Mau2-KO 基因敲除小鼠

1. Peng, Yin, Zhu, Ying, Wu, Lin, Deng, Fang. 2023. Clinical study and genetic analysis of Cornelia de Lange syndrome caused by a novel MAU2 gene variant in a Chinese boy. In Molecular genetics & genomic medicine, 12, e2318. doi:10.1002/mgg3.2318. https://pubmed.ncbi.nlm.nih.gov/37962004/

2. Hassan, Manal M, Li, Donghui, Han, Younghun, Roberts, Lewis R, Amos, Christopher I. 2024. Genome-wide association study identifies high-impact susceptibility loci for HCC in North America. In Hepatology (Baltimore, Md.), 80, 87-101. doi:10.1097/HEP.0000000000000800. https://pubmed.ncbi.nlm.nih.gov/38381705/

3. Minina, Elena A, Reza, Salim Hossain, Gutierrez-Beltran, Emilio, Bozhkov, Peter V, Moschou, Panagiotis N. 2017. The Arabidopsis homolog of Scc4/MAU2 is essential for embryogenesis. In Journal of cell science, 130, 1051-1063. doi:10.1242/jcs.196865. https://pubmed.ncbi.nlm.nih.gov/28137757/

4. Smith, Terence Gordon, Laval, Steve, Chen, Fangli, Strachan, Tom, Peters, Heiko. 2014. Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects. In Genesis (New York, N.Y. : 2000), 52, 687-94. doi:10.1002/dvg.22780. https://pubmed.ncbi.nlm.nih.gov/24700590/