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Model of WRN function in HR. DNA damage, replication, or repair can... | Download Scientific Diagram
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A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity | PNAS
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Targeting G-quadruplex for rescuing impaired chondrogenesis in WRN-deficient stem cells | Cell & Bioscience | Full Text
![Cancers | Free Full-Text | WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype Cancers | Free Full-Text | WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype](https://pub.mdpi-res.com/cancers/cancers-12-01319/article_deploy/html/images/cancers-12-01319-g001-550.jpg?1591375907)
Cancers | Free Full-Text | WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype
![Association of epigenetic inactivation of the WRN gene with anticancer drug sensitivity in cervical cancer cells Association of epigenetic inactivation of the WRN gene with anticancer drug sensitivity in cervical cancer cells](https://www.spandidos-publications.com/article_images/or/28/4/OR-28-04-1146-g00.jpg)
Association of epigenetic inactivation of the WRN gene with anticancer drug sensitivity in cervical cancer cells
![CDK2 phosphorylation of Werner protein (WRN) contributes to WRN's DNA double‐strand break repair pathway choice - Lee - 2021 - Aging Cell - Wiley Online Library CDK2 phosphorylation of Werner protein (WRN) contributes to WRN's DNA double‐strand break repair pathway choice - Lee - 2021 - Aging Cell - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/cdb89477-9ff1-40e1-9b08-f889e206880a/acel13484-toc-0001-m.jpg?trick=1702162526187)
CDK2 phosphorylation of Werner protein (WRN) contributes to WRN's DNA double‐strand break repair pathway choice - Lee - 2021 - Aging Cell - Wiley Online Library
The WRN gene and protein structure with a graphic representation of the... | Download Scientific Diagram
![WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations | Human Genetics WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations | Human Genetics](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs00439-010-0832-5/MediaObjects/439_2010_832_Fig1_HTML.gif)
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations | Human Genetics
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Acetylation of Werner protein at K1127 and K1117 is important for nuclear trafficking and DNA repair - ScienceDirect
![WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects - Yokote - 2017 - Human Mutation - Wiley Online Library WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects - Yokote - 2017 - Human Mutation - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/63528994-1e26-4fff-b9bc-dab0df206ec4/humu23128-fig-0001-m.jpg)
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects - Yokote - 2017 - Human Mutation - Wiley Online Library
![The Werner Syndrome Helicase-Nuclease--One Protein, Many Mysteries | Science of Aging Knowledge Environment The Werner Syndrome Helicase-Nuclease--One Protein, Many Mysteries | Science of Aging Knowledge Environment](https://www.science.org/cms/10.1126/sageke.2002.13.re2/asset/ecf2f8f3-b35a-421e-9240-d46f810e2492/assets/graphic/132002re2f1.jpeg)
The Werner Syndrome Helicase-Nuclease--One Protein, Many Mysteries | Science of Aging Knowledge Environment
![Association of epigenetic inactivation of the WRN gene with anticancer drug sensitivity in cervical cancer cells Association of epigenetic inactivation of the WRN gene with anticancer drug sensitivity in cervical cancer cells](https://www.spandidos-publications.com/article_images/or/28/4/OR-28-04-1146-g02.jpg)
Association of epigenetic inactivation of the WRN gene with anticancer drug sensitivity in cervical cancer cells
![The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases: Trends in Genetics The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases: Trends in Genetics](https://www.cell.com/cms/attachment/84e03b46-2583-4b52-881b-58d41dded69e/gr1.jpg)
The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases: Trends in Genetics
![Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A | Scientific Reports Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-021-88325-1/MediaObjects/41598_2021_88325_Fig5_HTML.png)
Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A | Scientific Reports
DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activities | Aging
![WRN mutation update. The 35 exons of WRN gene locus and WRN protein are... | Download Scientific Diagram WRN mutation update. The 35 exons of WRN gene locus and WRN protein are... | Download Scientific Diagram](https://www.researchgate.net/publication/309404797/figure/fig1/AS:582381900124160@1515862073017/WRN-mutation-update-The-35-exons-of-WRN-gene-locus-and-WRN-protein-are-shown.png)