Actions of estrogens on glial cells: Implications for neuroprotection von Arevalo, María-Angeles, Santos-Galindo, María, Bellini, María-José, Azcoitia, Iñigo, Garcia-Segura, Luis M.

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Selective Estrogen Receptor Modulators Decrease Reactive Astrogliosis in the Injured Brain: Effects of Aging and Prolonged Depletion of Ovarian Hormones von Barreto, George, Santos-Galindo, María, Diz-Chaves, Yolanda, Pernía, Olga, Carrero, Paloma, Azcoitia, Iñigo, Garcia-Segura, Luis M

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Differential regulation of Kidins220 isoforms in Huntington's disease von Sebastián‐Serrano, Álvaro, Simón‐García, Ana, Belmonte‐Alfaro, Alicia, Pose‐Utrilla, Julia, Santos‐Galindo, María, del Puerto, Ana, García‐Guerra, Lucía, Hernández, Ivó H., Schiavo, Giampietro, Campanero, Miguel R., Lucas, José J., Iglesias, Teresa

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Faulty splicing and cytoskeleton abnormalities in Huntington's disease von Fernández-Nogales, Marta, Santos-Galindo, María, Hernández, Ivó H., Cabrera, Jorge R., Lucas, José J.

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Selective estrogen receptor modulators as brain therapeutic agents von Arevalo, María Angeles, Santos-Galindo, María, Lagunas, Natalia, Azcoitia, Iñigo, Garcia-Segura, Luis M

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Tau‐positive nuclear indentations in P301S tauopathy mice von Fernández‐Nogales, Marta, Santos‐Galindo, María, Merchán‐Rubira, Jesús, Hoozemans, Jeroen J. M., Rábano, Alberto, Ferrer, Isidro, Avila, Jesús, Hernández, Félix, Lucas, José J.

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P2X7 Receptor Upregulation in Huntington’s Disease Brains von Ollà, Ivana, Santos-Galindo, María, Elorza, Ainara, Lucas, José J.

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IN VIVO INTERROGATION OF THE CONTRIBUTION OF SPECIFIC SPLICING FACTORS TO PATHOLOGICAL MIS-SPLICING IN HUNTINGTON´S DISEASE von Lozano-Muñoz, David, Elorza, Ainara, Santos-Galindo, María, Lucas, José

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Sex differences in the inflammatory response of primary astrocytes to lipopolysaccharide von Santos-Galindo, María, Acaz-Fonseca, Estefanía, Bellini, María J, Garcia-Segura, Luis M

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Role of astroglia in the neuroplastic and neuroprotective actions of estradiol von Azcoitia, Iñigo, Santos-Galindo, María, Arevalo, María A., Garcia-Segura, Luis M.

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Huntington's disease is a four-repeat tauopathy with tau nuclear rods von Fernández-Nogales, Marta, Cabrera, Jorge R, Santos-Galindo, María, Hoozemans, Jeroen J M, Ferrer, Isidro, Rozemuller, Annemieke J M, Hernández, Félix, Avila, Jesús, Lucas, José J

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Huntington's disease-specific mis-splicing unveils key effector genes and altered splicing factors von Elorza, Ainara, Márquez, Yamile, Cabrera, Jorge R, Sánchez-Trincado, José Luis, Santos-Galindo, María, Hernández, Ivó H, Picó, Sara, Díaz-Hernández, Juan I, García-Escudero, Ramón, Irimia, Manuel, Lucas, José J

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Pathogenic SREK1 decrease in Huntington's disease lowers TAF1 mimicking X-linked dystonia parkinsonism von Hernández, Ivó H, Cabrera, Jorge R, Santos-Galindo, María, Sánchez-Martín, Manuel, Domínguez, Verónica, García-Escudero, Ramón, Pérez-Álvarez, María J, Pintado, Belén, Lucas, José J

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Pathogenic Mis-splicing of CPEB4 in Schizophrenia von Ollà, Ivana, Pardiñas, Antonio F., Parras, Alberto, Hernández, Ivó H., Santos-Galindo, María, Picó, Sara, Callado, Luis F., Elorza, Ainara, Rodríguez-López, Claudia, Fernández-Miranda, Gonzalo, Belloc, Eulàlia, Walters, James T.R., O’Donovan, Michael C., Méndez, Raúl, Toma, Claudio, Meana, J. Javier, Owen, Michael J., Lucas, José J.

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Gonadal hormones and the control of reactive gliosis von Arevalo, María Angeles, Santos-Galindo, María, Acaz-Fonseca, Estefanía, Azcoitia, Iñigo, Garcia-Segura, Luis M.

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The neuroprotective transcription factor ATF5 is decreased and sequestered into polyglutamine inclusions in Huntington’s disease von Hernández, Ivó H., Torres-Peraza, Jesús, Santos-Galindo, María, Ramos-Morón, Eloísa, Fernández-Fernández, M. Rosario, Pérez-Álvarez, María J., Miranda-Vizuete, Antonio, Lucas, José J.

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Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing von Parras, Alberto, Anta, Héctor, Santos-Galindo, María, Swarup, Vivek, Elorza, Ainara, Nieto-González, José L., Picó, Sara, Hernández, Ivó H., Díaz-Hernández, Juan I., Belloc, Eulàlia, Rodolosse, Annie, Parikshak, Neelroop N., Peñagarikano, Olga, Fernández-Chacón, Rafael, Irimia, Manuel, Navarro, Pilar, Geschwind, Daniel H., Méndez, Raúl, Lucas, José J.

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Huntington's disease-specific mis-splicing unveils key effector genes and altered splicing factors von Elorza, Ainara, Márquez, Yamile, Cabrera, Jorge, Sánchez-Trincado, José Luis, Santos-Galindo, María, Hernández, Ivó H, Picó, Sara, Díaz-Hernández, Juan I, García-Escudero, Ramón, Irimia Martínez, Manuel, Lucas, José J

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CPEB alteration and aberrant transcriptome-polyadenylation lead to a treatable SLC19A3 deficiency in Huntington's disease von Picó, Sara, Parras, Alberto, Santos Galindo, María, Pose Utrilla, Julia, Castro, Margarita, Fraga, Enrique, Hernández, Ivo H, Elorza, Ainara, Anta, Héctor, Wang, Nan, Martí Sánchez, Laura, Belloc, Eulàlia, Garcia Esparcia, Patricia, Garrido, Juan J, Ferrer, Isidro, Macías García, Daniel, Mir, Pablo, Artuch, Rafael, Pérez, Belén, Hernández, Félix, Navarro, Pilar, López Sendón, José Luis, Iglesias, Teresa, Yang, X. William, Méndez, Raúl, Lucas, José J

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Faulty splicing and cytoskeleton abnormalities in H untington's disease von Fernández‐Nogales, Marta, Santos‐Galindo, María, Hernández, Ivó H., Cabrera, Jorge R., Lucas, José J.

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