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HomeHealth NewsAddressing a rare genetic disorder characterized by rapid aging in children

Addressing a rare genetic disorder characterized by rapid aging in children

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Fig. 1. Delayed repair of nuclear envelope rupture in HGPS cells. Credit: PNAS Nexus (2024). DOI: 10.1093/pnasnexus/pgae527

Researchers at Nano Life Science Institute (WPI-NanoLSI), Kanazawa University, have discovered how a protein called lamin A helps repair the protective barrier around a cell’s DNA. The findings reveal lamin A’s unique role…

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