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H Sakuraba

Showing results (11-20 of 128) with videos related to

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Biochemical and Biophysical Research Communications|December 13, 1996
Metabolism of glyoxylate, the end product of purin degradation, in liver peroxisomes of fresh water fishH Sakuraba, S Fujiwara, T Noguchi
Archives of Biochemistry and Biophysics|May 1, 1991
Purification and characterization of peroxisomal apo and holo alanine:glyoxylate aminotransferase from bird liverH Sakuraba, S Fujiwara, T Noguchi
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.
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.
Clinical Genetics|May 1, 1987
Effect of vitamin E and ticlopidine on platelet aggregation in Fabry's diseaseH Sakuraba, T Igarashi, T Shibata, et al.
Biochimica Et Biophysica Acta|October 19, 1999
The NAD-dependent glutamate dehydrogenase from the hyperthermophilic archaeon Pyrobaculum islandicum: cloning, sequencing, and expression of the enzyme gene(1)C Kujo, H Sakuraba, N Nunoura, et al.
Biochemical and Biophysical Research Communications|April 30, 1993
The major mutation among Japanese patients with infantile Tay-Sachs disease: a G-to-T transversion at the acceptor site of intron 5 of the beta-hexosaminidase alpha geneA Tanaka, H Sakuraba, G Isshiki, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|February 1, 1997
[alpha-Galactosidase gene mutation and its expression product in Fabry disease (alpha-galactosidase deficiency)]T Okumiya, T Takata, M Sasaki, et al.
European Journal of Biochemistry|September 5, 2001
A novel hyperthermophilic archaeal glyoxylate reductase from Thermococcus litoralis. Characterization, gene cloning, nucleotide sequence and expression in Escherichia coliT Ohshima, N Nunoura-Kominato, T Kudome, et al.
Pageof 13

Showing results (11-20 of 128) with videos related to

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Pageof 13
Biochemical and Biophysical Research Communications|December 13, 1996
Metabolism of glyoxylate, the end product of purin degradation, in liver peroxisomes of fresh water fishH Sakuraba, S Fujiwara, T Noguchi
Archives of Biochemistry and Biophysics|May 1, 1991
Purification and characterization of peroxisomal apo and holo alanine:glyoxylate aminotransferase from bird liverH Sakuraba, S Fujiwara, T Noguchi
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.
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.
Clinical Genetics|May 1, 1987
Effect of vitamin E and ticlopidine on platelet aggregation in Fabry's diseaseH Sakuraba, T Igarashi, T Shibata, et al.
Biochimica Et Biophysica Acta|October 19, 1999
The NAD-dependent glutamate dehydrogenase from the hyperthermophilic archaeon Pyrobaculum islandicum: cloning, sequencing, and expression of the enzyme gene(1)C Kujo, H Sakuraba, N Nunoura, et al.
Biochemical and Biophysical Research Communications|April 30, 1993
The major mutation among Japanese patients with infantile Tay-Sachs disease: a G-to-T transversion at the acceptor site of intron 5 of the beta-hexosaminidase alpha geneA Tanaka, H Sakuraba, G Isshiki, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|February 1, 1997
[alpha-Galactosidase gene mutation and its expression product in Fabry disease (alpha-galactosidase deficiency)]T Okumiya, T Takata, M Sasaki, et al.
European Journal of Biochemistry|September 5, 2001
A novel hyperthermophilic archaeal glyoxylate reductase from Thermococcus litoralis. Characterization, gene cloning, nucleotide sequence and expression in Escherichia coliT Ohshima, N Nunoura-Kominato, T Kudome, et al.
Pageof 13