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Association of functional FEN1 genetic variants and haplotypes and breast cancer risk
ISSN号:0378-1119
期刊名称:Gene
时间:2014.3.15
页码:42-45
相关项目:影响转录因子c-Myc结合的功能性遗传变异系统发掘及其与肝癌易感性的关系研究
作者:
Zhou, Changchun|Yuan, Qipeng|Zhou, Liqing|Yang, Ming|
同期刊论文项目
影响转录因子c-Myc结合的功能性遗传变异系统发掘及其与肝癌易感性的关系研究
期刊论文 29
同项目期刊论文
Functional MDM4 rs4245739 genetic variant, alone and in combination with P53 Arg72Pro polymorphism,
Association of a Genetic Variation in a miR-191 Binding Site in MDM4 with Risk of Esophageal Squamou
Functional BCL-2 regulatory genetic variants contribute to susceptibility of esophageal squamous cel
miR-190a inhibits epithelial–mesenchymal transition of hepatoma cells via targeting the long non-cod
Leukocyte telomere length-related rs621559 and rs398652 genetic variants influence risk of HBV-relat
The ALDH7A1 genetic polymorphisms contribute to development of esophageal squamous cell carcinoma.
The interaction of APEX1 variant with polycyclic aromatic hydrocarbons on increasing chromosome dama
A functional BRCA1 coding sequence genetic variant contributes to risk of esophageal squamous cell c
Functional FEN1 genetic variants and haplotypes are associated with glioma risk
Role of EGFR SNPs in survival of advanced lung adenocarcinoma patients treated with Gefitinib
Interleukin-23 receptor genetic variants contribute to susceptibility of multiple cancers
The identification of an ESCC susceptibility SNP rs920778 that regulates the expression of lncRNA HO
Association of a functional RAD52 genetic variant locating in a miRNA binding site with risk of HBV-
Association of the functional BCL-2 rs2279115 genetic variant and small cell lung cancer.
The identification of two regulatory ESCC susceptibility genetic variants in the TERT-CLPTM1L loci.
fMiRNA-192 and miRNA-204 Directly Suppress lncRNA HOTTIP and Interrupt GLS1-Mediated Glutaminolysis
Down-regulation of 5S rRNA by miR-150 and miR-383 enhances c-Myc–rpL11 interaction and inhibits prol
A functional lncRNA HOTAIR genetic variant contributes to gastric cancer susceptibility.
A Regulatory MDM4 Genetic Variant Locating in the Binding Sequence of Multiple MicroRNAs Contributes
Silencing of Long Noncoding RNA MALAT1 by miR-101 and miR-217 Inhibits Proliferation, Migration, and
The functional TP53 rs1042522 and MDM4 rs4245739 genetic variants contribute to Non-Hodgkin Lymphoma
A RAD52 genetic variant located in a miRNA binding site is associated with glioma risk in Han Chines
1p34.2 rs621559 and 14q21 rs398652 leukocyte telomere length-related genetic variants contribute to
Identification of an SCLC susceptibility rs7963551 genetic polymorphism in a previously GWAS-identif