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American Journal of Hematology|May 1, 1986
Activation of platelet function in Fabry's diseaseT Igarashi, H Sakuraba, Y SuzukiClinical Genetics|May 1, 1987
Effect of vitamin E and ticlopidine on platelet aggregation in Fabry's diseaseH Sakuraba, T Igarashi, T Shibata, et al.Human Genetics|April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry diseaseS Ishii, H Sakuraba, Y SuzukiClinical Genetics|April 1, 1986
Cardiovascular manifestations in Fabry's disease. A high incidence of mitral valve prolapse in hemizygotes and heterozygotesH Sakuraba, Y Yanagawa, T Igarashi, et al.Biochemical and Biophysical Research Communications|March 16, 1990
Expression, glycosylation, and intracellular distribution of human beta-galactosidase in recombinant baculovirus-infected Spodoptera frugiperda cellsK Itoh, A Oshima, H Sakuraba, et al.Biochemical and Biophysical Research Communications|December 30, 1993
Characterization of a mutant alpha-galactosidase gene product for the late-onset cardiac form of Fabry diseaseS Ishii, R Kase, H Sakuraba, et al.Biochimica Et Biophysica Acta|April 24, 1995
The functional role of glutamine-280 and threonine-282 in human alpha-galactosidaseS Ishii, R Kase, H Sakuraba, et al.Journal of Biochemistry|July 1, 1981
Beta-galactosidase-neuraminidase deficiency: restoration of beta-galactosidase activity by protease inhibitorsY Suzuki, H Sakuraba, K Hayashi, et al.Biochemical and Biophysical Research Communications|March 27, 1996
Aggregation of the inactive form of human alpha-galactosidase in the endoplasmic reticulumS Ishii, R Kase, T Okumiya, et al.Brain & Development|September 1, 1991
A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reactionH Sakuraba, K Ishii, M Shimmoto, et al.Pageof 507