RNA Isolation from Human Stem Cell–Derived Retinal Organoids
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Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-3918-4_1
Reference30 articles.
1. Kallman A, Capowski EE, Wang J et al (2020) Investigating cone photoreceptor development using patient-derived NRL null retinal organoids. Commun Biol 1:82. https://doi.org/10.1038/s42003-020-0808-5
2. Watson A, Lako M (2023) Retinal organoids provide unique insights into molecular signatures of inherited retinal disease throughout retinogenesis. J Anat 2:186–203. https://doi.org/10.1111/joa.13768
3. Jones MK, Orozco LD, Qin H et al (2023) Integration of human stem cell-derived in vitro systems and mouse preclinical models identifies complex pathophysiologic mechanisms in retinal dystrophy. Front Cell Dev Biol:1252547. https://doi.org/10.3389/fcell.2023.1252547
4. Bocquet B, Borday C, Erkilic N et al (2023) TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa. JCI Insight. https://doi.org/10.1172/jci.insight.169426
5. Sanjurjo-Soriano C, Jimenez-Medina C, Erkilic N et al (2023) USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids. HGG Adv 4:100229. https://doi.org/10.1016/j.xhgg.2023.100229
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