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Journal Abstract Search

169 related items for PubMed ID: 1830215

  • 1. Formation of cyclobutane thymine dimers photosensitized by pyridopsoralens: quantitative and qualitative distribution within DNA.
    Moysan A, Viari A, Vigny P, Voituriez L, Cadet J, Moustacchi E, Sage E.
    Biochemistry; 1991 Jul 23; 30(29):7080-8. PubMed ID: 1830215
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  • 2. Selective DNA thymine dimerization during UVA irradiation in the presence of a saturated pyridopsoralen.
    Guillo LA, Blais J, Vigny P, Spassky A.
    Photochem Photobiol; 1995 Apr 23; 61(4):331-5. PubMed ID: 7740076
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  • 3. Formation of cyclobutane thymine dimers photosensitized by pyridopsoralens: a triplet-triplet energy transfer mechanism.
    Costalat R, Blais J, Ballini JP, Moysan A, Cadet J, Chalvet O, Vigny P.
    Photochem Photobiol; 1990 Mar 23; 51(3):255-62. PubMed ID: 2356222
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  • 4. Formation of cyclobutane thymine dimers from UVA photosensitization of pyridopsoralen monoadducted DNA.
    Guillo LA, Beylot B, Vigny P, Spassky A.
    Photochem Photobiol; 1996 Aug 23; 64(2):349-55. PubMed ID: 8760575
    [Abstract] [Full Text] [Related]

  • 5. The trans-syn-I thymine dimer bends DNA by approximately 22 degrees and unwinds DNA by approximately 15 degrees.
    Wang CI, Taylor JS.
    Chem Res Toxicol; 1993 Aug 23; 6(4):519-23. PubMed ID: 8374051
    [Abstract] [Full Text] [Related]

  • 6. Production of cis-syn thymine-thymine cyclobutane dimer oligonucleotide in the presence of acetone photosensitizer.
    Mu W, Han Q, Luo Z, Wang Y.
    Anal Biochem; 2006 Jun 01; 353(1):117-23. PubMed ID: 16581009
    [Abstract] [Full Text] [Related]

  • 7. Inter-strand photoproducts are produced in high yield within A-DNA exposed to UVC radiation.
    Douki T, Laporte G, Cadet J.
    Nucleic Acids Res; 2003 Jun 15; 31(12):3134-42. PubMed ID: 12799441
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  • 8. Chemical synthesis and translesion replication of a cis-syn cyclobutane thymine-uracil dimer.
    Takasawa K, Masutani C, Hanaoka F, Iwai S.
    Nucleic Acids Res; 2004 Jun 15; 32(5):1738-45. PubMed ID: 15020710
    [Abstract] [Full Text] [Related]

  • 9. Formation of the main UV-induced thymine dimeric lesions within isolated and cellular DNA as measured by high performance liquid chromatography-tandem mass spectrometry.
    Douki T, Court M, Sauvaigo S, Odin F, Cadet J.
    J Biol Chem; 2000 Apr 21; 275(16):11678-85. PubMed ID: 10766787
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  • 10. Fluorescence quantum yield determination of pyrimidine (6-4) pyrimidone photoadducts.
    Blais J, Douki T, Vigny P, Cadet J.
    Photochem Photobiol; 1994 Apr 21; 59(4):402-4. PubMed ID: 8022882
    [Abstract] [Full Text] [Related]

  • 11. Solar UV radiation-induced DNA Bipyrimidine photoproducts: formation and mechanistic insights.
    Cadet J, Grand A, Douki T.
    Top Curr Chem; 2015 Apr 21; 356():249-75. PubMed ID: 25370518
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  • 18. The photochemistry of thymine in frozen aqueous solution: trimeric and minor dimeric products.
    Shetlar MD, Basus VJ.
    Photochem Photobiol; 2013 Apr 21; 89(3):631-9. PubMed ID: 23237383
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  • 19. Solution-state structure of a DNA dodecamer duplex containing a Cis-syn thymine cyclobutane dimer, the major UV photoproduct of DNA.
    McAteer K, Jing Y, Kao J, Taylor JS, Kennedy MA.
    J Mol Biol; 1998 Oct 09; 282(5):1013-32. PubMed ID: 9753551
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  • 20. [Mechanisms of targeted frameshift mutations--insertion formation under error-prone or SOS synthesis of DNA containing CIS-SYN cyncyclobutane thymine dimers].
    Grebneva EA.
    Mol Biol (Mosk); 2014 Oct 09; 48(4):531-42. PubMed ID: 25842840
    [Abstract] [Full Text] [Related]

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