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H Sakuraba

Showing results (1-10 of 128) with videos related to

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Rinsho Byori. the Japanese Journal of Clinical Pathology|June 1, 1994
[Molecular genetics of inherited metabolic diseases--its application to the investigation of pathogenesis and the diagnosis of Fabry disease]H Sakuraba
Brain & Development|January 1, 1983
Biochemical analysis of cerebrum of fetal rat X-irradiated in utero--DNA, RNA, superoxide dismutase and lipid peroxide--H Sakuraba, H Tanaka
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Fabry disease (alpha-galactosidase deficiency)]T Okumiya, H Sakuraba
The Journal of Biological Chemistry|January 6, 1995
Alcohol:NAD+ oxidoreductase is present in rat liver peroxisomesH Sakuraba, T Noguchi
American Journal of Hematology|May 1, 1986
Activation of platelet function in Fabry's diseaseT Igarashi, H Sakuraba, Y Suzuki
Archives of Biochemistry and Biophysics|May 1, 1994
Identification of chicken liver mitochondrial alanine:2-oxoglutarate aminotransferase and its response to starvationS Fujiwara, H Sakuraba, T Noguchi
Biochemical and Biophysical Research Communications|June 15, 1989
Alanine:glyoxylate aminotransferase is present as the apoenzyme in the peroxisomes of chicken kidneyH Sakuraba, S Fujiwara, T Noguchi
Human Genetics|April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry diseaseS Ishii, H Sakuraba, Y Suzuki
Biochemical and Biophysical Research Communications|May 15, 1991
Intraperoxisomal form of alanine:glyoxylate aminotransferase in the peroxisomes of bird kidneyH Sakuraba, S Fujiwara, T Noguchi
Biochemical and Biophysical Research Communications|November 30, 1989
Response of hepatic alanine:glyoxylate aminotransferase 1 to hormone differs among mammaliaS Hayashi, H Sakuraba, T Noguchi
Pageof 13

Showing results (1-10 of 128) with videos related to

Sort By:
Pageof 13
Rinsho Byori. the Japanese Journal of Clinical Pathology|June 1, 1994
[Molecular genetics of inherited metabolic diseases--its application to the investigation of pathogenesis and the diagnosis of Fabry disease]H Sakuraba
Brain & Development|January 1, 1983
Biochemical analysis of cerebrum of fetal rat X-irradiated in utero--DNA, RNA, superoxide dismutase and lipid peroxide--H Sakuraba, H Tanaka
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Fabry disease (alpha-galactosidase deficiency)]T Okumiya, H Sakuraba
The Journal of Biological Chemistry|January 6, 1995
Alcohol:NAD+ oxidoreductase is present in rat liver peroxisomesH Sakuraba, T Noguchi
American Journal of Hematology|May 1, 1986
Activation of platelet function in Fabry's diseaseT Igarashi, H Sakuraba, Y Suzuki
Archives of Biochemistry and Biophysics|May 1, 1994
Identification of chicken liver mitochondrial alanine:2-oxoglutarate aminotransferase and its response to starvationS Fujiwara, H Sakuraba, T Noguchi
Biochemical and Biophysical Research Communications|June 15, 1989
Alanine:glyoxylate aminotransferase is present as the apoenzyme in the peroxisomes of chicken kidneyH Sakuraba, S Fujiwara, T Noguchi
Human Genetics|April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry diseaseS Ishii, H Sakuraba, Y Suzuki
Biochemical and Biophysical Research Communications|May 15, 1991
Intraperoxisomal form of alanine:glyoxylate aminotransferase in the peroxisomes of bird kidneyH Sakuraba, S Fujiwara, T Noguchi
Biochemical and Biophysical Research Communications|November 30, 1989
Response of hepatic alanine:glyoxylate aminotransferase 1 to hormone differs among mammaliaS Hayashi, H Sakuraba, T Noguchi
Pageof 13