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S Akaboshi

Showing results (51-60 of 64) with videos related to

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Brain & Development|April 17, 1998
Increased levels of GM2 ganglioside in fibroblasts from a patient with juvenile Niemann-Pick disease type CY Watanabe, S Akaboshi, G Ishida, et al.
Brain & Development|April 9, 1998
Accumulation of cholesterol and GM2 ganglioside in cells cultured in the presence of progesterone: an implication for the basic defect in Niemann-Pick disease type CM Sato, S Akaboshi, T Katsumoto, et al.
Chemical & Pharmaceutical Bulletin|May 1, 1985
Studies on topical antiinflammatory corticosteroids. I. Syntheses and vasoconstrictive activities of 11 beta,17 alpha,21-trihydroxy-6 alpha-methyl-1,4-pregnadiene-3,20-dione 17-ester and 17,21-diester derivativesS Sugai, T Okazaki, Y Kajiwara, et al.
Chemical & Pharmaceutical Bulletin|April 1, 1986
Studies on topical antiinflammatory corticosteroids. II. Synthesis and vasoconstrictive activity of 11 beta,17 alpha,21-trihydroxy-6 alpha-methyl-1,4-pregnadiene-3,20-dione 17-methoxy- and (methylthio)acetatesS Sugai, T Okazaki, Y Kajiwara, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan|October 1, 1985
[Studies on spasmolytics. VII. Pharmacological properties of 4-benziloyloxy- and 4-(Xanthene-9-carbonyloxy)-1-(1,3-dioxolan-2- ylmethyl)-1- methylpiperidinium salts]S Sugai, Y Kajiwara, T Kawada, et al.
Chemical & Pharmaceutical Bulletin|February 1, 1985
Structure-activity relationship of 3- and 4-acyloxy-1-(1,3-dioxolan-4-ylmethyl)piperidine derivativesS Yoshida, S Sugai, Y Kajiwara, et al.
American Journal of Medical Genetics|February 5, 1998
Ataxia-telangiectasia without immunodeficiency: novel point mutations within and adjacent to the phosphatidylinositol 3-kinase-like domainM Toyoshima, T Hara, H Zhang, et al.
American Journal of Human Genetics|January 1, 1994
Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysisY Suzuki, N Shimozawa, S Yajima, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Prenatal diagnosis of succinate semialdehyde dehydrogenase deficiency in non-identical twinsI A Aligianis, P A Farndon, R G F Gray, et al.
American Journal of Medical Genetics|March 9, 1999
Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cystH Zhang, T Yamamoto, E Nanba, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Brain & Development|April 17, 1998
Increased levels of GM2 ganglioside in fibroblasts from a patient with juvenile Niemann-Pick disease type CY Watanabe, S Akaboshi, G Ishida, et al.
Brain & Development|April 9, 1998
Accumulation of cholesterol and GM2 ganglioside in cells cultured in the presence of progesterone: an implication for the basic defect in Niemann-Pick disease type CM Sato, S Akaboshi, T Katsumoto, et al.
Chemical & Pharmaceutical Bulletin|May 1, 1985
Studies on topical antiinflammatory corticosteroids. I. Syntheses and vasoconstrictive activities of 11 beta,17 alpha,21-trihydroxy-6 alpha-methyl-1,4-pregnadiene-3,20-dione 17-ester and 17,21-diester derivativesS Sugai, T Okazaki, Y Kajiwara, et al.
Chemical & Pharmaceutical Bulletin|April 1, 1986
Studies on topical antiinflammatory corticosteroids. II. Synthesis and vasoconstrictive activity of 11 beta,17 alpha,21-trihydroxy-6 alpha-methyl-1,4-pregnadiene-3,20-dione 17-methoxy- and (methylthio)acetatesS Sugai, T Okazaki, Y Kajiwara, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan|October 1, 1985
[Studies on spasmolytics. VII. Pharmacological properties of 4-benziloyloxy- and 4-(Xanthene-9-carbonyloxy)-1-(1,3-dioxolan-2- ylmethyl)-1- methylpiperidinium salts]S Sugai, Y Kajiwara, T Kawada, et al.
Chemical & Pharmaceutical Bulletin|February 1, 1985
Structure-activity relationship of 3- and 4-acyloxy-1-(1,3-dioxolan-4-ylmethyl)piperidine derivativesS Yoshida, S Sugai, Y Kajiwara, et al.
American Journal of Medical Genetics|February 5, 1998
Ataxia-telangiectasia without immunodeficiency: novel point mutations within and adjacent to the phosphatidylinositol 3-kinase-like domainM Toyoshima, T Hara, H Zhang, et al.
American Journal of Human Genetics|January 1, 1994
Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysisY Suzuki, N Shimozawa, S Yajima, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Prenatal diagnosis of succinate semialdehyde dehydrogenase deficiency in non-identical twinsI A Aligianis, P A Farndon, R G F Gray, et al.
American Journal of Medical Genetics|March 9, 1999
Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cystH Zhang, T Yamamoto, E Nanba, et al.
Pageof 7