Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Vicente Llorens"'
Autor:
Vicente Llorens
Publikováno v:
Nueva Revista de Filología Hispánica, Vol 7, Iss 1/2 (1953)
En este número no se incluyeron resúmenes ni palabras clave.
Externí odkaz:
https://doaj.org/article/e631a1f916fa4aa9b23f66e6636629b1
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:
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, José Vicente Llorens, María Dolores Moltó, Cristina Solana-Manrique, Francisco Sanz, Nuria Paricio
Publikováno v:
Insights into Human Neurodegeneration: Lessons Learnt from Drosophila ISBN: 9789811322174
Neurodegenerative diseases (NDs) constitute a very important problem in our current society, as they are usually associated with the aging process. NDs are devastating disorders that lead to severe disabilities and ultimately to death and have a cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87d06623c13848a35b4f062d55a49fa6
https://doi.org/10.1007/978-981-13-2218-1_15
https://doi.org/10.1007/978-981-13-2218-1_15
Autor:
José Vicente Llorens, Sirena Soriano, Pablo Calap-Quintana, Pilar Gonzalez-Cabo, María Dolores Moltó
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 13 (2019)
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
Publikováno v:
International Journal of Molecular Sciences
Drosophila melanogaster has been for over a century the model of choice of several neurobiologists to decipher the formation and development of the nervous system as well as to mirror the pathophysiological conditions of many human neurodegenerative
Autor:
Javier González-Fernández, Pablo Calap-Quintana, J. A. Navarro, José Vicente Llorens, M. J. Martínez-Sebastián, María Dolores Moltó
Publikováno v:
BioMed Research International
Calap-Quintana, Pablo Navarro, Juan A. González-Fernández, Javier Martínez Sebastián, María José Moltó Ruiz, María Dolores Llorens Llorens, Jose Vte. 2018 Drosophila melanogaster models of Friedreich's ataxia Biomed Research International 2018
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
BioMed Research International, Vol 2018 (2018)
Calap-Quintana, Pablo Navarro, Juan A. González-Fernández, Javier Martínez Sebastián, María José Moltó Ruiz, María Dolores Llorens Llorens, Jose Vte. 2018 Drosophila melanogaster models of Friedreich's ataxia Biomed Research International 2018
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
BioMed Research International, Vol 2018 (2018)
Friedreich’s ataxia (FRDA) is a rare inherited recessive disorder affecting the central and peripheral nervous systems and other extraneural organs such as the heart and pancreas. This incapacitating condition usually manifests in childhood or adol
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Publikováno v:
JBIC Journal of Biological Inorganic Chemistry. 20:1229-1238
Synthesis of ecdysone, the key hormone that signals the termination of larval growth and the initiation of metamorphosis in insects, is carried out in the prothoracic gland by an array of iron-containing cytochrome P450s, encoded by the halloween gen