Showing results (111-120 of 161) with videos related to

Sort By:
Pageof 17
The Journal of Biological Chemistry|May 15, 2012
The Q motif of Fanconi anemia group J protein (FANCJ) DNA helicase regulates its dimerization, DNA binding, and DNA repair functionYuliang Wu, Joshua A Sommers, Jason A Loiland, et al.
Cancer Research|July 23, 2013
Werner syndrome helicase has a critical role in DNA damage responses in the absence of a functional fanconi anemia pathwayMonika Aggarwal, Taraswi Banerjee, Joshua A Sommers, et al.
The Journal of Biological Chemistry|June 5, 2014
Novel function of the Fanconi anemia group J or RECQ1 helicase to disrupt protein-DNA complexes in a replication protein A-stimulated mannerJoshua A Sommers, Taraswi Banerjee, Twila Hinds, et al.
Nucleic Acids Research|January 18, 2006
Cockayne syndrome group B protein has novel strand annealing and exchange activitiesMeltem Muftuoglu, Sudha Sharma, Tina Thorslund, et al.
The Journal of Biological Chemistry|May 12, 2005
RECQ1 helicase interacts with human mismatch repair factors that regulate genetic recombinationKevin M Doherty, Sudha Sharma, Laura A Uzdilla, et al.
The Journal of Biological Chemistry|January 20, 2009
FANCJ uses its motor ATPase to destabilize protein-DNA complexes, unwind triplexes, and inhibit RAD51 strand exchangeJoshua A Sommers, Nina Rawtani, Rigu Gupta, et al.
Oncogene|February 28, 2003
The transcriptional response after oxidative stress is defective in Cockayne syndrome group B cellsKasper J Kyng, Alfred May, Robert M Brosh, et al.
The Journal of Biological Chemistry|December 29, 2005
Inhibition of Werner syndrome helicase activity by benzo[a]pyrene diol epoxide adducts can be overcome by replication protein ASaba Choudhary, Kevin M Doherty, Christopher J Handy, et al.
Communications Biology|April 13, 2026
Rare genetic diseases associated with G-quadruplex-induced replication stressLauren M Herr, Swagata Mukhopadhyay, Olivia M Anderson, 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.
Pageof 17