1. Cuevas, Elisa, Holder, Daniel L, Alshehri, Ashwak H, Lakowski, Jörn, Sowden, Jane C. 2021. NRL-/- gene edited human embryonic stem cells generate rod-deficient retinal organoids enriched in S-cone-like photoreceptors. In Stem cells (Dayton, Ohio), 39, 414-428. doi:10.1002/stem.3325. https://pubmed.ncbi.nlm.nih.gov/33400844/
2. Liu, Zhiquan, Chen, Siyu, Lo, Chien-Hui, Wang, Qing, Sun, Yang. 2024. All-in-one AAV-mediated Nrl gene inactivation rescues retinal degeneration in Pde6a mice. In JCI insight, 9, . doi:10.1172/jci.insight.178159. https://pubmed.ncbi.nlm.nih.gov/39499900/
3. Thorson, Molly T, Wei, Stephanie E, Johnson, Craig, Arshavsky, Vadim Y, Pearring, Jillian N. 2023. Nrl:CreERT2 mouse model to induce mosaic gene expression in rod photoreceptors. In Frontiers in molecular neuroscience, 16, 1161127. doi:10.3389/fnmol.2023.1161127. https://pubmed.ncbi.nlm.nih.gov/37181654/
4. Iarossi, Giancarlo, Sinibaldi, Lorenzo, Passarelli, Chiara, Bartuli, Andrea, Buzzonetti, Luca. 2022. A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients. In Diagnostics (Basel, Switzerland), 12, . doi:10.3390/diagnostics12092183. https://pubmed.ncbi.nlm.nih.gov/36140584/
5. Moore, Spencer M, Skowronska-Krawczyk, Dorota, Chao, Daniel L. 2020. Targeting of the NRL Pathway as a Therapeutic Strategy to Treat Retinitis Pigmentosa. In Journal of clinical medicine, 9, . doi:10.3390/jcm9072224. https://pubmed.ncbi.nlm.nih.gov/32668775/
6. Farjo, Q, Jackson, A, Pieke-Dahl, S, Richards, J E, Swaroop, A. . Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration. In Genomics, 45, 395-401. doi:. https://pubmed.ncbi.nlm.nih.gov/9344665/
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