Structural basis for nuclear import selectivity of pioneer transcription factor SOX2 by Jagga, Bikshapathi, Edwards, Megan, Pagin, Miriam, Wagstaff, Kylie M., Aragão, David, Roman, Noelia, Nanson, Jeffrey D., Raidal, Shane R., Dominado, Nicole, Stewart, Murray, Jans, David A., Hime, Gary R., Nicolis, Silvia K., Basler, Christopher F., Forwood, Jade K.

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Mapping the Global Chromatin Connectivity Network for Sox2 Function in Neural Stem Cell Maintenance by Bertolini, Jessica A., Favaro, Rebecca, Zhu, Yanfen, Pagin, Miriam, Ngan, Chew Yee, Wong, Chee Hong, Tjong, Harianto, Vermunt, Marit W., Martynoga, Ben, Barone, Cristiana, Mariani, Jessica, Cardozo, Marcos Julián, Tabanera, Noemi, Zambelli, Federico, Mercurio, Sara, Ottolenghi, Sergio, Robson, Paul, Creyghton, Menno P., Bovolenta, Paola, Pavesi, Giulio, Guillemot, Francois, Nicolis, Silvia K., Wei, Chia-Lin

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Deconstructing Sox2 Function in Brain Development and Disease by Mercurio, Sara, Serra, Linda, Pagin, Miriam, Nicolis, Silvia K

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Sox2 conditional mutation in mouse causes ataxic symptoms, cerebellar vermis hypoplasia, and postnatal defects of Bergmann glia by Cerrato, Valentina, Mercurio, Sara, Leto, Ketty, Fucà, Elisa, Hoxha, Eriola, Bottes, Sara, Pagin, Miriam, Milanese, Marco, Ngan, Chew‐Yee, Concina, Giulia, Ottolenghi, Sergio, Wei, Chia‐Lin, Bonanno, Giambattista, Pavesi, Giulio, Tempia, Filippo, Buffo, Annalisa, Nicolis, Silvia K.

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FOS Rescues Neuronal Differentiation of Sox2-Deleted Neural Stem Cells by Genome-Wide Regulation of Common SOX2 and AP1(FOS-JUN) Target Genes by Pagin, Miriam, Pernebrink, Mattias, Pitasi, Mattia, Malighetti, Federica, Ngan, Chew-Yee, Ottolenghi, Sergio, Pavesi, Giulio, Cantù, Claudio, Nicolis, Silvia K.

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Sox2 controls neural stem cell self‐renewal through a Fos‐centered gene regulatory network by Pagin, Miriam, Pernebrink, Mattias, Giubbolini, Simone, Barone, Cristiana, Sambruni, Gaia, Zhu, Yanfen, Chiara, Matteo, Ottolenghi, Sergio, Pavesi, Giulio, Wei, Chia‐Lin, Cantù, Claudio, Nicolis, Silvia K.

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Sox2‐dependent maintenance of mouse oligodendroglioma involves the Sox2‐mediated downregulation of Cdkn2b, Ebf1, Zfp423, and Hey2 by Barone, Cristiana, Buccarelli, Mariachiara, Alessandrini, Francesco, Pagin, Miriam, Rigoldi, Laura, Sambruni, Irene, Favaro, Rebecca, Ottolenghi, Sergio, Pallini, Roberto, Ricci‐Vitiani, Lucia, Malatesta, Paolo, Nicolis, Silvia K.

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Genomic glucocorticoid action in embryonic mouse neural stem cells by Berry, Kimberly J., Chandran, Uma, Mu, Fangping, Deochand, Dinesh K., Lei, T., Pagin, Miriam, Nicolis, Silvia K., Monaghan-Nichols, A. Paula, Rogatsky, Inez, DeFranco, Donald B.

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S ox2 conditional mutation in mouse causes ataxic symptoms, cerebellar vermis hypoplasia, and postnatal defects of B ergmann glia by Cerrato, Valentina, Mercurio, Sara, Leto, Ketty, Fucà, Elisa, Hoxha, Eriola, Bottes, Sara, Pagin, Miriam, Milanese, Marco, Ngan, Chew‐Yee, Concina, Giulia, Ottolenghi, Sergio, Wei, Chia‐Lin, Bonanno, Giambattista, Pavesi, Giulio, Tempia, Filippo, Buffo, Annalisa, Nicolis, Silvia K.

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Sox2-Dependent 3D Chromatin Interactomes in Transcription, Neural Stem Cell Proliferation and Neurodevelopmental Diseases by Wei, Chia-Lin, Nicolis, Silvia K, Zhu, Yanfen, Pagin, Miriam

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