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H Sakuraba

Showing results (81-90 of 128) with videos related to

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The American Journal of Cardiology|July 1, 1996
Immunofluorescence analysis of trihexosylceramide accumulated in the hearts of variant hemizygotes and heterozygotes with Fabry diseaseK Itoh, T Takenaka, S Nakao, et al.
Human Gene Therapy|December 28, 1999
Retrovirus-mediated transfer of human alpha-galactosidase A gene to human CD34+ hematopoietic progenitor cellsN Takiyama, J T Dunigan, M J Vallor, et al.
FEBS Letters|December 12, 1997
Generation and characterization of transgenic mice expressing a human mutant alpha-galactosidase with an R301Q substitution causing a variant form of Fabry diseaseM Shimmoto, R Kase, K Itoh, et al.
Biochimica Et Biophysica Acta|June 6, 2000
Characterization of two alpha-galactosidase mutants (Q279E and R301Q) found in an atypical variant of Fabry diseaseR Kase, U Bierfreund, A Klein, et al.
The Journal of Biological Chemistry|January 15, 1993
Purification and characterization of human lysosomal protective protein expressed in stably transformed Chinese hamster ovary cellsK Itoh, N Takiyama, R Kase, et al.
Biochimica Et Biophysica Acta|February 16, 1994
Human alpha-galactosidase gene expression: significance of two peptide regions encoded by exons 1-2 and 6S Ishii, R Kase, H Sakuraba, et al.
Oncogene|January 20, 2009
Contribution of sialidase NEU1 to suppression of metastasis of human colon cancer cells through desialylation of integrin beta4T Uemura, K Shiozaki, K Yamaguchi, et al.
Extremophiles : Life Under Extreme Conditions|January 4, 2001
Glutamate dehydrogenase from the aerobic hyperthermophilic archaeon Aeropyrum pernix K1: enzymatic characterization, identification of the encoding gene, and phylogenetic implicationsM W Bhuiya, H Sakuraba, C Kujo, et al.
Biochimica Et Biophysica Acta|June 19, 1998
Immunohistochemical characterization of transgenic mice highly expressing human lysosomal alpha-galactosidaseR Kase, M Shimmoto, K Itoh, et al.
Biochemical and Biophysical Research Communications|July 16, 1990
Partial deletion of human alpha-galactosidase A gene in Fabry disease: direct repeat sequences as a possible cause of slipped mispairingY Fukuhara, H Sakuraba, A Oshima, et al.
Pageof 13

Showing results (81-90 of 128) with videos related to

Sort By:
Pageof 13
The American Journal of Cardiology|July 1, 1996
Immunofluorescence analysis of trihexosylceramide accumulated in the hearts of variant hemizygotes and heterozygotes with Fabry diseaseK Itoh, T Takenaka, S Nakao, et al.
Human Gene Therapy|December 28, 1999
Retrovirus-mediated transfer of human alpha-galactosidase A gene to human CD34+ hematopoietic progenitor cellsN Takiyama, J T Dunigan, M J Vallor, et al.
FEBS Letters|December 12, 1997
Generation and characterization of transgenic mice expressing a human mutant alpha-galactosidase with an R301Q substitution causing a variant form of Fabry diseaseM Shimmoto, R Kase, K Itoh, et al.
Biochimica Et Biophysica Acta|June 6, 2000
Characterization of two alpha-galactosidase mutants (Q279E and R301Q) found in an atypical variant of Fabry diseaseR Kase, U Bierfreund, A Klein, et al.
The Journal of Biological Chemistry|January 15, 1993
Purification and characterization of human lysosomal protective protein expressed in stably transformed Chinese hamster ovary cellsK Itoh, N Takiyama, R Kase, et al.
Biochimica Et Biophysica Acta|February 16, 1994
Human alpha-galactosidase gene expression: significance of two peptide regions encoded by exons 1-2 and 6S Ishii, R Kase, H Sakuraba, et al.
Oncogene|January 20, 2009
Contribution of sialidase NEU1 to suppression of metastasis of human colon cancer cells through desialylation of integrin beta4T Uemura, K Shiozaki, K Yamaguchi, et al.
Extremophiles : Life Under Extreme Conditions|January 4, 2001
Glutamate dehydrogenase from the aerobic hyperthermophilic archaeon Aeropyrum pernix K1: enzymatic characterization, identification of the encoding gene, and phylogenetic implicationsM W Bhuiya, H Sakuraba, C Kujo, et al.
Biochimica Et Biophysica Acta|June 19, 1998
Immunohistochemical characterization of transgenic mice highly expressing human lysosomal alpha-galactosidaseR Kase, M Shimmoto, K Itoh, et al.
Biochemical and Biophysical Research Communications|July 16, 1990
Partial deletion of human alpha-galactosidase A gene in Fabry disease: direct repeat sequences as a possible cause of slipped mispairingY Fukuhara, H Sakuraba, A Oshima, et al.
Pageof 13