Hoxd13-flox 基因敲除小鼠

1. Guo, Xiaoyan, Shi, Tengfei, Lin, Mingrui, Zhang, Yiyuan. . A Nonsense Mutation in HOXD13 Gene from A Chinese Family with Non-Syndromic Synpolydactyly. In The Tohoku journal of experimental medicine, 249, 93-100. doi:10.1620/tjem.249.93. https://pubmed.ncbi.nlm.nih.gov/31611522/

2. Apfelbaum, April A, Wu, Feinan, Hawkins, Allegra G, Sarthy, Jay F, Lawlor, Elizabeth R. . EWS::FLI1 and HOXD13 Control Tumor Cell Plasticity in Ewing Sarcoma. In Clinical cancer research : an official journal of the American Association for Cancer Research, 28, 4466-4478. doi:10.1158/1078-0432.CCR-22-0384. https://pubmed.ncbi.nlm.nih.gov/35653119/

3. Kurban, Mazen, Wajid, Muhammad, Petukhova, Lynn, Shimomura, Yutaka, Christiano, Angela M. 2011. A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance. In Journal of human genetics, 56, 701-6. doi:10.1038/jhg.2011.84. https://pubmed.ncbi.nlm.nih.gov/21814222/

4. Zhong, Zhenbin, Shan, Ming, Wang, Ji, Ren, Yanlv, Pang, Da. 2015. HOXD13 methylation status is a prognostic indicator in breast cancer. In International journal of clinical and experimental pathology, 8, 10716-24. doi:. https://pubmed.ncbi.nlm.nih.gov/26617782/