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Effect of mechanical strain on the collagen VI pericellular matrix in anterior cruciate ligament fibroblasts. [electronic resource] by
- Sardone, Francesca
- Traina, Francesco
- Tagliavini, Francesca
- Pellegrini, Camilla
- Merlini, Luciano
- Squarzoni, Stefano
- Santi, Spartaco
- Neri, Simona
- Faldini, Cesare
- Maraldi, Nadir
- Sabatelli, Patrizia
Producer: 20140513
In:
Journal of cellular physiology vol. 229
Availability: No items available.
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7.
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DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions. [electronic resource] by
- Caporali, Leonardo
- Bello, Luca
- Tagliavini, Francesca
- La Morgia, Chiara
- Maresca, Alessandra
- Di Vito, Lidia
- Liguori, Rocco
- Valentino, Maria Lucia
- Cecchin, Diego
- Pegoraro, Elena
- Carelli, Valerio
Producer: 20190314
In:
Brain : a journal of neurology vol. 141
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8.
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Aggresome-Autophagy Involvement in a Sarcopenic Patient with Rigid Spine Syndrome and a p.C150R Mutation in FHL1 Gene. [electronic resource] by
- Sabatelli, Patrizia
- Castagnaro, Silvia
- Tagliavini, Francesca
- Chrisam, Martina
- Sardone, Francesca
- Demay, Laurence
- Richard, Pascale
- Santi, Spartaco
- Maraldi, Nadir M
- Merlini, Luciano
- Sandri, Marco
- Bonaldo, Paolo
Producer: 20140905
In:
Frontiers in aging neuroscience vol. 6
Availability: No items available.
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9.
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Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury response. [electronic resource] by
- Sardone, Francesca
- Santi, Spartaco
- Tagliavini, Francesca
- Traina, Francesco
- Merlini, Luciano
- Squarzoni, Stefano
- Cescon, Matilde
- Wagener, Raimund
- Maraldi, Nadir Mario
- Bonaldo, Paolo
- Faldini, Cesare
- Sabatelli, Patrizia
Producer: 20180221
In:
Matrix biology : journal of the International Society for Matrix Biology vol. 55
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10.
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Melanocytes from Patients Affected by Ullrich Congenital Muscular Dystrophy and Bethlem Myopathy have Dysfunctional Mitochondria That Can be Rescued with Cyclophilin Inhibitors. [electronic resource] by
- Zulian, Alessandra
- Tagliavini, Francesca
- Rizzo, Erika
- Pellegrini, Camilla
- Sardone, Francesca
- Zini, Nicoletta
- Maraldi, Nadir Mario
- Santi, Spartaco
- Faldini, Cesare
- Merlini, Luciano
- Petronilli, Valeria
- Bernardi, Paolo
- Sabatelli, Patrizia
Producer: 20141205
In:
Frontiers in aging neuroscience vol. 6
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11.
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NIM811, a cyclophilin inhibitor without immunosuppressive activity, is beneficial in collagen VI congenital muscular dystrophy models. [electronic resource] by
- Zulian, Alessandra
- Rizzo, Erika
- Schiavone, Marco
- Palma, Elena
- Tagliavini, Francesca
- Blaauw, Bert
- Merlini, Luciano
- Maraldi, Nadir Mario
- Sabatelli, Patrizia
- Braghetta, Paola
- Bonaldo, Paolo
- Argenton, Francesco
- Bernardi, Paolo
Producer: 20150603
In:
Human molecular genetics vol. 23
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12.
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Novel mutations in DNA2 associated with myopathy and mtDNA instability. [electronic resource] by
- Ronchi, Dario
- Liu, Changwei
- Caporali, Leonardo
- Piga, Daniela
- Li, Hongzhi
- Tagliavini, Francesca
- Valentino, Maria Lucia
- Ferrò, Maria Teresa
- Bini, Paola
- Zheng, Li
- Carelli, Valerio
- Shen, Binghui
- Comi, Giacomo Pietro
Producer: 20200512
In:
Annals of clinical and translational neurology vol. 6
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13.
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Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models. [electronic resource] by
- Iannielli, Angelo
- Bido, Simone
- Folladori, Lucrezia
- Segnali, Alice
- Cancellieri, Cinzia
- Maresca, Alessandra
- Massimino, Luca
- Rubio, Alicia
- Morabito, Giuseppe
- Caporali, Leonardo
- Tagliavini, Francesca
- Musumeci, Olimpia
- Gregato, Giuliana
- Bezard, Erwan
- Carelli, Valerio
- Tiranti, Valeria
- Broccoli, Vania
Producer: 20190527
In:
Cell reports vol. 22
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14.
