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Frontiers in Genetics|November 7, 2014
Molecular and cellular functions of the FANCJ DNA helicase defective in cancer and in Fanconi anemiaRobert M Brosh, Sharon B CantorExperimental Gerontology|February 7, 2002
Roles of the Werner syndrome protein in pathways required for maintenance of genome stabilityRobert M Brosh, Vilhelm A BohrMutation Research|January 2, 2013
Disease-causing missense mutations in human DNA helicase disordersAvvaru N Suhasini, Robert M BroshDNA Repair|November 2, 2020
DNA helicases and their roles in cancerSrijita Dhar, Arindam Datta, Robert M BroshGenetics|July 29, 2016
Biochemical Activities and Genetic Functions of the Drosophila melanogaster Fancm Helicase in DNA RepairNoelle-Erin Romero, Steven W Matson, Jeff SekelskyThe Journal of Biological Chemistry|February 1, 2006
The DNA binding activity of MutL is required for methyl-directed mismatch repair in Escherichia coliAdam Robertson, Steven R Pattishall, Steven W MatsonThe Journal of Biological Chemistry|May 7, 2014
The UvrD303 hyper-helicase exhibits increased processivityMatthew J Meiners, Kambiz Tahmaseb, Steven W MatsonJournal of Molecular Biology|August 8, 2006
Unwinding of forked DNA structures by UvrDChris J Cadman, Steven W Matson, Peter McGlynnThe Journal of Biological Chemistry|April 17, 2002
Biochemical characterization of the DNA substrate specificity of Werner syndrome helicaseRobert M Brosh, Juwaria Waheed, Joshua A SommersMolecular and Cellular Biology|April 23, 2008
FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stabilityYuliang Wu, Kazuo Shin-ya, Robert M BroshPageof 17