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RPS3A positively regulates the mitochondrial function of human periaortic adipose tissue and is associated with coronary artery diseases 期刊论文
CELL DISCOVERY, 2018, 卷号: 4
作者:  Zeng, Rong;  Mu, Wenjuan;  Zou, Ying;  He, Yi;  Tang, Yan
收藏  |  浏览/下载:12/0  |  提交时间:2019/12/05
GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity 期刊论文
GENETICS IN MEDICINE, 2017, 卷号: 19, 期号: 8
作者:  Chen, Xue;  Sheng, Xunlun;  Zhuang, Wenjuan;  Sun, Xiantao;  Liu, Guohua
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/05
BEYOND: A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase III Study of First-Line Carboplatin/Paclitaxel Plus Bevacizumab or Placebo in Chinese Patients With Advanced or Recurrent Nonsquamous Non-Small-Cell Lung Cancer 期刊论文
JOURNAL OF CLINICAL ONCOLOGY, 2015, 卷号: 33, 期号: 19
作者:  Zhou, Caicun;  Wu, Yi-Long;  Chen, Gongyan;  Liu, Xiaoqing;  Zhu, Yunzhong
收藏  |  浏览/下载:1/0  |  提交时间:2019/12/19
Mutation of kri1l causes definitive hematopoiesis failure via PERK-dependent excessive autophagy induction 期刊论文
CELL RESEARCH, 2015, 卷号: 25, 期号: 8
作者:  Jia, Xiao-E;  Ma, Ke;  Xu, Tao;  Gao, Lei;  Wu, Shuang
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/19
Identification of CHIP as a Novel Causative Gene for Autosomal Recessive Cerebellar Ataxia 期刊论文
PLOS ONE, 2013, 卷号: 8, 期号: 12
作者:  Shi, Yuting;  Wang, Junling;  Li, Jia-Da;  Ren, Haigang;  Guan, Wenjuan
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/19
BEYOND: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTRE, PHASE III STUDY OF FIRST-LINE CARBOPLATIN/PACLITAXEL (CP) PLUS BEVACIZUMAB (BV) OR PLACEBO (PL) IN CHINESE PATIENTS WITH ADVANCED OR RECURRENT NON-SQUAMOUS NON-SMALL CELL LUNG CANCER (NSCLC) 会议论文
作者:  Zhou, Caicun;  Chen, Gongyan;  Liu, Xiaoqing;  Zhu, Yunzhong;  Lu, Shun
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/19
The Purkinje Neuron Acts as a Central Regulator of Spatially and Functionally Distinct Cerebellar Precursors 期刊论文
DEVELOPMENTAL CELL, 2013, 卷号: 27, 期号: 3
作者:  Fleming, Jonathan T.;  He, Wenjuan;  Hao, Chuanming;  Ketova, Tatiana;  Pan, Fong C.
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/19
Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis 期刊论文
Zhonghua Yixue Yichuanxue Zazhi, 2005, 卷号: 22, 期号: 1
作者:  Qiu Wen-juan (wenjuan_qiu@sina.com);  Zhang Ya-fen;  Pan Jun;  Ye Jun;  Liu Xiao-qing
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/27


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