The (6–4) photoproduct of thymine–thymine induces targeted substitution mutations in mammalian cells

By Kamiya Hiroyuki   Iwai Shigenori   Kasai Hiroshi  

Nucleic Acids Research, Vol. 26, Iss. 11, 1998-06 ,pp. : 2611-2617

Oxford University Press

Access to resources Recommend Favorite

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

By Rochette Patrick J.   Therrien Jean‐Philippe   Drouin Régen   Perdiz Daniel  

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

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Essential dynamics of DNA containing a cis.syn cyclobutane thymine dimer lesion

By Yamaguchi Hiroshi   van Aalten Daan M. F.  

Nucleic Acids Research, Vol. 26, Iss. 8, 1998-04 ,pp. : 1939-1946

Oxford University Press

Access to resources Recommend Favorite