نتایج جستجو برای: high risk genotypes
تعداد نتایج: 2801279 فیلتر نتایج به سال:
Although Romania has one of the highest incidence of cervical cancer in Europe (30 new cases/100 000 women), little is known about the distribution of the human papillomaviruses (HPV) genotypes in this population. We seek to determine the distribution of HPV genotypes in women with normal and abnormal cervical cytology. We analyzed 460 cervical cytology specimens from women who self-referred to...
A case-control study was conducted for analyzing the genetic polymorphisms of phase II metabolic enzymes in 97 patients with lung cancer and 197 healthy subjects from Han ethnic group of Hunan Province located in Central South China. The results showed that the frequencies of glutathione S-transferase (GST) M1-null (GSTM1-) or GSTT1-null (GSTT1-) genotype alone, or combined form of both in lung...
To examine the joint effect of multiple loci on disease risk, many case-control association studies used "gene-dose analyses." However, some researchers defined high-risk genotypes (or alleles) as those that have higher genotypic (allelic) frequencies in the case group compared with the control group in the study. This will lead to the total number of the "high-risk" genotypes (alleles) tending...
The role of the familial breast cancer susceptibility genes, BRCA1 and BRCA2, in the homologous recombination pathway for DNA double-strand break (DSB) repair suggests that the mechanisms involved in DNA DSB repair are of particular etiological importance during breast tumorigenesis. However, there is currently no evidence for an association between breast cancer and the other DSB repair pathwa...
Abstract Background Ischemic stroke (IS) is the most leading cause of morbidity and mortality worldwide. Micro RNA (miRNA) genetic variants have been identified as a part IS non-modifiable risk markers. This study aims to identify possible association rs2910164 C > G pre-miRNA-146a rs3746444 A pre-miRNA-499 with increased risk. C-reactive protein (CRP) was studied one mediators disturbance i...
In order to evaluate genetic diversity and determine genetic relationship of 64 Kabuli chickpea genotypes under late season drought stress, an experimental design was carried out in a simple lattice design (8×8) in 2011 on the research field of college of Agriculture and natural resource of Tehran University. Based on factor analysis, four factors were selected that in total 81 percent of the t...
p21 plays an important role in modulating cell cycle control, inducing apoptosis, and inhibiting cell growth, subsequently affecting cancer risk. We investigated the association between two putatively functional single-nucleotide polymorphisms (SNPs) of p21 (p21 C98A and p21 C70T) among 1282 patients diagnosed with incident squamous cell carcinoma of the head and neck (SCCHN) and risk of second...
conclusions considering the high rates of relapse, more attention should be paid to reasons for relapse. it seems necessary that both clinical and psychological approaches would be undertaken simultaneously. background relapse prevention is a medical intervention designed for educating cognitive and behavioral skills to avoid continued drug abuse and relapse. objectives this study examined high...
school is the first social institution which affects adolescents' lives, and it determines their opportunities, life quality and behavior. thus, the aim of this study was to determine the relationship between students' bonds with their school and multiple health risk behaviors amongst high school students in kerman city, iran.in this cross-sectional study, high school students of all levels par...
The Runt-related transcription factors (RUNX), mitogen-activated protein kinase (MAPK) 1 and eukaryotic translation initiation factor 4E (eIF4E) are potentially involved in tumorigenesis. We evaluated genetic variation in RUNX1 (40 tagSNPs), RUNX2 (19 tagSNPs), RUNX3 (9 tagSNPs), MAPK1 (6 tagSNPs), eIF4E (3 tagSNPs), eIF4EBP2 (2 tagSNP) and eIF4EBP3 (2 tagSNPs) to determine associations with co...
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