CNTN4调节GluR1在听神经病谱系障碍中的致病机制研究

81900948
2019
H1404.听觉异常与平衡障碍
门美超
青年科学基金项目
副教授
中南大学
20万元
动物模型;听神经病谱系障碍;致病病机制;CNTN4;GluR1
2020-01-01到2022-12-31
  • 中英文摘要
  • 结题摘要
  • 结题报告
  • 项目成果
  • 项目参与人
查看更多信息请先登录或注册
查看更多信息请先登录或注册
查看更多信息请先登录或注册
重置
序号 标题 类型 作者
1 MITF Is Mutated in Type 1 Waardenburg Syndrome With Unusual Phenotype 期刊论文 Wu Li;Yong Feng;Hongsheng Chen;Chufeng He;Lingyun Mei;Xue Zhong Liu;Meichao Men
2 Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism 期刊论文 Dai Wenting;Li Jia-Da;Zhao Yaguang;Wu Jiayu;Jiang Fang;Chen Dan-Na;Zheng Ruizhi;Men Meichao
3 Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism 期刊论文 Men Meichao;Wu Jiayu;Zhao Yaguang;Xing Xiaoliang;Jiang Fang;Zheng Ruizhi;Li Jia-Da
4 Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort 期刊论文 Li Jia-Da;Wu Jiayu;Zhao Yaguang;Wang Xinying;Jiang Fang;Hou Qiao;Chen Dan-Na;Zheng Ruizhi;Yu Renhe;Zhou Wei;Men Meichao
5 Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism 期刊论文 Meichao Men;Xinying Wang;Jiayu Wu;Wang Zeng;Fang Jiang;Ruizhi Zheng;Jia-Da Li
查看更多信息请先登录或注册

相关项目

趋势报告

经验分享