Pls1-KO 基因敲除小鼠

1. Xu, Liangpu, Wang, Xinrui, Li, Jia, Huang, Hailong, Cao, Hua. 2023. A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. In Clinical genetics, 103, 413-423. doi:10.1111/cge.14283. https://pubmed.ncbi.nlm.nih.gov/36537221/

2. Clergeot, P H, Gourgues, M, Cots, J, Notteghem, J L, Lebrun, M H. . PLS1, a gene encoding a tetraspanin-like protein, is required for penetration of rice leaf by the fungal pathogen Magnaporthe grisea. In Proceedings of the National Academy of Sciences of the United States of America, 98, 6963-8. doi:. https://pubmed.ncbi.nlm.nih.gov/11391010/

3. Schrauwen, Isabelle, Melegh, Béla I, Chakchouk, Imen, Melegh, Béla, Leal, Suzanne M. 2019. Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma. In European journal of human genetics : EJHG, 27, 869-878. doi:10.1038/s41431-019-0372-y. https://pubmed.ncbi.nlm.nih.gov/30872814/

4. Morgan, Anna, Koboldt, Daniel C, Barrie, Elizabeth S, Dell'Orco, Daniele, Girotto, Giorgia. 2019. Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss. In Human mutation, 40, 2286-2295. doi:10.1002/humu.23891. https://pubmed.ncbi.nlm.nih.gov/31397523/