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Niels de Wind

Showing results (61-70 of 78) with videos related to

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Heliyon|July 24, 2023
<i>Rev1</i> deficiency induces a metabolic shift in MEFs that can be manipulated by the NAD<sup>+</sup> precursor nicotinamide ribosideSharath Anugula, Zhiquan Li, Yuan Li, et al.
The Journal of Cell Biology|April 15, 2015
Excision of translesion synthesis errors orchestrates responses to helix-distorting DNA lesionsAnastasia Tsaalbi-Shtylik, Cristina Ferrás, Bea Pauw, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 22, 2018
Adjuvant Treatment for <i>POLE</i> Proofreading Domain-Mutant Cancers: Sensitivity to Radiotherapy, Chemotherapy, and Nucleoside AnaloguesInge C Van Gool, Emily Rayner, Elisabeth M Osse, et al.
Molecular Carcinogenesis|December 5, 2013
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicityMichael T Parsons, Phillip J Whiley, Jonathan Beesley, et al.
Scientific Reports|October 4, 2017
Rev1 contributes to proper mitochondrial function via the PARP-NAD<sup>+</sup>-SIRT1-PGC1α axisNima Borhan Fakouri, Jon Ambæk Durhuus, Christine Elisabeth Regnell, et al.
American Journal of Physiology. Endocrinology and Metabolism|February 14, 2022
Rev1 deficiency induces replication stress to cause metabolic dysfunction differently in males and femalesWietse In Het Panhuis, Anastasia Tsaalbi-Shtylik, Milena Schönke, et al.
Scientific Reports|March 8, 2018
Author Correction: Rev1 contributes to proper mitochondrial function via the PARP-NAD<sup>+</sup>-SIRT1-PGC1α axisNima Borhan Fakouri, Jon Ambæk Durhuus, Christine Elisabeth Regnell, et al.
Human Mutation|July 4, 2012
Functional characterization of MLH1 missense variants identified in Lynch syndrome patientsSofie Dabros Andersen, Sascha Emilie Liberti, Anne Lützen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2020
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndromeMark Drost, Yvonne Tiersma, Dylan Glubb, et al.
Nucleic Acids Research|July 19, 2015
FANCD2 and REV1 cooperate in the protection of nascent DNA strands in response to replication stressYeran Yang, Zhenbo Liu, Fengli Wang, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Heliyon|July 24, 2023
<i>Rev1</i> deficiency induces a metabolic shift in MEFs that can be manipulated by the NAD<sup>+</sup> precursor nicotinamide ribosideSharath Anugula, Zhiquan Li, Yuan Li, et al.
The Journal of Cell Biology|April 15, 2015
Excision of translesion synthesis errors orchestrates responses to helix-distorting DNA lesionsAnastasia Tsaalbi-Shtylik, Cristina Ferrás, Bea Pauw, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 22, 2018
Adjuvant Treatment for <i>POLE</i> Proofreading Domain-Mutant Cancers: Sensitivity to Radiotherapy, Chemotherapy, and Nucleoside AnaloguesInge C Van Gool, Emily Rayner, Elisabeth M Osse, et al.
Molecular Carcinogenesis|December 5, 2013
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicityMichael T Parsons, Phillip J Whiley, Jonathan Beesley, et al.
Scientific Reports|October 4, 2017
Rev1 contributes to proper mitochondrial function via the PARP-NAD<sup>+</sup>-SIRT1-PGC1α axisNima Borhan Fakouri, Jon Ambæk Durhuus, Christine Elisabeth Regnell, et al.
American Journal of Physiology. Endocrinology and Metabolism|February 14, 2022
Rev1 deficiency induces replication stress to cause metabolic dysfunction differently in males and femalesWietse In Het Panhuis, Anastasia Tsaalbi-Shtylik, Milena Schönke, et al.
Scientific Reports|March 8, 2018
Author Correction: Rev1 contributes to proper mitochondrial function via the PARP-NAD<sup>+</sup>-SIRT1-PGC1α axisNima Borhan Fakouri, Jon Ambæk Durhuus, Christine Elisabeth Regnell, et al.
Human Mutation|July 4, 2012
Functional characterization of MLH1 missense variants identified in Lynch syndrome patientsSofie Dabros Andersen, Sascha Emilie Liberti, Anne Lützen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2020
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndromeMark Drost, Yvonne Tiersma, Dylan Glubb, et al.
Nucleic Acids Research|July 19, 2015
FANCD2 and REV1 cooperate in the protection of nascent DNA strands in response to replication stressYeran Yang, Zhenbo Liu, Fengli Wang, et al.
Pageof 8