Research Article

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09/21/2015
Adiponectin; Coronary heart disease; Inflammatory factor; Ischemia factor; Osteoprotegerin

This study aimed to explore serum adiponectin and osteoprotegerin levels in patients with coronary heart disease (CHD) and their correlation with inflammatory and ischemia factors. From September 2010 to Augest 2010, 347 CHD patients were enrolled for a retrospective analysis. Serum lipoprotein phospholipase A2 (Lp-PLA2), hypersensitive C-reactive protein (hs-CRP), ischemia modified albumin ( ... more

H.L. Zhang; X. Jin
10/28/2015
APOA-I; APOE; Coronary heart disease; HDL-C; High-density lipoprotein cholesterol; Polymorphism

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 of rs4420638 to ... more

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; S.W. Duan
03/28/2016
Coronary heart disease; Gene polymorphism; Methylene tetrahydrofolate reductase; Serum homocysteine levels

The aim of the current study was to explore the correlation between serum homocysteine (HCY) levels and the methylene tetrahydrofolate reductase (MTHFR) gene 677C/T polymorphism and coronary heart disease (CHD). We consecutively enrolled 208 patients with CHD confirmed by CTA or coronary angiography from our hospital. An additional 200 healthy volunteers were enrolled as the control ... more

Y.Y. Chen; B.N. Wang; X.P. Yu; Y.Y. Chen; B.N. Wang; X.P. Yu; Y.Y. Chen; B.N. Wang; X.P. Yu
03/04/2016
Coronary heart disease; N-acetyltransferase-2; Polymerase chain reaction; Polymorphism; Rapid acetylator genotype; Slow acetylator genotype

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 = 41) subgroups. DNA samples ... more

J.D. Sun; H. Yuan; H.Q. Hu; H.M. Yu; J.D. Sun; H. Yuan; H.Q. Hu; H.M. Yu
12/28/2015
Apolipoprotein A-V; Apolipoprotein C-III; Coronary heart disease; Polymorphism; Single nucleotide polymorphisms; Triglycerides

The aim of this study was to investigate correlations between apolipoprotein A-V (APOA5) -1131T>C and apolipoprotein C-III (APOC3) -455T>C polymorphisms and coronary heart disease (CHD). PubMed, Ovid, Cochrane Library, Embase, China National Knowledge Infrastructure, and Wanfang databases were searched using combinations of keywords relating to these polymorphisms ... more

Y. Sun; R.B. Zhou; D.M. Chen
10/09/2015
Coronary heart disease; Han Chinese population; Matrix metalloproteinase; Polymorphism

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 polymorphisms were associated with CHD in Han Chinese. Our case ... more

C.M. Wang; H.D. Ye; Y.R. Li; Q.X. Hong; L.L. Tang; A.N. Zhou; M.Q. Xu; S.W. Duan
03/11/2016
male; Mutation; Polymerase chain reaction; Steroid-resistant nephrotic syndrome; WT1

Mutations in the Wilms’ tumor gene, WT1, can lead to syndromic steroid-resistant nephrotic syndrome and isolated steroid-resistant nephrotic syndrome. WT1 mutations have been identified in the majority of children with Denys-Drash or Frasier syndrome. WT1 mutations have not previously been identified in boys with sporadic isolated steroid-resistant nephrotic ... more

Y. Yang; F. Zhao; X. Tu; Z. Yu; Y. Yang; F. Zhao; X. Tu; Z. Yu
12/02/2016
Asian Continental Ancestry Group; Child; Chromosome Deletion; Chromosomes, Human, Pair 2; Fingers; Heart Defects, Congenital; Hedgehog Proteins; Humans; Karyotype; male; Syndactyly; Waardenburg Syndrome

Reports of terminal and interstitial deletions of the long arm of chromosome 2 are rare in the literature. Here, we present a case report concerning a Chinese boy with a 47,XYY karyotype and a de novo deletion comprising approximately 5 Mb between 2q35 and q36.1, along with syndactyly, type III Waardenburg syndrome, and congenital heart disease. High-resolution chromosome analysis to detect ... more

D. Wang; G.F. Ren; H.Z. Zhang; C.Y. Yi; Z.J. Peng
12/02/2016
Animal Shells; Animals; Bivalvia; Breeding; Evolution, Molecular; Female; Fresh Water; Genetic variation; Genetics, Population; male; Microsatellite Repeats; Phenotype; Phylogeny; Quantitative trait loci

Four Hyriopsis cumingii populations, a breeding population (BP), a cultured population (FP), two wild populations from Poyang Lake (PY) and Dongting Lake (DT), and an H. schlegelii population were collected (JX), and the first filial generations (F1) were bred synchronously. The shell nacre polymorphisms, population genetic diversity, and genetic structures of the F1 of each population were ... more

L.M. Wu; Z.Y. Bai; X.J. Liu; C. Jin; H. Yin; J.L. Li
2016 Dec 19
Animals; Animals, Genetically Modified; Apoptosis Regulatory Proteins; Crosses, Genetic; Drosophila melanogaster; Drosophila Proteins; Gene Expression Regulation, Developmental; Gene Knockdown Techniques; Humans; male; Membrane Proteins; Neurons; Proto-Oncogene Proteins c-bcl-2; Sequence Homology, Amino Acid; Transgenes

Lifeguard is an integral transmembrane protein that modulates FasL-mediated apoptosis by interfering with the activation of caspase 8. It is evolutionarily conserved, with homologues present in plants, nematodes, zebra fish, frog, chicken, mouse, monkey, and human. The Lifeguard homologue in Drosophila, CG3814, contains the Bax inhibitor-1 family motif of unknown function. Downregulation of ... more

P.G. M'Angale; B.E. Staveley

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