Hps4-flox 基因敲除小鼠

1. Li, Yueru, Geng, Xin, Bao, Lisui, Dunham, Rex, Liu, Zhanjiang. 2017. A deletion in the Hermansky-Pudlak syndrome 4 (Hps4) gene appears to be responsible for albinism in channel catfish. In Molecular genetics and genomics : MGG, 292, 663-670. doi:10.1007/s00438-017-1302-8. https://pubmed.ncbi.nlm.nih.gov/28289846/

2. Kuratomi, Go, Saito, Atsushi, Ozeki, Yuji, Ohmori, Kenichi, Akiyama, Kazufumi. 2013. Association of the Hermansky-Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects. In BMC psychiatry, 13, 276. doi:10.1186/1471-244X-13-276. https://pubmed.ncbi.nlm.nih.gov/24168225/

3. Martina, José A, Moriyama, Kengo, Bonifacino, Juan S. 2003. BLOC-3, a protein complex containing the Hermansky-Pudlak syndrome gene products HPS1 and HPS4. In The Journal of biological chemistry, 278, 29376-84. doi:. https://pubmed.ncbi.nlm.nih.gov/12756248/

4. Suzuki, Tamio, Li, Wei, Zhang, Qing, Swank, Richard T, Spritz, Richard A. 2002. Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene. In Nature genetics, 30, 321-4. doi:. https://pubmed.ncbi.nlm.nih.gov/11836498/

5. Yu, Hailan, Luo, Nan, Sun, Lichao, Liu, Dong. 2012. HPS4/SABRE regulates plant responses to phosphate starvation through antagonistic interaction with ethylene signalling. In Journal of experimental botany, 63, 4527-38. doi:10.1093/jxb/ers131. https://pubmed.ncbi.nlm.nih.gov/22615140/