Enzymes of Ketone Body Utilization in Human Tissues: Protein and Messenger RNA Levels of Succinyl-Coenzyme A (CoA):3-Ketoacid CoA Transferase and Mitochondrial and Cytosolic Acetoacetyl-CoA Thiolases

Toshiyuki Fukao, Xiang‐Qian Song, Grant A. Mitchell, +4

Pediatric Research

Cellular EnzymologyBiochemistryNatural SciencesMedicinePhysiology +10

Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT): Cloning of the Human SCOT Gene, Tertiary Structural Modeling of the Human SCOT Monomer, and Characterization of Three Pathogenic Mutations

Toshiyuki Fukao, Grant A. Mitchell, Xiang‐Qian Song, +10

Genomics

Human Scot MonomerMedicineGeneticsPathogenesisSuccinyl-coa:3-ketoacid Coa Transferase +10

Blood-induced bone loss in murine hemophilic arthropathy is prevented by blocking the iRhom2/ADAM17/TNF-α pathway

Coline Haxaire, Narine Hakobyan, Tania Pannellini, +12

Blood

Liver-Specific Silencing of the Human Gene Encoding Succinyl-CoA: 3-Ketoacid CoA Transferase

Kenji E. Orii, Toshiyuki Fukao, Xiang‐Qian Song, +2

The Tohoku Journal of Experimental Medicine

Oxidative StressProtein ExpressionScot Gene ExpressionBiochemical GeneticsHepatotoxicity +22

Mucopolysaccharidosis type II (Hunter disease): Identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patients

Kazuko Sukegawa, Shunji Tomatsu, Toshiyuki Fukao, +6

Human Mutation

Characterization of N93S, I312T, and A333P missense mutations in two Japanese families with mitochondrial acetoacetyl-CoA thiolase deficiency

Toshiyuki Fukao, Haruki Nakamura, Xiang‐Qian Song, +8

Human Mutation

Charging load forecasting of electric vehicle charging station based on support vector regression

Qiming Sun, Jihong Liu, Xiaoxue Rong, +4

Intelligent ForecastingForecasting MethodologyElectrical EngineeringEv ChargingEngineering +10

Functional conservation of HIV-1 Vpr and variability in a mother–child pair of long-term non-progressors

Yuqi Zhao, Mingzhong Chen, Bin Wang, +5

Virus Research

Viral PersistenceHuman RetrovirusImmunodeficienciesImmunologyAntiviral Response +10

Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele

Kazuko Sukegawa, Xiang‐Qian Song, Mitsuo Masuno, +9

Human Mutation

GeneticsImmunologyPathologyMolecular GeneticsDisease Gene Identification +14

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: Two pathogenic mutations, V133E and C456F, in Japanese siblings

Xiang‐Qian Song, Toshiyuki Fukao, H. Watanabe, +5

Human Mutation