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Soluble CX3CL1 gene therapy improves cone survival and function in mouse models of retinitis pigmentosa
Retinitis pigmentosa (RP) is a disease that initially presents as night blindness due to genetic deficits in the rod photoreceptors of the retina. Rods then die, causing dysfunction and death of cone photoreceptors, the cell type that mediates high acuity and color vision, ultimately leading to blin...
Shranjeno v:
| izdano v: | Proc Natl Acad Sci U S A |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
National Academy of Sciences
2019
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6525490/ https://ncbi.nlm.nih.gov/pubmed/31036641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1901787116 |
| Oznake: |
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