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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 inhibitor
M 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 protein
H 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 disease
T 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 galactosialidosis
N 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 boy
T 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 cases
K 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 enzymes
Y Naganawa, K Itoh, M Shimmoto, et al.
The Journal of Biological Chemistry
|
March 28, 1998
Lysenin, a novel sphingomyelin-specific binding protein
A 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 litoralis
S Koga, I Yoshioka, H Sakuraba, et al.
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Search research articles
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Showing results (71-80 of 128) with videos related to
Sort By:
Page
of 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 inhibitor
M 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 protein
H 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 disease
T 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 galactosialidosis
N 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 boy
T 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 cases
K 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 enzymes
Y Naganawa, K Itoh, M Shimmoto, et al.
The Journal of Biological Chemistry
|
March 28, 1998
Lysenin, a novel sphingomyelin-specific binding protein
A 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 litoralis
S Koga, I Yoshioka, H Sakuraba, et al.
Page
of 13