Mutagenicity of a Unique Thymine-Thymine Dimer or Thymine-Thymine Pyrimidine Pyrimidone (6–4) Photoproduct in Mammalian Cells

By Gentil A.   Le Page F.   Borden A.   Sarasin A.  

Nucleic Acids Research, Vol. 24, Iss. 10, 1996-01 ,pp. : 1837-1840

Oxford University Press

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UVA‐induced cyclobutane pyrimidine dimers form predominantly at thymine–thymine dipyrimidines and correlate with the mutation spectrum in rodent cells

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Nucleic Acids Research, Vol. 31, Iss. 11, 2003-06 ,pp. : 2786-2794

Oxford University Press

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The contribution of thymine—thymine interactions to the stability of folded dimeric quadruplexes

By Keniry Max A.   Owen Elisabeth A.  

Nucleic Acids Research, Vol. 25, Iss. 21, 1997-11 ,pp. : 4389-4392

Oxford University Press

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Solution-state Structure of a DNA Dodecamer Duplex Containing a Cis-Syn Thymine Cyclobutane Dimer, the Major UV Photoproduct of DNA

By McAteer K.   Jing Y.   Kao J.     Kennedy M.A.  

Journal of Molecular Biology, Vol. 282, Iss. 5, 1998-10 ,pp. : 1013-1032

Academic Press

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Studies on the Effect of Thymine-Mercury-Thymine Stem as a Structural or Functional Motif in DNAzymes

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Nucleosides, Nucleotides & Nucleic Acids, Vol. 33, Iss. 10, 2014-10 ,pp. : 645-655

Taylor & Francis Ltd

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