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Müller Glia Activation in Response to Inherited Retinal Degeneration Is Highly Varied and Disease-Specific
Despite different aetiologies, most inherited retinal disorders culminate in photoreceptor loss, which induces concomitant changes in the neural retina, one of the most striking being reactive gliosis by Müller cells. It is typically assumed that photoreceptor loss leads to an upregulation of glial...
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| Vydáno v: | PLoS One |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4368159/ https://ncbi.nlm.nih.gov/pubmed/25793273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0120415 |
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