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K Ikeya

Showing results (11-20 of 19) with videos related to

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American Journal of Medical Genetics|March 13, 1995
Somatic mosaicism for a DMD gene deletionK Saito, K Ikeya, E Kondo, et al.
Acta Neuropathologica|August 1, 1997
Localization of laminin subunits in the central nervous system in Fukuyama congenital muscular dystrophy: an immunohistochemical investigationT Yamamoto, N Shibata, M Kanazawa, et al.
No to Hattatsu = Brain and Development|July 1, 1989
[Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA]K Saito, A Tanaka, T Harada, et al.
American Journal of Medical Genetics|June 1, 1992
Molecular genetic and immunological analysis of dystrophin of a young patient with X-linked muscular dystrophyK Ikeya, K Saito, K Hayashi, et al.
No to Hattatsu = Brain and Development|July 1, 1993
[Clinical significance of dystrophin test for patients with various neuromuscular diseases--immunofluorescence and immunoblot analyses of dystrophin abnormalities]K Ikeya, K Saito, A Yamauchi, et al.
American Journal of Human Genetics|April 1, 1991
Human CYP1A1 gene: cosegregation of the enzyme inducibility phenotype and an RFLPD D Petersen, C E McKinney, K Ikeya, et al.
American Journal of Medical Genetics|May 26, 1998
Prenatal diagnosis of Fukuyama type congenital muscular dystrophy in eight Japanese families by haplotype analysis using new markers closest to the geneK Saito, E Kondo-Iida, Y Kawakita, et al.
American Journal of Medical Genetics|May 19, 2000
Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophyK Saito, M Osawa, Z P Wang, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|February 26, 2008
Intensive granulocyte and monocyte adsorption versus intravenous prednisolone in patients with severe ulcerative colitis: an unblinded randomised multi-centre controlled studyH Hanai, T Iida, K Takeuchi, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
American Journal of Medical Genetics|March 13, 1995
Somatic mosaicism for a DMD gene deletionK Saito, K Ikeya, E Kondo, et al.
Acta Neuropathologica|August 1, 1997
Localization of laminin subunits in the central nervous system in Fukuyama congenital muscular dystrophy: an immunohistochemical investigationT Yamamoto, N Shibata, M Kanazawa, et al.
No to Hattatsu = Brain and Development|July 1, 1989
[Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA]K Saito, A Tanaka, T Harada, et al.
American Journal of Medical Genetics|June 1, 1992
Molecular genetic and immunological analysis of dystrophin of a young patient with X-linked muscular dystrophyK Ikeya, K Saito, K Hayashi, et al.
No to Hattatsu = Brain and Development|July 1, 1993
[Clinical significance of dystrophin test for patients with various neuromuscular diseases--immunofluorescence and immunoblot analyses of dystrophin abnormalities]K Ikeya, K Saito, A Yamauchi, et al.
American Journal of Human Genetics|April 1, 1991
Human CYP1A1 gene: cosegregation of the enzyme inducibility phenotype and an RFLPD D Petersen, C E McKinney, K Ikeya, et al.
American Journal of Medical Genetics|May 26, 1998
Prenatal diagnosis of Fukuyama type congenital muscular dystrophy in eight Japanese families by haplotype analysis using new markers closest to the geneK Saito, E Kondo-Iida, Y Kawakita, et al.
American Journal of Medical Genetics|May 19, 2000
Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophyK Saito, M Osawa, Z P Wang, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|February 26, 2008
Intensive granulocyte and monocyte adsorption versus intravenous prednisolone in patients with severe ulcerative colitis: an unblinded randomised multi-centre controlled studyH Hanai, T Iida, K Takeuchi, et al.
Pageof 2