Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rosanna Carroccia"'
Autor:
Antonio Cuneo, Giovanni Guerra, Gianluigi Castoldi, Rosanna Carroccia, Alessia Tieghi, Matteo G. Della Porta, Barbara Castagnari, Maria Ciccone, Gian Matteo Rigolin, Francesco Cavazzini, Letizia Zenone Bragotti
Publikováno v:
British Journal of Haematology. 120:953-959
The urokinase-type plasminogen activator (uPA) system, which consists of a proteinase (uPA), a receptor (uPAR or CD87) and inhibitors, is involved in proteolysis, cell migration, tissue remodelling, angiogenesis and cell adhesion. Recent findings sug
Autor:
Pasquale Montagna, Britta Baumann, Rosanna Carroccia, Nico Fuhrmann, Michela Rugolo, Giovanna Cenacchi, Simone Schaich, Anna Ghelli, Monika Papke, Raffaele Lodi, Rocco Liguori, Bernd Wissinger, Valerio Carelli, Marcel V. Alavi, Piero Barboni, Richard J. Youle, Maria Pia Giannoccaro, Laura Bucchi, Simone Schimpf, Lora Longanesi, Claudia Zanna, Caterina Tonon, Maria Lucia Valentino, Sabine Tippmann, Luisa Iommarini
Publikováno v:
Human molecular genetics. 20(10)
Dominant optic atrophy (DOA) is genetically heterogeneous and pathogenic mutations have been identified in the OPA1 and OPA3 genes, both encoding for mitochondrial proteins. We characterized clinical and laboratory features in a large OPA1-negative f
Autor:
Rafael Garesse, Carmen Ayuso, Bernd Wissinger, Katell Beauvais, Luisa Iommarini, Joaquiotan Arenas, Dominique Figarella-Branger, Yolanda Campos, Valerio Carelli, Chiara La Morgia, Miguel A. Martín, Alain Furby, Michela Rugolo, Andrea Cossarizza, Claudia Zanna, Pascal Reynier, Pascale Marcorelles, Maria Liguori, Henry Rivera, Jesús González de la Aleja, Pasquale Montagna, María Esther Gallardo, Guy Lenaers, Robert Schwarzenbacher, Rosanna Carroccia, Patrizia Amati-Bonneau, Franck Letournel, Dominique Bonneau, Rocco Liguori, Belén Bornstein, Anne Boissiere, Maria Lucia Valentino, Christophe Verny, Pierre Labauge
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2008, 131 (Pt 2), pp.338-51. ⟨10.1093/brain/awm298⟩
Brain-A Journal of Neurology, 2008, 131 (Pt 2), pp.338-51. ⟨10.1093/brain/awm298⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Brain-A Journal of Neurology, Oxford University Press (OUP), 2008, 131 (Pt 2), pp.338-51. ⟨10.1093/brain/awm298⟩
Brain-A Journal of Neurology, 2008, 131 (Pt 2), pp.338-51. ⟨10.1093/brain/awm298⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License.-- et al.
Mutations in OPA1, a dynamin-related GTPase involved in mitochondrial fusion, cristae organization and control of apo
Mutations in OPA1, a dynamin-related GTPase involved in mitochondrial fusion, cristae organization and control of apo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeca1b2b92e1571ea516c89c32dd04b4
https://www.hal.inserm.fr/inserm-00293604
https://www.hal.inserm.fr/inserm-00293604
Autor:
Marina Mattiazzi, Marcello Amadori, Luisa Iommarini, Simonetta Sangiorgi, Alessandra Maresca, Lucia Lanzi, Rosanna Carroccia, Maria Lucia Valentino, Valerio Carelli, Chiara La Morgia, Sabrina Farne, B. Foscarini, Marzio Bellan
Ocular involvement is a prevalent feature in mitochondrial diseases. Leber's hereditary optic neuropathy (LHON) and dominant optic atrophy (DOA) are both non-syndromic optic neuropathies with a mitochondrial etiology. LHON is associated with point mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9176ccbfeeaf8f4863359a132b97fa8b
http://hdl.handle.net/11585/47819
http://hdl.handle.net/11585/47819
Autor:
Gian Matteo, Rigolin, Alessia, Tieghi, Maria, Ciccone, Letizia Zenone, Bragotti, Francesco, Cavazzini, Matteo, Della Porta, Barbara, Castagnari, Rosanna, Carroccia, Giovanni, Guerra, Antonio, Cuneo, Gianluigi, Castoldi
The urokinase-type plasminogen activator (uPA) system, which consists of a proteinase (uPA), a receptor (uPAR or CD87) and inhibitors, is involved in proteolysis, cell migration, tissue remodelling, angiogenesis and cell adhesion. Recent findings sug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::eff67f862c8529f9e60106639071be54
http://hdl.handle.net/11392/1208024
http://hdl.handle.net/11392/1208024
Autor:
Bernd Wissinger, Piero Barboni, Luisa Iommarini, Costanza Lamperti, Rocco Liguori, Caterina Tonon, Rosanna Carroccia, Maria Lucia Valentino, Massimo Zeviani, Valerio Carelli, Chiara La Morgia, Susanne Kohl, Pasquale Montagna, Leonardo Caporali, Eleonora Lamantea, Alessandra Maresca, Michele Carbonelli, Raffaele Lodi
Publikováno v:
Mitochondrion. 11:645
Autor:
Fabio Pizza, L. Badiali De Giorgi, F. Coccolo, Rita Rinaldi, M. Zavatta, Maria Lucia Valentino, Rosanna Carroccia, C. La Morgia, Valerio Carelli, Elisa Baldin, Aurelia Santoro, L. Tarantino, Giovanna Cenacchi
Publikováno v:
Neuromuscular Disorders. 17:771
Autor:
Raffaele Lodi, Rosanna Carroccia, Valerio Carelli, Federico Sadun, Piero Barboni, Patrizia Avoni, C. La Morgia, Marzio Bellan, M. Villanova, Agostino Baruzzi, Rocco Liguori, Caterina Tonon
Publikováno v:
Neuromuscular Disorders. 17:891
Autor:
Valerio Carelli, Chiara La Morgia, Luisa Iommarini, Rosanna Carroccia, Marina Mattiazzi, Simonetta Sangiorgi, Sabrina Farne’, Alessandra Maresca, Beatrice Foscarini, Lucia Lanzi, Marcello Amadori, Marzio Bellan, Maria Valentino
Publikováno v:
Bioscience Reports; Jun2007, Vol. 27 Issue 1-3, p173-184, 12p
Autor:
Piero Barboni, Roberto Vetrugno, Pasquale Montagna, Antonio Torroni, C. La Morgia, Luisa Iommarini, Raffaele Lodi, Claudia Zanna, Sara Vidoni, Maria Pala, Barbara Mostacci, Anna Olivieri, Michela Rugolo, Alessandro Achilli, Rosanna Carroccia, Valerio Carelli, Rocco Liguori, Caterina Tonon
Publikováno v:
CIÊNCIAVITAE
ResearcherID
ResearcherID
Objective: To investigate the mechanisms underlying myoclonus in Leber hereditary optic neuropathy (LHON). Methods: Five patients and one unaffected carrier from two Italian families bearing the homoplasmic 11778/ND4 and 3460/ND1 mutations underwent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ee6e0a1a17fb1ebcab64b1c128adb28
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000253776100005&KeyUID=WOS:000253776100005
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000253776100005&KeyUID=WOS:000253776100005