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...
Objective: Recent genome-wide association studies of colorectal cancer (CRC) have identified rs69832...
Genome-wide association studies (GWAS) of colorectal cancer (CRC) have been conducted primarily in E...
Objective To evaluate the relationship between the rs10795668 single nucleotide polymorphism (SNP) a...
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...
Context The incidence of colorectal cancer has significantly increased in Iran during the ...
Colorectal cancer (CRC) is the third most common cancer type in the Western world. Over one million...
Purpose: Functional variants in the peroxisome proliferator-activated receptor gamma (PPARG) and PPA...
Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide, and has a strong herit...
Ke Xu,1 Hong Dai,2 Shaolong Wang,1 Jie Zhang,1 Tao Liu1 1Department of Oncology, The First Affiliat...
Known genetic loci explain only a small proportion of the familial relative risk of colorectal cance...
Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide, and has a strong herit...
<div><h3>Background</h3><p>Colorectal cancer (CRC) is the third common cancer and the fourth leading...
BACKGROUND: A common single nucleotide polymorphism (SNP), rs10795668, located at 10p14, was first i...
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...
Genome-wide association studies (GWAS) of colorectal cancer (CRC) have been conducted primarily in E...
Objective To evaluate the relationship between the rs10795668 single nucleotide polymorphism (SNP) a...
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...
Context The incidence of colorectal cancer has significantly increased in Iran during the ...
Colorectal cancer (CRC) is the third most common cancer type in the Western world. Over one million...
Purpose: Functional variants in the peroxisome proliferator-activated receptor gamma (PPARG) and PPA...
Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide, and has a strong herit...
Ke Xu,1 Hong Dai,2 Shaolong Wang,1 Jie Zhang,1 Tao Liu1 1Department of Oncology, The First Affiliat...
Known genetic loci explain only a small proportion of the familial relative risk of colorectal cance...
Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide, and has a strong herit...
<div><h3>Background</h3><p>Colorectal cancer (CRC) is the third common cancer and the fourth leading...
BACKGROUND: A common single nucleotide polymorphism (SNP), rs10795668, located at 10p14, was first i...
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...
Genome-wide association studies (GWAS) of colorectal cancer (CRC) have been conducted primarily in E...
Objective To evaluate the relationship between the rs10795668 single nucleotide polymorphism (SNP) a...