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CORC

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Identification and Fine Mapping of the Recessive Gene BK-5, Which Affects Cell Wall Biosynthesis and Plant Brittleness in Maize 期刊论文
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 卷号: 23, 期号: 2
作者:  Li, Qigui;  Nie, Shujun;  Li, Gaoke;  Du, Jiyuan;  Ren, Ruchang
收藏  |  浏览/下载：0/0  |  提交时间：2024/03/07
Oridonin inhibits DNMT3A R882 mutation-driven clonal hematopoiesis and leukemia by inducing apoptosis and necroptosis 期刊论文
CELL DEATH DISCOVERY, 2021, 卷号: 7, 期号: 1, 页码: 12
作者:  Liao, Min;  Dong, Qiongye;  Chen, Ruiqing;  Xu, Liqian;  Jiang, Yuxuan
收藏  |  浏览/下载：33/0  |  提交时间：2021/12/01
Mutation-induced remodeling of the BfmRS two-component system in Pseudomonas aeruginosa clinical isolates 期刊论文
SCIENCE SIGNALING, 2020, 卷号: 13, 期号: 656, 页码: 21
作者:  Cao, Qiao
收藏  |  浏览/下载：131/0  |  提交时间：2020/12/24
Identification of a missense ARSA mutation in metachromatic leukodystrophy and its potential pathogenic mechanism 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 页码: 11
作者:  Guo, Liyuan;  Jin, Bo;  Zhang, Yidan;  Wang, Jing
收藏  |  浏览/下载：26/0  |  提交时间：2020/10/22
Non-disruptive mutation in TP53 DNA-binding domain is a beneficial factor of esophageal squamous cell carcinoma 期刊论文
ANNALS OF TRANSLATIONAL MEDICINE, 2020, 卷号: 8
作者:  Huang, Minran;  Jin, Jiaoyue;  Zhang, Fanrong;  Wu, Yingxue;  Xu, Chenyang
收藏  |  浏览/下载：29/0  |  提交时间：2020/11/26
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
Hereditary spastic paraplegia associated with a rare IFIH1 mutation: a case report and literature review 期刊论文
HEREDITAS, 2019, 卷号: 156, 期号: 1
作者:  Chen, Jiajun;  Li, Jia;  Liu, Nan;  Shi, Tianji;  Xu, Chuan
收藏  |  浏览/下载：8/0  |  提交时间：2019/12/05
Identification and functional characterization of a novel missense mutation in FRMD7 responsible for idiopathic congenital nystagmus 期刊论文
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2019, 卷号: 51, 期号: 2
作者:  Wang, Min;  Lu, Boyang;  Wang, Zhe;  Wang, Chengyan
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05
Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification 期刊论文
Brain & Development, 2019, 卷号: Vol.41 No.1, 页码: 29-35
作者:  Shi, Chang-he;  Zhang, Shuo;  Yang, Zhi-hua;  Liu, Yu-tao;  Li, Yu-sheng
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/17
MISSENSE MUTATION IN PRKCQ IS ASSOCIATED WITH CROHN'S DISEASE. 期刊论文
Journal of digestive diseases, 2019
作者:  Yuwei Zhang;  Xiaoying Xu;  Jie Zhang;  Xin Yao;  Chao Lu
收藏  |  浏览/下载：18/0  |  提交时间：2019/12/17

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