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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 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.Biochemical and Biophysical Research Communications|December 22, 1999
Mutations of the IL-12 receptor beta2 chain gene in atopic subjectsE Matsui, H Kaneko, T Fukao, et al.Clinical Genetics|April 1, 1992
Biochemical investigation of a Brazilian patient with a defect in mitochondrial acetoacetylcoenzyme-A thiolaseM Wajner, M T Sanseverino, R Giugliani, et al.Journal of Inherited Metabolic Disease|November 9, 2006
Effect of Hunter disease (mucopolysaccharidosis type II) mutations on molecular phenotypes of iduronate-2-sulfatase: enzymatic activity, protein processing and structural analysisK Sukegawa-Hayasaka, Z Kato, H Nakamura, et al.Biochemical and Biophysical Research Communications|August 30, 1991
Evidence for a structural mutation (347Ala to Thr) in a German family with 3-ketothiolase deficiencyT Fukao, S Yamaguchi, S Tomatsu, et al.Scandinavian Journal of Immunology|November 26, 2003
Semiquantitative evaluation of mRNAs for the membranous form of immunoglobulin heavy chain is useful for investigating the etiology in CVIDT Terada, H Kaneko, T Fukao, et al.Human Mutation|January 1, 1993
Molecular studies of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in the two original familiesT Fukao, S Yamaguchi, C R Scriver, et al.Zhonghua Yi Xue Za Zhi|May 9, 2017
[Correlation between the clinical symptoms and the activation pattern of brain neurons in patients with obsessive-compulsive disorder]Q H Niu, J L Cheng, X Q Song, et al.Pageof 14