Showing results (11-20 of 133) with videos related to
Sort By:
Pageof 14
Neurochemical Research|July 21, 2004
NF-kappaB prevents TNF-alpha-induced apoptosis in an oligodendrocyte cell lineMakoto Hamanoue, Akira Yoshioka, Toya Ohashi, et al.International Journal of Otolaryngology|November 14, 2013
Long-term effect of enzyme replacement therapy with fabry diseaseManabu Komori, Yuika Sakurai, Hiromi Kojima, et al.Journal of Human Genetics|April 17, 2019
Mutation spectrum of α-Galactosidase gene in Japanese patients with Fabry diseaseMasahisa Kobayashi, Toya Ohashi, Eiko Kaneshiro, et al.Clinical Therapeutics|December 2, 2010
Successful pregnancy and lactation outcome in a patient with Gaucher disease receiving enzyme replacement therapy, and the subsequent distribution and excretion of imiglucerase in human breast milkYoshiki Sekijima, Toya Ohashi, Satoshi Ohira, et al.Pediatric Neurology|December 17, 2009
Gaucher disease patient with myoclonus epilepsy and a novel mutationAsako Tajima, Toya Ohashi, Shin-Ichiro Hamano, et al.The Journal of Gene Medicine|October 2, 2004
Widespread gene transduction to the central nervous system by adenovirus in utero: implication for prenatal gene therapy to brain involvement of lysosomal storage diseaseJin-Song Shen, Xing-Li Meng, Hiroshi Maeda, et al.Molecular Genetics and Metabolism|December 4, 2013
A practical fluorometric assay method to measure lysosomal acid lipase activity in dried blood spots for the screening of cholesteryl ester storage disease and Wolman diseaseTakenori Dairaku, Takeo Iwamoto, Minami Nishimura, et al.Molecular Genetics and Metabolism|August 11, 2007
Influence of antibody formation on reduction of globotriaosylceramide (GL-3) in urine from Fabry patients during agalsidase beta therapyToya Ohashi, Mio Sakuma, Teruo Kitagawa, et al.Molecular Genetics and Metabolism|July 28, 2024
Restoration of peripheral neuropathy in Fabry mice via intrathecal administration of an adeno-associated virus vector encoding mGLA cDNATakashi Higuchi, Yohta Shimada, Yukari Takahashi, et al.Molecular Genetics and Metabolism|January 1, 2018
Chaperone effect of sulfated disaccharide from heparin on mutant iduronate-2-sulfatase in mucopolysaccharidosis type IIHiroo Hoshina, Yohta Shimada, Takashi Higuchi, et al.Pageof 14