Specific photoreceptor cell fate pathways are differentially altered in NR2E3-associated diseases

Author:

Aísa-Marín Izarbe,Rovira Quirze,Díaz Noelia,Calvo-López Laura,Vaquerizas Juan M.,Marfany Gemma

Funder

Generalitat de Catalunya

Universitat de Barcelona

Gobierno de España Ministerio de Ciencia e Innovación

Medical Research Council

The Company of Biologists

Publisher

Elsevier BV

Reference82 articles.

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2. Data on the generation of two Nr2e3 mouse models by CRISPR / Cas9D10A nickase;Aísa-Marín;Data Br.,2020

3. A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse;Akhmedov;Proc. Natl. Acad. Sci. USA,2000

4. Crystallins in the eye: function and pathology;Andley;Prog. Retin. Eye Res.,2007

5. Identification of a common non-apoptotic cell death mechanism in hereditary retinal degeneration;Arango-Gonzalez;PLoS One,2014

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal development;Journal of Clinical Investigation;2024-04-23

2. Histogenesis: Cone Photoreceptor Development;Reference Module in Neuroscience and Biobehavioral Psychology;2024

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