Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Benedetta Ermon"'
Autor:
Benedetta Ermon, Claudia B. Volpato, Giada Cattelan, Rosamaria Silipigni, Marina Di Segni, Chiara Cantaloni, Michela Casella, Peter P. Pramstaller, Giulio Pompilio, Elena Sommariva, Viviana Meraviglia, Alessandra Rossini
Publikováno v:
Stem Cell Research, Vol 32, Iss , Pp 78-82 (2018)
Arrhythmogenic Cardiomyopathy (ACM) is an inherited cardiac disease characterized by arrhythmias and fibro-fatty replacement in the ventricular myocardium. Causative mutations are mainly reported in desmosomal genes, especially in plakophilin2 (PKP2)
Externí odkaz:
https://doaj.org/article/8bb11ce4299e44879ecaf8ca8701780a
Autor:
Chiara Volani, Alessandra Pagliaro, Johannes Rainer, Giuseppe Paglia, Benedetta Porro, Ilaria Stadiotti, Luisa Foco, Elisa Cogliati, Adolfo Paolin, Costanza Lagrasta, Caterina Frati, Emilia Corradini, Angela Falco, Theresa Matzinger, Anne Picard, Benedetta Ermon, Silvano Piazza, Marzia De Bortoli, Claudio Tondo, Réginald Philippe, Andrea Medici, Alexandros A. Lavdas, Michael J.F. Blumer, Giulio Pompilio, Elena Sommariva, Peter P. Pramstaller, Jakob Troppmair, Viviana Meraviglia, Alessandra Rossini
Arrhythmogenic cardiomyopathy (ACM) is a genetic disease associated with sudden cardiac death and cardiac fibro-fatty replacement. Over the last years, several works have demonstrated that different epigenetic enzymes can affect not only gene express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59b6d8e1b9d647f3df6704da41212a30
http://hdl.handle.net/10281/387586
http://hdl.handle.net/10281/387586
Autor:
Chiara Cantaloni, Viviana Meraviglia, Giada Cattelan, Giulio Pompilio, Marina Di Segni, Michela Casella, Alessandra Rossini, Benedetta Ermon, Peter P. Pramstaller, Claudia B. Volpato, Elena Sommariva, Rosamaria Silipigni
Publikováno v:
Stem Cell Research, Vol 32, Iss, Pp 78-82 (2018)
Stem Cell Research
Stem Cell Research
Arrhythmogenic Cardiomyopathy (ACM) is an inherited cardiac disease characterized by arrhythmias and fibro-fatty replacement in the ventricular myocardium. Causative mutations are mainly reported in desmosomal genes, especially in plakophilin2 (PKP2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c7f7a05be508bf621a118bae8ed0864
https://doi.org/10.1016/j.scr.2018.09.003
https://doi.org/10.1016/j.scr.2018.09.003