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CORC

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Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia 期刊论文
Archives of Oral Biology, 2019, 卷号: Vol.100, 页码: 49-56
作者:  Tingting Zhang;  Jing Wu;  Xiaoxue Zhao;  Feifei Hou;  Tengfei Ma
收藏  |  浏览/下载：31/0  |  提交时间：2019/12/17
Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia. 期刊论文
Archives of oral biology, 2019, 卷号: Vol.100, 页码: 49-56
作者:  Tingting Zhang;  Jing Wu;  Xiaoxue Zhao;  Feifei Hou;  Tengfei Ma
收藏  |  浏览/下载：15/0  |  提交时间：2019/12/17
Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review 期刊论文
MEDICINE, 2018, 卷号: 97, 期号: 32
作者:  Ma, Dan;  Wang, Xuxia;  Guo, Jun;  Zhang, Jun;  Cai, Tao
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/11
A novel gene mutation of Runx2 in cleidocranial dysplasia 期刊论文
JOURNAL OF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY-MEDICAL SCIENCES, 2017, 卷号: 37, 期号: 5
作者:  Peng, You-jian;  Chen, Qiao-yun;  Fu, Dong-jie;  Liu, Zhi-ming;  Mao, Tian-tian
收藏  |  浏览/下载：8/0  |  提交时间：2019/12/05
颅锁骨发育不全综合征一例 期刊论文
中华医学杂志, 2014, 卷号: 94, 期号: 26, 页码: 2078-2079
作者:  李淼;  李培强;  张晓敏
收藏  |  浏览/下载：3/0  |  提交时间：2016/09/05
The microtubule-associated protein DCAMKL1 regulates osteoblast function via repression of Runx2 期刊论文
JOURNAL OF EXPERIMENTAL MEDICINE, 2013, 卷号: 210, 期号: 9, 页码: 1793-1806
作者:  Zou, WG;  Greenblatt, MB;  Brady, N;  Lotinun, S;  Zhai, B
收藏  |  浏览/下载：39/0  |  提交时间：2015/07/22
Novel RUNX2 frameshift mutations in Chinese patients with cleidocranial dysplasia 期刊论文
EUROPEAN JOURNAL OF ORAL SCIENCES, 2013, 卷号: 121, 期号: 3
作者:  Huang, Yanyu;  Song, Yaling;  Zhang, Chenzheng;  Chen, Guoxin;  Wang, Shihua
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05
CHIP promotes Runx2 degradation and negatively regulates osteoblast differentiation 期刊论文
2010, 2010
Li, Xueni; Huang, Mei; Zheng, Huiling; Wang, Yinyin; Ren, Fangli; Shang, Yu; Zhai, Yonggong; Irwin, David M.; Shi, Yuguang; Chen, Di; Chang, Zhijie
收藏  |  浏览/下载：7/0
A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia 期刊论文
GENETICS AND MOLECULAR RESEARCH, 2010, 卷号: 9, 期号: 1, 页码: 41-47
作者:  Wang, G. X.;  Sun, R. P.;  Song, F. L.
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/26
[Clinical and image features, and identification of pathogenic gene mutation of two cleidocranial dysplasia families]. 期刊论文
Zhonghua er ke za zhi = Chinese journal of pediatrics, 2010, 卷号: 48, 期号: 11
作者:  Wang, Guang-xin;  Ma, Li-xia;  Xu, Wan-feng;  Song, Feng-ling;  Sun, Ruo-peng
收藏  |  浏览/下载：11/0  |  提交时间：2019/12/26

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