Hasil Pencarian - Dario Melgari

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  1. 1
    T-Type Calcium Channels: A Mixed Blessing

    T-Type Calcium Channels: A Mixed Blessing oleh Dario Melgari, Anthony Frosio, Serena Calamaio, Gaia A. Marzi, Carlo Pappone, Ilaria Rivolta

    Diterbitkan 2022-08-01
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  2. 2
    Action potential clamp and pharmacology of the variant 1 Short QT Syndrome T618I hERG K⁺ channel.

    Action potential clamp and pharmacology of the variant 1 Short QT Syndrome T618I hERG K⁺ channel. oleh Aziza El Harchi, Dario Melgari, Yi Hong Zhang, Henggui Zhang, Jules C Hancox

    Diterbitkan 2012-01-01
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  3. 3
    Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome

    Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome oleh Dario Melgari, Serena Calamaio, Anthony Frosio, Rachele Prevostini, Luigi Anastasia, Carlo Pappone, Ilaria Rivolta

    Diterbitkan 2023-04-01
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  4. 4
    Propranolol Attenuates Late Sodium Current in a Long QT Syndrome Type 3-Human Induced Pluripotent Stem Cell Model

    Propranolol Attenuates Late Sodium Current in a Long QT Syndrome Type 3-Human Induced Pluripotent Stem Cell Model oleh Sayako Hirose, Takeru Makiyama, Dario Melgari, Dario Melgari, Yuta Yamamoto, Yuta Yamamoto, Yimin Wuriyanghai, Fumika Yokoi, Suguru Nishiuchi, Takeshi Harita, Mamoru Hayano, Hirohiko Kohjitani, Jingshan Gao, Asami Kashiwa, Misato Nishikawa, Jie Wu, Jie Wu, Jun Yoshimoto, Kazuhisa Chonabayashi, Seiko Ohno, Yoshinori Yoshida, Minoru Horie, Minoru Horie, Takeshi Kimura

    Diterbitkan 2020-08-01
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  5. 5
    Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly

    Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly oleh Junichi Ozawa, Seiko Ohno, Dario Melgari, Qi Wang, Megumi Fukuyama, Futoshi Toyoda, Takeru Makiyama, Masao Yoshinaga, Hiroshi Suzuki, Akihiko Saitoh, Tomohiko Ai, Minoru Horie

    Diterbitkan 2022-11-01
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  6. 6
    Novel <i>SCN5A</i> p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths

    Novel <i>SCN5A</i> p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths oleh Michelle M. Monasky, Emanuele Micaglio, Giuseppe Ciconte, Ilaria Rivolta, Valeria Borrelli, Andrea Ghiroldi, Sara D’Imperio, Anna Binda, Dario Melgari, Sara Benedetti, Predrag Mitrovic, Luigi Anastasia, Valerio Mecarocci, Žarko Ćalović, Giorgio Casari, Carlo Pappone

    Diterbitkan 2021-04-01
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  7. 7
    Alterations of the Sialylation Machinery in Brugada Syndrome

    Alterations of the Sialylation Machinery in Brugada Syndrome oleh Andrea Ghiroldi, Giuseppe Ciconte, Pasquale Creo, Adriana Tarantino, Dario Melgari, Sara D’Imperio, Marco Piccoli, Federica Cirillo, Emanuele Micaglio, Michelle M. Monasky, Anthony Frosio, Emanuela T. Locati, Gabriele Vicedomini, Ilaria Rivolta, Carlo Pappone, Luigi Anastasia

    Diterbitkan 2022-10-01
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  8. 8
    Unravelling Novel <i>SCN5A</i> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

    Unravelling Novel <i>SCN5A</i> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights oleh Anthony Frosio, Emanuele Micaglio, Ivan Polsinelli, Serena Calamaio, Dario Melgari, Rachele Prevostini, Andrea Ghiroldi, Anna Binda, Paola Carrera, Marco Villa, Flavio Mastrocinque, Silvia Presi, Raffaele Salerno, Antonio Boccellino, Luigi Anastasia, Giuseppe Ciconte, Stefano Ricagno, Carlo Pappone, Ilaria Rivolta

    Diterbitkan 2023-10-01
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