Works matching AU Rajan, Deepa S.


Results: 8
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    Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22627-w
    By:
    • Kour, Sukhleen;
    • Rajan, Deepa S.;
    • Fortuna, Tyler R.;
    • Anderson, Eric N.;
    • Ward, Caroline;
    • Lee, Youngha;
    • Lee, Sangmoon;
    • Shin, Yong Beom;
    • Chae, Jong-Hee;
    • Choi, Murim;
    • Siquier, Karine;
    • Cantagrel, Vincent;
    • Amiel, Jeanne;
    • Stolerman, Elliot S.;
    • Barnett, Sarah S.;
    • Cousin, Margot A.;
    • Castro, Diana;
    • McDonald, Kimberly;
    • Kirmse, Brian;
    • Nemeth, Andrea H.
    Publication type:
    Article
    5

    SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration.

    Published in:
    Acta Neuropathologica, 2023, v. 146, n. 3, p. 477, doi. 10.1007/s00401-023-02607-8
    By:
    • Fortuna, Tyler R.;
    • Kour, Sukhleen;
    • Chimata, Anuradha Venkatakrishnan;
    • Muiños-Bühl, Anixa;
    • Anderson, Eric N.;
    • Nelson IV, Charlie H.;
    • Ward, Caroline;
    • Chauhan, Om;
    • O'Brien, Casey;
    • Rajasundaram, Dhivyaa;
    • Rajan, Deepa S.;
    • Wirth, Brunhilde;
    • Singh, Amit;
    • Pandey, Udai Bhan
    Publication type:
    Article
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