Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Giovanna Longo"'
Autor:
Mariella Errede, Tiziana Annese, Valentina Petrosino, Giovanna Longo, Francesco Girolamo, Ignazio de Trizio, Antonio d’Amati, Antonio Uccelli, Nicole Kerlero de Rosbo, Daniela Virgintino
Publikováno v:
Fluids and Barriers of the CNS, Vol 19, Iss 1, Pp 1-25 (2022)
Abstract Background In myelin oligodendrocyte glycoprotein (MOG)-induced experimental autoimmune encephalomyelitis (EAE), several areas of demyelination are detectable in mouse cerebral cortex, where neuroinflammation events are associated with scarc
Externí odkaz:
https://doaj.org/article/b14b931f4de7414d962d612c7471b1e3
Autor:
Donato Gemmati, Giovanna Longo, Ines Gallo, Juliana Araujo Silva, Paola Secchiero, Giorgio Zauli, Stefania Hanau, Angelina Passaro, Patrizia Pellegatti, Stefano Pizzicotti, Maria Luisa Serino, Ajay Vikram Singh, Veronica Tisato
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Development and worldwide availability of safe and effective vaccines against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) to fight severe symptoms of coronavirus disease 2019 (COVID-19) and block the pandemic have been a
Externí odkaz:
https://doaj.org/article/8a869b0e6cc345f19fd14baf505efb82
Autor:
Beatrice Berti, Giovanna Longo, Francesco Mari, Stefano Doccini, Ilaria Piccolo, Maria Alice Donati, Francesca Moro, Renzo Guerrini, Filippo M. Santorelli, Vittoria Petruzzella
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-6 (2021)
Abstract Background Charcot-Marie-Tooth disease (CMT) type 4B3 (CMT4B3) is a rare form of genetic neuropathy associated with variants in the MTMR5/SBF1 gene. MTMR5/SBF1 is a pseudophosphatase predicted to regulate endo-lysosomal trafficking in tandem
Externí odkaz:
https://doaj.org/article/762fb8ebeadd421d96de715d7615d7df
Autor:
Francesco Girolamo, Ignazio de Trizio, Mariella Errede, Giovanna Longo, Antonio d’Amati, Daniela Virgintino
Publikováno v:
Fluids and Barriers of the CNS, Vol 18, Iss 1, Pp 1-26 (2021)
Abstract Central nervous system diseases involving the parenchymal microvessels are frequently associated with a ‘microvasculopathy’, which includes different levels of neurovascular unit (NVU) dysfunction, including blood–brain barrier alterat
Externí odkaz:
https://doaj.org/article/1bde4cf505784ecea40649b4d178d328
Autor:
Angelica Bianco, Alessio Valletti, Giovanna Longo, Luigi Bisceglia, Julio Montoya, Sonia Emperador, Silvana Guerriero, Vittoria Petruzzella
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-4 (2018)
Abstract Objectives Leber’s hereditary optic neuropathy (LHON) is a mitochondrial genetic disease characterized by a variable and reduced penetrance. Individuals carrying a primary LHON-causing mitochondrial DNA (mtDNA) mutation may either remain a
Externí odkaz:
https://doaj.org/article/4e84867cd39546fdad35c467d4ae1865
Autor:
Mariella Errede, Domenica Mangieri, Giovanna Longo, Francesco Girolamo, Ignazio de Trizio, Antonella Vimercati, Gabriella Serio, Karl Frei, Roberto Perris, Daniela Virgintino
Publikováno v:
Fluids and Barriers of the CNS, Vol 15, Iss 1, Pp 1-17 (2018)
Abstract Background Nanotubular structures, denoted tunneling nanotubes (TNTs) have been described in recent times as involved in cell-to-cell communication between distant cells. Nevertheless, TNT-like, long filopodial processes had already been des
Externí odkaz:
https://doaj.org/article/e341a26eb24f41f999a416bf4ee6313d
Autor:
Francesco Girolamo, Mariella Errede, Giovanna Longo, Tiziana Annese, Carlotta Alias, Giovanni Ferrara, Sara Morando, Maria Trojano, Nicole Kerlero de Rosbo, Antonio Uccelli, Daniela Virgintino
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0213508 (2019)
During experimental autoimmune encephalomyelitis (EAE), a model for multiple sclerosis associated with blood-brain barrier (BBB) disruption, oligodendrocyte precursor cells (OPCs) overexpress proteoglycan nerve/glial antigen 2 (NG2), proliferate, and
Externí odkaz:
https://doaj.org/article/051588aa48ba4900929b713be3ffb83c
Autor:
Veronica Tisato, Giovanni Zuliani, Marco Vigliano, Giovanna Longo, Eugenia Franchini, Paola Secchiero, Giorgio Zauli, Elvezia Maria Paraboschi, Ajay Vikram Singh, Maria Luisa Serino, Beatrice Ortolani, Amedeo Zurlo, Cristina Bosi, Antonio Greco, Davide Seripa, Rosanna Asselta, Donato Gemmati
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0193867 (2018)
Cognitive impairments of different aetiology share alterations in iron and lipid homeostasis with mutual relationships. Since iron and cholesterol accumulation impact on neurodegenerative disease, the associated gene variants are appealing candidate
Externí odkaz:
https://doaj.org/article/8f7ab293289341be94c86e4027bbf3e5
Autor:
Paola Zanfardino, Giovanna Longo, Alessandro Amati, Federica Morani, Ernesto Picardi, Francesco Girolamo, Mariella Pafundi, Sharon N Cox, Caterina Manzari, Apollonia Tullo, Stefano Doccini, Filippo M Santorelli, Vittoria Petruzzella
Publikováno v:
Human Molecular Genetics. 32:333-350
Dominant mutations in ubiquitously expressed mitofusin 2 gene (MFN2) cause Charcot-Marie-Tooth type 2A (CMT2A; OMIM 609260), an inherited sensory-motor neuropathy that affects peripheral nerve axons. Mitofusin 2 protein has been found to take part in
Autor:
Antonio d’Amati, Francesco Girolamo, Ignazio de Trizio, Giovanna Longo, Daniela Virgintino, Mariella Errede
Publikováno v:
Fluids and Barriers of the CNS, Vol 18, Iss 1, Pp 1-26 (2021)
Fluids and Barriers of the CNS
Fluids and Barriers of the CNS
Central nervous system diseases involving the parenchymal microvessels are frequently associated with a ‘microvasculopathy’, which includes different levels of neurovascular unit (NVU) dysfunction, including blood–brain barrier alterations. To