Minar2-KO 基因敲除小鼠

1. Gao, Ge, Guo, Shuyu, Zhang, Quan, Zhang, Cuizhen, Peng, Gang. 2022. Kiaa1024L/Minar2 is essential for hearing by regulating cholesterol distribution in hair bundles. In eLife, 11, . doi:10.7554/eLife.80865. https://pubmed.ncbi.nlm.nih.gov/36317962/

2. Bademci, Guney, Lachgar-Ruiz, María, Deokar, Mangesh, Nasir, Jamal, Tekin, Mustafa. 2022. Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice. In Proceedings of the National Academy of Sciences of the United States of America, 119, e2204084119. doi:10.1073/pnas.2204084119. https://pubmed.ncbi.nlm.nih.gov/35727972/

3. Oluwole, Oluwafemi G, Esoh, Kevin K, Wonkam-Tingang, Edmond, Chimusa, Emile R, Wonkam, Ambroise. 2020. Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment. In Experimental biology and medicine (Maywood, N.J.), 246, 197-206. doi:10.1177/1535370220960388. https://pubmed.ncbi.nlm.nih.gov/32996353/