MS

N. Shimozawa, Takuhei Yamamoto, S. Takashima, 2020, Scientific Reports.