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Sox2 conditional mutation in mouse causes ataxic symptoms, cerebellar vermis hypoplasia, and postnatal defects of Bergmann glia.
Cerrato V, Mercurio S, Leto K, Fucà E, Hoxha E, Bottes S, Pagin M, Milanese M, Ngan CY, Concina G, Ottolenghi S, Wei CL, Bonanno G, Pavesi G, Tempia F, Buffo A, Nicolis SK. Cerrato V, et al. Among authors: ottolenghi s. Glia. 2018 Sep;66(9):1929-1946. doi: 10.1002/glia.23448. Epub 2018 May 6. Glia. 2018. PMID: 29732603 Free article.
Mapping the Global Chromatin Connectivity Network for Sox2 Function in Neural Stem Cell Maintenance.
Bertolini JA, Favaro R, Zhu Y, Pagin M, Ngan CY, Wong CH, Tjong H, Vermunt MW, Martynoga B, Barone C, Mariani J, Cardozo MJ, Tabanera N, Zambelli F, Mercurio S, Ottolenghi S, Robson P, Creyghton MP, Bovolenta P, Pavesi G, Guillemot F, Nicolis SK, Wei CL. Bertolini JA, et al. Among authors: ottolenghi s. Cell Stem Cell. 2019 Mar 7;24(3):462-476.e6. doi: 10.1016/j.stem.2019.02.004. Cell Stem Cell. 2019. PMID: 30849367 Free PMC article.
Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers.
Mariani J, Favaro R, Lancini C, Vaccari G, Ferri AL, Bertolini J, Tonoli D, Latorre E, Caccia R, Ronchi A, Ottolenghi S, Miyagi S, Okuda A, Zappavigna V, Nicolis SK. Mariani J, et al. Among authors: ottolenghi s. Nucleic Acids Res. 2012 Aug;40(14):6461-76. doi: 10.1093/nar/gks295. Epub 2012 Apr 11. Nucleic Acids Res. 2012. PMID: 22495934 Free PMC article.
167 results