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No to Hattatsu = Brain and Development
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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 particles
Y 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 inhibitors
T 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 lipofuscinosis
T Ohashi, Y Kanamoto, S Yamaguchi, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1988
Clinical and biochemical studies of Japanese neuronal ceroid-lipofuscinosis
Y 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 leukodystrophy
H 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 cDNA
K 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 disease
M Kobayashi, T Ohashi, M Sakuma, et al.
Page
of 31
Search research articles
Search
Showing results (121-130 of 307) with videos related to
Sort By:
Page
of 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 particles
Y 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 inhibitors
T 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 lipofuscinosis
T Ohashi, Y Kanamoto, S Yamaguchi, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1988
Clinical and biochemical studies of Japanese neuronal ceroid-lipofuscinosis
Y 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 leukodystrophy
H 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 cDNA
K 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 disease
M Kobayashi, T Ohashi, M Sakuma, et al.
Page
of 31