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T Fukao

Showing results (51-60 of 139) with videos related to

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The Journal of Experimental Medicine|June 22, 1999
Interleukin 12-dependent interferon gamma production by CD8alpha+ lymphoid dendritic cellsT Ohteki, T Fukao, K Suzue, et al.
Clinical and Experimental Immunology|April 17, 2004
Molecular analysis of B-cell differentiation in selective or partial IgA deficiencyT Asano, H Kaneko, T Terada, et al.
Pediatric Research|May 1, 1993
Biochemical and immunochemical study of seven families with 3-ketothiolase deficiency: diagnosis of heterozygotes using immunochemical determination of the ratio of mitochondrial acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase proteinsS Yamaguchi, A Sakai, T Fukao, et al.
Scandinavian Journal of Immunology|February 1, 1997
Reduced expression of the interferon-gamma messenger RNA in IgG2 deficiencyN Kondo, R Inoue, K Kasahara, et al.
Journal of Investigational Allergology & Clinical Immunology|July 1, 1997
Inhibition of interferon-gamma production from lymphocytes stimulated with food antigens by a beta 2-agonist, procaterol, in patients with food-sensitive atopic dermatitisN Kondo, M Shinbara, R Inoue, et al.
The Tohoku Journal of Experimental Medicine|June 1, 1992
Further analysis of mutant thiolase protein in fibroblasts from a Japanese boy with 3-ketothiolase deficiencyS Yamaguchi, T Fukao, M Kano, et al.
Journal of Biochemistry|August 1, 1989
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolaseT Fukao, K Kamijo, T Osumi, et al.
The Journal of Clinical Investigation|December 1, 1990
Molecular cloning and sequence of the complementary DNA encoding human mitochondrial acetoacetyl-coenzyme A thiolase and study of the variant enzymes in cultured fibroblasts from patients with 3-ketothiolase deficiencyT Fukao, S Yamaguchi, M Kano, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular basis of 3-ketothiolase deficiency: detection of gene mutations and expression of mutant cDNAs of mitochondrial acetoacetyl-CoA thiolaseT Fukao, S Yamaguchi, A Wakazono, et al.
Prenatal Diagnosis|March 1, 1996
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysisA Imamura, Y Suzuki, X Q Song, et al.
Pageof 14

Showing results (51-60 of 139) with videos related to

Sort By:
Pageof 14
The Journal of Experimental Medicine|June 22, 1999
Interleukin 12-dependent interferon gamma production by CD8alpha+ lymphoid dendritic cellsT Ohteki, T Fukao, K Suzue, et al.
Clinical and Experimental Immunology|April 17, 2004
Molecular analysis of B-cell differentiation in selective or partial IgA deficiencyT Asano, H Kaneko, T Terada, et al.
Pediatric Research|May 1, 1993
Biochemical and immunochemical study of seven families with 3-ketothiolase deficiency: diagnosis of heterozygotes using immunochemical determination of the ratio of mitochondrial acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase proteinsS Yamaguchi, A Sakai, T Fukao, et al.
Scandinavian Journal of Immunology|February 1, 1997
Reduced expression of the interferon-gamma messenger RNA in IgG2 deficiencyN Kondo, R Inoue, K Kasahara, et al.
Journal of Investigational Allergology & Clinical Immunology|July 1, 1997
Inhibition of interferon-gamma production from lymphocytes stimulated with food antigens by a beta 2-agonist, procaterol, in patients with food-sensitive atopic dermatitisN Kondo, M Shinbara, R Inoue, et al.
The Tohoku Journal of Experimental Medicine|June 1, 1992
Further analysis of mutant thiolase protein in fibroblasts from a Japanese boy with 3-ketothiolase deficiencyS Yamaguchi, T Fukao, M Kano, et al.
Journal of Biochemistry|August 1, 1989
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolaseT Fukao, K Kamijo, T Osumi, et al.
The Journal of Clinical Investigation|December 1, 1990
Molecular cloning and sequence of the complementary DNA encoding human mitochondrial acetoacetyl-coenzyme A thiolase and study of the variant enzymes in cultured fibroblasts from patients with 3-ketothiolase deficiencyT Fukao, S Yamaguchi, M Kano, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular basis of 3-ketothiolase deficiency: detection of gene mutations and expression of mutant cDNAs of mitochondrial acetoacetyl-CoA thiolaseT Fukao, S Yamaguchi, A Wakazono, et al.
Prenatal Diagnosis|March 1, 1996
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysisA Imamura, Y Suzuki, X Q Song, et al.
Pageof 14