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

No mutations in the XRCC2 gene in BRCA1/2-negative high-risk breast cancer families.

International journal of cancer - 1 Jan 2003

Rodríguez-López Raquel, Osorio Ana, Sánchez-Pulido Luis, De La Hoya Miguel, Barroso Alicia, Caldés Trinidad, Benítez Javier

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to BRCA1 Protein
Share to BRCA2 Protein
Share to Breast Neoplasms
Share to DNA, Neoplasm

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Germ-Line Mutation

Share to Ovarian Neoplasms

Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 12455067
DOI: 10.1002/ijc.10766

Genes

BRCA1
XRCC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No mutations in the XRCC2 gene in BRCA1/2-negative high-risk breast cancer families.PMID 12455067Read ↗

Rare mutations in XRCC2 increase the risk of breast cancer.Semantic proximity Read ↗

Rare variants in XRCC2 as breast cancer susceptibility alleles.Semantic proximity Read ↗

XRCC1 genetic polymorphism and breast cancer risk.Semantic proximity Read ↗

Classification of Missense Variants in XRCC2 by Functional Analysis: Implications for Breast Cancer Association Studies.Semantic proximity Read ↗

No association between BRCA2 N372H and breast cancer risk.Semantic proximity Read ↗

Absence of constitutional H2AX gene mutations in 101 hereditary breast cancer families.Semantic proximity Read ↗

A role for XRCC2 gene polymorphisms in breast cancer risk and survival.Semantic proximity Read ↗

Multiple skin cancers in adults with mutations in the XP-E (DDB2) DNA repair gene.Semantic proximity Read ↗

RAD52 S346X variant reduces breast cancer risk in BRCA2 mutation carriers.Semantic proximity Read ↗

Genetic variations in XRCC2 and XRCC3 are not associated with endometrial cancer risk.Semantic proximity Read ↗

TP53 and XRCC1 polymorphisms and breast cancer prognosis: a case-case study.Semantic proximity Read ↗

Polymorphisms in<i>RAD51, XRCC2</i>, and<i>XRCC3</i>Are Not Related to Breast Cancer RiskSemantic proximity Read ↗

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