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Did you mean pagni m[Author] (103 results)?
Structural basis for nuclear import selectivity of pioneer transcription factor SOX2.
Jagga B, Edwards M, Pagin M, Wagstaff KM, Aragão D, Roman N, Nanson JD, Raidal SR, Dominado N, Stewart M, Jans DA, Hime GR, Nicolis SK, Basler CF, Forwood JK. Jagga B, et al. Among authors: pagin m. Nat Commun. 2021 Jan 4;12(1):28. doi: 10.1038/s41467-020-20194-0. Nat Commun. 2021. PMID: 33397924 Free PMC article.
Genomic glucocorticoid action in embryonic mouse neural stem cells.
Berry KJ, Chandran U, Mu F, Deochand DK, Lei T, Pagin M, Nicolis SK, Monaghan-Nichols AP, Rogatsky I, DeFranco DB. Berry KJ, et al. Among authors: pagin m. Mol Cell Endocrinol. 2023 Mar 1;563:111864. doi: 10.1016/j.mce.2023.111864. Epub 2023 Jan 20. Mol Cell Endocrinol. 2023. PMID: 36690169 Free PMC 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: pagin m. 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.
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: pagin m. Glia. 2018 Sep;66(9):1929-1946. doi: 10.1002/glia.23448. Epub 2018 May 6. Glia. 2018. PMID: 29732603 Free article.
16 results