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H Sakuraba

Showing results (71-80 of 128) with videos related to

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Metabolism: Clinical and Experimental|March 22, 2000
Inhibition of progressive reduction of islet beta-cell mass in spontaneously diabetic Goto-Kakizaki rats by alpha-glucosidase inhibitorM Koyama, R Wada, H Mizukami, et al.
Brain & Development|May 1, 1993
A case of Duchenne muscular dystrophy with truncated dystrophin. Significance of a cysteine-rich domain for functional expression of dystrophin proteinH Sakuraba, S Hori, S Ohtani, et al.
The British Journal of Dermatology|August 27, 2005
Immunoelectron-microscopic detection of globotriaosylceramide accumulated in the skin of patients with Fabry diseaseT Kanekura, T Fukushige, A Kanda, et al.
Biochemical and Biophysical Research Communications|June 24, 1998
Protective protein/cathepsin A loss in cultured cells derived from an early-infantile form of galactosialidosis patients homozygous for the A1184-G transition (Y395C mutation)K Itoh, M Shimmoto, K Utsumi, et al.
Brain & Development|March 1, 1997
Molecular form and subcellular distribution of acid beta-galactosidase in fibroblasts from patients with GM1 gangliosidosis, Morquio B disease and galactosialidosisN Takiyama, K Itoh, M Shimmoto, et al.
Clinical Genetics|May 1, 1996
Coexistence of gene mutations causing Fabry disease and Duchenne muscular dystrophy in a Japanese boyT Takenaka, H Sakuraba, K Hashimoto, et al.
American Journal of Human Genetics|August 1, 1991
Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic casesK Yoshida, A Oshima, M Shimmoto, et al.
The Biochemical Journal|May 20, 1999
Stable expression of protective protein/cathepsin A-green fluorescent protein fusion genes in a fibroblastic cell line from a galactosialidosis patient. Model system for revealing the intracellular transport of normal and mutated lysosomal enzymesY Naganawa, K Itoh, M Shimmoto, et al.
The Journal of Biological Chemistry|March 28, 1998
Lysenin, a novel sphingomyelin-specific binding proteinA Yamaji, Y Sekizawa, K Emoto, et al.
Journal of Biochemistry|December 1, 2000
Biochemical characterization, cloning, and sequencing of ADP-dependent (AMP-forming) glucokinase from two hyperthermophilic archaea, Pyrococcus furiosus and Thermococcus litoralisS Koga, I Yoshioka, H Sakuraba, et al.
Pageof 13

Showing results (71-80 of 128) with videos related to

Sort By:
Pageof 13
Metabolism: Clinical and Experimental|March 22, 2000
Inhibition of progressive reduction of islet beta-cell mass in spontaneously diabetic Goto-Kakizaki rats by alpha-glucosidase inhibitorM Koyama, R Wada, H Mizukami, et al.
Brain & Development|May 1, 1993
A case of Duchenne muscular dystrophy with truncated dystrophin. Significance of a cysteine-rich domain for functional expression of dystrophin proteinH Sakuraba, S Hori, S Ohtani, et al.
The British Journal of Dermatology|August 27, 2005
Immunoelectron-microscopic detection of globotriaosylceramide accumulated in the skin of patients with Fabry diseaseT Kanekura, T Fukushige, A Kanda, et al.
Biochemical and Biophysical Research Communications|June 24, 1998
Protective protein/cathepsin A loss in cultured cells derived from an early-infantile form of galactosialidosis patients homozygous for the A1184-G transition (Y395C mutation)K Itoh, M Shimmoto, K Utsumi, et al.
Brain & Development|March 1, 1997
Molecular form and subcellular distribution of acid beta-galactosidase in fibroblasts from patients with GM1 gangliosidosis, Morquio B disease and galactosialidosisN Takiyama, K Itoh, M Shimmoto, et al.
Clinical Genetics|May 1, 1996
Coexistence of gene mutations causing Fabry disease and Duchenne muscular dystrophy in a Japanese boyT Takenaka, H Sakuraba, K Hashimoto, et al.
American Journal of Human Genetics|August 1, 1991
Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic casesK Yoshida, A Oshima, M Shimmoto, et al.
The Biochemical Journal|May 20, 1999
Stable expression of protective protein/cathepsin A-green fluorescent protein fusion genes in a fibroblastic cell line from a galactosialidosis patient. Model system for revealing the intracellular transport of normal and mutated lysosomal enzymesY Naganawa, K Itoh, M Shimmoto, et al.
The Journal of Biological Chemistry|March 28, 1998
Lysenin, a novel sphingomyelin-specific binding proteinA Yamaji, Y Sekizawa, K Emoto, et al.
Journal of Biochemistry|December 1, 2000
Biochemical characterization, cloning, and sequencing of ADP-dependent (AMP-forming) glucokinase from two hyperthermophilic archaea, Pyrococcus furiosus and Thermococcus litoralisS Koga, I Yoshioka, H Sakuraba, et al.
Pageof 13