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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Detaylı Bibliyografya
Yayımlandı:Int J Mol Sci
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2021
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC8231189/
https://ncbi.nlm.nih.gov/pubmed/34208383
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22126307
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