1. Kanzaki, Yuki, Fujita, Hirofumi, Sato, Keita, Morizane, Yuki, Ohuchi, Hideyo. . KCNJ13 Gene Deletion Impairs Cell Alignment and Phagocytosis in Retinal Pigment Epithelium Derived from Human-Induced Pluripotent Stem Cells. In Investigative ophthalmology & visual science, 61, 38. doi:10.1167/iovs.61.5.38. https://pubmed.ncbi.nlm.nih.gov/32437550/
2. Kanzaki, Yuki, Fujita, Hirofumi, Sato, Keita, Morizane, Yuki, Ohuchi, Hideyo. . Protrusion of KCNJ13 Gene Knockout Retinal Pigment Epithelium Due to Oxidative Stress-Induced Cell Death. In Investigative ophthalmology & visual science, 63, 29. doi:10.1167/iovs.63.12.29. https://pubmed.ncbi.nlm.nih.gov/36413373/
3. Schroeder, Marion, Peter, Virginie G, Gränse, Lotta, Rivolta, Carlo, Kjellström, Ulrika. 2022. A novel phenotype associated with the R162W variant in the KCNJ13 gene. In Ophthalmic genetics, 43, 500-507. doi:10.1080/13816810.2022.2068041. https://pubmed.ncbi.nlm.nih.gov/35477418/
4. Kabra, Meha, Shahi, Pawan K, Wang, Yuyuan, Saha, Krishanu, Pattnaik, Bikash R. 2023. Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathy. In The Journal of clinical investigation, 133, . doi:10.1172/JCI171356. https://pubmed.ncbi.nlm.nih.gov/37561581/
5. Shahi, Pawan K, Hermans, Dalton, Sinha, Divya, Gamm, David M, Pattnaik, Bikash R. 2019. Gene Augmentation and Readthrough Rescue Channelopathy in an iPSC-RPE Model of Congenital Blindness. In American journal of human genetics, 104, 310-318. doi:10.1016/j.ajhg.2018.12.019. https://pubmed.ncbi.nlm.nih.gov/30686507/
6. Yin, Wenguang, Kim, Hyun-Taek, Wang, ShengPeng, Offermanns, Stefan, Stainier, Didier Y R. 2018. The potassium channel KCNJ13 is essential for smooth muscle cytoskeletal organization during mouse tracheal tubulogenesis. In Nature communications, 9, 2815. doi:10.1038/s41467-018-05043-5. https://pubmed.ncbi.nlm.nih.gov/30022023/