Showing results (71-80 of 135) with videos related to
Sort By:
Pageof 14
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.Journal of Periodontal Research|September 8, 2011
Early microbial succession in redeveloping dental biofilms in periodontal health and diseaseF R Teles, R P Teles, N G Uzel, 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.World Journal of Gastroenterology|March 24, 2016
Clinical observation of (125)I-labeled anti-alpha fetoprotein antibody radioimmunotherapy in hepatocellular carcinomaY D Wu, K Z Yang, D N Zhou, et al.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.Zhonghua Yi Xue Za Zhi|August 14, 2023
[The influence of interaction between polygenic risk score and intestinal fungal microbiota on the risk of schizophrenia]X X Yuan, Y Sun, L J Pang, et al.Zhonghua Yi Xue Za Zhi|October 12, 2021
[Effect of the correlation between gut microbiota and folic acid in first-episode schizophrenia]Y Miao, X Li, X X Yuan, 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.Pageof 14