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CORC

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Genome-wide association analyses based on whole-genome sequencing of Protosalanx hyalocranius provide insights into sex determination of Salangid fishes 期刊论文
MOLECULAR ECOLOGY RESOURCES, 2020, 页码: 12
作者:  Li, Yu-Long;  Xing, Teng-Fei;  Liu, Jin-Xian
收藏  |  浏览/下载：23/0  |  提交时间：2020/09/24
Development of a PVY Resistant Flue-Cured Tobacco Line via EMS Mutagenesis of eIF4E 期刊论文
AGRONOMY-BASEL, 2020, 卷号: 10, 期号: 1
作者:  Zhao, Lu;  Li, Wenzheng;  Wang, Bingwu;  Gao, Yulong;  Sui, Xueyi
收藏  |  浏览/下载：13/0  |  提交时间：2022/03/01
Development of a nornicotine-reduced flue-cured tobacco line via EMS mutagenesis of nicotine N-demethylase genes 期刊论文
PLANT SIGNALING & BEHAVIOR, 2020, 卷号: 15, 期号: 2
作者:  Song, Zhongbang;  Sui, Xueyi;  Li, Meiyun;  Gao, Yulong;  Li, Wenzheng
收藏  |  浏览/下载：15/0  |  提交时间：2022/03/01
A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family 期刊论文
JOURNAL OF HUMAN GENETICS, 2019, 卷号: 64, 期号: 7
作者:  Yi, Haoan;  Zha, Xu;  Zhu, Yuechun;  Lv, Jin;  Hu, Shouzhi
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/04
A Nonsense Mutation in COL4A4 Gene Causing Isolated Hematuria in Either Heterozygous or Homozygous State 期刊论文
FRONTIERS IN GENETICS, 2019, 卷号: 10
作者:  Yang, Cheng;  Song, Yuan;  Chen, Zhaowei;  Yuan, Xiaohan;  Chen, Xinhua
收藏  |  浏览/下载：24/0  |  提交时间：2019/12/05
A new novel nonsense mutation in AIPL1 in a LCA4 family 期刊论文
2019, 卷号: 40, 期号: 4, 页码: 380-384
作者:  Wan, Ling[1];  Xiang, Li[2];  Wang, Haixin[3];  Shi, Yi[3];  Jiang, Dan[3]
收藏  |  浏览/下载：8/0  |  提交时间：2019/12/16
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel nonsense mutation in AVP-NPII gene 期刊论文
2019, 卷号: 18, 期号: 2, 页码: 1309-1314
作者:  Yang, Hongbo;  Yan, Kemin;  Wang, Linjie;  Gong, Fengying;  Jin, Zimeng
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03
A Novel FECH Mutation Causes Erythropoietic Protoporphyria with Severe Liver Dysfunction 期刊论文
HEPATITIS MONTHLY, 2018, 卷号: 18, 期号: 11
作者:  Chi, Xiumei;  Xu, Fang;  Wang, Xiaomei;  He, Xiuting;  Qi, Yue
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05
The Novel Pathogenic Mutation c.849dupT in BRCA2 Contributes to the Nonsense-Mediated mRNA Decay of BRCA2 in Familial Breast Cancer 期刊论文
JOURNAL OF BREAST CANCER, 2018, 卷号: 21, 期号: 3
作者:  Li, Sanrong;  Ma, Jing;  Hu, Caiying;  Zhang, Xing;  Xiao, Deyong
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/05
A novel nonsense mutation in MYO15A is associated with non-syndromic hearing loss: a case report 期刊论文
2018, 卷号: 19
作者:  Ma, Di[1];  Shen, Shanshan[1];  Gao, Hui[1];  Guo, Hui[1];  Lin, Yumei[1]
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/23

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