Works matching AU Ma, Duan

Results: 123

Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.

Published in:

2017

By:

Yanyan Qian;
Deyong Xiao;
Xiao Guo;
Hongbo Chen;
Lili Hao;
Xiaojing Ma;
Guoying Huang;
Duan Ma;
Huijun Wang;
Qian, Yanyan;
Xiao, Deyong;
Guo, Xiao;
Chen, Hongbo;
Hao, Lili;
Ma, Xiaojing;
Huang, Guoying;
Ma, Duan;
Wang, Huijun

Publication type:

journal article

Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss.

Published in:

2016

By:

Jiongjiong Hu;
Fei Liu;
Wenjun Xia;
Lili Hao;
Jun Lan;
Zhenghua Zhu;
Jing Ye;
Duan Ma;
Zhaoxin Ma;
Hu, Jiongjiong;
Liu, Fei;
Xia, Wenjun;
Hao, Lili;
Lan, Jun;
Zhu, Zhenghua;
Ye, Jing;
Ma, Duan;
Ma, Zhaoxin

Publication type:

journal article

New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss.

Published in:

Human Mutation, 2017, v. 38, n. 10, p. 1421, doi. 10.1002/humu.23285

By:

Xia, Wenjun;
Hu, Jiongjiong;
Liu, Fei;
Ma, Jing;
Sun, Shaoyang;
Zhang, Jin;
Jin, Kaiyue;
Huang, Jianbo;
Jiang, Nan;
Wang, Xu;
Li, Wen;
Ma, Zhaoxin;
Ma, Duan

Publication type:

Article

Identification of hub genes and potential molecular mechanisms in MSS/MSI classifier primary colorectal cancer based on multiple datasets.

Published in:

Discover Oncology, 2024, v. 15, n. 1, p. 1, doi. 10.1007/s12672-024-01148-0

By:

Qiao, Xia;
Ma, Duan;
Zhang, Xu

Publication type:

Article

Innovative Bio‐based Hydrogel Microspheres Micro‐Cage for Neutrophil Extracellular Traps Scavenging in Diabetic Wound Healing.

Published in:

Advanced Science, 2024, v. 11, n. 21, p. 1, doi. 10.1002/advs.202401195

By:

Xiao, Yongqiang;
Ding, Tao;
Fang, He;
Lin, Jiawei;
Chen, Lili;
Ma, Duan;
Zhang, Tianyu;
Cui, Wenguo;
Ma, Jing

Publication type:

Article

Determination of long non-coding RNAs associated with EZH2 in neuroblastoma by RIP-seq, RNA-seq and ChIP-seq.

Published in:

Oncology Letters, 2020, v. 20, n. 4, p. N.PAG

By:

Ye, Mujie;
Xie, Lulu;
Zhang, Jingjing;
Liu, Baihui;
Liu, Xiangqi;
He, Jiajun;
Ma, Duan;
Dong, Kuiran

Publication type:

Article

A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease.

Published in:

Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-30204-3

By:

Li, Shuolin;
Liu, Sida;
Chen, Weicheng;
Yuan, Yuan;
Gu, Ruoyi;
Song, Yangliu;
Li, Jian;
Cao, Yinyin;
Lin, Yixiang;
Xu, Jun;
Wang, Huijun;
Ma, Duan;
Ma, Xiaojing;
Sheng, Wei;
Huang, Guoying

Publication type:

Article

Correction: Ubiquitylation of MFHAS1 by the ubiquitin ligase praja2 promotes M1 macrophage polarization by activating JNK and p38 pathways.

Published in:

2018

By:

Zhong, Jing;
Wang, Huihui;
Chen, Wankun;
Sun, Zhirong;
Chen, Jiawei;
Xu, Yajun;
Weng, Meilin;
Shi, Qiqing;
Ma, Duan;
Miao, Changhong

Publication type:

Correction Notice

DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot.

