Notch Signal Mediates the Cross-Interaction between M2 Muscarinic Acetylcholine Receptor and Neuregulin/ErbB Pathway: Effects on Schwann Cell Proliferation

por Piovesana, Roberta, Pisano, Annalinda, Loreti, Simona, Ricordy, Ruggero, Talora, Claudio, Tata, Ada Maria
Publicado 2022

New Insights and Evidence on “Food Intolerances”: Non-Celiac Gluten Sensitivity and Nickel Allergic Contact Mucositis

por Greco, Nicoletta, Pisano, Annalinda, Mezzatesta, Laura, Pettinelli, Marta, Meacci, Arianna, Pignataro, Maria Gemma, Giordano, Carla, Picarelli, Antonio
Publicado 2023

Can IDO activity predict primary resistance to anti-PD-1 treatment in NSCLC?

por Botticelli, Andrea, Cerbelli, Bruna, Lionetto, Luana, Zizzari, Ilaria, Salati, Massimiliano, Pisano, Annalinda, Federica, Mazzuca, Simmaco, Maurizio, Nuti, Marianna, Marchetti, Paolo
Publicado 2018

Overexpression in metastatic breast cancer supports Syndecan-1 as a marker of invasiveness and poor prognosis

por Cerbelli, Bruna, Pisano, Annalinda, Pignataro, Maria Gemma, Pernazza, Angelina, Botticelli, Andrea, Carosi, Mariantonia, Costarelli, Leopoldo, Allegretti, Matteo, d’Amati, Giulia, Cordone, Iole
Publicado 2022

Mitochondrial Energetics and Ca(2+)-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy

por Lombardi, Maria, Lazzeroni, Davide, Pisano, Annalinda, Girolami, Francesca, Alfieri, Ottavio, La Canna, Giovanni, d’Amati, Giulia, Olivotto, Iacopo, Rimoldi, Ornella E., Foglieni, Chiara, Camici, Paolo G.
Publicado 2020

Neuromuscular magnetic stimulation counteracts muscle decline in ALS patients: results of a randomized, double-blind, controlled study

por Musarò, Antonio, Dobrowolny, Gabriella, Cambieri, Chiara, Onesti, Emanuela, Ceccanti, Marco, Frasca, Vittorio, Pisano, Annalinda, Cerbelli, Bruna, Lepore, Elisa, Ruffolo, Gabriele, Cifelli, Pierangelo, Roseti, Cristina, Giordano, Carla, Gori, Maria Cristina, Palma, Eleonora, Inghilleri, Maurizio
Publicado 2019

RNA‐seq profiling reveals different pathways between remodeled vessels and myocardium in hypertrophic cardiomyopathy

por Pisano, Annalinda, Pera, Loredana Le, Carletti, Raffaella, Cerbelli, Bruna, Pignataro, Maria G., Pernazza, Angelina, Ferre, Fabrizio, Lombardi, Maria, Lazzeroni, Davide, Olivotto, Iacopo, Rimoldi, Ornella E., Foglieni, Chiara, Camici, Paolo G., d'Amati, Giulia
Publicado 2022

Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations

por Perli, Elena, Fiorillo, Annarita, Giordano, Carla, Pisano, Annalinda, Montanari, Arianna, Grazioli, Paola, Campese, Antonio F., Di Micco, Patrizio, Tuppen, Helen A., Genovese, Ilaria, Poser, Elena, Preziuso, Carmela, Taylor, Robert W., Morea, Veronica, Colotti, Gianni, d'Amati, Giulia
Publicado 2016

Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy

por Pippucci, Tommaso, Maresca, Alessandra, Magini, Pamela, Cenacchi, Giovanna, Donadio, Vincenzo, Palombo, Flavia, Papa, Valentina, Incensi, Alex, Gasparre, Giuseppe, Valentino, Maria Lucia, Preziuso, Carmela, Pisano, Annalinda, Ragno, Michele, Liguori, Rocco, Giordano, Carla, Tonon, Caterina, Lodi, Raffaele, Parmeggiani, Antonia, Carelli, Valerio, Seri, Marco
Publicado 2015

Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure

por Pisano, Annalinda, Cerbelli, Bruna, Perli, Elena, Pelullo, Maria, Bargelli, Valentina, Preziuso, Carmela, Mancini, Massimiliano, He, Langping, Bates, Matthew GD, Lucena, Joaquin R, Della Monica, Paola Lilla, Familiari, Giuseppe, Petrozza, Vincenzo, Nediani, Chiara, Taylor, Robert W, d’Amati, Giulia, Giordano, Carla
Publicado 2016

The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells

por Perli, Elena, Giordano, Carla, Pisano, Annalinda, Montanari, Arianna, Campese, Antonio F, Reyes, Aurelio, Ghezzi, Daniele, Nasca, Alessia, Tuppen, Helen A, Orlandi, Maurizia, Di Micco, Patrizio, Poser, Elena, Taylor, Robert W, Colotti, Gianni, Francisci, Silvia, Morea, Veronica, Frontali, Laura, Zeviani, Massimo, d'Amati, Giulia
Publicado 2014

Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement

por Perli, Elena, Pisano, Annalinda, Glasgow, Ruth I. C., Carbo, Miriam, Hardy, Steven A., Falkous, Gavin, He, Langping, Cerbelli, Bruna, Pignataro, Maria Gemma, Zacara, Elisabetta, Re, Federica, Della Monica, Paola Lilla, Morea, Veronica, Bonnen, Penelope E., Taylor, Robert W., d’Amati, Giulia, Giordano, Carla
Publicado 2019

Myosins and MyomiR Network in Patients with Obstructive Hypertrophic Cardiomyopathy

por Foglieni, Chiara, Lombardi, Maria, Lazzeroni, Davide, Zerboni, Riccardo, Lazzarini, Edoardo, Bertoli, Gloria, Pisano, Annalinda, Girolami, Francesca, Andolfo, Annapaola, Magagnotti, Cinzia, Peretto, Giovanni, Sartorio, Carmem L., Olivotto, Iacopo, La Canna, Giovanni, Alfieri, Ottavio, Rimoldi, Ornella E., Barile, Lucio, d’Amati, Giulia, Camici, Paolo G.
Publicado 2022

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy

por Giordano, Carla, Iommarini, Luisa, Giordano, Luca, Maresca, Alessandra, Pisano, Annalinda, Valentino, Maria Lucia, Caporali, Leonardo, Liguori, Rocco, Deceglie, Stefania, Roberti, Marina, Fanelli, Francesca, Fracasso, Flavio, Ross-Cisneros, Fred N., D’Adamo, Pio, Hudson, Gavin, Pyle, Angela, Yu-Wai-Man, Patrick, Chinnery, Patrick F., Zeviani, Massimo, Salomao, Solange R., Berezovsky, Adriana, Belfort, Rubens, Ventura, Dora Fix, Moraes, Milton, Moraes Filho, Milton, Barboni, Piero, Sadun, Federico, De Negri, Annamaria, Sadun, Alfredo A., Tancredi, Andrea, Mancini, Massimiliano, d’Amati, Giulia, Loguercio Polosa, Paola, Cantatore, Palmiro, Carelli, Valerio
Publicado 2014