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Journal Abstract Search

99 related items for PubMed ID: 13954619

  • 1. The biochemical function of biotin. V. Further studies on beta-methylcrotonyl CoA carboxylase.
    HIMES RH, YOUNG DL, RINGELMANN E, LYNEN F.
    Biochem Z; 1963; 337():48-61. PubMed ID: 13954619
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  • 3. Biotin uptake into human peripheral blood mononuclear cells increases early in the cell cycle, increasing carboxylase activities.
    Stanley JS, Mock DM, Griffin JB, Zempleni J.
    J Nutr; 2002 Jul; 132(7):1854-9. PubMed ID: 12097659
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  • 4. A simple method for the preparation of antibodies to the mitochondrial biotin-dependent carboxylases.
    McKeon C, Wolf B.
    Experientia; 1982 Feb 15; 38(2):281-2. PubMed ID: 6120854
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  • 5. Primary cultures of astrocytes from rat as a model for biotin deficiency in nervous tissue.
    Rodríguez-Pombo P, Sweetman L, Ugarte M.
    Mol Chem Neuropathol; 1992 Feb 15; 16(1-2):33-44. PubMed ID: 1520405
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  • 7. Differential effects of biotin deficiency and replenishment on rat liver pyruvate and propionyl-CoA carboxylases and on their mRNAs.
    Rodríguez-Meléndez R, Pérez-Andrade ME, Díaz A, Deolarte A, Camacho-Arroyo I, Cicerón I, Ibarra I, Velázquez A.
    Mol Genet Metab; 1999 Jan 15; 66(1):16-23. PubMed ID: 9973543
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  • 8. Multiple carboxylase deficiency: clinical and biochemical improvement following neonatal biotin treatment.
    Wolf B, Hsia YE, Sweetman L, Feldman G, Boychuk RB, Bart RD, Crowell DH, Di Mauro RM, Nyhan WL.
    Pediatrics; 1981 Jul 15; 68(1):113-8. PubMed ID: 6787561
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  • 9. High-performance liquid chromatographic determination of four kinds of biotin-containing carboxylase.
    Oizumi J, Hayakawa K.
    J Chromatogr; 1990 Jul 13; 529(1):55-63. PubMed ID: 1976648
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  • 10. The relationship between plasma biotin concentration and circulating leucocyte beta-methylcrotonyl-CoA carboxylase and propionyl-CoA carboxylase.
    Bartlett K, Horsburgh T, Gompertz D.
    Clin Sci (Lond); 1980 Jan 13; 58(1):111-4. PubMed ID: 7353348
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  • 11. Biotin-reversible neurodegenerative disease in infancy.
    Low LC, Stephenson JB, Bartlett K, Seakins JW, Shaikh SA.
    Aust Paediatr J; 1986 Feb 13; 22(1):65-8. PubMed ID: 3087340
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  • 13. Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome.
    Bannwart C, Wermuth B, Baumgartner R, Suormala T, Weismann UN.
    J Inherit Metab Dis; 1992 Feb 13; 15(6):863-8. PubMed ID: 1293382
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  • 14. Purification and characterization of 3-methylcrotonyl-CoA carboxylase from somatic embryos of Daucus carota.
    Chen Y, Wurtele ES, Wang X, Nikolau BJ.
    Arch Biochem Biophys; 1993 Aug 15; 305(1):103-9. PubMed ID: 8393642
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  • 15. Enzyme studies in combined carboxylase deficiency.
    Bartlett K, Ghneim HK, Stirk JH, Wastell HJ, Sherratt HS, Leonard JV.
    Ann N Y Acad Sci; 1985 Aug 15; 447():235-51. PubMed ID: 2861780
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  • 19. 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 15; 13(11):1275-9. PubMed ID: 514693
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  • 20. Five patients with a biotin-responsive defect in holocarboxylase formation: evaluation of responsiveness to biotin therapy in vivo and comparative biochemical studies in vitro.
    Suormala T, Fowler B, Duran M, Burtscher A, Fuchshuber A, Tratzmüller R, Lenze MJ, Raab K, Baur B, Wick H, Baumgartner R.
    Pediatr Res; 1997 May 15; 41(5):666-73. PubMed ID: 9128289
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