Published in:

BMC Medical Genomics, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8794-6-46

By:

Wei Sheng;
Yanyan Qian;
Huijun Wang;
Xiaojing Ma;
Ping Zhang;
Lianwei Diao;
Quan An;
Long Chen;
Duan Ma;
Guoying Huang

Publication type:

Article

Low expression of TFPI-2 associated with poor survival outcome in patients with breast cancer.

Published in:

BMC Cancer, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2407-13-118

By:

Cheng Xu;
Huijun Wang;
Hongyu He;
Fengyun Zheng;
Yating Chen;
Jin Zhang;
Xiaoyan Lin;
Duan Ma;
Hongwei Zhang

Publication type:

Article

Low expression of TFPI-2 associated with poor survival outcome in patients with breast cancer.

Published in:

2013

By:

Xu, Cheng;
Wang, Huijun;
He, Hongyu;
Zheng, Fengyun;
Chen, Yating;
Zhang, Jin;
Lin, Xiaoyan;
Ma, Duan;
Zhang, Hongwei

Publication type:

journal article

miRNA-135a promotes breast cancer cell migration and invasion by targeting HOXA10.

Published in:

2012

By:

Chen, Yating;
Zhang, Jin;
Wang, Huijun;
Zhao, Jiayi;
Xu, Cheng;
Du, Yingying;
Luo, Xin;
Zheng, Fengyun;
Liu, Rui;
Zhang, Hongwei;
Ma, Duan

Publication type:

journal article

The interaction between ubiquitin C-terminal hydrolase 37 and glucose-regulated protein 78 in hepatocellular carcinoma.

Published in:

Molecular & Cellular Biochemistry, 2012, v. 359, n. 1/2, p. 59, doi. 10.1007/s11010-011-0999-7

By:

Fang, Ying;
Mu, Jingui;
Ma, Yushui;
Ma, Duan;
Fu, Da;
Shen, Xizhong

Publication type:

Article

Regulation of intracellular decorin via proteasome degradation in rat mesangial cells.

Published in:

Journal of Cellular Biochemistry, 2010, v. 111, n. 4, p. 1010, doi. 10.1002/jcb.22789

By:

Wu, Huijuan;
Jiang, Weina;
Zhang, Yan;
liu, Ye;
Zhao, Zhonghua;
Guo, Muyi;
Ma, Duan;
Zhang, Zhigang

Publication type:

Article

A novel loss-of-function heterozygous BRCA2 c.8946_8947delAG mutation found in a Chinese woman with family history of breast cancer.

Published in:

Journal of Cancer Research & Clinical Oncology, 2017, v. 143, n. 4, p. 631, doi. 10.1007/s00432-016-2327-9

By:

Ma, Jing;
Yang, Jichun;
Jian, Wenjing;
Wang, Xianming;
Xiao, Deyong;
Xia, Wenjun;
Xiong, Likuan;
Ma, Duan

Publication type:

Article

Effects of Tissue Factor Pathway Inhibitor-2 Expression on Biological Behavior of BeWo and JEG-3 Cell Lines.

Published in:

Clinical & Applied Thrombosis/Hemostasis, 2012, v. 18, n. 5, p. 526, doi. 10.1177/1076029611429785

By:

Zhou, Qiongjie;
Xiong, Yu;
Chen, Yan;
Du, Yingying;
Zhang, Jin;
Mu, Jingui;
Guo, Qisang;
Wang, Huijun;
Ma, Duan;
Li, Xiaotian

Publication type:

Article

Aberrant Hypermethylation of Aldehyde Dehydrogenase 2 Promoter Upstream Sequence in Rats with Experimental Myocardial Infarction.

Published in:

BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/503692

By:

Wang, Peng;
Shen, Cheng;
Diao, Lei;
Yang, Zhiyin;
Fan, Fan;
Wang, Cong;
Liu, Xiangwei;
Sun, Xiaolei;
Dong, Zhen;
Zhu, Hong;
Ma, Xin;
Cao, Quan;
Zhao, Xiaona;
Ma, Duan;
Zou, Yunzeng;
Hu, Kai;
Sun, Aijun;
Ge, Junbo

Publication type:

Article

The effect of multiple single nucleotide polymorphisms in the folic Acid pathway genes on homocysteine metabolism.

