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

Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease.

Clinical and experimental immunology - 1 Oct 2010

Colobran R, Pedrosa E, Carretero-Iglesia L, Juan M

Abstract excerpt

Genome copy number changes (copy number variations: CNVs) include inherited, de novo and somatically acquired deviations from a diploid state within a particular chromosomal segment. CNVs are frequent in higher eukaryotes and associated with a substantial portion of inherited and acquired risk for various human diseases. CNVs are distributed widely in the genomes of apparently healthy individuals and thus...

Read the complete abstract on PubMed

Topics

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

Share to Chemokine CCL3
Share to Chemokine CCL4
Share to Gene Dosage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Profiling

Share to Genetic Variation

Share to Genome, Human

Share to Multigene Family

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 20659124
DOI: 10.1111/j.1365-2249.2010.04224.x
PMCID: PMC2990928

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease.PMID 20659124Read ↗

Population structure in copy number variation and SNPs in the CCL4L chemokine gene.Semantic proximity Read ↗

HIV-1/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5.Semantic proximity Read ↗

Gene copy number regulates the production of the human chemokine CCL3-L1Semantic proximity Read ↗

Lower copy numbers of the chemokine CCL3L1 gene in patients with chronic hepatitis C.Semantic proximity Read ↗

Population-wide copy number variation calling using variant call format files from 6,898 individualsSemantic proximity Read ↗

Copy number variation: new insights in genome diversity.Semantic proximity Read ↗

Copy number variation in autoimmunity--importance hidden in complexity?Semantic proximity Read ↗

CCL3L1 copy number variation and susceptibility to HIV-1 infection: a meta-analysis.Semantic proximity Read ↗

Human copy number variation and complex genetic disease.Semantic proximity Read ↗

[Copy-number variation: a new pattern of structural diversity in genome].Semantic proximity Read ↗

Copy number variants, diseases and gene expression.Semantic proximity Read ↗

An MLPA-based approach for high-resolution genotyping of disease-related multi-allelic CNVs.Semantic proximity Read ↗

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