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Journal Abstract Search

214 related items for PubMed ID: 17616348

  • 1. Catabolism of L-phenylalanine and L-tyrosine by Rhodobacter sphaeroides OU5 occurs through 3,4-dihydroxyphenylalanine.
    Ranjith NK, Sasikala Ch, Ramana ChV.
    Res Microbiol; 2007; 158(6):506-11. PubMed ID: 17616348
    [Abstract] [Full Text] [Related]

  • 2. Purification and characterization of 3,4-dihydroxyphenylalanine oxidative deaminase from Rhodobacter sphaeroides OU5.
    Ranjith NK, Ramana ChV, Sasikala Ch.
    Can J Microbiol; 2008 Oct; 54(10):829-34. PubMed ID: 18923551
    [Abstract] [Full Text] [Related]

  • 3. Dopa oxidation and tyrosine oxygenation by human melanoma tyrosinase.
    Jergil B, Lindbladh C, Rorsman H, Rosengren E.
    Acta Derm Venereol; 1983 Oct; 63(6):468-75. PubMed ID: 6198834
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  • 5. L-Tryptophan catabolism by Rubrivivax benzoatilyticus JA2 occurs through indole 3-pyruvic acid pathway.
    Kumavath RN, Ramana ChV, Sasikala Ch.
    Biodegradation; 2010 Sep; 21(5):825-32. PubMed ID: 20217460
    [Abstract] [Full Text] [Related]

  • 6. Translational incorporation of L-3,4-dihydroxyphenylalanine into proteins.
    Ozawa K, Headlam MJ, Mouradov D, Watt SJ, Beck JL, Rodgers KJ, Dean RT, Huber T, Otting G, Dixon NE.
    FEBS J; 2005 Jun; 272(12):3162-71. PubMed ID: 15955073
    [Abstract] [Full Text] [Related]

  • 7. Rhodethrin: a novel indole terpenoid ether produced by Rhodobacter sphaeroides has cytotoxic and phytohormonal activities.
    Ranjith NK, Sasikala Ch, Ramana ChV.
    Biotechnol Lett; 2007 Sep; 29(9):1399-402. PubMed ID: 17636389
    [Abstract] [Full Text] [Related]

  • 8. Tyrosinase activity in the medium of human melanoma cell cultures.
    Jergil B, Lindbladh C, Rorsman H, Rosengren E.
    Acta Derm Venereol; 1983 Sep; 63(3):205-8. PubMed ID: 6192632
    [Abstract] [Full Text] [Related]

  • 9. [DOPA-DOPP-transaminases of rat brain in vitro].
    Gey KF.
    Helv Physiol Pharmacol Acta; 1967 Sep; 25(2):CR187-9. PubMed ID: 5588161
    [No Abstract] [Full Text] [Related]

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  • 11. The hydroxylation of phenylalanine and tyrosine: a comparison with salicylate and tryptophan.
    Maskos Z, Rush JD, Koppenol WH.
    Arch Biochem Biophys; 1992 Aug 01; 296(2):521-9. PubMed ID: 1321588
    [Abstract] [Full Text] [Related]

  • 12. Metabolism of L-phenylalanine and L-tyrosine by the phototrophic bacterium Rhodobacter capsulatus.
    Sáez LP, Castillo F, Caballero FJ.
    Curr Microbiol; 1999 Jan 01; 38(1):51-6. PubMed ID: 9841783
    [Abstract] [Full Text] [Related]

  • 13. Human phenylalanine hydroxylase is activated by H2O2: a novel mechanism for increasing the L-tyrosine supply for melanogenesis in melanocytes.
    Schallreuter KU, Wazir U, Kothari S, Gibbons NC, Moore J, Wood JM.
    Biochem Biophys Res Commun; 2004 Sep 10; 322(1):88-92. PubMed ID: 15313177
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  • 15. Contributions of conserved serine and tyrosine residues to catalysis, ligand binding, and cofactor processing in the active site of tyrosine ammonia lyase.
    Schroeder AC, Kumaran S, Hicks LM, Cahoon RE, Halls C, Yu O, Jez JM.
    Phytochemistry; 2008 May 10; 69(7):1496-506. PubMed ID: 18346767
    [Abstract] [Full Text] [Related]

  • 16. Phenylalanine as substrate for tyrosine hydroxylase in bovine adrenal chromaffin cells.
    Fukami MH, Haavik J, Flatmark T.
    Biochem J; 1990 Jun 01; 268(2):525-8. PubMed ID: 1973034
    [Abstract] [Full Text] [Related]

  • 17. Application of liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the analysis of stable isotope enrichments of phenylalanine and tyrosine.
    Meesters RJ, Wolfe RR, Deutz NE.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Jan 01; 877(1-2):43-9. PubMed ID: 19036645
    [Abstract] [Full Text] [Related]

  • 18. Aromatic amino acid aminotransferase activity and indole-3-acetic acid production by associative nitrogen-fixing bacteria.
    Pedraza RO, Ramírez-Mata A, Xiqui ML, Baca BE.
    FEMS Microbiol Lett; 2004 Apr 01; 233(1):15-21. PubMed ID: 15043864
    [Abstract] [Full Text] [Related]

  • 19. Double mutant of Aspergillus oryzae for improved production of L-dopa (3,4-dihydroxyphenyl-L-alanine) from L-tyrosine.
    Ali S, Haq IU, Qadeer MA, Rajoka MI.
    Biotechnol Appl Biochem; 2005 Oct 01; 42(Pt 2):143-9. PubMed ID: 15727563
    [Abstract] [Full Text] [Related]

  • 20. The effect of phenylalanine on DOPA synthesis in PC12 cells.
    DePietro FR, Fernstrom JD.
    Neurochem Res; 1998 Jul 01; 23(7):1011-20. PubMed ID: 9690745
    [Abstract] [Full Text] [Related]

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