Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mónica Feijóo-Cuaresma"'
Autor:
Said Lhamyani, Adriana-Mariel Gentile, Rosa M. Giráldez-Pérez, Mónica Feijóo-Cuaresma, Silvana Yanina Romero-Zerbo, Mercedes Clemente-Postigo, Hatem Zayed, Wilfredo Oliva-Olivera, Francisco Javier Bermúdez-Silva, Julián Salas, Carlos López Gómez, Abdelkrim Hmadcha, Nabil Hajji, Gabriel Olveira, Francisco J. Tinahones, Rajaa El Bekay
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 26, Iss , Pp 401-416 (2021)
MicroRNAs (miRNAs) are promising drug targets for obesity and metabolic disorders. Recently, miRNA mimics are providing a unique mechanism of action that guides the process for drug development and sets out the context of their therapeutic applicatio
Externí odkaz:
https://doaj.org/article/322e93f98c5a4bea87e9981e94c70da2
Autor:
Carlos López Gómez, Said Lhamyani, Mercedes Clemente-Postigo, Adriana-Mariel Gentile, Rosa M. Giráldez-Pérez, Nabil Hajji, Rajaa El Bekay, Abdelkrim Hmadcha, Julián Salas, Silvana Y. Romero-Zerbo, Francisco Javier Bermúdez-Silva, Gabriel Olveira, Wilfredo Oliva Olivera, Hatem Zayed, Francisco J. Tinahones, Mónica Feijóo-Cuaresma
Publikováno v:
Molecular Therapy. Nucleic Acids
Molecular Therapy: Nucleic Acids, Vol 26, Iss, Pp 401-416 (2021)
Molecular Therapy: Nucleic Acids, Vol 26, Iss, Pp 401-416 (2021)
MicroRNAs (miRNAs) are promising drug targets for obesity and metabolic disorders. Recently, miRNA mimics are providing a unique mechanism of action that guides the process for drug development and sets out the context of their therapeutic applicatio
Autor:
Rosa M. Giráldez-Pérez, Nabil Hajji, Francisco Javier Bermúdez-Silva, Rajaa El Bekay, Mónica Feijóo-Cuaresma, Gabriel Olveira Fuster, Said Lhamyani, Adriana-Mariel Gentile, Julián Salas, Carlos López Gómez, Wilfredo Oliva Olivera, Francisco J. Tinahones, Hatem Zayed, Silvana Y. Romero-Zerbo, Mercedes Clemente-Postigo
microRNAs are promising drug targets in obesity and metabolic disorders. miR-21 expression is upregulated in obese white adipose tissue (WAT); however, its physiological role in WAT has not been fully explored. We aimed to dissect the underlying mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a26c99d1690dc85b27141a0697a4d2d
https://doi.org/10.1101/2020.10.27.20219915
https://doi.org/10.1101/2020.10.27.20219915
Autor:
Salvador Guirado, Yolanda de Diego-Otero, Raúl Heredia, Rosa M. Giráldez-Pérez, M. Ángeles Real, Mónica Feijóo-Cuaresma, M. Nieves Ávila
Publikováno v:
Journal of Comparative Neurology. 521:894-911
Fragile X syndrome (FXS), the most common form of inherited mental retardation, is caused by the loss of the Fmr1 gene product, fragile X mental retardation protein. Here we analyze the immunohistochemical expression of calcium-binding proteins in th