نتائج البحث - Nithya Selvan

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  1. 1
    A mutant O-GlcNAcase as a probe to reveal global dynamics of protein O-GlcNAcylation during <i>Drosophila</i> embryonic development

    A mutant O-GlcNAcase as a probe to reveal global dynamics of protein O-GlcNAcylation during <i>Drosophila</i> embryonic development حسب Daniel Mariappa, Nithya Selvan, Vladimir S. Borodkin, Jana Alonso, Andrew T. Ferenbach, Claire Shepherd, Iva Navrátilová, Daan M. F. van Aalten

    منشور في 2015
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  2. 2
    Preclinical efficacy and safety of AAVrh10-based plakophilin-2 gene therapy (LX2020) as a treatment for arrhythmogenic cardiomyopathy

    Preclinical efficacy and safety of AAVrh10-based plakophilin-2 gene therapy (LX2020) as a treatment for arrhythmogenic cardiomyopathy حسب Jing Zhang, Erika J. Gutiérrez-Lara, Aryanne Do, Lena Nguyen, Anju Nair, Nithya Selvan, Tim Fenn, Eric Adler, Richie Khanna, Farah Sheikh

    منشور في 2025
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  3. 3
    A mutant O-GlcNAcase enriches Drosophila developmental regulators

    A mutant O-GlcNAcase enriches Drosophila developmental regulators حسب Nithya Selvan, Ritchie Williamson, Daniel Mariappa, David G. Campbell, Robert Gourlay, Andrew T. Ferenbach, Tonia Aristotelous, Iva Hopkins-Navratilova, Matthias Trost, Daan M. F. van Aalten

    منشور في 2017
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  4. 4
    O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling

    O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling حسب Nithya Selvan, Stephan George, Fatema Serajee, Marie Shaw, Lynne Hobson, Vera M. Kalscheuer, Nripesh Prasad, Shawn Levy, Juliet Taylor, Salim Aftimos, Charles E. Schwartz, Ahm M. Huq, Jozef Gécz, Lance Wells

    منشور في 2018
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  5. 5
    Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability

    Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability حسب Krithika Vaidyanathan, Tejasvi Niranjan, Nithya Selvan, Chin Fen Teo, Melanie May, Sneha Patel, Brent Weatherly, Cindy Skinner, John M. Opitz, John C. Carey, David Viskochil, Jozef Gécz, Marie Shaw, Yunhui Peng, Emil Alexov, Tao Wang, Charles E. Schwartz, Lance Wells

    منشور في 2017
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