Transcription factors SOX4 and SOX11 function redundantly to regulate the development of mouse retinal ganglion cells

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Abstract

Background: Roles of SoxC genes in the development of retinal ganglion cells (RGCs) are unknown at present. Results: Targeted deletion of Sox4 and Sox11 in retina results in a complete loss of RGCs. Conclusion: Sox4 and Sox11 function redundantly to regulate RGC development. Significance: These findings highlight the essential role of SoxC genes in retinal development. © 2013 by The American Society.

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APA

Jiang, Y., Ding, Q., Xie, X., Libby, R. T., Lefebvre, V., & Gan, L. (2013). Transcription factors SOX4 and SOX11 function redundantly to regulate the development of mouse retinal ganglion cells. Journal of Biological Chemistry, 288(25), 18429–18438. https://doi.org/10.1074/jbc.M113.478503

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