Foxi3-KO 基因敲除小鼠

1. Thawani, Ankita, Maunsell, Helen R, Zhang, Hongyuan, Ankamreddy, Harinarayana, Groves, Andrew K. 2023. The Foxi3 transcription factor is necessary for the fate restriction of placodal lineages at the neural plate border. In Development (Cambridge, England), 150, . doi:10.1242/dev.202047. https://pubmed.ncbi.nlm.nih.gov/37756587/

2. Xing, Xiao-Liang, Zeng, Ziqiang, Wang, Yana, Pan, Bo, Huang, Xueshuang. . Identification of potential molecular mechanism related to craniofacial dysmorphism caused by FOXI3 deficiency. In Molecular genetics & genomic medicine, 12, e2411. doi:10.1002/mgg3.2411. https://pubmed.ncbi.nlm.nih.gov/38433559/

3. Shirokova, Vera, Jussila, Maria, Hytönen, Marjo K, Thesleff, Irma, Mikkola, Marja L. 2013. Expression of Foxi3 is regulated by ectodysplasin in skin appendage placodes. In Developmental dynamics : an official publication of the American Association of Anatomists, 242, 593-603. doi:10.1002/dvdy.23952. https://pubmed.ncbi.nlm.nih.gov/23441037/

4. Jussila, Maria, Aalto, Anne J, Sanz Navarro, Maria, Mikkola, Marja L, Thesleff, Irma. 2015. Suppression of epithelial differentiation by Foxi3 is essential for molar crown patterning. In Development (Cambridge, England), 142, 3954-63. doi:10.1242/dev.124172. https://pubmed.ncbi.nlm.nih.gov/26450968/

5. Hasten, Erica, Morrow, Bernice E. 2019. Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome. In PLoS genetics, 15, e1008301. doi:10.1371/journal.pgen.1008301. https://pubmed.ncbi.nlm.nih.gov/31412026/