Sdr9c7-flox 基因敲除小鼠

1. Shigehara, Yohya, Okuda, Shujiro, Nemer, Georges, Kurban, Mazen, Shimomura, Yutaka. . Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis. In Human molecular genetics, 25, 4484-4493. doi:10.1093/hmg/ddw277. https://pubmed.ncbi.nlm.nih.gov/28173123/

2. Kiener, Sarah, Castilla, Eloy, Jagannathan, Vidhya, Welle, Monika, Leeb, Tosso. 2023. SDR9C7 missense variant in a Chihuahua with non-epidermolytic ichthyosis. In Animal genetics, 54, 562-565. doi:10.1111/age.13319. https://pubmed.ncbi.nlm.nih.gov/36967672/

3. Youssefian, Leila, Niaziorimi, Fatemeh, Saeidian, Amir Hossein, Vahidnezhad, Hassan, Uitto, Jouni. 2021. Knockdown of SDR9C7 Impairs Epidermal Barrier Function. In The Journal of investigative dermatology, 141, 1754-1764.e1. doi:10.1016/j.jid.2020.11.030. https://pubmed.ncbi.nlm.nih.gov/33422619/