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T Fukao

Showing results (91-100 of 139) with videos related to

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International Archives of Allergy and Immunology|April 18, 2001
Reduced interferon-gamma production and mutations of the interleukin-12 receptor beta(2) chain gene in atopic subjectsN Kondo, E Matsui, H Kaneko, et al.
Journal of Investigational Allergology & Clinical Immunology|July 29, 2005
Characterization of T-cell clones specific to ovomucoid from patients with egg-white allergyM Kondo, K Suzuki, R Inoue, et al.
Journal of Inherited Metabolic Disease|May 7, 2005
Two novel mutations in mitochondrial acetoacetyl-CoA thiolase deficiencyL Mrázová, T Fukao, K Hálovd, et al.
Human Mutation|January 1, 1995
Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patientsK Sukegawa, S Tomatsu, T Fukao, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiencyG T Berry, T Fukao, G A Mitchell, et al.
Prenatal Diagnosis|May 1, 1996
Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiencyT Fukao, X Q Song, H Watanabe, et al.
Biochemical and Biophysical Research Communications|January 28, 1994
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)K Isogai, K Sukegawa, S Tomatsu, et al.
Pediatric Research|November 1, 1991
Prenatal diagnosis and neonatal monitoring of a fetus with glutaric aciduria type II due to electron transfer flavoprotein (beta-subunit) deficiencyS Yamaguchi, N Shimizu, T Orii, et al.
Human Mutation|July 22, 1998
Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: two pathogenic mutations, V133E and C456F, in Japanese siblingsX Q Song, T Fukao, H Watanabe, et al.
Pageof 14

Showing results (91-100 of 139) with videos related to

Sort By:
Pageof 14
International Archives of Allergy and Immunology|April 18, 2001
Reduced interferon-gamma production and mutations of the interleukin-12 receptor beta(2) chain gene in atopic subjectsN Kondo, E Matsui, H Kaneko, et al.
Journal of Investigational Allergology & Clinical Immunology|July 29, 2005
Characterization of T-cell clones specific to ovomucoid from patients with egg-white allergyM Kondo, K Suzuki, R Inoue, et al.
Journal of Inherited Metabolic Disease|May 7, 2005
Two novel mutations in mitochondrial acetoacetyl-CoA thiolase deficiencyL Mrázová, T Fukao, K Hálovd, et al.
Human Mutation|January 1, 1995
Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patientsK Sukegawa, S Tomatsu, T Fukao, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiencyG T Berry, T Fukao, G A Mitchell, et al.
Prenatal Diagnosis|May 1, 1996
Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiencyT Fukao, X Q Song, H Watanabe, et al.
Biochemical and Biophysical Research Communications|January 28, 1994
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)K Isogai, K Sukegawa, S Tomatsu, et al.
Pediatric Research|November 1, 1991
Prenatal diagnosis and neonatal monitoring of a fetus with glutaric aciduria type II due to electron transfer flavoprotein (beta-subunit) deficiencyS Yamaguchi, N Shimizu, T Orii, et al.
Human Mutation|July 22, 1998
Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: two pathogenic mutations, V133E and C456F, in Japanese siblingsX Q Song, T Fukao, H Watanabe, et al.
Pageof 14