Ikuo Kawashima
Setagaya, 1568506, Japan
Last Updated: 09/26/2026
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Found 10 publications
Enzyme replacement therapy using a modified α-N-acetylgalactosaminidase to suppress progressive glycolipid accumulation and escape from antidrug antibody formation in young human NAGA-transgenic/Gla-knockout mice.
Journal: Molecular genetics and metabolism
Published: March 10, 2025
HGS Promotes Tumor Growth, Whereas the Coiled-Coil Domain and Its Oligopeptide of HGS Suppress It.
Journal: International journal of molecular sciences
Published: December 21, 2024
Phosphacan acts as a repulsive cue in murine and rat cerebellar granule cells in a TAG-1/GD3 rafts-dependent manner.
Journal: Journal of neurochemistry
Published: July 28, 2022
PKCδ deficiency inhibits fetal development and is associated with heart elastic fiber hyperplasia and lung inflammation in adult PKCδ knockout mice.
Journal: PloS one
Published: December 08, 2020
Methods for the Preparation of Anti-ganglioside Monoclonal Antibodies.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: June 22, 2018
Differences in cleavage of globotriaosylceramide and its derivatives accumulated in organs of young Fabry mice following enzyme replacement therapy.
Journal: Molecular genetics and metabolism
Published: July 24, 2016
Fabry disease: biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitution.
Journal: Molecular genetics and metabolism
Published: November 05, 2011
Lyso-GM2 ganglioside: a possible biomarker of Tay-Sachs disease and Sandhoff disease.
Journal: PloS one
Published: October 15, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026