Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Marta Guerrero‐Valero"'
Autor:
Elena Melgarejo De La Peña, Marta Guerrero-Valero, Jaime Mulero Franco, Maria Dolores Ledesma
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S609- (2023)
Externí odkaz:
https://doaj.org/article/4738ae26889b44e89d2464578ec6953c
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S925-S926 (2023)
Externí odkaz:
https://doaj.org/article/49d444cdb7c24b7d8c62df242fd480e9
Autor:
Álvaro Casadomé-Perales, Sara Naya, Elisa Fernández-Martínez, Bea G. Mille, Marta Guerrero-Valero, Héctor Peinado, Francesc X. Guix, Carlos G. Dotti, Ernest Palomer
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 6, p 5986 (2023)
Ageing is associated with notorious alterations in neurons, i.e., in gene expression, mitochondrial function, membrane degradation or intercellular communication. However, neurons live for the entire lifespan of the individual. One of the reasons why
Externí odkaz:
https://doaj.org/article/d0efd33f36e74584bf1203b371322caa
Autor:
Alessandra Bolino, Françoise Piguet, Valeria Alberizzi, Marta Pellegatta, Cristina Rivellini, Marta Guerrero‐Valero, Roberta Noseda, Chiara Brombin, Alessandro Nonis, Patrizia D'Adamo, Carla Taveggia, Stefano Carlo Previtali
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 12, Pp 1438-1454 (2016)
Abstract Charcot–Marie–Tooth (CMT) neuropathies are highly heterogeneous disorders caused by mutations in more than 70 genes, with no available treatment. Thus, it is difficult to envisage a single suitable treatment for all pathogenetic mechanis
Externí odkaz:
https://doaj.org/article/c9084326117846fcb36a849fe5607d3a
Autor:
Roberta Noseda, Marta Guerrero-Valero, Valeria Alberizzi, Stefano C Previtali, Diane L Sherman, Marilena Palmisano, Richard L Huganir, Klaus-Armin Nave, Ana Cuenda, Maria Laura Feltri, Peter J Brophy, Alessandra Bolino
Publikováno v:
PLoS Biology, Vol 14, Iss 4, p e1002440 (2016)
Microtubule-based kinesin motors have many cellular functions, including the transport of a variety of cargos. However, unconventional roles have recently emerged, and kinesins have also been reported to act as scaffolding proteins and signaling mole
Externí odkaz:
https://doaj.org/article/0c85f8955fe04ce2ad1d8bafe0230402
Autor:
Silvia Cipriani, Marta Guerrero‐Valero, Stefano Tozza, Edward Zhao, Veith Vollmer, Danique Beijer, Matt Danzi, Cristina Rivellini, Dejan Lazarevic, Giovanni Battista Pipitone, Bianca Rose Grosz, Costanza Lamperti, Stefania Bianchi Marzoli, Paola Carrera, Marcella Devoto, Chiara Pisciotta, Davide Pareyson, Marina Kennerson, Stefano C. Previtali, Stephan Zuchner, Steven S. Scherer, Fiore Manganelli, Martin Bähler, Alessandra Bolino
Publikováno v:
European journal of neurologyREFERENCES. 30(2)
Charcot-Marie-Tooth disease (CMT) is a heterogeneous group of disorders caused by mutations in at least 100 genes. However, approximately 60% of cases with axonal neuropathies (CMT2) still remain without a genetic diagnosis. We aimed at identifying n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df087f59a36e550dbf68e45a32da7fd9
https://pubmed.ncbi.nlm.nih.gov/36260368
https://pubmed.ncbi.nlm.nih.gov/36260368
Autor:
Gaëtan Chicanne, Francesca Bianchi, Linda Sawade, Ivan de Curtis, Ubaldo Del Carro, Yesim Parman, Marta Guerrero-Valero, Roberta Di Guardo, Davide Pareyson, Valeria Alberizzi, Bernard Payrastre, Federica Grandi, Silvia Cipriani, Angelo Schenone, Alessandra Bolino, Volker Haucke
Publikováno v:
Proc Natl Acad Sci U S A
Charcot-Marie-Tooth type 4B1 (CMT4B1) is a severe autosomal recessive demyelinating neuropathy with childhood onset, caused by loss-of-function mutations in the myotubularin-related 2 (MTMR2) gene. MTMR2 is a ubiquitously expressed catalytically acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cdec724fd3719cb7bff8dddbaf9c0f2
http://hdl.handle.net/11567/1057661
http://hdl.handle.net/11567/1057661
Autor:
Roberta Noseda, Stefano C. Previtali, Chiara Brombin, Marta Pellegatta, Françoise Piguet, Valeria Alberizzi, Cristina Rivellini, Marta Guerrero-Valero, Alessandra Bolino, Carla Taveggia, Alessandro Nonis, Patrizia D'Adamo
Publikováno v:
EMBO Molecular Medicine
Charcot–Marie–Tooth (CMT) neuropathies are highly heterogeneous disorders caused by mutations in more than 70 genes, with no available treatment. Thus, it is difficult to envisage a single suitable treatment for all pathogenetic mechanisms. Axona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::030b584375e47484e50751e590187be6
https://doi.org/10.15252/emmm.201606349
https://doi.org/10.15252/emmm.201606349
Autor:
Stefano C. Previtali, Richard L. Huganir, Marilena Palmisano, Alessandra Bolino, Valeria Alberizzi, Peter J. Brophy, Klaus-Armin Nave, Ana Cuenda, Roberta Noseda, Diane L. Sherman, Marta Guerrero-Valero, Maria Laura Feltri
Publikováno v:
PLoS Biology
Noseda, R, Guerrero-Valero, M, Alberizzi, V, Previtali, S C, Sherman, D, Palmisano, M, Huganir, R L, Nave, K-A, Cuenda, A, Feltri, M L, Brophy, P & Bolino, A 2016, ' Kif13b Regulates PNS and CNS Myelination Through the Dlg1 Scaffold ', PLoS Biology, vol. 14, no. 4 . https://doi.org/10.1371/journal.pbio.1002440
PLoS Biology, Vol 14, Iss 4, p e1002440 (2016)
Noseda, R, Guerrero-Valero, M, Alberizzi, V, Previtali, S C, Sherman, D, Palmisano, M, Huganir, R L, Nave, K-A, Cuenda, A, Feltri, M L, Brophy, P & Bolino, A 2016, ' Kif13b Regulates PNS and CNS Myelination Through the Dlg1 Scaffold ', PLoS Biology, vol. 14, no. 4 . https://doi.org/10.1371/journal.pbio.1002440
PLoS Biology, Vol 14, Iss 4, p e1002440 (2016)
Microtubule-based kinesin motors have many cellular functions, including the transport of a variety of cargos. However, unconventional roles have recently emerged, and kinesins have also been reported to act as scaffolding proteins and signaling mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f9a659265c84b017da4721441ddc12f
https://hdl.handle.net/11858/00-001M-0000-002C-1084-C11858/00-001M-0000-002C-1086-8
https://hdl.handle.net/11858/00-001M-0000-002C-1084-C11858/00-001M-0000-002C-1086-8