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Aging|June 21, 2012
DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activitiesTakashi Tadokoro, Tomasz Kulikowicz, Lale Dawut, et al.
DNA Repair|April 16, 2013
Functional deficit associated with a missense Werner syndrome mutationTakashi Tadokoro, Ivana Rybanska-Spaeder, Tomasz Kulikowicz, et al.
Molecular Biology of the Cell|July 4, 2008
WRN is required for ATM activation and the S-phase checkpoint in response to interstrand cross-link-induced DNA double-strand breaksWen-Hsing Cheng, Diana Muftic, Meltem Muftuoglu, et al.
Biochimica Et Biophysica Acta|August 14, 2012
RAPADILINO RECQL4 mutant protein lacks helicase and ATPase activityDeborah L Croteau, Marie L Rossi, Jennifer Ross, et al.
Nucleic Acids Research|August 5, 2004
Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome proteinCayetano von Kobbe, Jeanine A Harrigan, Valérie Schreiber, et al.
Molecular and Cellular Biology|November 13, 2003
Central role for the Werner syndrome protein/poly(ADP-ribose) polymerase 1 complex in the poly(ADP-ribosyl)ation pathway after DNA damageCayetano von Kobbe, Jeanine A Harrigan, Alfred May, et al.
The Journal of Biological Chemistry|March 29, 2002
Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteinsCayetano von Kobbe, Parimal Karmakar, Lale Dawut, et al.
Nucleic Acids Research|January 19, 2010
Human RECQL5beta stimulates flap endonuclease 1Elzbieta Speina, Lale Dawut, Mohammad Hedayati, et al.
Molecular Cell|June 18, 2004
The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2Patricia L Opresko, Marit Otterlei, Jesper Graakjaer, et al.
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