Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maria Paglione"'
Autor:
Arnau Llobet Rosell, Maria Paglione, Jonathan Gilley, Magdalena Kocia, Giulia Perillo, Massimiliano Gasparrini, Lucia Cialabrini, Nadia Raffaelli, Carlo Angeletti, Giuseppe Orsomando, Pei-Hsuan Wu, Michael P Coleman, Andrea Loreto, Lukas Jakob Neukomm
Publikováno v:
eLife, Vol 11 (2022)
Axon degeneration contributes to the disruption of neuronal circuit function in diseased and injured nervous systems. Severed axons degenerate following the activation of an evolutionarily conserved signaling pathway, which culminates in the activati
Externí odkaz:
https://doaj.org/article/a4f6256968184f2f948689f95a99de09
Autor:
Arnau Llobet Rosell, Maria Paglione, Jonathan Gilley, Magdalena Kocia, Giulia Perillo, Massimiliano Gasparrini, Lucia Cialabrini, Nadia Raffaelli, Carlo Angeletti, Giuseppe Orsomando, Pei-Hsuan Wu, Michael P Coleman, Andrea Loreto, Lukas Jakob Neukomm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3cbe7b57d6e717407580501a1af4496
https://doi.org/10.7554/elife.80245.sa2
https://doi.org/10.7554/elife.80245.sa2
Autor:
Federica Belluti, Andrea Tarozzi, Alessandra Bisi, Angela Rampa, Maria Paglione, Francesca Seghetti, Elia Di Schiavi, Loreto Martínez-González, Silvia Gobbi, Concepción Pérez, Rita Maria Concetta Di Martino, Ana Martínez, Letizia Pruccoli
Publikováno v:
ACS Chemical Neuroscience
ACS chemical neuroscience 11 (2020): 2728–2740. doi:10.1021/acschemneuro.0c00363
info:cnr-pdr/source/autori:Di Martino, Rita Maria Concetta; Pruccoli, Letizia; Bisi, Alessandra; Gobbi, Silvia; Rampa, Angela; Martinez, Ana; Pérez, Concepción; Martinez-Gonzalez, Loreto; Paglione, Maria; Di Schiavi, Elia; Seghetti, Francesca; Tarozzi, Andrea; Belluti, Federica/titolo:Novel Curcumin-Diethyl Fumarate Hybrid as a Dualistic GSK-3? Inhibitor%2FNrf2 Inducer for the Treatment of Parkinson's Disease/doi:10.1021%2Facschemneuro.0c00363/rivista:ACS chemical neuroscience/anno:2020/pagina_da:2728/pagina_a:2740/intervallo_pagine:2728–2740/volume:11
Digital.CSIC. Repositorio Institucional del CSIC
instname
ACS chemical neuroscience 11 (2020): 2728–2740. doi:10.1021/acschemneuro.0c00363
info:cnr-pdr/source/autori:Di Martino, Rita Maria Concetta; Pruccoli, Letizia; Bisi, Alessandra; Gobbi, Silvia; Rampa, Angela; Martinez, Ana; Pérez, Concepción; Martinez-Gonzalez, Loreto; Paglione, Maria; Di Schiavi, Elia; Seghetti, Francesca; Tarozzi, Andrea; Belluti, Federica/titolo:Novel Curcumin-Diethyl Fumarate Hybrid as a Dualistic GSK-3? Inhibitor%2FNrf2 Inducer for the Treatment of Parkinson's Disease/doi:10.1021%2Facschemneuro.0c00363/rivista:ACS chemical neuroscience/anno:2020/pagina_da:2728/pagina_a:2740/intervallo_pagine:2728–2740/volume:11
Digital.CSIC. Repositorio Institucional del CSIC
instname
26 p.-8 fig.-2 tab.-1 graph. abst.-+9 p. mat. supl.-10 fig.-2 tab.
