4.3 Review Book Chapter

Axon Regeneration in the Mammalian Optic Nerve

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DOI: 10.1146/annurev-vision-022720-094953

关键词

retinal ganglion cells; axon regeneration; survival; KLF; mTOR; oncomodulin

资金

  1. National Institutes of Health [P30EY026877, R01-EY026766, R01EY024481, R01EY027881, R01EY026939, R01EY021526]
  2. Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
  3. Medical Technology Enterprise Consortium
  4. Gilbert Vision Restoration Initiative
  5. Research to Prevent Blindness, Inc.
  6. US Department of Defense Congressionally Directed Medical Research Program [W81XWH16-1-0043]
  7. National Institute of Child Health and Development Intellectual and Developmental Disabilities Research Centers [HD018655]
  8. National Eye Institute [P30EY026877, R01-EY026766, R01EY024481, R01EY027881, R01EY026939, R01EY021526]

向作者/读者索取更多资源

The damage or loss of retinal ganglion cells (RGCs) and their axons accounts for the visual functional defects observed after traumatic injury, in degenerative diseases such as glaucoma, or in compressive optic neuropathies such as from optic glioma. By using optic nerve crush injury models, recent studies have revealed the cellular and molecular logic behind the regenerative failure of injured RGC axons in adult mammals and suggested several strategies with translational potential. This review summarizes these findings and discusses challenges for developing clinically applicable neural repair strategies.

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