Published in:

2014

By:

Liang, Shuang;
Zhou, Yuanpeng;
Wang, Huijun;
Qian, Yanyan;
Ma, Duan;
Tian, Weidong;
Persaud-Sharma, Vishwani;
Yu, Chen;
Ren, Yunyun;
Zhou, Shufeng;
Li, Xiaotian

Publication type:

Journal Article

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss.

Published in:

PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0126602

By:

Liu, Fei;
Hu, Jiongjiong;
Xia, Wenjun;
Hao, Lili;
Ma, Jing;
Ma, Duan;
Ma, Zhaoxin

Publication type:

Article

Quantitative Proteomic Analysis of Serum from Pregnant Women Carrying a Fetus with Conotruncal Heart Defect Using Isobaric Tags for Relative and Absolute Quantitation (iTRAQ) Labeling.

Published in:

PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111645

By:

Zhang, Ying;
Kang, Yuan;
Zhou, Qiongjie;
Zhou, Jizi;
Wang, Huijun;
Jin, Hong;
Liu, Xiaohui;
Ma, Duan;
Li, Xiaotian

Publication type:

Article

Psychiatric Illness and Intellectual Disability in the Prader–Willi Syndrome with Different Molecular Defects - A Meta Analysis.

Published in:

PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072640

By:

Yang, Lin;
Zhan, Guo-dong;
Ding, Jun-jie;
Wang, Hui-jun;
Ma, Duan;
Huang, Guo-ying;
Zhou, Wen-hao

Publication type:

Article

Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11).

Published in:

PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055178

By:

Qing Sang;
Xukun Yan;
Huan Wang;
Ruizhi Feng;
Xiang Fei;
Duan Ma;
Qinghe Xing;
Qiaoli Li;
Xinzhi Zhao;
Li Jin;
Lin He;
Huawei Li;
Lei Wang

Publication type:

Article

Characteristic Face: A Key Indicator for Direct Diagnosis of 22q11.2 Deletions in Chinese Velocardiofacial Syndrome Patients.

Published in:

PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054404

By:

Dandan Wu;
Yang Chen;
Chen Xu;
Ke Wang;
Huijun Wang;
Fengyun Zheng;
Duan Ma;
Guomin Wang

Publication type:

Article

The Induction of MicroRNA Targeting IRS-1 Is Involved in the Development of Insulin Resistance under Conditions of Mitochondrial Dysfunction in Hepatocytes.

Published in:

PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0017343

By:

Hyun Su Ryu;
Seung-Yoon Park;
Duan Ma;
Jin Zhang;
Wan Lee

Publication type:

Article

DNA methylation status of TBX20 in patients with tetralogy of Fallot.

Published in:

BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0534-3

By:

Gong, Juan;
Sheng, Wei;
Ma, Duan;
Huang, Guoying;
Liu, Fang

Publication type:

Article

Epigallocatechin‐3‐O‐gallate ameliorates oxidative stress‐induced chondrocyte dysfunction and exerts chondroprotective effects via the Keap1/Nrf2/ARE signaling pathway.

Published in:

Chemical Biology & Drug Design, 2022, v. 100, n. 1, p. 108, doi. 10.1111/cbdd.14056

By:

Zhu, Wenrun;
Tang, Han;
Cao, Lu;
Zhang, Jin;
Li, Juncheng;
Ma, Duan;
Guo, Changan

Publication type:

Article

Detection of RASA1 mutations in patients with sporadic Sturge-Weber syndrome.

Published in:

Child's Nervous System, 2011, v. 27, n. 4, p. 603, doi. 10.1007/s00381-010-1258-z

By:

Zhou, Qin;
Zheng, Jia-wei;
Yang, Xiu-juan;
Wang, Hui-jun;
Ma, Duan;
Qin, Zhong-ping

Publication type:

Article

Modulating Autophagy Improves Cardiac Function in a Rat Model of Early-Stage Dilated Cardiomyopathy.

