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浏览/检索结果: 共4条，第1-4条 帮助 限定条件 发表日期：2016     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 A novel splice donor site mutation in epha2 caused congenital cataract in a chinese family 期刊论文 Indian journal of ophthalmology, 2016, 卷号: 64, 期号: 5, 页码: 364-368 作者:  Bu, Juan;  He, Sijie;  Wang, Lejin;  Li, Jiankang;  Liu, Jing 收藏  |  浏览/下载：46/0  |  提交时间：2019/05/09 Autosomal dominant congenital cataract  Epha2  Splice donor site mutation  Whole exome sequencing   A Land Plant-Specific Transcription Factor Directly Enhances Transcription of a Pathogenic Noncoding RNA Template by DNA-Dependent RNA Polymerase II 期刊论文 PLANT CELL, 2016 Wang, Ying; Qu, Jie; Ji, Shaoyi; Wallace, Andrew J.; Wu, Jian; Li, Yi; Gopalan, Venkat; Ding, Biao 收藏  |  浏览/下载：5/0  |  提交时间：2017/12/03 5S RIBOSOMAL-RNA  HEPATITIS-DELTA VIRUS  VIROID-HOST INTERACTIONS  ZINC FINGERS  ARABIDOPSIS-THALIANA  PROTEIN VIRP1  REPLICATION  COMPLEX  TFIIIA  ASSOCIATION   Germline mutations in the VHL gene associated with 3 different renal lesions in a Chinese von Hippel-Lindau disease family 期刊论文 CANCER BIOLOGY & THERAPY, 2016 Yuan, Ping; Sun, Qipeng; Liang, Hao; Wang, Wenjun; Li, Ling; Wang, Ye; Deng, Huan; Lai, Luhua; Chen, Xiaoli; Zhou, Xiangfu 收藏  |  浏览/下载：2/0  |  提交时间：2017/12/03 Clear cell renal cell carcinoma  multilocular cystic renal cell carcinoma  mutation  von Hippel-Lindau disease  VHL  CELL CARCINOMA  PHEOCHROMOCYTOMA  EXPERIENCE  DIAGNOSIS  PATHOLOGY  NEOPLASIA  VARIANTS  COMPLEX   Rare Genetic Variants of the Transthyretin Gene Are Associated with Alzheimer’s Disease in Han Chinese 期刊论文 Molecular Neurobiology, 2016, 卷号: **, 期号: **, 页码: published online 作者:  Xiang Q;  Bi R[*];  Zheng C;  Fang YR;  Yao GY[*] 收藏  |  浏览/下载：29/0  |  提交时间：2016/10/11 Alzheimer’sdisease  TTR  Rarevariant  Genetic association  Aβ-bindingability