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T Fukao

Showing results (61-70 of 139) with videos related to

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International Immunology|February 7, 2001
Fate of the mutated IgG2 heavy chain: lack of expression of mutated membrane-bound IgG2 on the B cell surface in selective IgG2 deficiencyT Terada, H Kaneko, T Fukao, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|March 10, 2004
RNA editing of interleukin-12 receptor beta2, 2451 C-to-U (Ala 604 Val) conversion, associated with atopyN Kondo, E Matsui, H Kaneko, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Succinyl-CoA:3-ketoacid transferase (SCOT) deficiency in a new patient homozygous for an R217X mutationN Longo, T Fukao, R Singh, et al.
Prenatal Diagnosis|April 1, 1995
Prenatal diagnosis in a family with mitochondrial acetoacetyl-coenzyme A thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection methodT Fukao, A Wakazono, X Q Song, et al.
European Journal of Pediatrics|December 3, 1998
Perinatal mumps associated with bronchiolitis and respiratory distressT Fukao, A Hirano, K Nakamura, et al.
Journal of Investigational Allergology & Clinical Immunology|March 26, 2008
Protein-losing enteropathy associated with egg allergy in a 5-month-old boyM Kondo, T Fukao, K Omoya, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|April 7, 2004
Construction of a comparative RFLP map of Echinochloa crus-galli toward QTL analysis of flooding toleranceT Fukao, A H Paterson, M A Hussey, et al.
European Journal of Pediatrics|September 8, 2001
Lysinuric protein intolerance in siblings: complication of systemic lupus erythematosus in the elder sisterM Aoki, T Fukao, Y Fujita, et al.
European Journal of Clinical Investigation|December 19, 2002
Molecular study of electron transfer flavoprotein alpha-subunit deficiency in two Japanese children with different phenotypes of glutaric acidemia type IIE Purevjav, M Kimura, Y Takusa, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Molecular cloning of cDNA for human mitochondrial acetoacetyl-CoA thiolase and molecular analysis of 3-ketothiolase deficiencyT Fukao, S Yamaguchi, H Nagasawa, et al.
Pageof 14

Showing results (61-70 of 139) with videos related to

Sort By:
Pageof 14
International Immunology|February 7, 2001
Fate of the mutated IgG2 heavy chain: lack of expression of mutated membrane-bound IgG2 on the B cell surface in selective IgG2 deficiencyT Terada, H Kaneko, T Fukao, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|March 10, 2004
RNA editing of interleukin-12 receptor beta2, 2451 C-to-U (Ala 604 Val) conversion, associated with atopyN Kondo, E Matsui, H Kaneko, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Succinyl-CoA:3-ketoacid transferase (SCOT) deficiency in a new patient homozygous for an R217X mutationN Longo, T Fukao, R Singh, et al.
Prenatal Diagnosis|April 1, 1995
Prenatal diagnosis in a family with mitochondrial acetoacetyl-coenzyme A thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection methodT Fukao, A Wakazono, X Q Song, et al.
European Journal of Pediatrics|December 3, 1998
Perinatal mumps associated with bronchiolitis and respiratory distressT Fukao, A Hirano, K Nakamura, et al.
Journal of Investigational Allergology & Clinical Immunology|March 26, 2008
Protein-losing enteropathy associated with egg allergy in a 5-month-old boyM Kondo, T Fukao, K Omoya, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|April 7, 2004
Construction of a comparative RFLP map of Echinochloa crus-galli toward QTL analysis of flooding toleranceT Fukao, A H Paterson, M A Hussey, et al.
European Journal of Pediatrics|September 8, 2001
Lysinuric protein intolerance in siblings: complication of systemic lupus erythematosus in the elder sisterM Aoki, T Fukao, Y Fujita, et al.
European Journal of Clinical Investigation|December 19, 2002
Molecular study of electron transfer flavoprotein alpha-subunit deficiency in two Japanese children with different phenotypes of glutaric acidemia type IIE Purevjav, M Kimura, Y Takusa, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Molecular cloning of cDNA for human mitochondrial acetoacetyl-CoA thiolase and molecular analysis of 3-ketothiolase deficiencyT Fukao, S Yamaguchi, H Nagasawa, et al.
Pageof 14