Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Andrea Urpi"'
Autor:
Emma Puighermanal, Marta Luna-Sánchez, Alejandro Gella, Gunter van der Walt, Andrea Urpi, María Royo, Paula Tena-Morraja, Isabella Appiah, Maria Helena de Donato, Fabien Menardy, Patrizia Bianchi, Anna Esteve-Codina, Laura Rodríguez-Pascau, Cristina Vergara, Mercè Gómez-Pallarès, Giovanni Marsicano, Luigi Bellocchio, Marc Martinell, Elisenda Sanz, Sandra Jurado, Francesc Xavier Soriano, Pilar Pizcueta, Albert Quintana
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-21 (2024)
Abstract Mutations in mitochondrial energy-producing genes lead to a heterogeneous group of untreatable disorders known as primary mitochondrial diseases (MD). Leigh syndrome (LS) is the most common pediatric MD and is characterized by progressive ne
Externí odkaz:
https://doaj.org/article/622861ac6cc14a5babd24370dd72d435
Autor:
Alejandro Gella, Patricia Prada-Dacasa, Montserrat Carrascal, Andrea Urpi, Melania González-Torres, Joaquin Abian, Elisenda Sanz, Albert Quintana
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Defects in mitochondrial function lead to severe neuromuscular orphan pathologies known as mitochondrial disease. Among them, Leigh Syndrome is the most common pediatric presentation, characterized by symmetrical brain lesions, hypotonia, motor and r
Externí odkaz:
https://doaj.org/article/2ee59d68877041839468b29143c278fb
Autor:
Pablo Machuca-Márquez, Laura Sánchez-Benito, Fabien Menardy, Andrea Urpi, Richard D. Palmiter, Elisenda Sanz, Isabella Appiah, Albert Quintana
Passive motion can induce kinetosis (motion sickness, MS) in susceptible individuals. MS is an evolutionary conserved mechanism caused by mismatches between motion-related sensory information and past visual and motion memory, triggering a malaise ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95efeed42b64d28fa6e3873b22b4a75d
https://doi.org/10.1101/2021.09.08.459510
https://doi.org/10.1101/2021.09.08.459510
Autor:
Andrea Urpi, Rubèn López-Vales, Joana Garcia-Garcia, Jesús Amo-Aparicio, Albert Quintana, Anna Esteve-Codina, Isaac Francos-Quijorna, Marta Gut
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Theranostics
Universitat Autònoma de Barcelona
Theranostics
Background: Microglia and macrophages adopt a pro-inflammatory phenotype after spinal cord injury (SCI), what is thought to contribute to secondary tissue degeneration. We previously reported that this is due, in part, to the low levels of anti-infla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07a227ef69329ed79fa47808c92acd5d
https://ddd.uab.cat/record/250526
https://ddd.uab.cat/record/250526
Publikováno v:
Bio Protoc
Respiratory dysfunction is among the main cause of severe and fatal pathologies worldwide. The use of effective experimental models and methodologies for the study of the pulmonary pathophysiology is necessary to prevent, control and cure these disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6168e9b0d00063c571b24a5f2b59142
https://pubmed.ncbi.nlm.nih.gov/33659401
https://pubmed.ncbi.nlm.nih.gov/33659401
Autor:
Alejandro Gella, Patricia Prada-Dacasa, Montserrat Carrascal, Andrea Urpi, Melania González-Torres, Joaquin Abian, Elisenda Sanz, Albert Quintana
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Frontiers in Cell and Developmental Biology
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Frontiers in Cell and Developmental Biology
Defects in mitochondrial function lead to severe neuromuscular orphan pathologies known as mitochondrial disease. Among them, Leigh Syndrome is the most common pediatric presentation, characterized by symmetrical brain lesions, hypotonia, motor and r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b660ca4628b53ade4118a79aa9d25874
https://pubmed.ncbi.nlm.nih.gov/32850799
https://pubmed.ncbi.nlm.nih.gov/32850799