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CORC

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A Virtual Ultrasonography Simulator for Skill Training Using Magnetic-Inertial Probe Tracking 期刊论文
IEEE-ASME TRANSACTIONS ON MECHATRONICS, 2023, 页码: 10
作者:  Wang, Heng;  Dong, Shuda;  Yang, Qi;  Han, Jiancheng;  He, Ze'an
收藏  |  浏览/下载：2/0  |  提交时间：2023/11/17
Conjugation of Hemoglobin and Mannan Markedly Improves the Immunogenicity of Domain III of the Zika Virus E Protein: Structural and Immunological Study 期刊论文
BIOCONJUGATE CHEMISTRY, 2021, 卷号: 32, 期号: 2, 页码: 328-338
作者:  Qi, Jinming;  He, Yunxia;  Shen, Lijuan;  Yu, Weili;  Hu, Tao
收藏  |  浏览/下载：17/0  |  提交时间：2021/08/31
Deficiency of lrp4 in zebrafish and human LRP4 mutation induce aberrant activation of Jagged-Notch signaling in fin and limb development 期刊论文
CELLULAR AND MOLECULAR LIFE SCIENCES, 2019, 卷号: 76, 期号: 1, 页码: 163-178
作者:  Tian, Jing;  Shao, Jinhui;  Liu, Cong;  Hou, Hsin-Yu;  Chou, Chih-Wei
收藏  |  浏览/下载：66/0  |  提交时间：2019/07/01
European Heart Rhythm Association consensus document on management of arrhythmias and cardiac electronic devices in the critically ill and post-surgery patient, endorsed by Heart Rhythm Society , Asia Pacific Heart Rhythm Society , Cardiac Arrhythmia Society of Southern Africa , and Latin American Heart Rhythm Society 期刊论文
EP Europace, 2019, 卷号: Vol.21 No.1, 页码: 7-8
作者:  Giuseppe Boriani;  Laurent Fauchier;  Luis Aguinaga;  James M Beattie;  Carina Blomstrom Lundqvist
收藏  |  浏览/下载：33/0  |  提交时间：2019/02/25
TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice 期刊论文
Human Molecular Genetics, 2019, 卷号: Vol.28 No.4, 页码: 539-547
作者:  Nan Yang;  Nan Wu;  Ling Zhang;  Yanxue Zhao;  Jiaqi Liu
收藏  |  浏览/下载：43/0  |  提交时间：2019/12/17
Iron deficiency in pulmonary arterial hypertension associated with congenital heart disease. 期刊论文
Scandinavian cardiovascular journal, 2019, 页码: 1-18
作者:  Xue Yu;  Yi Zhang;  Qin Luo;  Zhihong Liu;  Zhihui Zhao
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/13
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. 期刊论文
Genetics in medicine : official journal of the American College of Medical Genetics, 2019
作者:  Jiaqi Liu;  Nan Wu;  Nan Yang;  Kazuki Takeda;  Weisheng Chen
收藏  |  浏览/下载：48/0  |  提交时间：2019/12/13
TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文
Genetics in Medicine, 2019
作者:  Jiaqi Liu;  Nan Wu;  Deciphering Disorders Involving Scoliosis and COmorbidities study, Nan Yang;  Kazuki Takeda;  Weisheng Chen
收藏  |  浏览/下载：40/0  |  提交时间：2019/12/13
Identification and characterization of NF1 and non-NF1 congenital pseudarthrosis of the tibia based on germline NF1 variants: genetic and clinical analysis of 75 patients. 期刊论文
Orphanet journal of rare diseases, 2019, 卷号: 14, 期号: 1, 页码: 221
作者:  Zhu, Guanghui;  Zheng, Yu;  Liu, Yaoxi;  Yan, An;  Hu, Zhengmao
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/27
Three-Dimensional Printing of a Complex Aortic Anomaly 期刊论文
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2018, 期号: 141
作者:  Sun, Xiaoning;  Zhu, Kai;  Zhang, Weijia;  Zhang, Hongqiang;  Hu, Fazong
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05

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