Published in:

Cardiology, 2013, v. 125, n. 1, p. 60, doi. 10.1159/000348308

By:

Xie, Kun;
Jin, Bo;
Li, Yong;
Luo, Xinping;
Zhu, Jun;
Ma, Duan;
Shi, Haiming

Publication type:

Article

Genome-wide methylation analysis reveals differentially methylated CpG sites and altered expression of heart development-associated genes in fetuses with cardiac defects.

Published in:

Experimental & Therapeutic Medicine, 2021, v. 22, n. 3, p. N.PAG, doi. 10.3892/etm.2021.10464

By:

Zhou, Jizi;
Xiong, Yu;
Dong, Xinran;
Wang, Huijun;
Qian, Yanyan;
Ma, Duan;
Li, Xiaotian

Publication type:

Article

A hidden proteome encoded by circRNAs in human placentas: Implications for uncovering preeclampsia pathogenesis.

Published in:

Clinical & Translational Medicine, 2024, v. 14, n. 7, p. 1, doi. 10.1002/ctm2.1759

By:

Zhao, Huanqiang;
Xiong, Yu;
Zhou, Zixiang;
Xu, Qixin;
Zi, Yang;
Zheng, Xiujie;
Chen, Shiguo;
Xiao, Xirong;
Gong, Lili;
Xu, Huangfang;
Liu, Lidong;
Lu, Huiqing;
Cui, Yutong;
Shao, Shuyi;
Zhang, Jin;
Ma, Jing;
Zhou, Qiongjie;
Ma, Duan;
Li, Xiaotian

Publication type:

Article

WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.

Published in:

Clinical & Translational Medicine, 2022, v. 12, n. 7, p. 1, doi. 10.1002/ctm2.941

By:

Hao, Lili;
Ma, Jing;
Wu, Feizhen;
Ma, Xiaojing;
Qian, Maoxiang;
Sheng, Wei;
Yan, Tizhen;
Tang, Ning;
Jiang, Xin;
Zhang, Bowen;
Xiao, Deyong;
Qian, Yanyan;
Zhang, Jin;
Jiang, Nan;
Zhou, Wenhao;
Chen, Weicheng;
Ma, Duan;
Huang, Guoying

Publication type:

Article

Single‐cell transcriptomics reveals pathogenic dysregulation of previously unrecognised chondral stem/progenitor cells in children with microtia.

Published in:

Clinical & Translational Medicine, 2022, v. 12, n. 2, p. 1, doi. 10.1002/ctm2.702

By:

Ma, Jing;
Zhang, Yu;
Yan, Zijun;
Wu, Peixuan;
Li, Chenlong;
Yang, Run;
Lu, Xinyu;
Chen, Xin;
He, Aijuan;
Fu, Yaoyao;
Ma, Duan;
Tian, Weidong;
Zhang, Tianyu

Publication type:

Article

Comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 7, p. 393, doi. 10.1038/jhg.2014.40

By:

Wang, Yanlin;
Wen, Zujia;
Shen, Jiawei;
Cheng, Weiwei;
Li, Jun;
Qin, Xiaolan;
Ma, Duan;
Shi, Yongyong

Publication type:

Article

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

Published in:

Human Molecular Genetics, 2017, v. 26, n. 16, p. 3234, doi. 10.1093/hmg/ddx232

By:

Zhaoxin Ma;
Wenjun Xia;
Fei Liu;
Jing Ma;
Shaoyang Sun;
Jin Zhang;
Nan Jiang;
Xu Wang;
Jiongjiong Hu;
Duan Ma

Publication type:

Article

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

Published in:

Human Molecular Genetics, 2017, v. 26, n. 2, p. 383, doi. 10.1093/hmg/ddw394

By:

Zhaoxin Ma;
Wenjun Xia;
Fei Liu;
Jing Ma;
Shaoyang Sun;
Jin Zhang;
Nan Jiang;
Xu Wang;
Jiongjiong Hu;
Duan Ma

Publication type:

Article

A novel adiponectin receptor agonist (AdipoAI) ameliorates type 2 diabetes‐associated periodontitis by enhancing autophagy in osteoclasts.

