Werner syndrome: MedlinePlus Genetics
Acetylation of Werner protein at K1127 and K1117 is important for nuclear trafficking and DNA repair - ScienceDirect
The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases: Trends in Genetics
Mutation Database
The WRN gene and its putative association with human ageing
Genes | Free Full-Text | Research on Werner Syndrome: Trends from Past to Present and Future Prospects
A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity | PNAS
Targeting G-quadruplex for rescuing impaired chondrogenesis in WRN-deficient stem cells | Cell & Bioscience | Full Text
Representation of the WRN protein and summary of the most common WRN... | Download Scientific Diagram
Werner syndrome helicase - Wikipedia
International Registry of Werner Syndrome / WRN Gene
Frontiers | Structural mechanisms of human RecQ helicases WRN and BLM
WRN Gene - GeneCards | WRN Protein | WRN Antibody
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 (WRN) gene variants and their association with altered function and age-associated diseases
Werner Syndrome ATP Dependent Helicase - an overview | ScienceDirect Topics
Genetic correction of Werner syndrome gene reveals impaired pro‐angiogenic function and HGF insufficiency in mesenchymal stem cells - Tu - 2020 - Aging Cell - Wiley Online Library
WRN Helicase Activity Assay Kit
The Role of WRN Helicase/Exonuclease in DNA Replication | IntechOpen
Werner syndrome - Wikipedia
WRN Antibody (NB100-471): Novus Biologicals
Enigmatic role of WRN-RECQL helicase in DNA repair and its implications in cancer
File:WRN location.png - Wikimedia Commons
The Role of WRN Helicase/Exonuclease in DNA Replication | IntechOpen
Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A | Scientific Reports
