Showing 1 - 2 results of 2 for search '"WRN"', query time: 0.02s Refine Results
  1. 1
    Werner Syndrome Caused by Homozygous Frameshift Variant c.1578del in WRN

    Werner Syndrome Caused by Homozygous Frameshift Variant c.1578del in WRN by Jovita Patricija Druta, Gunda Petraitytė, Aušra Sasnauskienė, Eglė Preikšaitienė

    Published 2024-12-01
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  2. 2
    Amelioration of premature aging in Werner syndrome stem cells by targeting SHIP/AKT pathway

    Amelioration of premature aging in Werner syndrome stem cells by targeting SHIP/AKT pathway by Hei-Yin Tam, Jiaxing Liu, Tsz-Ching Yiu, Adrian On-Wah Leung, Chang Li, Shen Gu, Owen Rennert, Boxian Huang, Hoi-Hung Cheung

    Published 2025-01-01
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