Published in:

Journal of Periodontal Research, 2022, v. 57, n. 2, p. 381, doi. 10.1111/jre.12969

By:

Wu, Xingwen;
Sun, Yang;
Cui, Renjie;
Qiu, Wei;
Zhang, Jin;
Hu, Zhekai;
Bi, Wei;
Yang, Fei;
Ma, Duan;
Van Dyke, Thomas;
Tu, Qisheng;
Yu, Youcheng;
Chen, Jake

Publication type:

Article

Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.

Published in:

Clinical Genetics, 2019, v. 96, n. 5, p. 402, doi. 10.1111/cge.13606

By:

Rao, Jia;
Liu, Xiaorong;
Mao, Jianhua;
Tang, Xiaoshan;
Shen, Qian;
Li, Guomin;
Sun, Li;
Bi, Yunli;
Wang, Xiang;
Qian, Yanyan;
Wu, Bingbing;
Wang, Huijun;
Zhou, Wenhao;
Ma, Duan;
Zheng, Bixia;
Shen, Ying;
Chen, Zhi;
Luan, Jiangwei;
Wang, Xiaowen;
Wang, Mo

Publication type:

Article

Novel TRRAP mutation causes autosomal dominant non‐syndromic hearing loss.

Published in:

Clinical Genetics, 2019, v. 96, n. 4, p. 300, doi. 10.1111/cge.13590

By:

Xia, Wenjun;
Hu, Jiongjiong;
Ma, Jing;
Huang, Jianbo;
Wang, Xu;
Jiang, Nan;
Zhang, Jin;
Ma, Zhaoxin;
Ma, Duan

Publication type:

Article

MicroRNA-125b-2 overexpression represses ectodermal differentiation of mouse embryonic stem cells.

Published in:

International Journal of Molecular Medicine, 2015, v. 36, n. 2, p. 355, doi. 10.3892/ijmm.2015.2238

By:

SHANSHAN DENG;
YANLI ZHANG;
CHUNDI XU;
DUAN MA

Publication type:

Article

microRNA expression profiling of heart tissue during fetal development.

Published in:

International Journal of Molecular Medicine, 2014, v. 33, n. 5, p. 1250, doi. 10.3892/ijmm.2014.1691

By:

JIZI ZHOU;
XINRAN DONG;
QIONGJIE ZHOU;
HUIJUN WANG;
YANYAN QIAN;
WEIDONG TIAN;
DUAN MA;
XIAOTIAN LI

Publication type:

Article

Association between mRNA levels of DNMT1, DNMT3A, DNMT3B, MBD2 and LINE-1 methylation status in infants with tetralogy of Fallot.

Published in:

International Journal of Molecular Medicine, 2013, v. 32, n. 3, p. 694, doi. 10.3892/ijmm.2013.1427

By:

WEI SHENG;
YANYAN QIAN;
HUIJUN WANG;
XIAOJING MA;
PING ZHANG;
LONG CHEN;
DUAN MA;
GUOYING HUANG

Publication type:

Article

PolyA RT-PCR-based quantification of microRNA by using universal TaqMan probe.

Published in:

Biotechnology Letters, 2012, v. 34, n. 4, p. 627, doi. 10.1007/s10529-011-0813-3

By:

Luo, Xin;
Zhang, Jin;
Wang, Huijun;
Du, Yingying;
Yang, Lu;
Zheng, Fengyun;
Ma, Duan

Publication type:

Article

The Genotype and Expression of the TGFβ2 Gene in Children With Congenital Conotruncal Defects.

