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H Sakuraba

Showing results (111-120 of 128) with videos related to

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Annals of Neurology|March 1, 1992
GM1 gangliosidosis in adults: clinical and molecular analysis of 16 Japanese patientsK Yoshida, A Oshima, H Sakuraba, et al.
The New England Journal of Medicine|August 3, 1995
An atypical variant of Fabry's disease in men with left ventricular hypertrophyS Nakao, T Takenaka, M Maeda, et al.
Clinical Nephrology|February 1, 1997
Subclinical Fabry's disease occurring in the context of IgA nephropathyO Kawamura, H Sakuraba, K Itoh, et al.
Glycoconjugate Journal|January 9, 1999
Alpha-galactosidase transgenic mouse: heterogeneous gene expression and posttranslational glycosylation in tissuesS Ishii, R Kase, H Sakuraba, et al.
Biochimica Et Biophysica Acta|November 16, 1993
Cloning and sequence analysis of a full length cDNA encoding human mitochondrial 3-oxoacyl-CoA thiolaseH Abe, A Ohtake, S Yamamoto, et al.
Cell Structure and Function|April 1, 1994
Evidence for direct binding of intracellularly distributed ganglioside GM2 to isolated vimentin intermediate filaments in normal and Tay-Sachs disease human fibroblastsM Kotani, H Hosoya, H Kubo, et al.
Applied Microbiology and Biotechnology|October 18, 2003
Expression of foreign proteins in Escherichia coli by fusing with an archaeal FK506 binding proteinA Ideno, M Furutani, T Iwabuchi, et al.
Brain & Development|July 1, 1993
Prenatal diagnosis of GM2-gangliosidosis. Immunofluorescence analysis of ganglioside GM2 in cultured amniocytes by confocal laser scanning microscopyH Sakuraba, K Itoh, M Kotani, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 1999
Urinary excretion of the vitronectin receptor (integrin alpha V beta 3) in patients with Fabry diseaseK Utsumi, K Itoh, R Kase, et al.
Biochemical and Biophysical Research Communications|March 29, 1991
Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiencyP Hu, A J Reuser, H C Janse, et al.
Pageof 13

Showing results (111-120 of 128) with videos related to

Sort By:
Pageof 13
Annals of Neurology|March 1, 1992
GM1 gangliosidosis in adults: clinical and molecular analysis of 16 Japanese patientsK Yoshida, A Oshima, H Sakuraba, et al.
The New England Journal of Medicine|August 3, 1995
An atypical variant of Fabry's disease in men with left ventricular hypertrophyS Nakao, T Takenaka, M Maeda, et al.
Clinical Nephrology|February 1, 1997
Subclinical Fabry's disease occurring in the context of IgA nephropathyO Kawamura, H Sakuraba, K Itoh, et al.
Glycoconjugate Journal|January 9, 1999
Alpha-galactosidase transgenic mouse: heterogeneous gene expression and posttranslational glycosylation in tissuesS Ishii, R Kase, H Sakuraba, et al.
Biochimica Et Biophysica Acta|November 16, 1993
Cloning and sequence analysis of a full length cDNA encoding human mitochondrial 3-oxoacyl-CoA thiolaseH Abe, A Ohtake, S Yamamoto, et al.
Cell Structure and Function|April 1, 1994
Evidence for direct binding of intracellularly distributed ganglioside GM2 to isolated vimentin intermediate filaments in normal and Tay-Sachs disease human fibroblastsM Kotani, H Hosoya, H Kubo, et al.
Applied Microbiology and Biotechnology|October 18, 2003
Expression of foreign proteins in Escherichia coli by fusing with an archaeal FK506 binding proteinA Ideno, M Furutani, T Iwabuchi, et al.
Brain & Development|July 1, 1993
Prenatal diagnosis of GM2-gangliosidosis. Immunofluorescence analysis of ganglioside GM2 in cultured amniocytes by confocal laser scanning microscopyH Sakuraba, K Itoh, M Kotani, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 1999
Urinary excretion of the vitronectin receptor (integrin alpha V beta 3) in patients with Fabry diseaseK Utsumi, K Itoh, R Kase, et al.
Biochemical and Biophysical Research Communications|March 29, 1991
Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiencyP Hu, A J Reuser, H C Janse, et al.
Pageof 13