Showing results (1-10 of 2,098) with videos related to

Sort By:
Pageof 210
Brain & Development|September 1, 1996
Gene therapy in Duchenne muscular dystrophyK Inui, S Okada, G Dickson
Gene Therapy|June 1, 1996
Expression of full-length human dystrophin cDNA in mdx mouse muscle by HVJ-liposome injectionI Yanagihara, K Inui, G Dickson, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|September 1, 1993
[Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods]H Tsukamoto, K Inui, S Okada
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Krabbe disease (globoid cell leukodystrophy)]N Sakai, K Inui, S Okada
Gene Therapy|August 24, 1999
Enhanced expression of recombinant dystrophin following intramuscular injection of Epstein-Barr virus (EBV)-based mini-chromosome vectors in mdx miceH Tsukamoto, D Wells, S Brown, et al.
The Japanese Journal of Human Genetics|December 1, 1996
Allele frequencies of intragenic, and 5' and 3' markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophyH Tsukamoto, K Inui, H Fukushima, et al.
Biochemistry International|June 1, 1989
Impaired cholesterol esterification in cultured skin fibroblasts from patients with I-cell disease and pseudo-Hurler polydystrophyK Inui, J Nishimoto, S Okada, et al.
The Journal of Clinical Investigation|February 1, 1988
Metabolism of cerebroside sulfate and subcellular distribution of its metabolites in cultured skin fibroblasts from controls, metachromatic leukodystrophy, and globoid cell leukodystrophyK Inui, M Furukawa, S Okada, et al.
The Tohoku Journal of Experimental Medicine|August 1, 1980
Studies on alpha-ketoglutaric aciduria in type I glycogenosisH Kodama, S Okada, K Inui, et al.
American Journal of Human Genetics|September 1, 1991
GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patientsJ Nishimoto, E Nanba, K Inui, et al.
Pageof 210