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Showing results (191-200 of 276) with videos related to

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The Journal of Pediatrics|October 1, 1995
Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation groupA Poulos, J Christodoulou, C W Chow, et al.
Human Mutation|January 1, 1996
Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populationsA Yamagishi, S Tomatsu, S Fukuda, et al.
Acta Paediatrica Japonica : Overseas Edition|August 1, 1992
Neuroradiological findings in glutaric aciduria type I: report of four Japanese patientsH Nagasawa, S Yamaguchi, Y Suzuki, et al.
Brain & Development|April 13, 2000
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humansA Imamura, N Shimozawa, Y Suzuki, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications|August 3, 2001
Urinary organic acids in peroxisomal disorders: a simple screening methodS Yamaguchi, M Iga, M Kimura, et al.
Gene|May 14, 1990
Molecular basis of mucopolysaccharidosis type VII: replacement of Ala619 in beta-glucuronidase with ValS Tomatsu, K Sukegawa, Y Ikedo, et al.
Transplantation|June 29, 1999
Elimination of Kupffer cells and nafamostat mesilate rinse prevent reperfusion injury in liver grafts from agonal non-heart-beating donorsS Tsukamoto, N Ohkohchi, T Fukumori, et al.
Experimental Cell Research|May 25, 1997
Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group IIIK Okumoto, A Bogaki, K Tateishi, et al.
Human Molecular Genetics|April 1, 1995
Four novel mutations in mucopolysaccharidosis type VII including a unique base substitution in exon 10 of the beta-glucuronidase gene that creates a novel 5'-splice siteS Yamada, S Tomatsu, W S Sly, et al.
Biotherapy (Dordrecht, Netherlands)|January 1, 1994
Proliferative responses towards native, heat-denatured and pepsin-treated ovalbumin by peripheral blood mononuclear cells from patients with hen's egg-sensitive atopic dermatitisT Nishida, N Kondo, H Agata, et al.
Pageof 28

Showing results (191-200 of 276) with videos related to

Sort By:
Pageof 28
The Journal of Pediatrics|October 1, 1995
Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation groupA Poulos, J Christodoulou, C W Chow, et al.
Human Mutation|January 1, 1996
Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populationsA Yamagishi, S Tomatsu, S Fukuda, et al.
Acta Paediatrica Japonica : Overseas Edition|August 1, 1992
Neuroradiological findings in glutaric aciduria type I: report of four Japanese patientsH Nagasawa, S Yamaguchi, Y Suzuki, et al.
Brain & Development|April 13, 2000
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humansA Imamura, N Shimozawa, Y Suzuki, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications|August 3, 2001
Urinary organic acids in peroxisomal disorders: a simple screening methodS Yamaguchi, M Iga, M Kimura, et al.
Gene|May 14, 1990
Molecular basis of mucopolysaccharidosis type VII: replacement of Ala619 in beta-glucuronidase with ValS Tomatsu, K Sukegawa, Y Ikedo, et al.
Transplantation|June 29, 1999
Elimination of Kupffer cells and nafamostat mesilate rinse prevent reperfusion injury in liver grafts from agonal non-heart-beating donorsS Tsukamoto, N Ohkohchi, T Fukumori, et al.
Experimental Cell Research|May 25, 1997
Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group IIIK Okumoto, A Bogaki, K Tateishi, et al.
Human Molecular Genetics|April 1, 1995
Four novel mutations in mucopolysaccharidosis type VII including a unique base substitution in exon 10 of the beta-glucuronidase gene that creates a novel 5'-splice siteS Yamada, S Tomatsu, W S Sly, et al.
Biotherapy (Dordrecht, Netherlands)|January 1, 1994
Proliferative responses towards native, heat-denatured and pepsin-treated ovalbumin by peripheral blood mononuclear cells from patients with hen's egg-sensitive atopic dermatitisT Nishida, N Kondo, H Agata, et al.
Pageof 28