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浏览/检索结果: 共11条，第1-10条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Cryo-EM structure of human heptameric Pannexin 1 channel 期刊论文 CELL RESEARCH, 2020, 页码: 3 作者:  Qu, Ronggui;  Dong, Lili;  Zhang, Jilin;  Yu, Xuekui;  Wang, Lei 收藏  |  浏览/下载：18/0  |  提交时间：2020/07/01 Expression of ENPP3 in human cyclic endometrium: a novel molecule involved in embryo implantation 期刊论文 REPRODUCTION FERTILITY AND DEVELOPMENT, 2018, 卷号: 30, 期号: 10 作者:  Chen, Qianqian;  Xin, Aijie;  Qu, Ronggui;  Zhang, Wenbi;  Li, Lu 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05 endometrial receptivity  integrin-beta 3  LIF  window of implantation   Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest 期刊论文 AMERICAN JOURNAL OF HUMAN GENETICS, 2016, 卷号: 99, 期号: 3 作者:  Xu, Yao;  Shi, Yingli;  Fu, Jing;  Yu, Min;  Feng, Ruizhi 收藏  |  浏览/下载：16/0  |  提交时间：2019/12/05 Mutations in TUBB8 and Human Oocyte Meiotic Arrest 期刊论文 NEW ENGLAND JOURNAL OF MEDICINE, 2016, 卷号: 374, 期号: 3 作者:  Nogales, Eva;  Feng, Ruizhi;  Sang, Qing;  Kuang, Yanping;  Sun, Xiaoxi 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05 Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment 期刊论文 INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 84 作者:  Qu, Ronggui;  Sang, Qing;  Xu, Yao;  Feng, Ruizhi;  Jin, Li 收藏  |  浏览/下载：8/0  |  提交时间：2019/12/06 Congenital non-syndromic autosomal recessive deafness  Missense mutation  Myosin IIIA  Target sequencing   Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos 期刊论文 JOURNAL OF MEDICAL GENETICS, 2016, 卷号: 53, 期号: 10 作者:  Feng, Ruizhi;  Yan, Zheng;  Li, Bin;  Yu, Min;  Sang, Qing 收藏  |  浏览/下载：11/0  |  提交时间：2019/12/06 TUBB8  mutations  oocyte maturation arrest  female infertility   ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42 期刊论文 BIOLOGY OPEN, 2015, 卷号: 4, 期号: 4, 页码: 411-U11 作者:  Sang, Qing;  Li, Wen;  Xu, Yao;  Qu, Ronggui;  Xu, Zhigang 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/17 ILDR1  Deafness  Genetics   ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42 期刊论文 BIOLOGY OPEN, 2015, 卷号: 4, 期号: 4 作者:  Sang, Qing;  Li, Wen;  Xu, Yao;  Qu, Ronggui;  Xu, Zhigang 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/13 ILDR1  Deafness  Genetics   MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro 期刊论文 SCIENTIFIC REPORTS, 2015, 卷号: 5 作者:  Feng, Ruizhi;  Sang, Qing;  Zhu, Yan;  Fu, Wei;  Liu, Miao 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/19 Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment 期刊论文 MOLECULAR GENETICS AND GENOMICS, 2015, 卷号: 290, 期号: 3 作者:  Sang, Qing;  Mei, Honglin;  Kuermanhan, Ahan;  Feng, Ruizhi;  Guo, Luo 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/19 Hearing loss  Genetics  PTPRQ