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

PALB2 mutations in German and Russian patients with bilateral breast cancer.

Breast cancer research and treatment - 1 Apr 2011

Bogdanova Natalia, Sokolenko Anna P, Iyevleva Aglaya G, Abysheva Svetlana N, Blaut Magda, Bremer Michael, Christiansen Hans, Rave-Fränk Margret, Dörk Thilo, Imyanitov Evgeny N

Abstract excerpt

Since germline mutations in the PALB2 (Partner and Localizer of BRCA2) gene have been identified as breast cancer (BC) susceptibility alleles, the geographical spread and risks associated with PALB2 mutations are subject of intense investigation. Patients with bilateral breast cancer constitute a...

Read the complete abstract on PubMed

Topics

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

Share to Codon, Nonsense
Share to Fanconi Anemia Complementation Group N Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Frameshift Mutation

Share to Germ-Line Mutation

Share to Germany

Share to Mutation, Missense

Share to Russia

Share to Tumor Suppressor Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 21165770
DOI: 10.1007/s10549-010-1290-4
PMCID: PMC3291835

Genes

PALB2
BRCA2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21165770-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PALB2 mutations in German and Russian patients with bilateral breast cancer.PMID 21165770Read ↗

Spectrum of PALB2 germline mutations and characteristics of PALB2-related breast cancer: Screening of 16,501 unselected patients with breast cancer and 5890 controls by next-generation sequencing.Semantic proximity Read ↗

Mutation analysis of PALB2 gene in French breast cancer families.Semantic proximity Read ↗

Germline mutations of PALB2 gene in a sequential series of Chinese patients with breast cancer.Semantic proximity Read ↗

Rare germline mutations in PALB2 and breast cancer risk: a population-based study.Semantic proximity Read ↗

Prevalence of PALB2 mutations in breast cancer patients in multi-ethnic Asian population in Malaysia and Singapore.Semantic proximity Read ↗

Frequency and molecular characteristics of PALB2-associated cancers in Russian patients.Semantic proximity Read ↗

Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe.Semantic proximity Read ↗

Frequency of bilateral prophylactic and contra-lateral risk-reducing mastectomies in women with germline PALB2 variants.Semantic proximity Read ↗

PALB2 germline mutations in a large cohort of Middle Eastern breast-ovarian cancer patients.Semantic proximity Read ↗

Role of PALB2 Polymorphisms with Regard to Susceptibility to Female Breast Cancer Risk in the Chinese Population.Semantic proximity Read ↗

Molecular analysis of PALB2-associated breast cancers.Semantic proximity Read ↗

The PALB2 gene is a strong candidate for clinical testing in BRCA1- and BRCA2-negative hereditary breast cancer.Semantic proximity Read ↗

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