DDX3X syndrome: From clinical phenotypes to biological insights von Mueffling, Alexa, Garcia‐Forn, Marta, De Rubeis, Silvia

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Neuron type‐specific increase in lamin B1 contributes to nuclear dysfunction in Huntington’s disease von Alcalá‐Vida, Rafael, Garcia‐Forn, Marta, Castany‐Pladevall, Carla, Creus‐Muncunill, Jordi, Ito, Yoko, Blanco, Enrique, Golbano, Arantxa, Crespí‐Vázquez, Kilian, Parry, Aled, Slater, Guy, Samarajiwa, Shamith, Peiró, Sandra, Di Croce, Luciano, Narita, Masashi, Pérez‐Navarro, Esther

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Pharmacogenetic modulation of STEP improves motor and cognitive function in a mouse model of Huntington's disease von García-Forn, Marta, Martínez-Torres, Sara, García-Díaz Barriga, Gerardo, Alberch, Jordi, Milà, Montse, Azkona, Garikoitz, Pérez-Navarro, Esther

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Lamin B1 and nuclear morphology in peripheral cells as new potential biomarkers to follow treatment response in Huntington's disease von Garcia‐Forn, Marta, Castany‐Pladevall, Carla, Golbano, Arantxa, Pérez‐Pérez, Jesús, Brito, Verónica, Kulisevsky, Jaime, Pérez‐Navarro, Esther

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Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex von Salamon, Iva, Park, Yongkyu, Miškić, Terezija, Kopić, Janja, Matteson, Paul, Page, Nicholas F., Roque, Alfonso, McAuliffe, Geoffrey W., Favate, John, Garcia-Forn, Marta, Shah, Premal, Judaš, Miloš, Millonig, James H., Kostović, Ivica, De Rubeis, Silvia, Hart, Ronald P., Krsnik, Željka, Rasin, Mladen-Roko

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Neuronal diversity and stereotypy at multiple scales through whole brain morphometry von Liu, Yufeng, Jiang, Shengdian, Li, Yingxin, Zhao, Sujun, Yun, Zhixi, Zhao, Zuo-Han, Zhang, Lingli, Wang, Gaoyu, Chen, Xin, Manubens-Gil, Linus, Hang, Yuning, Gong, Qiaobo, Li, Yuanyuan, Qian, Penghao, Qu, Lei, Garcia-Forn, Marta, Wang, Wei, De Rubeis, Silvia, Wu, Zhuhao, Osten, Pavel, Gong, Hui, Hawrylycz, Michael, Mitra, Partha, Dong, Hongwei, Luo, Qingming, Ascoli, Giorgio A., Zeng, Hongkui, Liu, Lijuan, Peng, Hanchuan

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RTP801/REDD1 Is Involved in Neuroinflammation and Modulates Cognitive Dysfunction in Huntington's Disease von Pérez-Sisqués, Leticia, Solana-Balaguer, Júlia, Campoy-Campos, Genís, Martín-Flores, Núria, Sancho-Balsells, Anna, Vives-Isern, Marcel, Soler-Palazón, Ferran, Garcia-Forn, Marta, Masana, Mercè, Alberch, Jordi, Pérez-Navarro, Esther, Giralt, Albert, Malagelada, Cristina

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Linking Autism Risk Genes to Disruption of Cortical Development von Garcia-Forn, Marta, Boitnott, Andrea, Akpinar, Zeynep, De Rubeis, Silvia

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Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4 von Campisi, Laura, Chizari, Shahab, Ho, Jessica S. Y., Gromova, Anastasia, Arnold, Frederick J., Mosca, Lorena, Mei, Xueyan, Fstkchyan, Yesai, Torre, Denis, Beharry, Cindy, Garcia-Forn, Marta, Jiménez-Alcázar, Miguel, Korobeynikov, Vladislav A., Prazich, Jack, Fayad, Zahi A., Seldin, Marcus M., De Rubeis, Silvia, Bennett, Craig L., Ostrow, Lyle W., Lunetta, Christian, Squatrito, Massimo, Byun, Minji, Shneider, Neil A., Jiang, Ning, La Spada, Albert R., Marazzi, Ivan

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Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome von Boitnott, Andrea, Garcia-Forn, Marta, Ung, Dévina C., Niblo, Kristi, Mendonca, Danielle, Park, Yeaji, Flores, Michael, Maxwell, Sylvia, Ellegood, Jacob, Qiu, Lily R., Grice, Dorothy E., Lerch, Jason P., Rasin, Mladen-Roko, Buxbaum, Joseph D., Drapeau, Elodie, De Rubeis, Silvia