Published in:

Pediatric Cardiology, 2013, v. 34, n. 8, p. 1823, doi. 10.1007/s00246-013-0696-2

By:

Meng, Yingying;
Ma, Xiaojing;
Zhang, Jing;
Wang, Huijun;
Ma, Duan;
Huang, Guoying

Publication type:

Article

Noninvasive genetic testing for type IV collagen nephropathy using oral mucosa DNA sampling in children with haematuria.

Published in:

Renal Failure, 2024, v. 46, n. 2, p. 1, doi. 10.1080/0886022X.2024.2423845

By:

Liu, Jiaojiao;
Zhou, Dayin;
Wang, Xiaowen;
Shen, Tong;
Wang, Chunyan;
Dai, Rufeng;
Han, Xinli;
Huang, Lin;
Xu, Wenli;
Chen, Jing;
Zhai, Yihui;
Rao, Jia;
Ma, Duan;
Shen, Qian;
Xu, Hong

Publication type:

Article

Noninvasive genetic testing for type IV collagen nephropathy using oral mucosa DNA sampling in children with haematuria.

Published in:

Renal Failure, 2024, v. 46, n. 2, p. 1, doi. 10.1080/0886022X.2024.2423845

By:

Liu, Jiaojiao;
Zhou, Dayin;
Wang, Xiaowen;
Shen, Tong;
Wang, Chunyan;
Dai, Rufeng;
Han, Xinli;
Huang, Lin;
Xu, Wenli;
Chen, Jing;
Zhai, Yihui;
Rao, Jia;
Ma, Duan;
Shen, Qian;
Xu, Hong

Publication type:

Article

Laser beam melting 3D printing of Ti6Al4V based porous structured dental implants: fabrication, biocompatibility analysis and photoelastic study.

Published in:

Scientific Reports, 2017, p. 45360, doi. 10.1038/srep45360

By:

Yang, Fei;
Chen, Chen;
Zhou, QianRong;
Gong, YiMing;
Li, RuiXue;
Li, ChiChi;
Klämpfl, Florian;
Freund, Sebastian;
Wu, XingWen;
Sun, Yang;
Li, Xiang;
Schmidt, Michael;
Ma, Duan;
Yu, YouCheng

Publication type:

Article

The alternatively-included 11a sequence modifies the effects of Mena on actin cytoskeletal organization and cell behavior.

Published in:

Scientific Reports, 2016, p. 35298, doi. 10.1038/srep35298

By:

Balsamo, Michele;
Mondal, Chandrani;
Carmona, Guillaume;
McClain, Leslie M.;
Riquelme, Daisy N.;
Tadros, Jenny;
Ma, Duan;
Vasile, Eliza;
Condeelis, John S.;
Lauffenburger, Douglas A.;
Gertler, Frank B.

Publication type:

Article

Establishment and Phenotypic Analysis of the Novel Gaucher Disease Mouse Model With the Partially Humanized Gba1 Gene and F213I Mutation.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.892457

By:

Jia-ni Guo;
Ming Guan;
Nan Jiang;
Na Li;
Ya-jun Li;
Jin Zhang;
Duan Ma

Publication type:

Article

Long non-coding RNA SAP30-2:1 is downregulated in congenital heart disease and regulates cell proliferation by targeting HAND2.

Published in:

Frontiers of Medicine, 2021, v. 15, n. 1, p. 91, doi. 10.1007/s11684-020-0778-5

By:

Ma, Jing;
Chen, Shiyu;
Hao, Lili;
Sheng, Wei;
Chen, Weicheng;
Ma, Xiaojing;
Zhang, Bowen;
Ma, Duan;
Huang, Guoying

Publication type:

Article

Endogenous tissue factor pathway inhibitor in vascular smooth muscle cells inhibits arterial thrombosis.

Published in:

Frontiers of Medicine, 2017, v. 11, n. 3, p. 403, doi. 10.1007/s11684-017-0522-y

By:

Yang, Jichun;
Jin, Kaiyue;
Xiao, Jiajun;
Ma, Jing;
Ma, Duan

Publication type:

Article