Hasil Pencarian - Junya Awata

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  1. 1
    Single Cell Transcriptomic Analysis in a Mouse Model of Barth Syndrome Reveals Cell-Specific Alterations in Gene Expression and Intercellular Communication

    Single Cell Transcriptomic Analysis in a Mouse Model of Barth Syndrome Reveals Cell-Specific Alterations in Gene Expression and Intercellular Communication oleh Gayani Perera, Liam Power, Amy Larson, Christina J. Codden, Junya Awata, Rebecca Batorsky, Douglas Strathdee, Michael T. Chin

    Diterbitkan 2023-07-01
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  2. 2
    Corrigendum: a novel αB-crystallin R123W variant drives hypertrophic cardiomyopathy by promoting maladaptive calcium-dependent signal transduction

    Corrigendum: a novel αB-crystallin R123W variant drives hypertrophic cardiomyopathy by promoting maladaptive calcium-dependent signal transduction oleh Chun Chou, Gregory L. Martin, Gayani Perera, Junya Awata, Amy Larson, Robert Blanton, Robert Blanton, Michael T. Chin, Michael T. Chin

    Diterbitkan 2024-08-01
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  3. 3
    A novel αB-crystallin R123W variant drives hypertrophic cardiomyopathy by promoting maladaptive calcium-dependent signal transduction

    A novel αB-crystallin R123W variant drives hypertrophic cardiomyopathy by promoting maladaptive calcium-dependent signal transduction oleh Chun Chou, Gregory L. Martin, Gayani Perera, Junya Awata, Amy Larson, Robert Blanton, Robert Blanton, Michael T. Chin, Michael T. Chin

    Diterbitkan 2023-06-01
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  4. 4
    Intramuscular delivery of formulated RNA encoding six linked nanobodies is highly protective for exposures to three Botulinum neurotoxin serotypes

    Intramuscular delivery of formulated RNA encoding six linked nanobodies is highly protective for exposures to three Botulinum neurotoxin serotypes oleh Jean Mukherjee, Celinia A. Ondeck, Jacqueline M. Tremblay, Jacob Archer, Michelle Debatis, Alexa Foss, Junya Awata, Jesse H. Erasmus, Patrick M. McNutt, Charles B. Shoemaker

    Diterbitkan 2022-07-01
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  5. 5
    A Barth Syndrome Patient-Derived <i>D75H</i> Point Mutation in <i>TAFAZZIN</i> Drives Progressive Cardiomyopathy in Mice

    A Barth Syndrome Patient-Derived <i>D75H</i> Point Mutation in <i>TAFAZZIN</i> Drives Progressive Cardiomyopathy in Mice oleh Paige L. Snider, Elizabeth A. Sierra Potchanant, Zejin Sun, Donna M. Edwards, Ka-Kui Chan, Catalina Matias, Junya Awata, Aditya Sheth, P. Melanie Pride, R. Mark Payne, Michael Rubart, Jeffrey J. Brault, Michael T. Chin, Grzegorz Nalepa, Simon J. Conway

    Diterbitkan 2024-07-01
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