BackgroundColorectal cancer (CRC) is the third most common malignant tumor in the world. The morbidity and mortality rates in Western countries have decreased, but they are still on the rise in China. C10orf90 is associated with a variety of cancers, but the correlation between C10orf90 and CRC is not yet known.MethodsA total of 1,339 subjects were randomly enrolled in our study. After extracting their DNA, three single-nucleotide polymorphisms (SNPs) of C10orf90 were genotyped to analyze the potential relationship between these variants and CRC risk. PLINK software packages (version 1.07) were used to evaluate multiple genetic models by calculating the odds ratio (OR) and 95% confidence interval (95% CI). The best SNP–SNP interaction model...
In a genome-wide association study to identify loci associated with colorectal cancer (CRC) risk, w...
Dept. of Public Health/박사Background and purpose: Colorectal cancer (CRC) is a complex disease influe...
The common single-nucleotide polymorphism (SNP) rs3802842 at 11q23.1 has recently been reported to b...
BackgroundColorectal cancer (CRC) is the third most common malignant tumor in the world. The morbidi...
BackgroundColorectal cancer (CRC) is the third most common malignant tumor in the world. The morbidi...
Purpose: Functional variants in the peroxisome proliferator-activated receptor gamma (PPARG) and PPA...
Objective To evaluate the relationship between the rs10795668 single nucleotide polymorphism (SNP) a...
Context: The incidence of colorectal cancer has significantly increased in Iran during the last deca...
To identify common variants influencing colorectal cancer (CRC) risk, we performed a meta-analysis o...
Objective: Recent genome-wide association studies of colorectal cancer (CRC) have identified rs69832...
Ke Xu,1 Hong Dai,2 Shaolong Wang,1 Jie Zhang,1 Tao Liu1 1Department of Oncology, The First Affiliat...
OBJECTIVE: Genome-wide association studies have identified a large number of single nucleotide polym...
To identify new genetic factors for colorectal cancer (CRC), we conducted a genome-wide association ...
Background: X-ray cross-complementing group 1 (XRCC1) polymorphisms affect DNA repair capacity and m...
BACKGROUND: A common single nucleotide polymorphism (SNP), rs10795668, located at 10p14, was first i...
In a genome-wide association study to identify loci associated with colorectal cancer (CRC) risk, w...
Dept. of Public Health/박사Background and purpose: Colorectal cancer (CRC) is a complex disease influe...
The common single-nucleotide polymorphism (SNP) rs3802842 at 11q23.1 has recently been reported to b...
BackgroundColorectal cancer (CRC) is the third most common malignant tumor in the world. The morbidi...
BackgroundColorectal cancer (CRC) is the third most common malignant tumor in the world. The morbidi...
Purpose: Functional variants in the peroxisome proliferator-activated receptor gamma (PPARG) and PPA...
Objective To evaluate the relationship between the rs10795668 single nucleotide polymorphism (SNP) a...
Context: The incidence of colorectal cancer has significantly increased in Iran during the last deca...
To identify common variants influencing colorectal cancer (CRC) risk, we performed a meta-analysis o...
Objective: Recent genome-wide association studies of colorectal cancer (CRC) have identified rs69832...
Ke Xu,1 Hong Dai,2 Shaolong Wang,1 Jie Zhang,1 Tao Liu1 1Department of Oncology, The First Affiliat...
OBJECTIVE: Genome-wide association studies have identified a large number of single nucleotide polym...
To identify new genetic factors for colorectal cancer (CRC), we conducted a genome-wide association ...
Background: X-ray cross-complementing group 1 (XRCC1) polymorphisms affect DNA repair capacity and m...
BACKGROUND: A common single nucleotide polymorphism (SNP), rs10795668, located at 10p14, was first i...
In a genome-wide association study to identify loci associated with colorectal cancer (CRC) risk, w...
Dept. of Public Health/박사Background and purpose: Colorectal cancer (CRC) is a complex disease influe...
The common single-nucleotide polymorphism (SNP) rs3802842 at 11q23.1 has recently been reported to b...