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Raymond J Monnat

Showing results (21-30 of 81) with videos related to

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Micromachines|November 9, 2018
Development of a Whole Blood Paper-Based Device for Phenylalanine Detection in the Context of PKU Therapy MonitoringRobert Robinson, Liam Wong, Raymond J Monnat, et al.
DNA Repair|April 16, 2004
The Werner syndrome protein has separable recombination and survival functionsCristina Swanson, Yannick Saintigny, Mary J Emond, et al.
Cell Cycle (Georgetown, Tex.)|February 6, 2008
The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrestJulia M Sidorova, Nianzhen Li, Albert Folch, et al.
Nucleic Acids Research|August 28, 2007
Altered target site specificity variants of the I-PpoI His-Cys box homing endonucleaseJennifer L Eklund, Umut Y Ulge, Jennifer Eastberg, et al.
Human Molecular Genetics|August 9, 2014
Global and disease-associated genetic variation in the human Fanconi anemia gene familyKai J Rogers, Wenqing Fu, Joshua M Akey, et al.
Plos One|April 11, 2013
Spectrum and risk of neoplasia in Werner syndrome: a systematic reviewJulia M Lauper, Alison Krause, Thomas L Vaughan, et al.
Journal of Molecular Biology|May 22, 2003
Flexible DNA target site recognition by divergent homing endonuclease isoschizomers I-CreI and I-MsoIBrett Chevalier, Monique Turmel, Claude Lemieux, et al.
Molecular and Cellular Biology|September 21, 2002
Homologous recombination resolution defect in werner syndromeYannick Saintigny, Kate Makienko, Cristina Swanson, et al.
Nucleic Acids Research|January 21, 2009
Generation of single-chain LAGLIDADG homing endonucleases from native homodimeric precursor proteinsHui Li, Stefan Pellenz, Umut Ulge, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 2013
Essential role for Cdk2 inhibitory phosphorylation during replication stress revealed by a human Cdk2 knockin mutationBridget T Hughes, Julia Sidorova, Jherek Swanger, et al.
Pageof 9

Showing results (21-30 of 81) with videos related to

Sort By:
Pageof 9
Micromachines|November 9, 2018
Development of a Whole Blood Paper-Based Device for Phenylalanine Detection in the Context of PKU Therapy MonitoringRobert Robinson, Liam Wong, Raymond J Monnat, et al.
DNA Repair|April 16, 2004
The Werner syndrome protein has separable recombination and survival functionsCristina Swanson, Yannick Saintigny, Mary J Emond, et al.
Cell Cycle (Georgetown, Tex.)|February 6, 2008
The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrestJulia M Sidorova, Nianzhen Li, Albert Folch, et al.
Nucleic Acids Research|August 28, 2007
Altered target site specificity variants of the I-PpoI His-Cys box homing endonucleaseJennifer L Eklund, Umut Y Ulge, Jennifer Eastberg, et al.
Human Molecular Genetics|August 9, 2014
Global and disease-associated genetic variation in the human Fanconi anemia gene familyKai J Rogers, Wenqing Fu, Joshua M Akey, et al.
Plos One|April 11, 2013
Spectrum and risk of neoplasia in Werner syndrome: a systematic reviewJulia M Lauper, Alison Krause, Thomas L Vaughan, et al.
Journal of Molecular Biology|May 22, 2003
Flexible DNA target site recognition by divergent homing endonuclease isoschizomers I-CreI and I-MsoIBrett Chevalier, Monique Turmel, Claude Lemieux, et al.
Molecular and Cellular Biology|September 21, 2002
Homologous recombination resolution defect in werner syndromeYannick Saintigny, Kate Makienko, Cristina Swanson, et al.
Nucleic Acids Research|January 21, 2009
Generation of single-chain LAGLIDADG homing endonucleases from native homodimeric precursor proteinsHui Li, Stefan Pellenz, Umut Ulge, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 2013
Essential role for Cdk2 inhibitory phosphorylation during replication stress revealed by a human Cdk2 knockin mutationBridget T Hughes, Julia Sidorova, Jherek Swanger, et al.
Pageof 9