Chm-KO 基因敲除小鼠

1. Toualbi, Lyes, Toms, Maria, Almeida, Patrick Vingadas, Harbottle, Richard, Moosajee, Mariya. 2023. Gene Augmentation of CHM Using Non-Viral Episomal Vectors in Models of Choroideremia. In International journal of molecular sciences, 24, . doi:10.3390/ijms242015225. https://pubmed.ncbi.nlm.nih.gov/37894906/

2. Imani, Saber, Ijaz, Iqra, Shasaltaneh, Marzieh Dehghan, Cheng, Jingliang, Fu, Junjiang. 2018. Molecular genetics ‎characterization and homology modeling of the CHM gene mutation: A study on its association with choroideremia. In Mutation research. Reviews in mutation research, 775, 39-50. doi:10.1016/j.mrrev.2018.02.001. https://pubmed.ncbi.nlm.nih.gov/29555028/

3. Karali, Marianthi, Testa, Francesco, Di Iorio, Valentina, Simonelli, Francesca, Banfi, Sandro. 2022. Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy. In Scientific reports, 12, 20815. doi:10.1038/s41598-022-24636-1. https://pubmed.ncbi.nlm.nih.gov/36460718/

4. De Silva, Samantha R, Arno, Gavin, Robson, Anthony G, Webster, Andrew R, Mahroo, Omar A. 2020. The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies. In Progress in retinal and eye research, 82, 100898. doi:10.1016/j.preteyeres.2020.100898. https://pubmed.ncbi.nlm.nih.gov/32860923/