Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of a functional RAD52 genetic variant locating in a miRNA binding site with risk of HBV-related hepatocellular carcinoma.

Molecular carcinogenesis - 1 Sept 2015

Li Ziqiang, Guo Yuan, Zhou Liqing, Ge Yunxia, Wei Lili, Li Lichao, Zhou Changchun, Wei Jinyu, Yuan Qipeng, Li Jie, Yang Ming

Abstract excerpt

As an important member in homologous recombination repair, RAD52 plays a crucial part in maintaining genomic stability and prevent carcinogenesis. Several cancer susceptibility RAD52 single nucleotide polymorphisms (SNPs) have been identified previously. However, little or nothing has been known about the RAD52 SNPs and their functional significance in hepatitis B viruses (HBV)-related hepatocellular carcinoma...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Binding Sites
Share to Carcinoma, Hepatocellular

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hepatitis B, Chronic

Share to Hepatitis B virus

Share to Liver Neoplasms

Share to MicroRNAs

Share to Rad52 DNA Repair and Recombination Protein

Source

Identifiers

PMID: 24729511
DOI: 10.1002/mc.22156

Genes

RAD52

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of a functional RAD52 genetic variant locating in a miRNA binding site with risk of HBV-related hepatocellular carcinoma.PMID 24729511Read ↗

A RAD52 genetic variant located in a miRNA binding site is associated with glioma risk in Han Chinese.Semantic proximity Read ↗

RAD52 gene polymorphisms are associated with risk of colorectal cancer in a Chinese Han population.Semantic proximity Read ↗

Genetic variation in a hsa-let-7 binding site in RAD52 is associated with breast cancer susceptibility.Semantic proximity Read ↗

Polymorphisms of DNA repair genes in Korean hepatocellular carcinoma patients with chronic hepatitis B: possible implications on survival.Semantic proximity Read ↗

Genetic variants in NER pathway genes predict hepatitis B virus-related hepatocellular carcinoma survivalSemantic proximity Read ↗

A functional variant in the RAD51 3' UTR is associated with survival of hepatocellular carcinoma patients.Semantic proximity Read ↗

Genetic polymorphisms in DNA double-strand break repair genes XRCC5, XRCC6 and susceptibility to hepatocellular carcinoma.Semantic proximity Read ↗

Potentially functional genetic polymorphisms of USP45 and PRFP19 in the NER pathway genes predict HBV-related hepatocellular carcinoma survivalSemantic proximity Read ↗

Association between Single-Nucleotide Polymorphism in MicroRNA Target Site of DDB2 and Risk of Hepatocellular Carcinoma in a Southern Chinese Population.Semantic proximity Read ↗

Replication of genome wide association studies on hepatocellular carcinoma susceptibility loci in a Chinese population.Semantic proximity Read ↗

Identification of a novel heterozygous germline RAD52 missense mutation in a patient with gallbladder carcinoma: A case report.Semantic proximity Read ↗

Genetic variants within microRNA-binding site of RAD51B are associated with risk of cervical cancer in Chinese women.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.