Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Nuno Gonçalves-Anjo"'
Autor:
Hasier Eraña, Cristina Sampedro-Torres-Quevedo, Jorge M. Charco, Carlos M. Díaz-Domínguez, Francesca Peccati, Maitena San-Juan-Ansoleaga, Enric Vidal, Nuno Gonçalves-Anjo, Miguel A. Pérez-Castro, Ezequiel González-Miranda, Patricia Piñeiro, Leire Fernández-Veiga, Josu Galarza-Ahumada, Eva Fernández-Muñoz, Guiomar Perez de Nanclares, Glenn Telling, Mariví Geijo, Gonzalo Jiménez-Osés, Joaquín Castilla
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Prion diseases are a group of rapidly progressing neurodegenerative disorders caused by the misfolding of the endogenous prion protein (PrPC) into a pathogenic form (PrPSc). This process, despite being the central event underlying these diso
Externí odkaz:
https://doaj.org/article/a04d98f58ccd4cb2b901a29e2c563eae
Autor:
Jorge C. Pereira, Nuno Gonçalves-Anjo, Leonor Orge, Maria A. Pires, Sara Rocha, Luís Figueira, Ana C. Matos, João Silva, Paula Mendonça, Paulo Carvalho, Paula Tavares, Carla Lima, Anabela Alves, Alexandra Esteves, Maria L. Pinto, Isabel Pires, Adelina Gama, Roberto Sargo, Filipe Silva, Fernanda Seixas, Madalena Vieira-Pinto, Estela Bastos
Publikováno v:
Prion, Vol 17, Iss 1, Pp 75-81 (2023)
ABSTRACTAmong the transmissible spongiform encephalopathies (TSEs), chronic wasting disease (CWD) in cervids is now a rising concern in wildlife within Europe, after the detection of the first case in Norway in 2016, in a wild reindeer and until June
Externí odkaz:
https://doaj.org/article/d9f2eb4f7bc345e6a270a89303797f3b
Autor:
Hasier Eraña, Carlos M. Díaz-Domínguez, Jorge M. Charco, Enric Vidal, Ezequiel González-Miranda, Miguel A. Pérez-Castro, Patricia Piñeiro, Rafael López-Moreno, Cristina Sampedro-Torres-Quevedo, Leire Fernández-Veiga, Juan Tasis-Galarza, Nuria L. Lorenzo, Aileen Santini-Santiago, Melisa Lázaro, Sandra García-Martínez, Nuno Gonçalves-Anjo, Maitena San-Juan-Ansoleaga, Josu Galarza-Ahumada, Eva Fernández-Muñoz, Samanta Giler, Mikel Valle, Glenn C. Telling, Mariví Geijó, Jesús R. Requena, Joaquín Castilla
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-30 (2023)
Abstract Among transmissible spongiform encephalopathies or prion diseases affecting humans, sporadic forms such as sporadic Creutzfeldt–Jakob disease are the vast majority. Unlike genetic or acquired forms of the disease, these idiopathic forms oc
Externí odkaz:
https://doaj.org/article/63c13fcaea6249e3a04b3b8cea76b3ad
Autor:
Alexandra Esteves, Madalena Vieira-Pinto, Hélder Quintas, Leonor Orge, Adelina Gama, Anabela Alves, Fernanda Seixas, Isabel Pires, Maria de Lurdes Pinto, Ana Paula Mendonça, Carla Lima, Carla Neves Machado, João Carlos Silva, Paula Tavares, Filipe Silva, Estela Bastos, Jorge Pereira, Nuno Gonçalves-Anjo, Paulo Carvalho, Roberto Sargo, Ana Matos, Luís Figueira, Maria dos Anjos Pires
Publikováno v:
Animals, Vol 11, Iss 11, p 3028 (2021)
Wasting disease in small ruminants is frequently detected at slaughterhouses. The wasting disorder is manifested by the deterioration of the nutritional and physiological state of the animal indicated by thinness, emaciation, and cachexia. Evidence o
Externí odkaz:
