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

ARLTS1, MDM2 and RAD51 gene variations are associated with familial breast cancer.

Molecular biology reports - 1 Jan 2011

Akisik Elif, Yazici Hulya, Dalay Nejat

Abstract excerpt

Genetic factors that contribute to the risk of breast cancer are largely not known and association studies have revealed several genes with low penetrance risk alleles for breast cancer. Analysis of these genes may provide important information on the risk factors affecting carcinogenesis. Variations in the ARLTS1, RAD51 and MDM2 genes have been associated with increased risk of different cancer types but for...

Read the complete abstract on PubMed

Topics

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

Share to ADP-Ribosylation Factors
Share to Breast Neoplasms
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Gene Frequency

Share to Genetic Association Studies

Share to Proto-Oncogene Proteins c-mdm2

Share to Rad51 Recombinase

Source

Identifiers

PMID: 20358297
DOI: 10.1007/s11033-010-0113-3

Genes

MDM2
RAD51

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

ARLTS1, MDM2 and RAD51 gene variations are associated with familial breast cancer.PMID 20358297Read ↗

Polymorphism of DNA repair genes in breast cancerSemantic proximity Read ↗

BLM and RAD51 genes polymorphism and susceptibility to breast cancer.Semantic proximity Read ↗

Variants in DNA double-strand break repair genes and breast cancer susceptibility.Semantic proximity Read ↗

RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study.Semantic proximity Read ↗

DNA-repair genetic polymorphisms and risk of breast cancer in Cyprus.Semantic proximity Read ↗

DNA repair gene polymorphisms and susceptibility to familial breast cancer in a group of patients from Campinas, Brazil.Semantic proximity Read ↗

Polymorphisms in cancer susceptibility genes XRCC1, RAD51 and TP53 and the risk of breast cancer in Serbian women.Semantic proximity Read ↗

Breast cancer risk and common single nucleotide polymorphisms in homologous recombination DNA repair pathway genes XRCC2, XRCC3, NBS1 and RAD51.Semantic proximity Read ↗

RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability.Semantic proximity Read ↗

Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families.Semantic proximity Read ↗

Variation in the RAD51 gene and familial breast cancer.Semantic proximity Read ↗

Canine mammary tumor risk is associated with polymorphisms in RAD51 and STK11 genes.Semantic proximity Read ↗

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