CORC

浏览/检索结果: 共60条,第1-10条 帮助

已选(0)清除 条数/页:   排序方式:
Fuzuloparib Maintenance Therapy in Patients With Platinum-Sensitive, Recurrent Ovarian Carcinoma (FZOCUS-2): A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase III Trial 期刊论文
JOURNAL OF CLINICAL ONCOLOGY, 2022, 卷号: 40
作者:  Li, Ning;  Zhang, Youzhong;  Wang, Jing;  Zhu, Jianqing;  Wang, Li
收藏  |  浏览/下载:25/0  |  提交时间:2022/12/22
Somatic synonymous mutations in regulatory elements contribute to the genetic aetiology of melanoma 期刊论文
BMC MEDICAL GENOMICS, 2020, 卷号: 13
作者:  Zhang, Di;  Xia, Junfeng
收藏  |  浏览/下载:6/0  |  提交时间:2021/09/06
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:12/0  |  提交时间:2022/03/01
Androgen receptor gene mutations are associated with male infertility in Northeast China: Clinical features and identification of two novel mutations 期刊论文
ANDROLOGIA, 2019, 卷号: 51, 期号: 3
作者:  Li, Leilei;  Yang, Xiao;  Wang, Ruixue;  Liu, Xiaojun;  Yu, Yang
收藏  |  浏览/下载:26/0  |  提交时间:2019/12/05
Recurrent acute liver failure associated with novel SCYL1 mutation: A case report 期刊论文
WORLD JOURNAL OF CLINICAL CASES, 2019, 卷号: 7, 期号: 4
作者:  Li, Jia-Qi;  Gong, Jing-Yu;  Knisely, A. S.;  Zhang, Mei-Hong;  Wang, Jian-She
收藏  |  浏览/下载:19/0  |  提交时间:2019/12/05
COL6A1 mutation leading to Bethlem myopathy with recurrent hematuria: a case report 期刊论文
BMC NEUROLOGY, 2019, 卷号: 19, 期号: 1
作者:  Bao, Mengxin;  Mao, Fei;  Zhao, Zhangning;  Ma, Gaoting;  Xu, Guangjun
收藏  |  浏览/下载:8/0  |  提交时间:2019/12/11
Whole Genome Incorporation and Epigenetic Stability in a Newly Synthetic Allopolyploid of Gynogenetic Gibel Carp 期刊论文
GENOME BIOLOGY AND EVOLUTION, 2018, 卷号: 10, 期号: 9, 页码: 2394-2407
作者:  Shao, Guang-Ming;  Li, Xi-Yin;  Wang, Yang;  Wang, Zhong-Wei;  Li, Zhi
收藏  |  浏览/下载:52/0  |  提交时间:2019/07/02
Whole Genome Incorporation and Epigenetic Stability in a Newly Synthetic Allopolyploid of Gynogenetic Gibel Carp 期刊论文
GENOME BIOLOGY AND EVOLUTION, 2018, 卷号: 10, 期号: 9, 页码: 2394-2407
作者:  Gui, Jian-Fang;  Zhou, Li;  Zhang, Xiao-Juan;  Li, Zhi;  Wang, Zhong-Wei
收藏  |  浏览/下载:41/0  |  提交时间:2018/12/29
Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear Cataract 期刊论文
CURRENT EYE RESEARCH, 2018, 卷号: 43, 期号: 3
作者:  Wang, Kai Jie;  Zha, Xu;  Chen, Dou Dou;  Zhu, Si Quan
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/04
Co-Existence of Novel PDE6A Mutations and A Recurrent RPGR Mutation: A Potential Explanation for Phenotypic Diversity in Female RPGR Mutation Carriers 期刊论文
CURRENT MOLECULAR MEDICINE, 2018, 卷号: 18, 期号: 5
作者:  Chen, X.;  Sheng, X.;  Liu, G.;  Liu, Y.;  Li, H.
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/05


©版权所有 ©2017 CSpace - Powered by CSpace