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Clinica Chimica Acta; International Journal of Clinical Chemistry|April 29, 1988
A high-performance liquid chromatographic assay for acid ceramidase activity in cultured fibroblasts from patients with Farber's disease and from controlsK Mitsuo, T Kobayashi, N Shinnoh, et al.The Journal of Biological Chemistry|December 5, 1985
Hydrolysis of galactosylceramide is catalyzed by two genetically distinct acid beta-galactosidasesT Kobayashi, N Shinnoh, I Goto, et al.Journal of the Neurological Sciences|February 1, 1985
Fabry's disease with partially deficient hydrolysis of ceramide trihexosideT Kobayashi, J Kira, N Shinnoh, et al.Journal of Biochemistry|January 1, 1994
Glucosylceramide and glucosylsphingosine metabolism in cultured fibroblasts deficient in acid beta-glucosidase activityN Sasagasako, T Kobayashi, Y Yamaguchi, et al.Clinical Genetics|July 1, 1993
Prenatal diagnosis of congenital sialidosisN Sasagasako, S Miyahara, N Saito, et al.Journal of Inherited Metabolic Disease|October 14, 2000
Lovastatin does not correct the accumulation of very long-chain fatty acids in tissues of adrenoleukodystrophy protein-deficient miceT Yamada, N Shinnoh, T Taniwaki, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 1998
Expression and processing of recombinant human galactosylceramidaseS Nagano, T Yamada, N Shinnoh, et al.Biochemical and Biophysical Research Communications|June 15, 1994
Adrenoleukodystrophy gene encodes an 80 kDa membrane proteinT Kobayashi, T Yamada, T Yasutake, et al.Journal of the Neurological Sciences|July 1, 1995
Molecular analysis of X-linked adrenoleukodystrophy patientsT Yasutake, T Yamada, H Furuya, et al.Cell Biochemistry and Biophysics|May 2, 2001
Very-long-chain fatty acid metabolism in adrenoleukodystrophy protein-deficient miceT Yamada, N Shinnoh, A Kondo, et al.Pageof 3