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CORC

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Application of Three-Dimension Printing Nano-Carbonated-Hydroxylapatite to the Repair of Defects in Rabbit Bone 期刊论文
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2024, 卷号: 19, 页码: 15
作者:  Wang, Shujie;  Shao, Chunyan;  Zhao, Xingkai;  Guo, Yizhe;  Song, Houhui
收藏  |  浏览/下载：0/0  |  提交时间：2024/05/15
保水剂处理下呼伦贝尔地区燕麦草产量和营养成分差异分析 期刊论文
草业科学, 2023, 卷号: 40, 期号: 10, 页码: 2629-2638
作者:  周镇磊;  刘建明;  曹东;  刘宝龙;  张怀刚
收藏  |  浏览/下载：0/0  |  提交时间：2023/12/01
TBX6-associated congenital scoliosis (TACS) 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, 卷号: 21, 期号: 7
作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng
收藏  |  浏览/下载：63/0  |  提交时间：2019/12/05
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：45/0  |  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：39/0  |  提交时间：2019/12/13
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文
2019, 卷号: 21, 期号: 7, 页码: 1548-1558
作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng
收藏  |  浏览/下载：33/0  |  提交时间：2020/01/03
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease 期刊论文
HUMAN GENETICS, 2018, 卷号: 137, 期号: 6-7
作者:  Liu, Jiaqi;  Zhou, Yangzhong;  Liu, Sen;  Song, Xiaofei;  Yang, Xin-Zhuang
收藏  |  浏览/下载：22/0  |  提交时间：2019/12/05
DMXAA-pyranoxanthone hybrids enhance inhibition activities against human cancer cells with multi-target functions 期刊论文
2018, 卷号: 143, 页码: 1768
作者:  Liu, Jie[1];  Zhou, Fan[1];  Zhang, Lei[1];  Wang, Huailing[2];  Zhang, Jianrun[1]
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/23
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease 期刊论文
2018, 卷号: 137, 期号: 6-7, 页码: 553-567
作者:  Liu, Jiaqi;  Zhou, Yangzhong;  Liu, Sen;  Song, Xiaofei;  Yang, Xin-Zhuang
收藏  |  浏览/下载：9/0  |  提交时间：2020/01/03
Comparative analysis of serum proteome in congenital scoliosis patients with TBX6 haploinsufficiency - a first report pointing to lipid metabolism 期刊论文
2018, 卷号: 22, 期号: 1, 页码: 533-545
作者:  Zhu, Qiankun;  Wu, Nan;  Liu, Gang;  Zhou, Yangzhong;  Liu, Sen
收藏  |  浏览/下载：10/0  |  提交时间：2020/01/03

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