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Journal Abstract Search

102 related items for PubMed ID: 711858

  • 21. 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; 74(4):476-83. PubMed ID: 11749052
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  • 26. Structure of the PCCA gene and distribution of mutations causing propionic acidemia.
    Campeau E, Desviat LR, Leclerc D, Wu X, Pérez B, Ugarte M, Gravel RA.
    Mol Genet Metab; 2001 Dec; 74(1-2):238-47. PubMed ID: 11592820
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  • 27. Stimulation of propionyl CoA and beta-methylcrotonyl CoA carboxylase activities in human leukocytes and cultured fibroblasts by biotin.
    Wolf B, Rosenberg LE.
    Pediatr Res; 1979 Nov; 13(11):1275-9. PubMed ID: 514693
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  • 28. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria.
    Dobson CM, Gradinger A, Longo N, Wu X, Leclerc D, Lerner-Ellis J, Lemieux M, Belair C, Watkins D, Rosenblatt DS, Gravel RA.
    Mol Genet Metab; 2006 Aug; 88(4):327-33. PubMed ID: 16697227
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  • 30. NTP Toxicology and Carcinogenesis Studies of Salicylazosulfapyridine (CAS No. 599-79-1) in F344/N Rats and B6C3F1 Mice (Gavage Studies).
    National Toxicology Program .
    Natl Toxicol Program Tech Rep Ser; 1997 May; 457():1-327. PubMed ID: 12587019
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  • 31. Genetics of propionic acidemia in a Mennonite-Amish kindred.
    Kidd JR, Wolf B, Hsia E, Kidd KK.
    Am J Hum Genet; 1980 Mar; 32(2):236-45. PubMed ID: 7386459
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  • 33. Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Treem WR, Shoup ME, Hale DE, Bennett MJ, Rinaldo P, Millington DS, Stanley CA, Riely CA, Hyams JS.
    Am J Gastroenterol; 1996 Nov; 91(11):2293-300. PubMed ID: 8931405
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  • 34. Overview of mutations in the PCCA and PCCB genes causing propionic acidemia.
    Ugarte M, Pérez-Cerdá C, Rodríguez-Pombo P, Desviat LR, Pérez B, Richard E, Muro S, Campeau E, Ohura T, Gravel RA.
    Hum Mutat; 1999 Nov; 14(4):275-82. PubMed ID: 10502773
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  • 35. Molecular basis for genetic complementation in propionyl CoA carboxylase deficiency.
    Wolf B.
    Exp Cell Res; 1980 Feb; 125(2):502-7. PubMed ID: 7353607
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  • 37. Genetic heterogeneity of propionic acidemia: analysis of 15 Japanese patients.
    Ohura T, Miyabayashi S, Narisawa K, Tada K.
    Hum Genet; 1991 May; 87(1):41-4. PubMed ID: 2037281
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  • 40. Coexistence of defective activity in glycine-cleavage reaction and propionyl-CoA carboxylase in the liver of a hyperglycinemic child.
    Nishimura Y, Tada K, Arakawa T.
    Tohoku J Exp Med; 1974 Jul; 113(3):267-71. PubMed ID: 4454060
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