Molecular strategies to treat inherited arrhythmias

Project Information

EU-rhythmy

Grant agreement ID: 669387

DOI 10.3030/669387

Project closed

EC signature date 5 October 2015

Start date 1 November 2015

End date 31 October 2021

Funded under

• EXCELLENT SCIENCE - European Research Council (ERC)

Total cost € 2 314 029,00

EU contribution € 2 314 029,00

Coordinated by

UNIVERSITA DEGLI STUDI DI PAVIA
Italy

CORDIS provides links to public deliverables and publications of HORIZON projects.

Links to deliverables and publications from FP7 projects, as well as links to some specific result types such as dataset and software, are dynamically retrieved from OpenAIRE .

Publications

Peer reviewed articles (5)

A Network of Macrophages Supports Mitochondrial Homeostasis in the Heart

Author(s): José Ángel Nicolás-Ávila; Ana Victoria Lechuga-Vieco; Lorena Esteban-Martínez; María Sánchez-Díaz; Elena Díaz-García; Demetrio J. Santiago; Andrea Rubio-Ponce; Jackson LiangYao Li; Jackson LiangYao Li; Akhila Balachander; Juan A. Quintana; Raquel Martínez-de-Mena; Beatriz Castejón-Vega; Andrés Pun-García; Paqui G. Través; Elena Bonzón-Kulichenko; Fernando García-Marqués; Lorena C
Published in: Cell, Issue Volume 183, Issue 1, 2020, Page(s) 94-109, ISSN 0092-8674
Publisher: Cell Press
DOI: 10.1016/j.cell.2020.08.031

Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia

Author(s): Francesco Lodola; Diego Morone; Marco Denegri; Rossana Bongianino; Hiroko Nakahama; Lucia Rutigliano; Rosanna Gosetti; Giulia Rizzo; Alessandra Vollero; Michelangelo Buonocore; Carlo Napolitano; Gianluigi Condorelli; Gianluigi Condorelli; Silvia G. Priori; Elisa Di Pasquale
Published in: Cell Death and Disease, Issue Volume 7, Issue 106, 2016, Page(s) Article number e2393, ISSN 2041-4889
Publisher: Nature Publishing Group
DOI: 10.1038/cddis.2016.304

Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2).

Author(s): Rossana Bongianino; Marco Denegri; Andrea Mazzanti; Francesco Lodola; Alessandra Vollero; Simona Boncompagni; Silvia Fasciano; Giulia Rizzo; Damiano Mangione; Serena Barbaro; Alessia Di Fonso; Carlo Napolitano; Alberto Auricchio; Feliciano Protasi; Silvia G. Priori
Published in: Circulation Research, Issue Volume 121, Issue 5,, 2017, Page(s) 525-536, ISSN 0009-7330
Publisher: Lippincott Williams & Wilkins Ltd.
DOI: 10.1161/circresaha.117.310882

Cardiac ryanodine receptor calcium release deficiency syndrome

Author(s): Bo Sun; Bo Sun; Jinjing Yao; Mingke Ni; Jinhong Wei; Xiaowei Zhong; Wenting Guo; Lin Zhang; Ruiwu Wang; Darrell D. Belke; Yong-Xiang Chen; Krystien V.V. Lieve; Anders Krogh Broendberg; Thomas M. Roston; Ivan Blankoff; Janneke A.E. Kammeraad; Johannes C. von Alvensleben; Julieta Lazarte; Alexander Vallmitjana; Loryn J. Bohne; Robert A. Rose; Raul Benitez; Leif Hove-Madsen; Carlo Napolitano; Robert
Published in: Science Translational Medicine, Issue Volume 13, Issue 5793, 2021, Page(s) Article number eaba7287, ISSN 1946-6234
Publisher: American Association for the Advancement of Science
DOI: 10.1126/scitranslmed.aba7287

Precision Medicine in Catecholaminergic Polymorphic Ventricular Tachycardia: JACC Focus Seminar 5/5.

Author(s): Silvia G. Priori; Silvia G. Priori; Andrea Mazzanti; Demetrio J. Santiago; Deni Kukavica; Alessandro Trancuccio; Jason C. Kovacic; Jason C. Kovacic; Jason C. Kovacic
Published in: Journal of the American College of Cardiology, Issue Volume 77, Issue 20, 2021, Page(s) 2592-2612, ISSN 0735-1097
Publisher: Elsevier BV
DOI: 10.1016/j.jacc.2020.12.073