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Association of a Genetic Variation in a miR-191 Binding Site in MDM4 with Risk of Esophageal Squamou
ISSN号:1932-6203
期刊名称:PLos One
时间:2013.5.28
页码:-
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:
Lu, Chao|Li, Helou|Yuan, Qipeng|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,
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
Association of functional FEN1 genetic variants and haplotypes and breast cancer risk
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