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Journal Abstract Search

200 related items for PubMed ID: 15890657

  • 1. Characterization of four variant forms of human propionyl-CoA carboxylase expressed in Escherichia coli.
    Jiang H, Rao KS, Yee VC, Kraus JP.
    J Biol Chem; 2005 Jul 29; 280(30):27719-27. PubMed ID: 15890657
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  • 2. Changes in the carboxyl terminus of the beta subunit of human propionyl-CoA carboxylase affect the oligomer assembly and catalysis: expression and characterization of seven patient-derived mutant forms of PCC in Escherichia coli.
    Chloupková M, Ravn K, Schwartz M, Kraus JP.
    Mol Genet Metab; 2000 Dec 29; 71(4):623-32. PubMed ID: 11136555
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  • 3. Propionic acidemia: analysis of mutant propionyl-CoA carboxylase enzymes expressed in Escherichia coli.
    Chloupkova M, Maclean KN, Alkhateeb A, Kraus JP.
    Hum Mutat; 2002 Jun 29; 19(6):629-40. PubMed ID: 12007220
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  • 4. Effect of PCCB gene mutations on the heteromeric and homomeric assembly of propionyl-CoA carboxylase.
    Muro S, Pérez B, Desviat LR, Rodríguez-Pombo P, Pérez-Cerdá C, Clavero S, Ugarte M.
    Mol Genet Metab; 2001 Dec 29; 74(4):476-83. PubMed ID: 11749052
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  • 5. Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations.
    Rivera-Barahona A, Navarrete R, García-Rodríguez R, Richard E, Ugarte M, Pérez-Cerda C, Pérez B, Gámez A, Desviat LR.
    Mol Genet Metab; 2018 Nov 29; 125(3):266-275. PubMed ID: 30274917
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  • 7. Crystal structure of the alpha(6)beta(6) holoenzyme of propionyl-coenzyme A carboxylase.
    Huang CS, Sadre-Bazzaz K, Shen Y, Deng B, Zhou ZH, Tong L.
    Nature; 2010 Aug 19; 466(7309):1001-5. PubMed ID: 20725044
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  • 10. Crystal structure of the beta-subunit of acyl-CoA carboxylase: structure-based engineering of substrate specificity.
    Diacovich L, Mitchell DL, Pham H, Gago G, Melgar MM, Khosla C, Gramajo H, Tsai SC.
    Biochemistry; 2004 Nov 09; 43(44):14027-36. PubMed ID: 15518551
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  • 11. Characterization of acetyl-CoA and propionyl-CoA carboxylases encoded by Leptospira interrogans serovar Lai: an initial biochemical study for leptospiral gluconeogenesis via anaplerotic CO(2) assimilation.
    Peng N, Zhong Y, Zhang Q, Zheng M, Zhao W, Jiang H, Yang C, Guo X, Zhao G.
    Acta Biochim Biophys Sin (Shanghai); 2012 Aug 09; 44(8):692-702. PubMed ID: 22710261
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  • 12. [Gene mutation analysis in patients with propionic acidemia].
    Hu YH, Han LS, Ye J, Qiu WJ, Zhang YF, Yang YL, Liu L, Ma HW, Gao XL, Gu XF.
    Zhonghua Er Ke Za Zhi; 2008 Jun 09; 46(6):416-20. PubMed ID: 19099776
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  • 13. Biochemical characterization of propionyl CoA carboxylase deficiency: heterogeneity within a single genetic complementation group.
    McKeon C, Eanes RZ, Wolf B.
    Biochem Genet; 1982 Feb 09; 20(1-2):77-94. PubMed ID: 7092804
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  • 16. Functional analysis of PCCB mutations causing propionic acidemia based on expression studies in deficient human skin fibroblasts.
    Pérez-Cerdá C, Clavero S, Pérez B, Rodríguez-Pombo P, Desviat LR, Ugarte M.
    Biochim Biophys Acta; 2003 May 20; 1638(1):43-9. PubMed ID: 12757933
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  • 20. Biochemical characterization of a Rhizobium etli monovalent cation-stimulated acyl-coenzyme A carboxylase with a high substrate specificity constant for propionyl-coenzyme A.
    Dunn MF, Araíza G, Mora J.
    Microbiology (Reading); 2004 Feb 20; 150(Pt 2):399-406. PubMed ID: 14766918
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