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Acetylation of Werner protein at K1127 and K1117 is important for nuclear trafficking and DNA repair - ScienceDirect
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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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Frontiers | Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming
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WRN suppresses p53/PUMA-induced apoptosis in colorectal cancer with microsatellite instability/mismatch repair deficiency | PNAS
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The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases: Trends in Genetics
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Cancers | Free Full-Text | WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype
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Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A | Scientific Reports
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WRN mutation update. The 35 exons of WRN gene locus and WRN protein are... | Download Scientific Diagram
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Targeting G-quadruplex for rescuing impaired chondrogenesis in WRN-deficient stem cells | Cell & Bioscience | Full Text
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Association of epigenetic inactivation of the WRN gene with anticancer drug sensitivity in cervical cancer cells
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CDK2 phosphorylation of Werner protein (WRN) contributes to WRN's DNA double‐strand break repair pathway choice - Lee - 2021 - Aging Cell - Wiley Online Library
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