R. Du

发表

BCAS2 interacts with HSF4 and negatively regulates its protein stability via ubiquitination.

Fei Liu, Tao Jiang, Mugen Liu, 2015, The international journal of biochemistry & cell biology.

HSF4 regulates DLAD expression and promotes lens de-nucleation.

Mugen Liu, D. W. Li, T. Ke, 2013, Biochimica et biophysica acta.

HSF4 is involved in DNA damage repair through regulation of Rad51.

Mugen Liu, D. W. Li, Stephen Archacki, 2012, Biochimica et biophysica acta.

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family

Mugen Liu, Stephen Archacki, Zhao-hui Tang, 2011, Neuroscience Letters.

Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome

R. Du, Jin Li, F. Ren, 2007, Frontiers of medicine in China.

Missense mutations in CSX/NKX2.5 are associated with atrial septal defects

Jing Li, R. Du, J. Yang, 2007 .

The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes.

R. Du, Zi-Fang Song, L. Tian, 2009, Biochemical and biophysical research communications.

Congenital long QT syndrome caused by the F275S KCNQ1 mutation: mechanism of impaired channel function.

R. Du, Xuelin Chen, Si-ming Guan, 2009, Biochemical and biophysical research communications.

Site-directed mutagenesis of long QT syndrome KCNQ1 gene in vitro

Bin Wang, R. Du, L. Tian, 2004, Yi chuan = Hereditas.

Inhibitory effect of rhynchophylline on human ether-a-go-go related gene channel.

Jing Li, R. Du, Guo-hui Yuan, 2005, Sheng li xue bao : [Acta physiologica Sinica].

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family

Ping Liu, Mugen Liu, T. Ke, 2005, Journal of Molecular Medicine.

Identification of a new lamin A/C mutation in a chinese family affected with atrioventricular block as the prominent phenotype

Mugen Liu, R. Du, Q. Wang, 2010, Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban.

Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1

Y. Liu, Mugen Liu, Zhao-hui Tang, 2013, Molecular vision.

MEF 2 A gene mutations and susceptibility to coronary artery disease in the Chinese population

R. Du, J. Li, L. Tian, 2014 .

Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome

R. Du, Wen Zhang, Yunting Lin, 2023, Frontiers in Genetics.

MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.

R. Du, J. Li, L. Tian, 2014, Genetics and Molecular Research.