Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Pablo Calap"'
Autor:
Diana C. Muñoz-Lasso, Belén Mollá, Pablo Calap-Quintana, José Luis García-Giménez, Federico V. Pallardo, Francesc Palau, Pilar Gonzalez-Cabo
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Abstract Abnormalities in actin cytoskeleton have been linked to Friedreich’s ataxia (FRDA), an inherited peripheral neuropathy characterised by an early loss of neurons in dorsal root ganglia (DRG) among other clinical symptoms. Despite all effort
Externí odkaz:
https://doaj.org/article/1c2e1b48290849ff8db4190d1f6da79c
Autor:
Laura Rodríguez-Pascau, Elena Britti, Pablo Calap-Quintana, Yi Na Dong, Cristina Vergara, Fabien Delaspre, Marta Medina-Carbonero, Jordi Tamarit, Federico V. Pallardó, Pilar Gonzalez-Cabo, Joaquim Ros, David R. Lynch, Marc Martinell, Pilar Pizcueta
Publikováno v:
Neurobiology of Disease, Vol 148, Iss , Pp 105162- (2021)
Friedreich ataxia (FRDA), the most common autosomal recessive ataxia, is characterized by degeneration of the large sensory neurons and spinocerebellar tracts, cardiomyopathy, and increased incidence in diabetes. The underlying pathophysiological mec
Externí odkaz:
https://doaj.org/article/d8901ebb28414e638a9b30b6d425544b
Autor:
Laura R. Rodríguez, Pablo Calap-Quintana, Tamara Lapeña-Luzón, Federico V. Pallardó, Stephan Schneuwly, Juan A. Navarro, Pilar Gonzalez-Cabo
Publikováno v:
Redox Biology, Vol 37, Iss , Pp 101762- (2020)
Friedreich ataxia (FRDA) is a neurodegenerative disorder characterized by neuromuscular and neurological manifestations. It is caused by mutations in the FXN gene, which results in loss of the mitochondrial protein frataxin. Endoplasmic Reticulum-mit
Externí odkaz:
https://doaj.org/article/7654ccea76264ec88bb2ffef946df062
Autor:
José Vicente Llorens, Sirena Soriano, Pablo Calap-Quintana, Pilar Gonzalez-Cabo, María Dolores Moltó
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Friedreich’s ataxia (FRDA) is a rare early-onset degenerative disease that affects both the central and peripheral nervous systems, and other extraneural tissues, mainly the heart and endocrine pancreas. This disorder progresses as a mixed sensory
Externí odkaz:
https://doaj.org/article/d200de270712460d8e2f39f1fbc14e75
Autor:
Laura R. Rodríguez, Tamara Lapeña, Pablo Calap-Quintana, María Dolores Moltó, Pilar Gonzalez-Cabo, Juan Antonio Navarro Langa
Publikováno v:
Antioxidants, Vol 9, Iss 8, p 664 (2020)
Friedreich’s ataxia is the commonest autosomal recessive ataxia among population of European descent. Despite the huge advances performed in the last decades, a cure still remains elusive. One of the most studied hallmarks of the disease is the inc
Externí odkaz:
https://doaj.org/article/3dc7c056f62f4e02a53a6b6ad3c07410
Autor:
Sirena Soriano, Pablo Calap-Quintana, José Vicente Llorens, Ismael Al-Ramahi, Lucía Gutiérrez, María José Martínez-Sebastián, Juan Botas, María Dolores Moltó
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0159209 (2016)
Friedreich's ataxia (FRDA), the most commonly inherited ataxia in populations of European origin, is a neurodegenerative disorder caused by a decrease in frataxin levels. One of the hallmarks of the disease is the accumulation of iron in several tiss
Externí odkaz:
https://doaj.org/article/c5f78dbb1899456b995509590addd8af
Autor:
Pablo Calap-Quintana, Sirena Soriano, José Vicente Llorens, Ismael Al-Ramahi, Juan Botas, María Dolores Moltó, María José Martínez-Sebastián
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132376 (2015)
Friedreich's ataxia (FRDA), the most common inherited ataxia in the Caucasian population, is a multisystemic disease caused by a significant decrease in the frataxin level. To identify genes capable of modifying the severity of the symptoms of fratax
Externí odkaz:
https://doaj.org/article/718b06bcbd2b49dfa7d036d168391ddf
Autor:
Pablo Calap-Quintana, Javier González-Fernández, Noelia Sebastiá-Ortega, José Vicente Llorens, María Dolores Moltó
Publikováno v:
International Journal of Molecular Sciences, Vol 18, Iss 7, p 1456 (2017)
Iron, copper and zinc are transition metals essential for life because they are required in a multitude of biological processes. Organisms have evolved to acquire metals from nutrition and to maintain adequate levels of each metal to avoid damaging e
Externí odkaz:
https://doaj.org/article/cc817b83cf3a45d89bbcdd2519e7a72b
Autor:
Francesc Palau, Belén Mollá, Federico V. Pallardo, Pilar Gonzalez-Cabo, Diana C. Muñoz-Lasso, Pablo Calap-Quintana, José Luis García-Giménez
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports
Digital.CSIC. Repositorio Institucional del CSIC
instname
Scientific Reports
Digital.CSIC. Repositorio Institucional del CSIC
instname
10 páginas, 3 figuras. Contiene material suplementario accesible en: https://doi.org/10.1038/s41598-020-62050-7
Abnormalities in actin cytoskeleton have been linked to Friedreich's ataxia (FRDA), an inherited peripheral neuropathy characterised
Abnormalities in actin cytoskeleton have been linked to Friedreich's ataxia (FRDA), an inherited peripheral neuropathy characterised
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0bf079744afed55d0942ff17d57f4b7
https://doaj.org/article/1c2e1b48290849ff8db4190d1f6da79c
https://doaj.org/article/1c2e1b48290849ff8db4190d1f6da79c
Autor:
Marta Medina-Carbonero, Pilar Pizcueta, David A. Lynch, Yi Na Dong, Laura Rodríguez-Pascau, Fabien Delaspre, Joaquim Ros, Elena Britti, Pilar Gonzalez-Cabo, Jordi Tamarit, Marc Martinell, Cristina Vergara, Pablo Calap-Quintana, Federico V. Pallardó
Publikováno v:
Repositorio Abierto de la UdL
Universitad de Lleida
Neurobiology of Disease, Vol 148, Iss, Pp 105162-(2021)
Universitad de Lleida
Neurobiology of Disease, Vol 148, Iss, Pp 105162-(2021)
Friedreich ataxia (FRDA), the most common autosomal recessive ataxia, is characterized by degeneration of the large sensory neurons and spinocerebellar tracts, cardiomyopathy, and increased incidence in diabetes. The underlying pathophysiological mec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a9585e690a79b4626b1b743126f6b63
https://hdl.handle.net/10459.1/72112
https://hdl.handle.net/10459.1/72112
