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

Survey of polymorphic sequence variation in the immediate 5' region of human DNA repair genes.

Mutation research - 1 Mar 2007

Mohrenweiser Harvey

Abstract excerpt

Systematic screens have revealed extensive DNA sequence variation existing in the human population. Studies of the role of polymorphic genetic variants in explaining the association of family history with risk of common disease have generally focused on variants predicted to disrupt protein structure and activity. Recent studies have identified genetic variation in the level of expression of many genes, variation...

Read the complete abstract on PubMed

Topics

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

Share to 5' Untranslated Regions
Share to Databases, Genetic
Share to DNA Repair

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Genetic Variation

Share to Polymorphism, Genetic

Share to Polymorphism, Single Nucleotide

Share to Regulatory Elements, Transcriptional

Source

Identifiers

PMID: 17161851
DOI: 10.1016/j.mrfmmm.2006.11.008

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

Survey of polymorphic sequence variation in the immediate 5' region of human DNA repair genes.PMID 17161851Read ↗

Searching for functional genetic variants in non-coding DNA.Semantic proximity Read ↗

Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes.Semantic proximity Read ↗

Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes.Semantic proximity Read ↗

Human DNA repair genesSemantic proximity Read ↗

Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans.Semantic proximity Read ↗

Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.Semantic proximity Read ↗

Single nucleotide polymorphisms in DNA repair genes and putative cancer risk.Semantic proximity Read ↗

A survey of genomic properties for the detection of regulatory polymorphisms.Semantic proximity Read ↗

Cis-regulatory mutations in human disease.Semantic proximity Read ↗

Coding variants in human double-strand break DNA repair genes.Semantic proximity Read ↗

The distribution of SNPs in human gene regulatory regions.Semantic proximity Read ↗

The importance and identification of regulatory polymorphisms and their mechanisms of action.Semantic proximity Read ↗

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