Common copathogenic factors, including oxidative stress and neuroinflammation, are found to play a vital role in the development of neurodegenerative disorders, including Alzheim
Common copathogenic factors, including oxidative stress and neuroinflammation, are found to play a vital role in the development of neurodegenerative disorders, including Alzheim
Autor:
Arnau, Llobet Rosell, Maria, Paglione, Jonathan, Gilley, Magdalena, Kocia, Giulia, Perillo, Massimiliano, Gasparrini, Lucia, Cialabrini, Nadia, Raffaelli, Carlo, Angeletti, Giuseppe, Orsomando, Pei-Hsuan, Wu, Michael P, Coleman, Andrea, Loreto, Lukas Jakob, Neukomm
Publikováno v:
eLife. 11
Axon degeneration contributes to the disruption of neuronal circuit function in diseased and injured nervous systems. Severed axons degenerate following the activation of an evolutionarily conserved signaling pathway, which culminates in the activati
Autor:
Flavia Trettel, Cristina Roseti, Rosalba Carrozzo, Teresa Rizza, Susanna Cogo, Anna Rita Bentivoglio, Claudia Carducci, Cristina Limatola, Alice Traversa, Gianfranco Bocchinfuso, Martina Venditti, Laura Civiero, Michela Di Nottia, Viviana Caputo, Eleonora Palma, Miriam Sciaccaluga, Ambra Lanzo, Maria Paglione, Luca Pannone, Manju A. Kurian, Serena Galosi, Simone Martinelli, Vincenzo Leuzzi, Lorenzo Stella, A Farrotti, Sergio Fucile, Laura Bernardini, Viviana Cordeddu, Joanne Ng, Marco Tartaglia, Elia Di Schiavi, Elisa Greggio, Andrea Ciolfi
Publikováno v:
Parkinsonism & related disorders 72 (2020): 75–79. doi:10.1016/j.parkreldis.2020.02.003
info:cnr-pdr/source/autori:Martinelli, Simone; Cordeddu, Viviana; Galosi, Serena; Lanzo, Ambra; Palma, Eleonora; Pannone, Luca; Ciolfi, Andrea; Di Nottia, Michela; Rizza, Teresa; Bocchinfuso, Gianfranco; Traversa, Alice; Caputo, Viviana; Farrotti, Andrea; Carducci, Claudia; Bernardini, Laura; Cogo, Susanna; Paglione, Maria; Venditti, Martina; Bentivoglio, Annarita; Ng, Joanne; Kurian, Manju A.; Civiero, Laura; Greggio, Elisa; Stella, Lorenzo; Trettel, Flavia; Sciaccaluga, Miriam; Roseti, Cristina; Carrozzo, Rosalba; Fucile, Sergio; Limatola, Cristina; Di Schiavi, Elia; Tartaglia, Marco; Leuzzi, Vincenzo/titolo:Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism/doi:10.1016%2Fj.parkreldis.2020.02.003/rivista:Parkinsonism & related disorders/anno:2020/pagina_da:75/pagina_a:79/intervallo_pagine:75–79/volume:72
info:cnr-pdr/source/autori:Martinelli, Simone; Cordeddu, Viviana; Galosi, Serena; Lanzo, Ambra; Palma, Eleonora; Pannone, Luca; Ciolfi, Andrea; Di Nottia, Michela; Rizza, Teresa; Bocchinfuso, Gianfranco; Traversa, Alice; Caputo, Viviana; Farrotti, Andrea; Carducci, Claudia; Bernardini, Laura; Cogo, Susanna; Paglione, Maria; Venditti, Martina; Bentivoglio, Annarita; Ng, Joanne; Kurian, Manju A.; Civiero, Laura; Greggio, Elisa; Stella, Lorenzo; Trettel, Flavia; Sciaccaluga, Miriam; Roseti, Cristina; Carrozzo, Rosalba; Fucile, Sergio; Limatola, Cristina; Di Schiavi, Elia; Tartaglia, Marco; Leuzzi, Vincenzo/titolo:Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism/doi:10.1016%2Fj.parkreldis.2020.02.003/rivista:Parkinsonism & related disorders/anno:2020/pagina_da:75/pagina_a:79/intervallo_pagine:75–79/volume:72
Objective To investigate the molecular cause(s) underlying a severe form of infantile-onset parkinsonism and characterize functionally the identified variants. Methods A trio-based whole exome sequencing (WES) approach was used to identify the candid
Publikováno v:
Journal of visualized experiments : JoVE. (157)
Axon degeneration is a shared feature in neurodegenerative disease and when nervous systems are challenged by mechanical or chemical forces. However, our understanding of the molecular mechanisms underlying axon degeneration remains limited. Injury-i
Publikováno v:
Journal of Visualized Experiments.
Axon degeneration is a shared feature in neurodegenerative disease and when nervous systems are challenged by mechanical or chemical forces. However, our understanding of the molecular mechanisms underlying axon degeneration remains limited. Injury-i
Autor:
Damiana Leo, Giuseppina Zampi, Ambra Lanzo, Elia Di Schiavi, Placido Illiano, Maria Paglione, Raul R. Gainetdinov
Publikováno v:
European journal of neuroscience
(2016): 1–8. doi:10.1111/ejn.13366
info:cnr-pdr/source/autori:Placido Illiano, Ambra Lanzo, Damiana Leo, Maria Paglione, Giuseppina Zampi, Raul R. Gainetdinov and Elia Di Schiavi/titolo:A Caenorhabditis elegans model to study dopamine transporter deficiency syndrome/doi:10.1111%2Fejn.13366/rivista:European journal of neuroscience (Print)/anno:2016/pagina_da:1/pagina_a:8/intervallo_pagine:1–8/volume
(2016): 1–8. doi:10.1111/ejn.13366
info:cnr-pdr/source/autori:Placido Illiano, Ambra Lanzo, Damiana Leo, Maria Paglione, Giuseppina Zampi, Raul R. Gainetdinov and Elia Di Schiavi/titolo:A Caenorhabditis elegans model to study dopamine transporter deficiency syndrome/doi:10.1111%2Fejn.13366/rivista:European journal of neuroscience (Print)/anno:2016/pagina_da:1/pagina_a:8/intervallo_pagine:1–8/volume
Dopamine transporter deficiency syndrome (DTDS) is a novel autosomal recessive disorder caused by mutations in the dopamine transporter (DAT), which leads to the partial or total loss of function of the protein. DTDS is a pharmacoresistant syndrome a