CDK2 phosphorylation of Werner protein (WRN) contributes to WRN's DNA double‐strand break repair pathway choice - Lee - 2021 - Aging Cell - Wiley Online Library
Werner syndrome helicase - Wikipedia
File:WRN location.png - Wikimedia Commons
Investigation of the core binding regions of human Werner syndrome and Fanconi anemia group J helicases on replication protein A | Scientific Reports
A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity | PNAS
Recent Advances in Understanding Werner Syndrome | F1000Research
The Role of WRN Helicase/Exonuclease in DNA Replication | IntechOpen
Recent Advances in Understanding Werner Syndrome | F1000Research
![PDF] The Heli-CASE of the Missing WRN Gene | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/6d5a3c2a5f3734e3c363e3dd76363c21cb3519bf/5-Figure2-1.png "PDF] The Heli-CASE of the Missing WRN Gene | Semantic Scholar")
PDF] The Heli-CASE of the Missing WRN Gene | Semantic Scholar
Genes | Free Full-Text | Research on Werner Syndrome: Trends from Past to Present and Future Prospects
Mutations in the WRN Gene in Mice Accelerate Mortality in a p53-Null Background | Molecular and Cellular Biology
A cascade leading to premature aging phenotypes including abnormal tumor profiles in Werner syndrome (Review)
Frontiers | Structural mechanisms of human RecQ helicases WRN and BLM
Anti-WRN | Bethyl Laboratories | Biomol.com
WRN Gene - GeneCards | WRN Protein | WRN Antibody
![PDF] The Heli-CASE of the Missing WRN Gene | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/6d5a3c2a5f3734e3c363e3dd76363c21cb3519bf/2-Figure1-1.png "PDF] The Heli-CASE of the Missing WRN Gene | Semantic Scholar")
PDF] The Heli-CASE of the Missing WRN Gene | Semantic Scholar
Targeting G-quadruplex for rescuing impaired chondrogenesis in WRN-deficient stem cells | Cell & Bioscience | Full Text
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
Cancers | Free Full-Text | WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype
Model of WRN function in HR. DNA damage, replication, or repair can... | Download Scientific Diagram
WRN mutation update. The 35 exons of WRN gene locus and WRN protein are... | Download Scientific Diagram
DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activities | Aging
The Werner Syndrome Helicase-Nuclease--One Protein, Many Mysteries | Science of Aging Knowledge Environment
