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Lawrence A Loeb

Showing results (91-100 of 122) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 3, 2012
Detection of ultra-rare mutations by next-generation sequencingMichael W Schmitt, Scott R Kennedy, Jesse J Salk, et al.
Molecular Cell|March 30, 2010
Frameshift mutagenesis and microsatellite instability induced by human alkyladenine DNA glycosylaseJoanna Klapacz, Gondichatnahalli M Lingaraju, Haiwei H Guo, et al.
Molecular Carcinogenesis|October 14, 2009
Werner syndrome gene variants in human sarcomasJessica J Hsu, Ashwini S Kamath-Loeb, Eitan Glick, et al.
Nature Genetics|March 4, 2008
DNA deletions and clonal mutations drive premature aging in mitochondrial mutator miceMarc Vermulst, Jonathan Wanagat, Gregory C Kujoth, 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.
Nature Genetics|March 6, 2007
Mitochondrial point mutations do not limit the natural lifespan of miceMarc Vermulst, Jason H Bielas, Gregory C Kujoth, et al.
Nucleic Acids Research|April 5, 2011
A random mutation capture assay to detect genomic point mutations in mouse tissueJocelyn H Wright, Kristina L Modjeski, Jason H Bielas, et al.
DNA Repair|September 17, 2005
Mitochondrial DNA integrity is not dependent on DNA polymerase-beta activityAlexis B Hansen, Nicholas B Griner, Jon P Anderson, et al.
The Journal of Biological Chemistry|March 20, 2003
Amino acid substitutions at conserved tyrosine 52 alter fidelity and bypass efficiency of human DNA polymerase etaEitan Glick, Janice S Chau, Kellie L Vigna, et al.
Nature Methods|April 8, 2015
Sequencing small genomic targets with high efficiency and extreme accuracyMichael W Schmitt, Edward J Fox, Marc J Prindle, et al.
Pageof 13

Showing results (91-100 of 122) with videos related to

Sort By:
Pageof 13
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2012
Detection of ultra-rare mutations by next-generation sequencingMichael W Schmitt, Scott R Kennedy, Jesse J Salk, et al.
Molecular Cell|March 30, 2010
Frameshift mutagenesis and microsatellite instability induced by human alkyladenine DNA glycosylaseJoanna Klapacz, Gondichatnahalli M Lingaraju, Haiwei H Guo, et al.
Molecular Carcinogenesis|October 14, 2009
Werner syndrome gene variants in human sarcomasJessica J Hsu, Ashwini S Kamath-Loeb, Eitan Glick, et al.
Nature Genetics|March 4, 2008
DNA deletions and clonal mutations drive premature aging in mitochondrial mutator miceMarc Vermulst, Jonathan Wanagat, Gregory C Kujoth, 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.
Nature Genetics|March 6, 2007
Mitochondrial point mutations do not limit the natural lifespan of miceMarc Vermulst, Jason H Bielas, Gregory C Kujoth, et al.
Nucleic Acids Research|April 5, 2011
A random mutation capture assay to detect genomic point mutations in mouse tissueJocelyn H Wright, Kristina L Modjeski, Jason H Bielas, et al.
DNA Repair|September 17, 2005
Mitochondrial DNA integrity is not dependent on DNA polymerase-beta activityAlexis B Hansen, Nicholas B Griner, Jon P Anderson, et al.
The Journal of Biological Chemistry|March 20, 2003
Amino acid substitutions at conserved tyrosine 52 alter fidelity and bypass efficiency of human DNA polymerase etaEitan Glick, Janice S Chau, Kellie L Vigna, et al.
Nature Methods|April 8, 2015
Sequencing small genomic targets with high efficiency and extreme accuracyMichael W Schmitt, Edward J Fox, Marc J Prindle, et al.
Pageof 13