Research Article

Related GMR Articles

Colorectal cancer; Gastric cancer; Single nucleotide polymorphism; susceptibility

Evidence suggests that some genetic variants are risk factors for both colorectal cancer (CRC) and gastric cancer (GC). Thus, we selected 12 reported single nucleotide polymorphisms (SNPs) from genome-wide association studies of CRC and conducted this case-control study to assess the associations between these SNPs and the risk for GC in a southern Chinese population. All SNPs were ... more

C.P. Zhou; H.Z. Pan; F.X. Li; N.Y. Hu; M. Li; X.X. Yang
Meat quality traits; MSTN gene; Rabbits; Single nucleotide polymorphism

We analyzed meat samples of nine pure lines of rabbit and its 37 hybrid combinations by sequencing and single-strand conformation polymorphism techniques to explore genetic polymorphisms of all the three exon regions and part of the 5'-regulatory region of the myostatin (MSTN) gene. Thus, we detected a single nucleotide mutation (T→C) on the 476 locus of the 5'-regulatory region ... more

X.B. Qiao; K.Y. Xu; B. Li; X. Luan; T. Xia; X.Z. Fan
BMP-2; COL6A1; Genetic association; Ossification of the posterior longitudinal ligament; Single nucleotide polymorphism

COL6A1 and BMP-2 genes have been implicated in ossification of the posterior longitudinal ligament (OPLL) susceptibility in Japanese and Chinese Han populations. However, no study has yet investigated the DNA of unaffected family members of patients with OPLL. This study investigated differences in genetic polymorphisms of BMP-2 and COL6A1 between Korean patients with ... more

K.H. Kim; S.U. Kuh; J.Y. Park; S.J. Lee; H.S. Park; D.K. Chin; K.S. Kim; Y.E. Cho
Apolipoprotein E; Chinese Hui population; Essential hypertension; Single nucleotide polymorphism

In the present study, the correlation of polymorphisms of the apolipoprotein E (apoE) gene with the susceptibility of essential hypertension (EH) was investigated. Single nucleotide polymorphisms of the apoE gene at the -491 A>T, +969 C>G, and +2836 G>A sites were determined in 221 non-EH individuals and 109 subjects with EH of Chinese Hui ethnicity using ... more

Y. Yang; J.R. Xu; X.M. Liu; J. Zhou; B. Yang; M. Li; Y.J. Wang
CYP2C9; Genotyping; Meloxicam; Single nucleotide polymorphism

The aim of this study was to investigate the effect of the CYP2C9*3 (CYP2C9 1075 A>C) polymorphism on meloxicam pharmacokinetics in a Chinese population. Twenty-four healthy volunteers were enrolled in this study. The pyrosequencing technique was used to identify polymorphisms of CYP2C9. The concentration of meloxicam in plasma was determined by a high-performance liquid chromatography ... more

M. Zhang; Y. Yang; G. Zhao; X. Di; L. Xu; N. Jiang; J. Xu; X. Xu
Hepatocellular carcinoma; Molecular marker; Single nucleotide polymorphism; susceptibility; XRCC1 gene

The human X-ray repair cross-complementing protein 1 (XRCC1) gene is a potentially gene determining hepatocellular carcinoma (HCC) susceptibility. The purpose of this study was to evaluate the association between XRCC1 and susceptibility to HCC. The association of XRCC1 polymorphisms with HCC susceptibility was investigated in 460 HCC patients and 463 controls ... more

X.F. Li; Y.X. Chen; W.W. Ye; X.F. Tao; J.H. Zhu; S. Wu; L.Q. Lou
Neovascular age-related macular degeneration; Polypoidal choroidal vasculopathy; Single nucleotide polymorphism; TLR3

Toll-like receptor 3 (TLR3) variants in mainland northern Chinese patients with polypoidal choroidal vasculopathy (PCV) and neovascular age-related macular degeneration (nAMD) were investigated. The complete genes of TLR3, including all exons and the promoter region, were assessed using direct sequencing technology of 284 unrelated mainland northern Chinese individuals: 96 nAMD patients, ... more

Y. Cheng; M.W. Li; H.P. Li; W.T. Zeng; P. Zhou; L.Z. Huang; X.X. Li; Y.Y. Sun
FGD1; Intellectual developmental disorders; Restriction fragment length polymorphism; Single nucleotide polymorphism; Single-strand conformation polymorphism

FGD1 encoding a guanine nucleotide exchange factor, specifically activates Rho GTPase cell division cycle 42 (Cdc42). Dysfunction of FGD1 causes Aarskog-Scott syndrome (MIM #305400), an X-linked disorder that may affect bone and intellectual development. However, the relationship between FGD1 and intellectual developmental disorders (IDD) remains unclear. The purpose of this study was to ... more

J.L. Li; Y.J. Li; K.J. Zhang; L. Lan; J.G. Shi; X. Yang; M.J. Zhang; F.C. Zhang; X.C. Gao
Hepatocellular carcinoma; Meta-analysis; Single nucleotide polymorphism; XRCC1-Arg280His

Hepatocellular carcinoma (HCC) is one of the most life-threatening malignancies worldwide. Defects in DNA repair genes may increase the risk of HCC. X-ray cross-complementing group 1 gene (XRCC1) is a major DNA repair gene involved in base excision re­pair. Recently, several studies have indicated that an association exists between XRCC1 polymorphism and HCC, ... more

W. Xu; S. Liu; L. Li; Z.Y. Shen; Y.L. Wu
Cancer; Cytosolic serine hydroxymethyltransferase C1420T; Meta-analysis; Single nucleotide polymorphism

Published data regarding the association between the cytosolic serine hydroxymethyltransferase (SHMT1) C1420T (Leu474Phe) polymorphism and solid tumor risk have shown inconclusive results. To derive a more precise estimation of the relationship, we performed a meta-analysis of 23 published studies that included 14,409 cancer cases and 16,996 controls. A comprehensive search was ... more

T.T. Zhao; L.L. Shen; X.L. Zhang; D.Y. Gu; Q. Zhang; X.Y. Huo; C.J. Tang; J.F. Chen