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Journal Abstract Search


85 related items for PubMed ID: 5650415

  • 1. Energy transfer in oligotyrosyl compounds: fluorescence quenching as a function of the ionization of the phenolic hydroxyl groups.
    Knopp JA, Longworth JW.
    Biochim Biophys Acta; 1968 Apr 09; 154(3):436-43. PubMed ID: 5650415
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  • 2. Energy transfer in poly-L-tyrosine as a function of the degree of ionization of the phenolic hydroxyls. IV. Calculations of theoretical transfer rates.
    ten Bosch JJ, Knopp JA.
    Biochim Biophys Acta; 1969 Apr 09; 188(2):173-84. PubMed ID: 5823021
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  • 3. PROTON-TRANSFER EFFECTS IN THE QUENCHING OF FLUORESCENCE OF TYROSINE COPOLYMERS.
    WEBER G, ROSENHECK K.
    Biopolym Symp; 1964 Apr 09; 13():333-41. PubMed ID: 14210457
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  • 10. Fluorescence studies with tyrosyl peptides.
    Edelhoch H, Perlman RL, Wilchek M.
    Biochemistry; 1968 Nov 09; 7(11):3893-900. PubMed ID: 5722258
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  • 11. Phenolic hydroxyl ionization in stem bromelain.
    Tachibana A, Murachi T.
    Biochemistry; 1966 Aug 09; 5(8):2756-63. PubMed ID: 5968581
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  • 12. Energy transfer: a spectroscopic ruler.
    Stryer L, Haugland RP.
    Proc Natl Acad Sci U S A; 1967 Aug 09; 58(2):719-26. PubMed ID: 5233469
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  • 13. Phenolic hydroxyl ionization in two subtilisins.
    Markland FS.
    J Biol Chem; 1969 Feb 25; 244(4):694-700. PubMed ID: 5768864
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  • 14. Fluorescence and protein structure. XVII. On the mechanism of peptide quenching.
    Cowgill RW.
    Biochim Biophys Acta; 1970 Jan 20; 200(1):18-25. PubMed ID: 5410718
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  • 17. Fluorescence and the structure of proteins. VII. Hydrogen-bonded phenols as fluorescence sinks.
    Cowgill RW.
    Bibl Laeger; 1966 Mar 14; 112(3):550-8. PubMed ID: 5912022
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