Zika virus induces FOXG1 nuclear displacement and downregulation in human neural progenitors

Congenital alterations in the levels of the transcription factor Forkhead box g1 (FOXG1) coding gene trigger “FOXG1 syndrome,” a spectrum that recapitulates birth defects found in the “congenital Zika syndrome,” such as microcephaly and other neurodevelopmental conditions. Here, we report that Zika...

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Detalles Bibliográficos
Autores principales: Lottini, Giulia, Baggiani, Matteo, Chesi, Giulia, D’Orsi, Beatrice, Quaranta, Paola, Lai, Michele, Pancrazi, Laura, Onorati, Marco, Pistello, Mauro, Freer, Giulia, Costa, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287670/
https://www.ncbi.nlm.nih.gov/pubmed/35714598
http://dx.doi.org/10.1016/j.stemcr.2022.05.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287670/
https://www.ncbi.nlm.nih.gov/pubmed/35714598
http://dx.doi.org/10.1016/j.stemcr.2022.05.008

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