Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anita Carija"'
Publikováno v:
Redox Biology, Vol 12, Iss , Pp 699-711 (2017)
Protein misfolding and aggregation have been associated with the onset of neurodegenerative disorders. Recent studies demonstrate that the aggregation process can result in a high diversity of protein conformational states, however the identity of th
Externí odkaz:
https://doaj.org/article/ccd9b27fac8e4947be2445fbdfc73ec4
Autor:
Anita Carija, Francisca Pinheiro, Jordi Pujols, Inês C. Brás, Diana Fernandes Lázaro, Carlo Santambrogio, Rita Grandori, Tiago F. Outeiro, Susanna Navarro, Salvador Ventura
Publikováno v:
Redox Biology, Vol 22, Iss , Pp - (2019)
The aggregation of α-synuclein (α-syn) into amyloid fibrils is a major pathological hallmark of Parkinson's disease (PD) and other synucleinopathies. The mechanisms underlying the structural transition of soluble and innocuous α-syn to aggregated
Externí odkaz:
https://doaj.org/article/1de474bdc01e470880d6ec847b05a0c5
Publikováno v:
Data in Brief, Vol 7, Iss , Pp 143-147 (2016)
Protein aggregation and amyloid formation is a hallmark of an increasing number of human disorders. Because protein aggregation is deleterious for the cell physiology and results in a decrease in overall cell fitness, it is thought that natural selec
Externí odkaz:
https://doaj.org/article/4b9962f2bf514c91baffb2a6a8c24f96
Publikováno v:
Cells, Vol 8, Iss 8, p 856 (2019)
The aggregation of proteins compromises cell fitness, either because it titrates functional proteins into non-productive inclusions or because it results in the formation of toxic assemblies. Accordingly, computational proteome-wide analyses suggest
Externí odkaz:
https://doaj.org/article/5cb23e1c13e1456bb3178996ca93c952
Autor:
Susanna Navarro, Jordi Pujols, Ernest Giralt, Samuel Peña-Díaz, Xavier Salvatella, Danilo González, Francesca Peccati, Diana F. Lázaro, Salvador Guardiola, Esther Dalfó, María Conde-Giménez, Tiago F. Outeiro, Javier Sancho, Jesús García, Mariona Sodupe, Salvador Ventura, Francisca Pinheiro, Anita Carija
Publikováno v:
Proceedings of the National Academy of Sciences. 115:10481-10486
Parkinson’s disease (PD) is characterized by a progressive loss of dopaminergic neurons, a process that current therapeutic approaches cannot prevent. In PD, the typical pathological hallmark is the accumulation of intracellular protein inclusions,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f1db49e4743fa279af6e4ffc3a895f6
https://doi.org/10.1073/pnas.1804198115
https://doi.org/10.1073/pnas.1804198115
Autor:
Jordi Pujols, Anita Carija, Tiago F. Outeiro, Susanna Navarro, Inês Caldeira Brás, Rita Grandori, Carlo Santambrogio, Salvador Ventura, Francisca Pinheiro, Diana F. Lázaro
Publikováno v:
Redox Biology
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Redox Biology, Vol 22, Iss, Pp-(2019)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Redox Biology, Vol 22, Iss, Pp-(2019)
The aggregation of α-synuclein (α-syn) into amyloid fibrils is a major pathological hallmark of Parkinson's disease (PD) and other synucleinopathies. The mechanisms underlying the structural transition of soluble and innocuous α-syn to aggregated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::443e55413154d26a3dd1fb43439d4fdb
https://hdl.handle.net/21.11116/0000-0003-6327-221.11116/0000-0003-6329-0
https://hdl.handle.net/21.11116/0000-0003-6327-221.11116/0000-0003-6329-0
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Cells, Vol 8, Iss 8, p 856 (2019)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Cells
Volume 8
Issue 8
Recercat. Dipósit de la Recerca de Catalunya
instname
Universitat Autònoma de Barcelona
Cells, Vol 8, Iss 8, p 856 (2019)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Cells
Volume 8
Issue 8
Recercat. Dipósit de la Recerca de Catalunya
instname
The aggregation of proteins compromises cell fitness, either because it titrates functional proteins into non-productive inclusions or because it results in the formation of toxic assemblies. Accordingly, computational proteome-wide analyses suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb636b2d2b04ac38bd154e9ad185d50a
https://ddd.uab.cat/record/216984
https://ddd.uab.cat/record/216984
Publikováno v:
J Vis Exp
Protein misfolding and aggregation into amyloid conformations have been related to the onset and progression of several neurodegenerative diseases. However, there is still little information about how insoluble protein aggregates exert their toxic ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e439eda74de6cc6af5078fe8b8e49fd
https://europepmc.org/articles/PMC6101985/
https://europepmc.org/articles/PMC6101985/
Publikováno v:
Redox Biology, Vol 12, Iss, Pp 699-711 (2017)
Redox Biology
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Redox Biology
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Protein misfolding and aggregation have been associated with the onset of neurodegenerative disorders. Recent studies demonstrate that the aggregation process can result in a high diversity of protein conformational states, however the identity of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::592525a4e7f710a14724f43f606b451c
https://ddd.uab.cat/record/186208
https://ddd.uab.cat/record/186208
Autor:
Ira Milosevic, Ellen Gerhardt, Caterina Masaracchia, Enrique Abad Gonzalez, Raquel Ramos Pinho, Giulia Rossetti, Claudio O. Fernández, Anna Villar-Piqué, Markus Zweckstetter, Anita Carija, Salvador Ventura, Debora Foguel, Paolo Carloni, Éva M. Szegö, Tomás Lopes da Fonseca, Luis Fonseca-Ornelas, Ricardo Sant'Anna, Tiago F. Outeiro
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America 113(42), E6506-E6515 (2016). doi:10.1073/pnas.1606791113
Proceedings of the National Academy of Sciences
Europe PubMed Central
Proceedings of the National Academy of Sciences of the United States of Amerca
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Proceedings of the National Academy of Sciences of the United States of America 113(42), E6506-E6515 (2016). doi:10.1073/pnas.1606791113
Proceedings of the National Academy of Sciences
Europe PubMed Central
Proceedings of the National Academy of Sciences of the United States of Amerca
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Synucleinopathies are a group of progressive disorders characterized by the abnormal aggregation and accumulation of α-synuclein (aSyn), an abundant neuronal protein that can adopt different conformations and biological properties. Recently, aSyn pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b082eb3f1b773cd6384717581e19dfa
https://hdl.handle.net/11858/00-001M-0000-002B-96CD-721.11116/0000-0002-4B71-B21.11116/0000-0002-4B72-A
https://hdl.handle.net/11858/00-001M-0000-002B-96CD-721.11116/0000-0002-4B71-B21.11116/0000-0002-4B72-A