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Results: 1-9 |
Results: 9
Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice
Authors: Huang, TT Carlson, EJ Kozy, HM Mantha, S Goodman, SI Ursell, PC Epstein, CJ
Citation: Tt. Huang et al., Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice, FREE RAD B, 31(9), 2001, pp. 1101-1110
IGF-1 and bFGF reduce glutaric acid and 3-hydroxyglutaric acid toxicity instriatal cultures
Authors: Bjugstad, KB Zawada, WM Goodman, SI Freed, CR
Citation: Kb. Bjugstad et al., IGF-1 and bFGF reduce glutaric acid and 3-hydroxyglutaric acid toxicity instriatal cultures, J INH MET D, 24(6), 2001, pp. 631-647
Binding, hydration, and decarboxylation of the reaction intermediate glutaconyl-coenzyme A by human glutaryl-CoA dehydrogenase
Authors: Westover, JB Goodman, SI Frerman, FE
Citation: Jb. Westover et al., Binding, hydration, and decarboxylation of the reaction intermediate glutaconyl-coenzyme A by human glutaryl-CoA dehydrogenase, BIOCHEM, 40(46), 2001, pp. 14106-14114
Age at symptom onset predicts severity of motor impairment and clinical outcome of glutaric acidemia type 1
Authors: Bjugstad, KB Goodman, SI Freed, CR
Citation: Kb. Bjugstad et al., Age at symptom onset predicts severity of motor impairment and clinical outcome of glutaric acidemia type 1, J PEDIAT, 137(5), 2000, pp. 681-686
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Authors: Enns, GM Bennett, MJ Hoppel, CL Goodman, SI Weisiger, K Ohnstad, C Golabi, M Packman, S
Citation: Gm. Enns et al., Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, J PEDIAT, 136(2), 2000, pp. 251-254
Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidation
Authors: Jones, PM Quinn, R Fennessey, PV Tjoa, S Goodman, SI Fiore, S Burlina, AB Rinaldo, P Boriack, RL Bennett, MJ
Citation: Pm. Jones et al., Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidation, CLIN CHEM, 46(2), 2000, pp. 149-155
Proton abstraction reaction, steady-state kinetics, and oxidation - Reduction potential of human glutaryl-CoA dehydrogenase
Authors: Dwyer, TM Rao, KS Goodman, SI Frerman, FE
Citation: Tm. Dwyer et al., Proton abstraction reaction, steady-state kinetics, and oxidation - Reduction potential of human glutaryl-CoA dehydrogenase, BIOCHEM, 39(37), 2000, pp. 11488-11499
Assignment of electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence in situ hybridization and somatic cell hybridization
Authors: Spector, EB Seltzer, WK Goodman, SI
Citation: Eb. Spector et al., Assignment of electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence in situ hybridization and somatic cell hybridization, MOL GEN MET, 67(4), 1999, pp. 364-367
Mitochondrial disease in superoxide dismutase 2 mutant mice
Authors: Melov, S Coskun, P Patel, M Tuinstra, R Cottrell, B Jun, AS Zastawny, TH Dizdaroglu, M Goodman, SI Huang, TT Miziorko, H Epstein, CJ Wallace, DC
Citation: S. Melov et al., Mitochondrial disease in superoxide dismutase 2 mutant mice, P NAS US, 96(3), 1999, pp. 846-851
Risultati: 1-9 |