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Increased translation as a novel pathogenic mechanism in Huntington's disease von Creus-Muncunill, Jordi, Badillos-Rodríguez, Raquel, Garcia-Forn, Marta, Masana, Mercè, Garcia-Díaz Barriga, Gerardo, Guisado-Corcoll, Anna, Alberch, Jordi, Malagelada, Cristina, Delgado-García, José M, Gruart, Agnès, Pérez-Navarro, Esther

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A subpopulation of cortical neurons altered by mutations in the autism risk gene DDX3X von Flores, Michael A, Garcia-Forn, Marta, von Mueffling, Alexa, Ola, Praise, Park, Yeaji, Boitnott, Andrea, De Rubeis, Silvia

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Lack of Annexin A6 Exacerbates Liver Dysfunction and Reduces Lifespan of Niemann-Pick Type C Protein–Deficient Mice von Meneses-Salas, Elsa, Garcia-Forn, Marta, Castany-Pladevall, Carla, Lu, Albert, Fajardo, Alba, Jose, Jaimy, Wahba, Mohamed, Bosch, Marta, Pol, Albert, Tebar, Francesc, Klein, Andrés D., Zanlungo, Silvana, Pérez-Navarro, Esther, Grewal, Thomas, Enrich, Carlos, Rentero, Carles

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Lack of Annexin A6 exacerbates liver dysfunction and reduces lifespan of Niemann-Pick type C protein-deficient mice von Meneses Salas, Elsa, Garcia-Forn, Marta, Castany Pladevall, Carla, Lu, Albert, Fajardo, Alba, Jose, Jaimy, Wahba, Mohamed, Bosch i Rodríguez, Marta, Pol i Sorolla, Albert, Tebar Ramon, Francesc, Klein, Andrés D, Zanlungo, Silvana, Pérez Navarro, Esther, Grewal, Thomas, Enrich Bastús, Carles, Rentero Alfonso, Carles

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Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4 von Campisi, Laura, Chizari, Shahab, Ho, Jessica S. Y., Gromova, Anastasia, Arnold, Frederick J., Mosca, Lorena, Mei, Xueyan, Fstkchyan, Yesai, Torre, Denis, Beharry, Cindy, Garcia-Forn, Marta, Jiménez-Alcázar, Miguel, Korobeynikov, Vladislav A., Prazich, Jack, Fayad, Zahi A., Seldin, Marcus M., De Rubeis, Silvia, Bennett, Craig L., Ostrow, Lyle W., Lunetta, Christian, Squatrito, Massimo, Byun, Minji, Shneider, Neil A., Jiang, Ning, La Spada, Albert R., Marazzi, Ivan

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Increased translation as a novel pathogenic mechanism in Huntington's disease von Creus Muncunill, Jordi, Badillos Rodríguez, Raquel, Garcia-Forn, Marta, Masana Nadal, Mercè, García-Díaz Barriga, Gerardo, Guisado Corcoll, Anna, Alberch i Vié, Jordi, 1959, Malagelada Grau, Cristina, Delgado García, José M, Gruart i Massó, Agnès, Pérez Navarro, Esther

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Pharmacogenetic Modulation of STEP improves motor and cognitive function in a mouse model of Huntington's disease von Garcia-Forn, Marta, Martínez Torres, Sara, García-Díaz Barriga, Gerardo, Alberch i Vié, Jordi, 1959, Milà i Recasens, Montserrat, Azkona, Garikoitz, Pérez Navarro, Esther

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Teaching case 3-2019: Are nuclear clefts or invaginations the niche of intranuclear inclusions in FTLD-TDP? von Molina Porcel, Laura, Pérez Navarro, Esther, Garcia-Forn, Marta, Westaway, David, Colom Cadena, Martí, Gelpi, Ellen

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Neuron type-specific increase in lamin B1 contributes to nuclear dysfunction in Huntington's disease von Alcalá Vida, Rafael, Garcia-Forn, Marta, Castany Pladevall, Carla, Creus Muncunill, Jordi, Ito, Yoko, Blanco, Enrique, Golbano, Arantxa, Crespí-Vázquez, Kilian, Parry, Aled, Slater, Guy, Samarajiwa, Shamith, Peiró, Sandra, Croce, Luciano Di, Narita, Masashi, Pérez Navarro, Esther

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Teaching case 3-2019: Are nuclear clefts or invaginations the niche of intranuclear inclusions in FTLD-TDP? von Molina-Porcel, Laura, Pérez-Navarro, Esther, García-Forn, Marta, Westaway, David, Colom-Cadena, Martí, Gelpi, Ellen

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