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Human Genetics

Human Genetics   Research Article

rs3918242 MMP9 gene polymorphism is associated with myocardial infarction in Mexican patients

Authors: J.M. Rodr�­guez-P�©rez1*, G. Vargas-Alarc�³n1*, R. Posadas-S�¡nchez2,T.X. Zagal-Jim�©nez1, R. Ort�­z-Alarc�³n1, B. Valente-Acosta1, C. Tovilla-Z�¡rate3, C. Nostroza-Hern�¡ndez1, O. P�©rez-M�©ndez1 and N. P�©rez-Hern�¡ndez1,4

Several studies have demonstrated that matrix metalloproteinases (MMPs) play a major role in atherosclerotic plaque disruption and lead to myocardial infarction (MI). We investigated the association between the MMP1 -1607 1G/2G (rs1799750), MMP3 -1612 5A/6A (rs3025058), and MMP9 -1562 C/T (rs3918242) polymorphisms and the risk of developing MI in a Mexica.. Read More»

Genet. Mol. Res. 15(1):
gmr.15017776
DOI:
10.4238/gmr.15017776
Human Genetics   Research Article

Assessment of the mutagenic, genotoxic and cytotoxic potential of the waters of the Preto River in the area influenced by S�£o Jos�© do Rio Preto, SP

Authors: L.R. Maschio

-.. Read More»

Genet. Mol. Res. 8(3):
vol8-3ta020
DOI:
10.4238/vol8-3ta020
Human Genetics   Research Article

Meta-analysis demonstrates association between TLR polymorphisms and rheumatoid arthritis

Authors: Y.H. Lee S.-C. Bae G.G. Song

We investigated whether Toll-like receptor (TLR) polymorphisms confer susceptibility to rheumatoid arthritis and whether they influence clinical characteristics of rheumatoid arthritis. Studies were considered relevant for our meta-analysis if at least two comparisons of an issue were available. Eleven studies with 2078 patients with rheumatoid arthritis .. Read More»

Genet. Mol. Res. 12(1):
2013.February.7.2
DOI:
10.4238/2013.February.7.2
Human Genetics   Research Article

Effects of probucol on cultured human umbilical vein endothelial cells injured by hypoxia/reoxygenation

Authors: Y.L. Chai, J.Z. Xu, Y.L. Zhang and G.T. Sheng

There is increasing evidence suggesting that endoplasmic reticulum stress (ERS) plays an important role in the initiation and development of atherosclerosis. This study was designed to examine the effect of probucol on cultured human umbilical vein endothelial cells (HUVECs) injured by hypoxia/reoxygenation (H/R) and the potential mechanisms involving ERS.. Read More»

Genet. Mol. Res. 15(1):
gmr.15016752
DOI:
10.4238/gmr.15016752
Human Genetics   Research Article

The role of smoking status and collagen IX polymorphisms in the susceptibility to cervical spondylotic myelopathy

Authors: Z.C. Wang, J.G. Shi, X.S. Chen, G.H. Xu, L.J. Li and L.S. Jia

We investigated a possible association of collagen IX tryptophan (Trp) alleles (Trp2 and Trp3) and smoking with cervical spondylotic myelopathy (CSM) in 172 Chinese patients and 176 age- and gender-matched controls. The smoking status was evaluated by smoking index (SI). The CSM cases had a significantly higher prevalence of T.. Read More»

Genet. Mol. Res. 11(2):
2012.May.9.2
DOI:
10.4238/2012.May.9.2
Human Genetics   Research Article

Association between GSTM1, GSTT1, and GSTP1 polymorphisms and gastric cancer risk, and their interactions with environmental factors

Authors: Z.H. Chen, J.F. Xian and L.P. Luo

Glutathione S-transferase (GST) is an important member of phase II metabolic enzymes; GSTM1, GSTT1, and GSTP1 belong to three subfamilies of the GST enzyme. Polymorphisms in GSTM1, GSTT1, and GSTP1 could affect detoxification processes, and increase individuals’ susceptibility to cancers. We aimed to investigate the asso.. Read More»

Genet. Mol. Res. 16(1):
gmr16018877
DOI:
10.4238/gmr16018877
Human Genetics   Research Article

Effect of ST2825 on the proliferation and apoptosis of human hepatocellular carcinoma cells

Authors: Y. Deng, J. Sun and L.D. Zhang

The purpose of this study was to investigate the effect of ST2825, an inhibitor of myeloid differentiation factor 88 (MyD88), on the proliferation and apoptosis of human hepatocellular carcinoma (HCC) cells as well as the potential mechanism and clinical significance of ST2825 in the treatment of HCC. Immunohistochemical staining with an MyD88 antibody wa.. Read More»

Genet. Mol. Res. 15(1):
gmr.15016826
DOI:
10.4238/gmr.15016826
Human Genetics   Research Article

Comparative study of 13 candidate genes applying multi-reference normalization to detect the expression of different fineness in skin tissues of wool sheep

Authors: Y.Z. Tian, T. Usman, K.C. Tian, J. Di, X.X. Huang, X.M. Xu, H. Tulafu, W.W. Wu, X.F. Fu, Y. Bai, M. Tuerxun and A. Maimaiti

Fiber diameter is a useful indicator of wool traits and it is the main determinant of wool quality and value. A comparative study was conducted to analyze the abundance and expression of 13 candidate genes using expression profile microarray analysis and to identify novel molecular markers associated with wool traits to provid.. Read More»

Genet. Mol. Res. 16(1):
gmr16018905
DOI:
10.4238/gmr16018905
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

Frequency of alterations in the MEFV gene and clinical signs in familial Mediterranean fever in Central Anatolia, Turkey

Authors: G.G. Ceylan, C. Ceylan and E. Ozturk

Familial Mediterranean fever is a recessive autoinflammatory disease that is frequent in Armenians, Jews, Arabs, and Turks. The MEFV gene is responsible for this disease. We looked for MEFV gene variations (polymorphism and mutations) in a population that resides in Central Anatolia, Turkey. DNA was extracted from peripheral b.. Read More»

Genet. Mol. Res. 11(2):
2012.May.7.4
DOI:
10.4238/2012.May.7.4