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Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome. [electronic resource] by
- La Morgia, Chiara
- Maresca, Alessandra
- Amore, Giulia
- Gramegna, Laura Ludovica
- Carbonelli, Michele
- Scimonelli, Emanuela
- Danese, Alberto
- Patergnani, Simone
- Caporali, Leonardo
- Tagliavini, Francesca
- Del Dotto, Valentina
- Capristo, Mariantonietta
- Sadun, Federico
- Barboni, Piero
- Savini, Giacomo
- Evangelisti, Stefania
- Bianchini, Claudio
- Valentino, Maria Lucia
- Liguori, Rocco
- Tonon, Caterina
- Giorgi, Carlotta
- Pinton, Paolo
- Lodi, Raffaele
- Carelli, Valerio
Producer: 20201204
In:
Scientific reports vol. 10
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15.
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Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy. [electronic resource] by
- Caporali, Leonardo
- Iommarini, Luisa
- La Morgia, Chiara
- Olivieri, Anna
- Achilli, Alessandro
- Maresca, Alessandra
- Valentino, Maria Lucia
- Capristo, Mariantonietta
- Tagliavini, Francesca
- Del Dotto, Valentina
- Zanna, Claudia
- Liguori, Rocco
- Barboni, Piero
- Carbonelli, Michele
- Cocetta, Veronica
- Montopoli, Monica
- Martinuzzi, Andrea
- Cenacchi, Giovanna
- De Michele, Giuseppe
- Testa, Francesco
- Nesti, Anna
- Simonelli, Francesca
- Porcelli, Anna Maria
- Torroni, Antonio
- Carelli, Valerio
Producer: 20180718
In:
PLoS genetics vol. 14
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16.
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DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism. [electronic resource] by
- Maresca, Alessandra
- Del Dotto, Valentina
- Capristo, Mariantonietta
- Scimonelli, Emanuela
- Tagliavini, Francesca
- Morandi, Luca
- Tropeano, Concetta Valentina
- Caporali, Leonardo
- Mohamed, Susan
- Roberti, Marina
- Scandiffio, Letizia
- Zaffagnini, Mirko
- Rossi, Jacopo
- Cappelletti, Martina
- Musiani, Francesco
- Contin, Manuela
- Riva, Roberto
- Liguori, Rocco
- Pizza, Fabio
- La Morgia, Chiara
- Antelmi, Elena
- Loguercio Polosa, Paola
- Mignot, Emmanuel
- Zanna, Claudia
- Plazzi, Giuseppe
- Carelli, Valerio
Producer: 20210813
In:
Human molecular genetics vol. 29
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17.
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ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy. [electronic resource] by
- Caporali, Leonardo
- Magri, Stefania
- Legati, Andrea
- Del Dotto, Valentina
- Tagliavini, Francesca
- Balistreri, Francesca
- Nasca, Alessia
- La Morgia, Chiara
- Carbonelli, Michele
- Valentino, Maria L
- Lamantea, Eleonora
- Baratta, Silvia
- Schöls, Ludger
- Schüle, Rebecca
- Barboni, Piero
- Cascavilla, Maria L
- Maresca, Alessandra
- Capristo, Mariantonietta
- Ardissone, Anna
- Pareyson, Davide
- Cammarata, Gabriella
- Melzi, Lisa
- Zeviani, Massimo
- Peverelli, Lorenzo
- Lamperti, Costanza
- Marzoli, Stefania B
- Fang, Mingyan
- Synofzik, Matthis
- Ghezzi, Daniele
- Carelli, Valerio
- Taroni, Franco
Producer: 20201013
In:
Annals of neurology vol. 88
Availability: No items available.
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18.
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SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder. [electronic resource] by
- Del Dotto, Valentina
- Ullah, Farid
- Di Meo, Ivano
- Magini, Pamela
- Gusic, Mirjana
- Maresca, Alessandra
- Caporali, Leonardo
- Palombo, Flavia
- Tagliavini, Francesca
- Baugh, Evan Harris
- Macao, Bertil
- Szilagyi, Zsolt
- Peron, Camille
- Gustafson, Margaret A
- Khan, Kamal
- La Morgia, Chiara
- Barboni, Piero
- Carbonelli, Michele
- Valentino, Maria Lucia
- Liguori, Rocco
- Shashi, Vandana
- Sullivan, Jennifer
- Nagaraj, Shashi
- El-Dairi, Mays
- Iannaccone, Alessandro
- Cutcutache, Ioana
- Bertini, Enrico
- Carrozzo, Rosalba
- Emma, Francesco
- Diomedi-Camassei, Francesca
- Zanna, Claudia
- Armstrong, Martin
- Page, Matthew
- Stong, Nicholas
- Boesch, Sylvia
- Kopajtich, Robert
- Wortmann, Saskia
- Sperl, Wolfgang
- Davis, Erica E
- Copeland, William C
- Seri, Marco
- Falkenberg, Maria
- Prokisch, Holger
- Katsanis, Nicholas
- Tiranti, Valeria
- Pippucci, Tommaso
- Carelli, Valerio
Producer: 20200724
In:
The Journal of clinical investigation vol. 130
Availability: No items available.
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