Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ignacio del Arco-Herrera"'
Publikováno v:
Human Technology, Vol 6, Iss 2, Pp 269-271 (2010)
Externí odkaz:
https://doaj.org/article/14865fbab69b44d99839e7fd79e5d009
Autor:
Fernando Rodríguez de Fonseca, Ignacio del Arco-Herrera, Yanina Romero-Zerbo, Lourdes Sanchez, Yolanda de Diego-Otero, Rajaa El Bekay, Juan Decara
Publikováno v:
Neuropsychopharmacology. 34:1011-1026
Fragile X syndrome is the most common genetic cause of mental disability. The mechanisms underlying the pathogenesis remain unclear and specific treatments are still under development. Previous studies have proposed an abnormal hypothalamic-pituitary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b3597c0a1c132eb154bd151459d69d8
https://doi.org/10.1038/npp.2008.152
https://doi.org/10.1038/npp.2008.152
Autor:
Juan Decara, Yolanda de Diego-Otero, Yanina Romero-Zerbo, Rajaa El Bekay, Ignacio del Arco-Herrera, Lourdes Sánchez-Salido, Fernando Rodríguez de Fonseca
Publikováno v:
European Journal of Neuroscience. 26:3169-3180
Fragile X syndrome is the most common form of inherited mental retardation in humans. It originates from the loss of expression of the Fragile X mental retardation 1 (FMR1) gene, which results in the absence of the Fragile X mental retardation protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b0844ebe9061fda52ac452234b879fd
https://doi.org/10.1111/j.1460-9568.2007.05939.x
https://doi.org/10.1111/j.1460-9568.2007.05939.x
Autor:
Lourdes Sánchez-Salido, Francisco Garcia-Guirado, Yolanda de Diego-Otero, Ignacio del Arco-Herrera, Rafaela Caballero-Andaluz, Teresa Ferrando-Lucas, Carolina Quintero-Navarro, Isabel Fernandez-Carvajal, Lucía Pérez-Costillas, R. Calvo-Medina
Publikováno v:
Trials
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
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This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0).
[Background]: Fragile X syndrome (FXS) is an inherited neurodevelopmental condition characterise
[Background]: Fragile X syndrome (FXS) is an inherited neurodevelopmental condition characterise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940cfa245747909aca12b5b601872c9f
https://pubmed.ncbi.nlm.nih.gov/25187257
https://pubmed.ncbi.nlm.nih.gov/25187257
Autor:
Yanina Romero-Zerbo, Lourdes Sánchez-Salido, Fernando Rodríguez de Fonseca, Yolanda de Diego-Otero, Rajaa El Bekay, Juan Decara, Ignacio del Arco-Herrera
Publikováno v:
Journal of pineal research. 46(2)
Fragile X syndrome is the most common form of inherited mental retardation. It is typically caused by a mutation of the Fragile X mental-retardation 1 (Fmr1) gene. To better understand the role of the Fmr1 gene and its gene product, the fragile X men
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d3dd29d9f8a81d6b00297a54e9a77a
https://pubmed.ncbi.nlm.nih.gov/19141086
https://pubmed.ncbi.nlm.nih.gov/19141086
Autor:
Rajaa, el Bekay, Yanina, Romero-Zerbo, Juan, Decara, Lourdes, Sanchez-Salido, Ignacio, Del Arco-Herrera, Fernando, Rodríguez-de Fonseca, Yolanda, de Diego-Otero
Publikováno v:
The European journal of neuroscience. 26(11)
Fragile X syndrome is the most common form of inherited mental retardation in humans. It originates from the loss of expression of the Fragile X mental retardation 1 (FMR1) gene, which results in the absence of the Fragile X mental retardation protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b2c78afd5798fde3f135208943e8f196
https://pubmed.ncbi.nlm.nih.gov/18005058
https://pubmed.ncbi.nlm.nih.gov/18005058