Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Vittoria Di Mauro"'
Disease modeling of a mutation in α‐actinin 2 guides clinical therapy in hypertrophic cardiomyopathy
Autor:
Maksymilian Prondzynski, Marc D Lemoine, Antonia TL Zech, András Horváth, Vittoria Di Mauro, Jussi T Koivumäki, Nico Kresin, Josefine Busch, Tobias Krause, Elisabeth Krämer, Saskia Schlossarek, Michael Spohn, Felix W Friedrich, Julia Münch, Sandra D Laufer, Charles Redwood, Alexander E Volk, Arne Hansen, Giulia Mearini, Daniele Catalucci, Christian Meyer, Torsten Christ, Monica Patten, Thomas Eschenhagen, Lucie Carrier
Publikováno v:
EMBO Molecular Medicine, Vol 14, Iss 8, Pp n/a-n/a (2022)
Externí odkaz:
https://doaj.org/article/20088ae3e8874325a43b88d720c8d7fd
Publikováno v:
Biomedicines, Vol 11, Iss 7, p 1907 (2023)
Due to their different biological functions, extracellular vesicles (EVs) have great potential from a therapeutic point of view. They are released by all cell types, carrying and delivering different kinds of biologically functional cargo. Under path
Externí odkaz:
https://doaj.org/article/99841ef86a9a4321a0de438e58987d5c
Autor:
Vittoria Di Mauro, Paola Ceriotti, Francesco Lodola, Nicolò Salvarani, Jessica Modica, Marie-Louise Bang, Andrea Mazzanti, Carlo Napolitano, Silvia G. Priori, Daniele Catalucci
Publikováno v:
Frontiers in Physiology, Vol 11 (2021)
Brugada syndrome (BrS) is an inherited arrhythmogenic disease that may lead to sudden cardiac death in young adults with structurally normal hearts. No pharmacological therapy is available for BrS patients. This situation highlights the urgent need t
Externí odkaz:
https://doaj.org/article/185089ae836f4f82a40fa10a9c2cfed3
Disease modeling of a mutation in α‐actinin 2 guides clinical therapy in hypertrophic cardiomyopathy
Autor:
Maksymilian Prondzynski, Marc D Lemoine, Antonia TL Zech, András Horváth, Vittoria Di Mauro, Jussi T Koivumäki, Nico Kresin, Josefine Busch, Tobias Krause, Elisabeth Krämer, Saskia Schlossarek, Michael Spohn, Felix W Friedrich, Julia Münch, Sandra D Laufer, Charles Redwood, Alexander E Volk, Arne Hansen, Giulia Mearini, Daniele Catalucci, Christian Meyer, Torsten Christ, Monica Patten, Thomas Eschenhagen, Lucie Carrier
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 12, Pp n/a-n/a (2019)
Abstract Hypertrophic cardiomyopathy (HCM) is a cardiac genetic disease accompanied by structural and contractile alterations. We identified a rare c.740C>T (p.T247M) mutation in ACTN2, encoding α‐actinin 2 in a HCM patient, who presented with lef
Externí odkaz:
https://doaj.org/article/3dc134090e7a4e27beee5c5b257be092
Publikováno v:
Non-coding RNA Research, Vol 3, Iss 1, Pp 12-19 (2018)
The cardiovascular system plays a pivotal role in regulating and maintaining homeostasis in the human body. Therefore any alteration in regulatory networks that orchestrate heart development as well as adaptation to physiological and environmental st
Externí odkaz:
https://doaj.org/article/1edbeb7aa22b4aa78b1106fcf8e29be1
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 16, p 8721 (2021)
Cardiomyopathies (CMPs) are a heterogeneous group of myocardial diseases accountable for the majority of cases of heart failure (HF) and/or sudden cardiac death (SCD) worldwide. With the recent advances in genomics, the original classification of CMP
Externí odkaz:
https://doaj.org/article/b49796feedc24616acc5bf852d4bdb2f
Autor:
Pietro Ameri, Gabriele Giacomo Schiattarella, Lia Crotti, Margherita Torchio, Edoardo Bertero, Daniele Rodolico, Maurizio Forte, Vittoria Di Mauro, Roberta Paolillo, Cristina Chimenti, Daniele Torella, Daniele Catalucci, Sebastiano Sciarretta, Cristina Basso, Ciro Indolfi, Cinzia Perrino
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1192 (2020)
Despite important advances in diagnosis and treatment, heart failure (HF) remains a syndrome with substantial morbidity and dismal prognosis. Although implementation and optimization of existing technologies and drugs may lead to better management of
Externí odkaz:
https://doaj.org/article/9c85ae495d3247fab743541576b719c4
Autor:
Jessica Modica, Vittoria Di Mauro, Maria Barandalla-Sobrados, Samuel Elias Pineda Chavez, Pierluigi Carullo, Simona Nemska, Achille Anselmo, Gianluigi Condorelli, Michele Iafisco, Michele Miragoli, Daniele Catalucci
Publikováno v:
Circulation (Online) 144 (2021): 1973–1976. doi:10.1161/CIRCULATIONAHA.121.055866
info:cnr-pdr/source/autori:Modica J.; Di Mauro V.; Barandalla-Sobrados M.; Chavez S.E.P.; Carullo P.; Nemska S.; Anselmo A.; Condorelli G.; Iafisco M.; Miragoli M.; Catalucci D./titolo:Nano-miR-133a Replacement Therapy Blunts Pressure Overload-Induced Heart Failure/doi:10.1161%2FCIRCULATIONAHA.121.055866/rivista:Circulation (Online)/anno:2021/pagina_da:1973/pagina_a:1976/intervallo_pagine:1973–1976/volume:144
info:cnr-pdr/source/autori:Modica J.; Di Mauro V.; Barandalla-Sobrados M.; Chavez S.E.P.; Carullo P.; Nemska S.; Anselmo A.; Condorelli G.; Iafisco M.; Miragoli M.; Catalucci D./titolo:Nano-miR-133a Replacement Therapy Blunts Pressure Overload-Induced Heart Failure/doi:10.1161%2FCIRCULATIONAHA.121.055866/rivista:Circulation (Online)/anno:2021/pagina_da:1973/pagina_a:1976/intervallo_pagine:1973–1976/volume:144
Here we provide the proof-of-concept for an unconventional and effective nanotechnology-based inhalation approach for delivery of a synthetic miRNA mimic via biocompatible and biodegradable calcium phosphate-based nanoparticles (CaPs) preferentially
Autor:
Marco Ronfini, Vittoria Di Mauro, Valentina Prando, Anais Franco Romero, Lolita Dokshokova, Andrea Armani, Giulia Favaro, Silvia Bertoli, Anna Di Bona, Mattia Albiero, Michele Guescini, Marco Sandri, Marco Mongillo, Tania Zaglia
Publikováno v:
Journal of Molecular and Cellular Cardiology. 173:32-33
Autor:
Ines Elia, Giulia Realini, Vittoria Di Mauro, Sara Borghi, Laura Bottoni, Salvatore Tornambè, Libero Vitiello, Stephen J. Weiss, Mario Chiariello, Annalaura Tamburrini, Salvatore Oliviero, Francesco Neri, Maurizio Orlandini, Federico Galvagni
During skeletal myogenesis, the zinc-finger transcription factors SNAI1 and SNAI2, are expressed in proliferating myoblasts and regulate the transition to terminally differentiated myotubes while repressing pro-differentiation genes. Here, we demonst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::670f494fa2b8b2ffd18e90a59af2a46b
https://hdl.handle.net/11577/3479720
https://hdl.handle.net/11577/3479720