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Serena Calamaio

Showing results (1-10 of 10) with videos related to

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International Journal of Molecular Sciences|September 9, 2022
T-Type Calcium Channels: A Mixed BlessingDario Melgari, Anthony Frosio, Serena Calamaio, et al.
International Journal of Molecular Sciences|April 13, 2023
Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada SyndromeDario Melgari, Serena Calamaio, Anthony Frosio, et al.
American Journal of Physiology. Cell Physiology|July 11, 2025
Functional reassessment of Nav1.5 T559A reveals loss-of-function in a variant commonly used as wild typeDario Melgari, Marco Villa, Anthony Frosio, et al.
Stem Cell Research|June 14, 2022
Generation of the induced pluripotent stem cell line UNIBSi017-A from an individual with cardiospondylocarpofacial syndrome and the MAP3K7 c.737-7A > G variantSerena Calamaio, Marialaura Serzanti, Silvia Morlino, et al.
Biomedicines|August 26, 2023
Human iPSC-Derived 3D Hepatic Organoids in a Miniaturized Dynamic Culture SystemSerena Calamaio, Marialaura Serzanti, Jennifer Boniotti, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 19, 2026
Exploring light chain cardiotoxicity in AL amyloidosis: impact on hiPSC-derived cardiomyocyte activitySerena Calamaio, Anthony Frosio, Dario Melgari, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|June 6, 2026
Integrated electrophysiological, cellular, and pharmacological profiling reveals variant-specific mechanisms in SCN4A-related myotoniaAnthony Frosio, Serena Calamaio, Serena Pagliarani, et al.
International Journal of Molecular Sciences|October 28, 2023
Unravelling Novel <i>SCN5A</i> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic InsightsAnthony Frosio, Emanuele Micaglio, Ivan Polsinelli, et al.
Epilepsia|September 25, 2023
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic dietJacopo C DiFrancesco, Francesca Ragona, Carmen Murano, et al.
European Heart Journal|July 30, 2024
NaV1.5 autoantibodies in Brugada syndrome: pathogenetic implicationsAdriana Tarantino, Giuseppe Ciconte, Dario Melgari, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
International Journal of Molecular Sciences|September 9, 2022
T-Type Calcium Channels: A Mixed BlessingDario Melgari, Anthony Frosio, Serena Calamaio, et al.
International Journal of Molecular Sciences|April 13, 2023
Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada SyndromeDario Melgari, Serena Calamaio, Anthony Frosio, et al.
American Journal of Physiology. Cell Physiology|July 11, 2025
Functional reassessment of Nav1.5 T559A reveals loss-of-function in a variant commonly used as wild typeDario Melgari, Marco Villa, Anthony Frosio, et al.
Stem Cell Research|June 14, 2022
Generation of the induced pluripotent stem cell line UNIBSi017-A from an individual with cardiospondylocarpofacial syndrome and the MAP3K7 c.737-7A > G variantSerena Calamaio, Marialaura Serzanti, Silvia Morlino, et al.
Biomedicines|August 26, 2023
Human iPSC-Derived 3D Hepatic Organoids in a Miniaturized Dynamic Culture SystemSerena Calamaio, Marialaura Serzanti, Jennifer Boniotti, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 19, 2026
Exploring light chain cardiotoxicity in AL amyloidosis: impact on hiPSC-derived cardiomyocyte activitySerena Calamaio, Anthony Frosio, Dario Melgari, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|June 6, 2026
Integrated electrophysiological, cellular, and pharmacological profiling reveals variant-specific mechanisms in SCN4A-related myotoniaAnthony Frosio, Serena Calamaio, Serena Pagliarani, et al.
International Journal of Molecular Sciences|October 28, 2023
Unravelling Novel <i>SCN5A</i> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic InsightsAnthony Frosio, Emanuele Micaglio, Ivan Polsinelli, et al.
Epilepsia|September 25, 2023
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic dietJacopo C DiFrancesco, Francesca Ragona, Carmen Murano, et al.
European Heart Journal|July 30, 2024
NaV1.5 autoantibodies in Brugada syndrome: pathogenetic implicationsAdriana Tarantino, Giuseppe Ciconte, Dario Melgari, et al.
Pageof 1