Sex-specific attenuation of photoreceptor degeneration by reserpine in a rhodopsin P23H rat model of autosomal dominant retinitis pigmentosa

Inherited retinal degenerations (IRDs) constitute a group of clinically and genetically diverse vision-impairing disorders. Retinitis pigmentosa (RP), the most common form of IRD, is characterized by gradual dysfunction and degeneration of rod photoreceptors, followed by the loss of cone photorecept...

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Principais autores:	Hyun Beom Song, Laura Campello, Anupam Mondal, Holly Y Chen, Milton A English, Michael Glen, Phillip Vanlandingham, Rafal Farjo, Anand Swaroop
Formato:	Artigo
Idioma:	Inglês
Publicado:	eLife Sciences Publications Ltd 2025-04-01
Series:	eLife
Assuntos:	small molecule drug retinal degeneration neuroprotection rhodopsin mutation retinitis pigmentosa
Acceso en liña:	https://elifesciences.org/articles/103888
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