Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa

Hereditary retinal degenerations like retinitis pigmentosa (RP) are among the leading causes of blindness in younger patients. To enable in vivo investigation of cellular and molecular mechanisms responsible for photoreceptor cell death and to allow testing of therapeutic strategies that could preve...

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Detalles Bibliográficos
Autores principales: Bielmeier, Christina B., Roth, Saskia, Schmitt, Sabrina I., Boneva, Stefaniya K., Schlecht, Anja, Vallon, Mario, Tamm, Ernst R., Ergün, Süleyman, Neueder, Andreas, Braunger, Barbara M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231189/
https://www.ncbi.nlm.nih.gov/pubmed/34208383
http://dx.doi.org/10.3390/ijms22126307

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231189/
https://www.ncbi.nlm.nih.gov/pubmed/34208383
http://dx.doi.org/10.3390/ijms22126307

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