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CORC

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Optimal strategy for enterprises' green technology innovation from the perspective of political competition 期刊论文
Journal of Cleaner Production, 2019, 卷号: 235, 页码: 930-942
作者:  Deng, Yaling;  You, Daming*;  Wang, Jingjing*
收藏  |  浏览/下载：12/0  |  提交时间：2019/12/03
Identification of a Premature Termination Mutation in the Proline-Rich Transmembrane Protein 2 Gene in a Chinese Family with Febrile Seizures 期刊论文
Molecular Neurobiology, 2016, 卷号: 53, 期号: 2, 页码: 835-841
作者:  Zheng, Wen;  Zhang, Jie;  Deng, Xiong;  Xiao, Jingjing;  Yuan, Lamei
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/03
Systematic Genetic Analysis of the SMPD1 Gene in Chinese Patients with Parkinson’s Disease 期刊论文
Molecular Neurobiology, 2016, 卷号: 53, 期号: 7, 页码: 5025-5029
作者:  Deng, Sheng;  Deng, Xiong;  Song, Zhi;  Xiu, Xiaofei;  Guo, Yi
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). 期刊论文
AUTOPHAGY, 2016, 卷号: 12, 期号: 1, 页码: 1-222
作者:  Klionsky, Daniel J.*;  Abdelmohsen, Kotb;  Abe, Akihisa;  Abedin, Md Joynal;  Abeliovich, Hagai
收藏  |  浏览/下载：91/0  |  提交时间：2019/12/03
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 期刊论文
Autophagy, 2016, 卷号: 12, 期号: 1, 页码: 1-222
作者:  Klionsky, Daniel J.*;  Abdelmohsen, Kotb;  Abe, Akihisa;  Abedin, Md Joynal;  Abeliovich, Hagai
收藏  |  浏览/下载：72/0  |  提交时间：2019/12/03
Identification of a novel GJA3 mutation in congenital nuclear cataract 期刊论文
Optometry and Vision Science, 2015, 卷号: 92, 期号: 3, 页码: 337-342
作者:  Yuan, Lamei;  Guo, Yi;  Yi, Junhui;  Xiao, Jingjing;  Yuan, Jinzhong
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03
The Role of Consolidative Radiotherapy after a Complete Response to Chemotherapy in the Treatment of Diffuse Large B-Cell Lymphoma in the Rituximab Era: Results from a Systematic Review with a Meta-Analysis 期刊论文
Acta haematologica, 2015, 卷号: 134, 期号: 2, 页码: 111-118
作者:  Hu, Chunhong;  Deng, Chao;  Zou, Wen;  Zhang, Guangsen;  Wang, Jingjing*
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03
Identification of a novel PHEX mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing 期刊论文
Biological Chemistry, 2015, 卷号: 396, 期号: 1, 页码: 27-33
作者:  Yuan, Lamei;  Wu, Song;  Xu, Hongbo;  Xiao, Jingjing;  Yang, Zhijian
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/03
A Novel COL4A5 Mutation Identified in a Chinese Han Family Using Exome Sequencing 期刊论文
Journal of Biomedicine and Biotechnology, 2014, 卷号: 2014, 期号: 4, 页码: 186048
作者:  Xiu, Xiaofei;  Yuan, Jinzhong;  Deng, Xiong;  Xiao, Jingjing;  Xu, Hongbo
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/03
Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing 期刊论文
Molecular Biology Reports, 2014, 卷号: 41, 期号: 6, 页码: 3631-3635
作者:  Guo, Yi;  Yuan, Jinzhong;  Liang, Hui;  Xiao, Jingjing;  Xu, Hongbo
收藏  |  浏览/下载：12/0  |  提交时间：2019/12/03

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