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Journal Abstract Search

123 related items for PubMed ID: 639329

  • 21. Biotin dependent carboxylase activities in normal human and multicarboxylase deficient patient fibroblasts: relationship to the biotin content of the culture medium.
    Marsac C, Gaudry M, Augereau C, Moncion A, Saudubray JM, Coudé FX, Munnich A.
    Clin Chim Acta; 1983 Apr; 129(2):119-28. PubMed ID: 6851156
    [Abstract] [Full Text] [Related]

  • 22. Defective biotin absorption in multiple carboxylase deficiency.
    Munnich A, Saudubray JM, Carré G, Coudé FX, Ogier H, Charpentier C, Frézal J.
    Lancet; 1981 Aug 01; 2(8240):263. PubMed ID: 6114319
    [No Abstract] [Full Text] [Related]

  • 23. Prenatal administration of biotin in biotin responsive multiple carboxylase deficiency.
    Roth KS, Yang W, Allan L, Saunders M, Gravel RA, Dakshinamurti K.
    Pediatr Res; 1982 Feb 01; 16(2):126-9. PubMed ID: 6799930
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  • 24. Plants contain multiple biotin enzymes: discovery of 3-methylcrotonyl-CoA carboxylase, propionyl-CoA carboxylase and pyruvate carboxylase in the plant kingdom.
    Wurtele ES, Nikolau BJ.
    Arch Biochem Biophys; 1990 Apr 01; 278(1):179-86. PubMed ID: 2321957
    [Abstract] [Full Text] [Related]

  • 25. Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset.
    Sherwood WG, Saunders M, Robinson BH, Brewster T, Gravel RA.
    J Pediatr; 1982 Oct 01; 101(4):546-50. PubMed ID: 6811711
    [Abstract] [Full Text] [Related]

  • 26. [3H]biotin-labeled proteins in cultured human skin fibroblasts from patients with pyruvate carboxylase deficiency.
    Robinson BH, Oei J, Saunders M, Gravel R.
    J Biol Chem; 1983 May 25; 258(10):6660-4. PubMed ID: 6406485
    [Abstract] [Full Text] [Related]

  • 27. Fatty-acid-responsive alopecia in multiple carboxylase deficiency.
    Munnich A, Saudubray JM, Coude FX, Charpentier C, Saurat JH, Frezal J.
    Lancet; 1980 May 17; 1(8177):1080-1. PubMed ID: 6103410
    [No Abstract] [Full Text] [Related]

  • 28. Biochemical evidence for diverse etiologies in biotin-responsive multiple carboxylase deficiency.
    Packman S, Caswell NM, Baker H.
    Biochem Genet; 1982 Feb 17; 20(1-2):17-28. PubMed ID: 6807281
    [Abstract] [Full Text] [Related]

  • 29. Biotin-responsive multiple carboxylase deficiency (MCD): deficient biotinidase activity associated with renal loss of biotin.
    Baumgartner ER, Suormala T, Wick H, Bonjour JP.
    J Inherit Metab Dis; 1984 Feb 17; 7 Suppl 2():123-5. PubMed ID: 6434862
    [No Abstract] [Full Text] [Related]

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  • 35. Infantile multiple carboxylase deficiency: evidence for normal intestinal absorption but renal loss of biotin.
    Baumgartner R, Suormala T, Wick H, Geisert J, Lehnert W.
    Helv Paediatr Acta; 1982 Feb 17; 37(5):499-502. PubMed ID: 6819258
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  • 39. Essential arginine residues in the active sites of propionyl CoA carboxylase and beta-methylcrotonyl CoA carboxylase.
    Wolf B, Kalousek F, Rosenberg LE.
    Enzyme; 1979 Feb 17; 24(5):302-6. PubMed ID: 510274
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