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

Loss, mutation and deregulation of L3MBTL4 in breast cancers.

Molecular cancer - 10 Aug 2010

Addou-Klouche Lynda, Adélaïde José, Finetti Pascal, Cervera Nathalie, Ferrari Anthony, Bekhouche Ismahane, Sircoulomb Fabrice, Sotiriou Christos, Viens Patrice, Moulessehoul Soraya, Bertucci François, Birnbaum Daniel, Chaffanet Max

Abstract excerpt

BACKGROUND: Many alterations are involved in mammary oncogenesis, including amplifications of oncogenes and losses of tumor suppressor genes (TSG). Losses may affect almost all chromosome arms and many TSGs remain to be identified. RESULTS: We studied 307 primary breast tumors and 47 breast cance...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Breast Neoplasms
Share to Chromosomes, Human, Pair 11

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Primers

Share to Down-Regulation

Share to Mutation

Share to Nucleic Acid Hybridization

Share to RNA, Messenger

Source

Open in PubMed Open full text

Identifiers

PMID: 20698951
DOI: 10.1186/1476-4598-9-213
PMCID: PMC2933619

Genes

ERBB2
YES1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20698951-2026-09-02.2. 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

Loss, mutation and deregulation of L3MBTL4 in breast cancers.PMID 20698951Read ↗

Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25.Semantic proximity Read ↗

Mapping of a breast cancer tumor suppressor gene locus to a 4-cM interval on chromosome 18q21.Semantic proximity Read ↗

Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes.Semantic proximity Read ↗

Deletion of 17p in cancers: Guilt by (p53) associationSemantic proximity Read ↗

A genome-wide map showing common regions of loss of heterozygosity/allelic imbalance in breast cancer.Semantic proximity Read ↗

Identification of Four Novel Human Genes Amplified and Overexpressed in Breast Carcinoma and Localized to the q11-q21.3 Region of Chromosome 17Semantic proximity Read ↗

Genetic variation in the chromosome 17q23 amplicon and breast cancer risk.Semantic proximity Read ↗

Genomic Markers for Ovarian Cancer at Chromosomes 1, 8 and 17 Revealed by Array CGH AnalysisSemantic proximity Read ↗

A possible tumor suppressor role of the KLF5 transcription factor in human breast cancer.Semantic proximity Read ↗

Correlation of allelic losses and clinicopathological factors in 504 primary breast cancers.Semantic proximity Read ↗

Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients.Semantic proximity Read ↗

Chromosome-breakage genomic instability and chromothripsis in breast cancer.Semantic proximity Read ↗

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