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Proceedings of the National Academy of Sciences of the United States of America|June 15, 2007
Werner syndrome protein interacts functionally with translesion DNA polymerasesAshwini S Kamath-Loeb, Li Lan, Satoshi Nakajima, et al.
The Journal of Biological Chemistry|February 22, 2012
The Werner syndrome exonuclease facilitates DNA degradation and high fidelity DNA polymerization by human DNA polymerase δAshwini S Kamath-Loeb, Jiang-Cheng Shen, Michael W Schmitt, et al.
The Journal of Biological Chemistry|October 19, 2004
The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834CAshwini S Kamath-Loeb, Piri Welcsh, Maureen Waite, et al.
The Journal of Biological Chemistry|July 4, 2008
The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomerSarah A Compton, Gökhan Tolun, Ashwini S Kamath-Loeb, et al.
Molecular Carcinogenesis|October 14, 2009
Werner syndrome gene variants in human sarcomasJessica J Hsu, Ashwini S Kamath-Loeb, Eitan Glick, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2019
A high-resolution landscape of mutations in the <i>BCL6</i> super-enhancer in normal human B cellsJiang-Cheng Shen, Ashwini S Kamath-Loeb, Brendan F Kohrn, et al.
The Journal of Biological Chemistry|June 15, 2014
Sphingosine, a modulator of human translesion DNA polymerase activityAshwini S Kamath-Loeb, Sharath Balakrishna, Dale Whittington, et al.
Leukemia Research|March 18, 2022
Accurate detection of subclonal variants in paired diagnosis-relapse acute myeloid leukemia samples by next generation Duplex SequencingAshwini S Kamath-Loeb, Jiang-Cheng Shen, Michael W Schmitt, et al.
Scientific Reports|March 10, 2017
Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotypeAshwini S Kamath-Loeb, Diego G Zavala-van Rankin, Jeny Flores-Morales, et al.
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