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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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
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Article
Acesso em linha: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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