Junko Matsuda

Kurashiki, Japan

Last Updated: 09/26/2026

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Found 27 publications

Siblings of hyaline fibromatosis syndrome with accumulation of sulfatide and GM3 ganglioside in addition to ceramide.

Siblings of hyaline fibromatosis syndrome with accumulation of sulfatide and GM3 ganglioside in addition to ceramide.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: June 11, 2025

Accumulation of prosaposin and progranulin around the subfornical organ induces polydipsia in SAP-D-deficient mice.

Accumulation of prosaposin and progranulin around the subfornical organ induces polydipsia in SAP-D-deficient mice.

Journal: Biochemistry and biophysics reports

Published: May 15, 2025

Vacuolar sterol β-glucosidase EGCrP2/Sgl1 deficiency in Cryptococcus neoformans: Dysfunctional autophagy and Mincle-dependent immune activation as targets of novel antifungal strategies.

Vacuolar sterol β-glucosidase EGCrP2/Sgl1 deficiency in Cryptococcus neoformans: Dysfunctional autophagy and Mincle-dependent immune activation as targets of novel antifungal strategies.

Journal: PLoS pathogens

Published: October 24, 2024

Promyelinating drugs ameliorate oligodendrocyte pathologies in a mouse model of Krabbe disease.

Promyelinating drugs ameliorate oligodendrocyte pathologies in a mouse model of Krabbe disease.

Journal: Molecular genetics and metabolism

Published: March 22, 2024

Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in Japan.

Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in Japan.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 10, 2023

Genetic ablation of Saposin-D in Krabbe disease eliminates psychosine accumulation but does not significantly improve demyelination.

Genetic ablation of Saposin-D in Krabbe disease eliminates psychosine accumulation but does not significantly improve demyelination.

Journal: Journal of neurochemistry

Published: February 23, 2023

Mass Spectrometry of Neutral Glycosphingolipids.

Mass Spectrometry of Neutral Glycosphingolipids.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: December 31, 2022

Bifunctional DEGS2 has higher hydroxylase activity toward substrates with very-long-chain fatty acids in the production of phytosphingosine ceramides.

Bifunctional DEGS2 has higher hydroxylase activity toward substrates with very-long-chain fatty acids in the production of phytosphingosine ceramides.

Journal: The Journal of biological chemistry

Published: September 20, 2022

The Urinary Bladder is Rich in Glycosphingolipids Composed of Phytoceramides.

The Urinary Bladder is Rich in Glycosphingolipids Composed of Phytoceramides.

Journal: Journal of lipid research

Published: March 12, 2022

Prevalence of patients with lysosomal storage disorders and peroxisomal disorders: A nationwide survey in Japan.

Prevalence of patients with lysosomal storage disorders and peroxisomal disorders: A nationwide survey in Japan.

Journal: Molecular genetics and metabolism

Published: February 24, 2021

Reduction in miR-219 expression underlies cellular pathogenesis of oligodendrocytes in a mouse model of Krabbe disease.

Reduction in miR-219 expression underlies cellular pathogenesis of oligodendrocytes in a mouse model of Krabbe disease.

Journal: Brain pathology (Zurich, Switzerland)

Published: September 16, 2020

Involvement of acid ceramidase in the degradation of bioactive N-acylethanolamines.

Involvement of acid ceramidase in the degradation of bioactive N-acylethanolamines.

Journal: Biochimica et biophysica acta. Molecular and cell biology of lipids

Published: September 03, 2020

Showing 1-12 of 27

Last Updated: 09/26/2026