Rang Xu

发表

Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family.

Kun Sun, Sun Chen, Bojian Li, 2021, Molecular genetics & genomic medicine.

Duplication and deletion of CFC1 associated with heterotaxy syndrome.

K. Sun, Sun Chen, Yuejuan Xu, 2015, DNA and cell biology.

Duplication and Deletion of 22q11 Associated with Anomalous Pulmonary Venous Connection

K. Sun, Sun Chen, Fen Li, 2018, Pediatric Cardiology.

A Potential Relationship among Beta-Defensins Haplotype, SOX7 Duplication and Cardiac Defects

K. Sun, Sun Chen, Yuejuan Xu, 2013, PloS one.

Inhibition of Cardiomyogenesis in Embryocarcinoma Cells Induced by Long-Term High Level of Glucose

K. Sun, Sun Chen, Rang Xu, 2016, Cellular Physiology and Biochemistry.

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

Qi-hua Fu, Sun Chen, E. Zhang, 2017, Scientific Reports.

In Silico Analyses Reveal the Relationship Between SIX1/EYA1 Mutations and Conotruncal Heart Defects

Sun Chen, Bojian Li, Rang Xu, 2017, Pediatric Cardiology.

Hypoxia inducible factor‐1α‐mediated activation of survivin in cervical cancer cells

G. Qian, S. Ge, Rang Xu, 2013, The journal of obstetrics and gynaecology research.

Tumor-specific, hypoxia-regulated, WW domain-containing oxidoreductase-expressing adenovirus inhibits human non-small cell lung cancer growth in vivo.

Ping Zhang, B. Dai, G. Qian, 2010, Human gene therapy.

TM7SF1 (GPR137B): a novel lysosome integral membrane protein

Lizhuo Wang, Jialin Gao, Rang Xu, 2012, Molecular Biology Reports.

Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect

K. Sun, Wei Wei, Fen Li, 2020, Clinical genetics.

Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects.

Jian Wang, K. Sun, Sun Chen, 2014, Molecular medicine reports.

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients

K. Sun, Sun Chen, Yang Liu, 2017, Molecular Genetics and Genomics.

Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays

Xuefan Gu, L. Liang, Yongguo Yu, 2020, Journal of Human Genetics.

Novel compound heterozygous CCDC40 mutations in a familial case of primary ciliary dyskinesia

Wei Wei, Rang Xu, Yurong Wu, 2022, Frontiers in Pediatrics.

Novel In-Frame Deletion Mutation in NOTCH1 in a Chinese Sporadic Case of Adams-Oliver Syndrome.

Rang Xu, Yurong Wu, Ling Yang, 2020, DNA and cell biology.

De novo disruptive heterozygous MMP21 variants are potential predisposing genetic risk factors in Chinese Han heterotaxy children

Sun Chen, Yuejuan Xu, JianMin Ye, 2022, Human Genomics.

A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

K. Sun, Sun Chen, E. Zhang, 2018, Journal of Translational Medicine.

LOF variants identifying candidate genes of laterality defects patients with congenital heart disease

K. Sun, Wei Wei, Sun Chen, 2022, PLoS genetics.

SOX7 suppresses endothelial-to-mesenchymal transitions by enhancing VE-cadherin expression during outflow tract development.

K. Sun, Sun Chen, Wei Wei, 2021, Clinical science.

Identification of candidate genes for congenital heart defects on proximal chromosome 8p

Sun Chen, Yuejuan Xu, K. Sun, 2016, Scientific Reports.

Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy.

K. Sun, Sun Chen, Yuejuan Xu, 2014, DNA and cell biology.

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

Jian Wang, K. Sun, Yuejuan Xu, 2011, BMC Medical Genetics.

Using exome sequencing to identify the cause of myocardial hypertrophy in a Chinese family.

K. Sun, Sun Chen, Ruixue Cao, 2015, Molecular medicine reports.

Sp1 and Sp3 regulate basal transcription of the survivin gene.

Ping Zhang, Jian Huang, G. Qian, 2007, Biochemical and biophysical research communications.

Patients Carrying 9q31.1-q32 Deletion Share Common Features with Cornelia de Lange Syndrome

J. Xie, K. Sun, Sun Chen, 2015, Cellular Physiology and Biochemistry.

Involvement of miR‐21 in resistance to daunorubicin by regulating PTEN expression in the leukaemia K562 cell line

Zhongwei Cao, Rang Xu, H. Bai, 2011, FEBS letters.

Tet inactivation disrupts YY1 binding and long-range chromatin interactions during embryonic heart development

Matthew C. Hill, Ping Zhang, Jiang Chang, 2019, Nature Communications.

Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion

Jian Zhang, Jian Wang, K. Sun, 2014, BMC Medical Genetics.

MicroRNA-21 regulates the sensitivity of diffuse large B-cell lymphoma cells to the CHOP chemotherapy regimen

Rang Xu, H. Bai, Chun Wang, 2013, International Journal of Hematology.

Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation

K. Sun, Sun Chen, Yuejuan Xu, 2021, Orphanet Journal of Rare Diseases.

Smilagenin Protects Dopaminergic Neurons in Chronic MPTP/Probenecid—Lesioned Parkinson’s Disease Models

Jianrong Xu, Xuan He, Lina Hou, 2019, Front. Cell. Neurosci..

Copy Number Variants and Exome Sequencing Analysis in Six Pairs of Chinese Monozygotic Twins Discordant for Congenital Heart Disease

K. Sun, Sun Chen, Yuejuan Xu, 2017, Twin Research and Human Genetics.

Exome sequencing identifies a FHOD3 p.S527del mutation in a Chinese family with hypertrophic cardiomyopathy

Wei Wei, Rang Xu, Yurong Wu, 2019, The journal of gene medicine.

TM7SF1 (GPR137B): a novel lysosome integral membrane protein

Lizhuo Wang, Rang Xu, Libing Xia, 2012, Molecular Biology Reports.

CITED2 Mutations in Conserved Regions Contribute to Conotruncal Heart Defects in Chinese Children.

Yuejuan Xu, Bojian Li, Rang Xu, 2017, DNA and cell biology.

A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

K. Sun, Sun Chen, E. Zhang, 2018, Journal of translational medicine.

Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects

K. Sun, Sun Chen, Yuejuan Xu, 2018, Genome Medicine.

Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects

K. Sun, Sun Chen, Yuejuan Xu, 2018, Genome Medicine.

MicroRNA-21 is involved in X-ray irradiation resistance in K562 leukaemia cells

S. Shao, Rang Xu, H. Bai, 2015, Hematology.

Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing.

K. Sun, Sun Chen, Yuejuan Xu, 2023, Genomics.

Tumor-specific, hypoxia-regulated, WW domain-containing oxidoreductase-expressing adenovirus inhibits human non-small cell lung cancer growth in vivo.

Ping Zhang, B. Dai, G. Qian, 2010, Human Gene Therapy.

ccdc141 is required for left-right axis development by regulating cilia formation in the Kupffer's vesicle of zebrafish.

Sun Chen, Rang Xu, Xuechao Jiang, 2024, Journal of genetics and genomics = Yi chuan xue bao.

In Silico Analyses Reveal the Relationship Between SIX1/EYA1 Mutations and Conotruncal Heart Defects

Sun Chen, Bojian Li, Rang Xu, 2017, Pediatric Cardiology.