https://doaj.org/article/8087d7768b3c49cea577bfb28b07f077
Autor:
Leonor Orge, Carla Lima, Carla Machado, Paula Tavares, Paula Mendonça, Paulo Carvalho, João Silva, Maria de Lurdes Pinto, Estela Bastos, Jorge Cláudio Pereira, Nuno Gonçalves-Anjo, Adelina Gama, Alexandra Esteves, Anabela Alves, Ana Cristina Matos, Fernanda Seixas, Filipe Silva, Isabel Pires, Luis Figueira, Madalena Vieira-Pinto, Roberto Sargo, Maria dos Anjos Pires
Publikováno v:
Biomolecules, Vol 11, Iss 3, p 466 (2021)
Transmissible Spongiform Encephalopathies (TSEs) or prion diseases are a fatal group of infectious, inherited and spontaneous neurodegenerative diseases affecting human and animals. They are caused by the conversion of cellular prion protein (PrPC) i
Externí odkaz:
https://doaj.org/article/9cb2a54b2e994f108c0397a3224e927a
Autor:
Jorge C. Pereira, Nuno Gonçalves-Anjo, Leonor Orge, Maria A. Pires, Sara Rocha, Luís Figueira, Ana C. Matos, João Silva, Paula Mendonça, Paulo Carvalho, Paula Tavares, Carla Lima, Anabela Alves, Alexandra Esteves, Maria L. Pinto, Isabel Pires, Adelina Gama, Roberto Sargo, Filipe Silva, Fernanda Seixas, Madalena Vieira-Pinto, Estela Bastos
Among the transmissible spongiform encephalopathies (TSEs), chronic wasting disease (CWD) in cervids is now a rising concern in wildlife within Europe, after the detection of the first case in Norway in 2016, in a wild reindeer and until June 2022 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64666645155d8eda41105f86ef9ddf7d
https://doi.org/10.1101/2022.08.16.504133
https://doi.org/10.1101/2022.08.16.504133
Autor:
Nuno Gonçalves-Anjo, João Requicha, Andreia Teixeira, Isabel Dias, Carlos Viegas, Estela Bastos
Publikováno v:
Journal of veterinary dentistry. 39(4)
Genetic variability is the main cause of phenotypic variation. Some variants may be associated with several diseases and can be used as risk biomarkers, identifying animals with higher susceptibility to develop the pathology. Genomic medicine uses th
Autor:
Nuno Gonçalves-Anjo, Estela Bastos, Carlos Alberto de Assis Viegas, Fátima Leite-Pinheiro, José Carlos Leitão, António Cortinhas, Teresa Bento, Isabel R. Dias
Publikováno v:
Meta Gene. 18:9-15
Autor:
Paulo Carvalho, Isabel Pires, Leonor Orge, Ana Cristina Matos, Alexandra Esteves, Jorge C. Pereira, Maria de Lurdes Pinto, Maria dos Anjos Pires, Nuno Gonçalves-Anjo, Paula Tavares, Carla Machado, Roberto Sargo, Filipe Silva, Fernanda Seixas, Paula Mendonça, Madalena Vieira-Pinto, Estela Bastos, Anabela Alves, Adelina Gama, João Silva, Carla Lima, L. Figueira
Publikováno v:
Biomolecules
Biomolecules, Vol 11, Iss 466, p 466 (2021)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Biomolecules, Vol 11, Iss 466, p 466 (2021)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Transmissible Spongiform Encephalopathies (TSEs) or prion diseases are a fatal group of infectious, inherited and spontaneous neurodegenerative diseases affecting human and animals. They are caused by the conversion of cellular prion protein (PrPC) i
Autor:
Marzena Dominiak, Nuno Gonçalves-Anjo, Jacek Matys, Kinga Grzech-Leśniak, BRITTO FALCÓN GUERRERO
Publikováno v:
International Dental Journal. 68:85-123