先天性巨结肠患者SEMA3C/D基因功能失活突变影响肠神经系统发育的细胞和分子机制
序号 | 标题 | 类型 | 作者 |
---|---|---|---|
1 | Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated with Hirschsprung Disease in Han Chinese | 期刊论文 | Su Lin|Shangguan Shaofang|Jiang Qian|Li Long| |
2 | 先天性巨结肠患者SEMA3C/SEMA3D基因错义突变对Semaphorin 3蛋白表达的影响 | 期刊论文 | 肖萍|苏琳|苗春越|李龙| |
3 | Genotyping analysis of 3 RET polymorphisms demonstrates low somatic mutation rate in Chinese Hirschsprung disease patients | 期刊论文 | Zhang Z, Jiang Q, Li Q, Cheng W, Qiao G, Xiao P,| |
4 | SEMA3C/SEMA3D基因错义突变对蛋白稳定性和受体亲合力的影响 | 期刊论文 | 李颀|肖萍|苏琳|李龙| |
5 | Functional Loss of Semaphorin 3C and/or Semaphorin 3D and Their Epistatic Interaction with Ret Are Critical to Hirschsprung Disease Liability | 期刊论文 | Gray JJ|Pachnis V|McCallion AS|Chakravarti A| |