Spatial Transcriptomic Analysis Reveals Regional Transcript Changes in Early and Late Stages of rd1 Model Mice with Retinitis Pigmentosa

Retinitis pigmentosa (RP) is the leading cause of inherited blindness with a genetically heterogeneous disorder. Currently, there is no effective treatment that can protect vision for those with RP. In recent decades, the rd1 mouse has been used to study the pathological mechanisms of RP. Molecular...

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Detalles Bibliográficos
Autores principales: Zhou, Ying, Sheng, Yuqi, Pan, Min, Tu, Jing, Zhao, Xiangwei, Ge, Qinyu, Lu, Zuhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573885/
https://www.ncbi.nlm.nih.gov/pubmed/37834317
http://dx.doi.org/10.3390/ijms241914869

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573885/
https://www.ncbi.nlm.nih.gov/pubmed/37834317
http://dx.doi.org/10.3390/ijms241914869

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