All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Heart

Microbial Genetics   Research Article

Maternal MTHFR C677T polymorphism and congenital heart defect risk in the Chinese Han population: a meta-analysis

Authors: K.H. Chen, L.L. Chen, W.G. Li, Y. Fang and G.Y. Huang

Numerous studies have evaluated the association between the maternal C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene and congenital heart defect (CHD) risk in the Chinese Han population. However, the specific association is still controversial. Six separate studies with 1089 subjects in the Chinese Han population on the relation.. Read More»

Genet. Mol. Res. 12(4):
2013.December.4.8
DOI:
10.4238/2013.December.4.8
Microbial Genetics   Research Article

Microdeletion on 17p11.2 in a Smith-Magenis syndrome patient with mental retardation and congenital heart defect: first report from China

Authors: C. Huang, Y.-F. Yang, H. Zhang, L. Xie, J.-L. Chen, J. Wang, Z.-P. Tan and H. Luo

Smith-Magenis syndrome (SMS) is a rare syndrome with multiple congenital malformations, including development and mental retardation, behavioral problems and a distinct facial appearance. SMS is caused by haploinsufficiency of RAI1 (deletion or mutation of RAI1). We describe an eight-year-old female Chinese patient with multiple malformations, congenital .. Read More»

Genet. Mol. Res. 11(3):
2012.August.13.5
DOI:
10.4238/2012.August.13.5
Medical Genetics   Research Article

Relationship between perioperative cardiovascular risk factors and bone marrow cells from patients undergoing coronary artery bypass grafting surgery

Authors: L. Zhang, R. Wang, C.-S. Xiao, Y. Wu and C.-Q. Gao

Cell therapy through the implantation of autologous bone marrow cells has long been used in clinical trials for the treatment of ischemic heart diseases. However, as the outcomes of cell implantation vary among patients, risk factors that might influence the level and function of bone marrow progenitor cells should be determin.. Read More»

Genet. Mol. Res. 14(4):
2015.November.25.11
DOI:
10.4238/2015.November.25.11
Human Genetics   Research Article

Lack of an association between matrix metalloproteinase polymorphisms and coronary heart disease in a Han Chinese population

Authors: C.M. Wang, H.D. Ye, Y.R. Li, Q.X. Hong, L.L. Tang, A.N. Zhou, M.Q. Xu and S.W. Duan

Coronary heart disease (CHD) has become a leading cause of human deaths worldwide. Recent studied showed that polymorphisms of the matrix metalloproteinase (MMP) genes played important roles in extracellular matrix remodeling and contribute to the pathogenesis of vascular diseases. Here, we investigated whether these MMP gene .. Read More»

Genet. Mol. Res. 14(4):
2015.October.9.14
DOI:
10.4238/2015.October.9.14
Human Genetics   Research Article

Significant interaction of APOE rs4420638 polymorphism with HDL-C and APOA-I levels in coronary heart disease in Han Chinese men

Authors: Y. Huang, H.D. Ye, X. Gao, S. Nie, Q.X. Hong, H.H. Ji, J. Sun, S.J. Zhou, B. Fei, K.Q. Li, J.K. Zhao, Z.P. Wang, M.Q. Xu and S.W. Duan

Apolipoprotein E (APOE) is recognized for its importance in lipoprotein metabolism and cardiovascular disease. We evaluated the association between APOE rs4420638 genotypes and circulating lipid concentrations along with the risk of coronary heart disease (CHD). We conducted a case-control study involving 1508 individuals to investigate the contribution o.. Read More»

Genet. Mol. Res. 14(4):
2015.October.28.3
DOI:
10.4238/2015.October.28.3
Human Genetics   Research Article

Association between angiotensin-converting enzyme insertion/deletion polymorphisms and the risk of heart disease: an updated meta-analysis

Authors: F.J. You and D.M. Shen

Insertion/deletion (I/D) polymorphisms of the gene encoding angiotensin converting enzyme (ACE) are a controversial risk factor for heart diseases (HDs). ACE I/D polymorphism has been reported to be associated with various cardiovascular diseases. However, some studies have presented conflicting results. In this study, we aim to explore the association be.. Read More»

Genet. Mol. Res. 15(1):
gmr.15017194
DOI:
10.4238/gmr.15017194
Human Genetics   Research Article

Association of N-acetyltransferase-2 polymorphism with an increased risk of coronary heart disease in a Chinese population

Authors: J.D. Sun, H. Yuan, H.Q. Hu and H.M. Yu

We investigated the possible correlations between N-acetyltransferase-2 (NAT2) gene polymorphisms and the risk of coronary heart disease (CHD). CHD patients (113) and healthy controls (118) were enrolled from the First People’s Hospital of Yuhang between January 2013 and June 2014. The patients were divided into mild CHD (N = 72) and severe CHD (N =.. Read More»

Genet. Mol. Res. 15(1):
gmr.15016954
DOI:
10.4238/gmr.15016954
Human Genetics   Research Article

Effect of atorvastatin on plasma NT-proBNP and inflammatory cytokine expression in patients with heart failure

Authors: H.Y. Duan, D.M. Liu, P. Qian, S.L. Wang, L.J. Yan, J.T. Wu, H.T. Yang, X.W. Fan, Y.J. Chu

The aim of this study was to explore the effect of atorvastatin intervention on plasma N-terminal pro-B-type natriuretic peptide (NT-proBNP) and inflammatory cytokine levels in patients with heart failure (HF). One hundred and twenty-three HF patients were selected from our hospital and randomly divided into control (N = 61) a.. Read More»

Genet. Mol. Res. 14(4):
2015.December.1.25
DOI:
10.4238/2015.December.1.25
Human Genetics   Research Article

Identification of molecular markers in patients with hypertensive heart disease accompanied with coronary artery disease

Authors: H. Pang, B. Han, Z.Y. Li and Q. Fu

We investigated the plasma hypersensitive C-reactive protein (hs-CRP), oxidized low-density lipoprotein (ox-LDL), and apelin levels in patients with hypertensive heart disease (HHD) plus coronary artery disease (CAD). Patients with hypertension hospitalized in Xuzhou Central Hospital were categorized into the HHD group and the HHD plus CAD group; 40 healt.. Read More»

Genet. Mol. Res. 14(1):
2015.January.15.12
DOI:
10.4238/2015.January.15.12
Human Genetics   Research Article

Resveratrol, an activator of SIRT1, upregulates AMPK and improves cardiac function in heart failure

Authors: X.S. Gu, Z.B. Wang, Z. Ye, J.P. Lei, L. Li, D.F. Su and X. Zheng

Reduced AMP-activated protein kinase (AMPK) expression has been shown to play a significant role in the cardiac dysfunction in heart failure. This study was designed to examine the effect of resveratrol, a potent activator of silent information regulator (SIRT1), on cardiac function and AMPK expression in heart failure. Adult .. Read More»

Genet. Mol. Res. 13(1):
http://dx.doi.org/2014.January.17.17
DOI:
http://dx.doi.org/10.4238/2014.January.17.17