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Showing results (121-130 of 307) with videos related to

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No to Hattatsu = Brain and Development|September 18, 2001
[Investigation to sequelae of acute encephalopathy]M Kurihara, Y Nakae, T Kohagisawa, et al.
Archives of Biochemistry and Biophysics|May 15, 1992
Succinate-dependent lipid peroxidation and its prevention by reduced ubiquinone in beef heart submitochondrial particlesY Eto, D Kang, E Hasegawa, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Type C Niemann-Pick disease fibroblasts and their transformed cell lines are hypersensitive to HMG-CoA reductase inhibitorsT Yamamoto, T Ohashi, T Tokoro, et al.
The Tohoku Journal of Experimental Medicine|April 1, 1986
Abnormal excretion of autofluorescent lipids in urine from patients with neuronal ceroid lipofuscinosisT Ohashi, Y Kanamoto, S Yamaguchi, et al.
American Journal of Medical Genetics. Supplement|January 1, 1988
Clinical and biochemical studies of Japanese neuronal ceroid-lipofuscinosisY Eto, T Tsuda, T Ohhashi, et al.
Biochemical and Biophysical Research Communications|January 30, 1990
Galactosylceramide and galactosylsphingosine loading studies in cultured skin fibroblasts in human and murine globoid cell leukodystrophyH Ida, K Kusano, H Suzuki, et al.
Biochemical and Biophysical Research Communications|March 15, 1985
Enzyme replacement with liposomes containing beta-galactosidase from Charonia lumpas in murine globoid cell leukodystrophy (twitcher)F Umezawa, Y Eto, T Tokoro, et al.
Biochemical and Biophysical Research Communications|November 24, 1999
Differentiation-induced insulin secretion from nonendocrine cells with engineered human proinsulin cDNAK Yamasaki, T Sasaki, M Nemoto, et al.
Human Cell|December 1, 1990
[Molecular basis of organic acidemia--propionic acidemia]T Tahara, Y Eto, J P Kraus, et al.
Journal of Inherited Metabolic Disease|January 19, 2008
Clinical manifestations and natural history of Japanese heterozygous females with Fabry diseaseM Kobayashi, T Ohashi, M Sakuma, et al.
Pageof 31

Showing results (121-130 of 307) with videos related to

Sort By:
Pageof 31
No to Hattatsu = Brain and Development|September 18, 2001
[Investigation to sequelae of acute encephalopathy]M Kurihara, Y Nakae, T Kohagisawa, et al.
Archives of Biochemistry and Biophysics|May 15, 1992
Succinate-dependent lipid peroxidation and its prevention by reduced ubiquinone in beef heart submitochondrial particlesY Eto, D Kang, E Hasegawa, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Type C Niemann-Pick disease fibroblasts and their transformed cell lines are hypersensitive to HMG-CoA reductase inhibitorsT Yamamoto, T Ohashi, T Tokoro, et al.
The Tohoku Journal of Experimental Medicine|April 1, 1986
Abnormal excretion of autofluorescent lipids in urine from patients with neuronal ceroid lipofuscinosisT Ohashi, Y Kanamoto, S Yamaguchi, et al.
American Journal of Medical Genetics. Supplement|January 1, 1988
Clinical and biochemical studies of Japanese neuronal ceroid-lipofuscinosisY Eto, T Tsuda, T Ohhashi, et al.
Biochemical and Biophysical Research Communications|January 30, 1990
Galactosylceramide and galactosylsphingosine loading studies in cultured skin fibroblasts in human and murine globoid cell leukodystrophyH Ida, K Kusano, H Suzuki, et al.
Biochemical and Biophysical Research Communications|March 15, 1985
Enzyme replacement with liposomes containing beta-galactosidase from Charonia lumpas in murine globoid cell leukodystrophy (twitcher)F Umezawa, Y Eto, T Tokoro, et al.
Biochemical and Biophysical Research Communications|November 24, 1999
Differentiation-induced insulin secretion from nonendocrine cells with engineered human proinsulin cDNAK Yamasaki, T Sasaki, M Nemoto, et al.
Human Cell|December 1, 1990
[Molecular basis of organic acidemia--propionic acidemia]T Tahara, Y Eto, J P Kraus, et al.
Journal of Inherited Metabolic Disease|January 19, 2008
Clinical manifestations and natural history of Japanese heterozygous females with Fabry diseaseM Kobayashi, T Ohashi, M Sakuma, et al.
Pageof 31