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Making Fe-Si-B amorphous powders as an effective catalyst for dye degradation by high-energy ultrasonic vibration 期刊论文
MATERIALS & DESIGN, 2020, 卷号: 194
作者:  Lv, Zhuwei;  Yan, Yuqiang;  Yuan, Chenchen;  Huang, Bo;  Yang, Can
收藏  |  浏览/下载:62/0  |  提交时间:2020/12/16
Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing 期刊论文
FRONTIERS IN PHARMACOLOGY, 2019, 卷号: 10
作者:  Wang, Dong;  Gao, Min;  Zhang, Kaihui;  Jin, Ruifeng;  Lv, Yuqiang
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/11
Generation of an induced pluripotent stem cell line (SDQLCHi003-a) from a patient with short rib-thoracic dysplasia syndrome type III carrying compound heterozygous mutations in DYNC2H1 期刊论文
STEM CELL RESEARCH, 2019, 卷号: 39
作者:  Zhang, Haiyan;  Ma, Yanyan;  Song, Fengling;  Yang, Xiaomeng;  Li, Yue
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/11
Novel Neonatal Variants of the Carbamoyl Phosphate Synthetase 1 Deficiency: Two Case Reports and Review of Literature 期刊论文
FRONTIERS IN GENETICS, 2019, 卷号: 10
作者:  Yan, Beibei;  Wang, Chao;  Zhang, Kaihui;  Zhang, Haiyan;  Gao, Min
收藏  |  浏览/下载:15/0  |  提交时间:2019/12/11
Establishment of a human induced pluripotent stem cell line (SDQLCHi004-A) from a patient with nemaline myopathy-4 disease carrying heterozygous mutation in TPM2 gene 期刊论文
STEM CELL RESEARCH, 2019, 卷号: 40
作者:  Ma, Yanyan;  Zhang, Haiyan;  Yang, Xiaomeng;  Li, Yue;  Guan, Jingyun
收藏  |  浏览/下载:14/0  |  提交时间:2019/12/11
An induced pluripotent stem cell line (SDQLCHi006-A) derived from a patient with maple syrup urine disease type Ib carrying compound heterozygous mutations of p.R168C and p.T322I in BCKDHB gene 期刊论文
STEM CELL RESEARCH, 2019, 卷号: 40
作者:  Li, Yue;  Zhang, Haiyan;  Yan, Beibei;  Ma, Yanyan;  Yang, Xiaomeng
收藏  |  浏览/下载:10/0  |  提交时间:2019/12/11
Effect of electroplating parameters on microstructure of copper coating on carbon fibers used for fabrication of aluminum matrix composite 会议论文
21st International Conference on Composite Materials, ICCM 2017, Xi'an, China, 2017-08-20
作者:  Sha, Jianjun;  Lv, Zhaozhao;  Zu, Yufei;  Zhang, Zhaofu;  Wang, Shouhao
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/02
Novel OFD1 frameshift mutation in a Chinese boy with Joubert syndrome: a case report and literature review 期刊论文
Clinical Dysmorphology, 2017, 卷号: 26, 期号: 3, 页码: 135-141
作者:  Kaihui.Zhang;  Chen.Meng;  Jing.Ma;  Min.Gao;  Yuqiang.Lv
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/11
Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking 期刊论文
CYTOGENETIC AND GENOME RESEARCH, 2017, 卷号: 152, 期号: 1, 页码: 1-8
作者:  Liu, Shu;  Zhang, Kaihui;  Song, Fengling;  Yang, Yali;  Lv, Yuqiang
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/12
The Simpler The Better: A Unified Approach to Predicting Original Taxi Demands based on Large-Scale Online Platforms 会议论文
KDD'17: PROCEEDINGS OF THE 23RD ACM SIGKDD INTERNATIONAL CONFERENCE ON KNOWLEDGE DISCOVERY AND DATA MINING, 2017-01-01
作者:  Tong, Yongxin;  Chen, Yuqiang;  Zhou, Zimu;  Chen, Lei;  Wang, Jie
收藏  |  浏览/下载:10/0  |  提交时间:2019/12/30


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