Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Angela Paggio"'
Autor:
Claudia Proto, Sara Manglaviti, Giuseppe Lo Russo, Marco Musca, Giulia Galli, Martina Imbimbo, Matteo Perrino, Nadia Cordua, Eliana Rulli, Zelmira Ballatore, Alessandro Dal Maso, Antonio Chella, Andrea Sbrana, Arsela Prelaj, Roberto Ferrara, Mario Occhipinti, Marta Brambilla, Alessandro De Toma, Laura Mazzeo, Teresa Beninato, Diego Signorelli, Giacomo Massa, Francesca Gabriella Greco, Giuseppina Calareso, Daniela Miliziano, Rosa Maria Di Mauro, Giulia Mella, Alessandra Lucarelli, Angela Paggio, Francesca Galli, Valter Torri, Filippo Guglielmo Maria de Braud, Giulia Pasello, Iacopo Petrini, Rossana Berardi, Monica Ganzinelli, Marina Chiara Garassino, Paolo Andrea Zucali
Publikováno v:
Journal of Thoracic Oncology.
Autor:
Fabio Di Lisa, Angela Paggio, Antonio Campo, Roberta Menabò, Diego De Stefani, Ildikò Szabò, Giulia Di Marco, Rosario Rizzuto, Vanessa Checchetto
Publikováno v:
Nature
Mitochondria provide chemical energy for endoergonic reactions in the form of ATP, and their activity must meet cellular energy requirements, but the mechanisms that link organelle performance to ATP levels are poorly understood. Here we confirm the
Publikováno v:
Biophysical Journal. 110(3)
Mitochondria are essential organelles that control a plethora of cellular functions, including ATP production, synthesis of intermediate metabolites, cellular signaling and regulation of cell fate. Their proper functioning is necessary to the health
Autor:
Simona Reina, Angela Paggio, Ildikò Szabò, Diego De Stefani, Rosario Rizzuto, Vito De Pinto, Vanessa Checchetto
Mitochondrial ion channels are of great importance to ensure the proper function of this bioenergetic organelle and to regulate cell fate. However, in many cases our knowledge concerning their molecular identity and regulation is still limited. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68cd745a32040ba50a9a3d80539a3d8d
http://hdl.handle.net/20.500.11769/61362
http://hdl.handle.net/20.500.11769/61362
Autor:
Thomas Langer, Thorsten Decker, Ines Lauria, Ricarda Richter-Dennerlein, Kavya Bakka, Angela Paggio, Maria Patron, Anne Korwitz, Mareike Mühlmeister, Ulrich Brandt, Elena I. Rugarli, Tim König, Simon E. Tröder, Rosario Rizzuto, Philipp A Lampe, Sergio Guerrero-Castillo, Diego De Stefani
Publikováno v:
Mol Cell
Molecular Cell, 64, 1, pp. 148-162
Molecular Cell, 64, 148-162
Molecular Cell, 64, 1, pp. 148-162
Molecular Cell, 64, 148-162
Item does not contain fulltext Mutations in subunits of mitochondrial m-AAA proteases in the inner membrane cause neurodegeneration in spinocerebellar ataxia (SCA28) and hereditary spastic paraplegia (HSP7). m-AAA proteases preserve mitochondrial pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86775fcfc9a16ac65450ff61970eb902
http://hdl.handle.net/11577/3206185
http://hdl.handle.net/11577/3206185
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1859:e93
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857:e62-e63
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857:e10-e11
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857:e70