CORC

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CORC

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Expert consensus on the diagnosis and treatment of NTRK gene fusion solid tumors in China 期刊论文
THORACIC CANCER, 2022
作者:  Xu, Chunwei;  Si, Lu;  Wang, Wenxian;  Li, Ziming;  Song, Zhengbo
收藏  |  浏览/下载：34/0  |  提交时间：2022/12/22
Immune evolution from preneoplasia to invasive lung adenocarcinomas and underlying molecular features 期刊论文
NATURE COMMUNICATIONS, 2021, 卷号: 12
作者:  Dejima, Hitoshi;  Hu, Xin;  Chen, Runzhe;  Zhang, Jiexin;  Fujimoto, Junya
收藏  |  浏览/下载：20/0  |  提交时间：2021/08/31
Joint Entropy-Assisted Graphene Oxide-Based Multiplexing Biosensing Platform for Simultaneous Detection of Multiple Proteases 期刊论文
ANALYTICAL CHEMISTRY, 2020, 卷号: 92, 期号: 22, 页码: 15042-15049
作者:  Zhang, Youwen;  Chen, Xiaohan;  Yuan, Shaoqing;  Wang, Liang;  Guan, Xiyun
收藏  |  浏览/下载：17/0  |  提交时间：2021/03/01
Molecular phylogeny and species delimitation of Stachyuraceae: Advocating a herbarium specimen-based phylogenomic approach in resolving species boundaries 期刊论文
JOURNAL OF SYSTEMATICS AND EVOLUTION, 2020, 卷号: 58, 期号: 5, 页码: 710-724
作者:  Su, Jun-Xia;  Dong, Cong-Cong;  Niu, Yan-Ting;  Lu, Li-Min;  Xu, Chao
收藏  |  浏览/下载：9/0  |  提交时间：2022/03/01
A CRISPR/LbCas12a-based method for highly efficient multiplex gene editing in Physcomitrella patens 期刊论文
PLANT JOURNAL, 2019, 页码: 10
作者:  Pu, Xiaojun;  Liu, Lina;  Li, Ping;  Huo, Heqiang;  Dong, Xiumei
收藏  |  浏览/下载：70/0  |  提交时间：2019/10/28
A novel heterozygous large deletion of MSH6 gene in a Chinese family with Lynch syndrome 期刊论文
GENE, 2019, 卷号: 704
作者:  Liu, Yuanyuan;  Wang, Mingwei;  Chen, Qiongrong;  Zheng, Qiaosong;  Li, Guangyu
收藏  |  浏览/下载：12/0  |  提交时间：2019/12/05
Accumulative effects of indoor air pollution exposure on leukocyte telomere length among non-smokers 期刊论文
ENVIRONMENTAL POLLUTION, 2017
Lin, Nan; Mu, Xinlin; Wang, Guilian; Ren, Yu' Su, Shu; Li, Zhiwen; Wang, Bin; Tao, Shu; ang
收藏  |  浏览/下载：110/0  |  提交时间：2017/12/03
An LMNB1 Duplication Caused Adult-Onset Autosomal Dominant Leukodystrophy in Chinese Family: Clinical Manifestations, Neuroradiology and Genetic Diagnosis 期刊论文
2017, 卷号: 10, 页码: 215
作者:  Dai, Yi;  Ma, Yaling;  Li, Shengde;  Banerjee, Santasree;  Liang, Shengran
收藏  |  浏览/下载：4/0  |  提交时间：2020/01/04
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents 期刊论文
Human Genetics, 2016, 卷号: 135, 期号: 8, 页码: 953-961
作者:  Yan, Denise;  Tekin, Demet;  Bademci, Guney;  Foster, Joseph, II;  Cengiz, F. Basak
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
Gene mutation of pachyonychia congenita II: A family case analysis 期刊论文
Journal of Xi'an Jiaotong University (Medical Sciences), 2016, 卷号: 37, 页码: 118-122
作者:  Liu, Ping;  Lu, Ning;  Su, Hui;  Li, Lin-Li;  Song, Jian-Wen
收藏  |  浏览/下载：3/0  |  提交时间：2019/11/26

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