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

Polymorphisms in the human DNA repair gene XPF.

Mutation research - 1 Aug 1999

Fan F, Liu C, Tavaré S, Arnheim N

Abstract excerpt

DNA sequence polymorphisms were sought in the coding region and at the exon-intron boundaries of the human XPF gene, which plays a role in nucleotide excision repair. Based on a survey of 38 individuals, we found six single nucleotide polymorphisms, one in the 5' non-coding region of the XPF gene, and five in the 2751 bp coding region. At each site, the frequency of the rarer allele varies from about 0.01 to over...

Read the complete abstract on PubMed

Topics

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

Share to DNA
Share to DNA-Binding Proteins
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Repair

Share to Gene Frequency

Share to Point Mutation

Share to Polymorphism, Genetic

Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 10479728
DOI: 10.1016/s1383-5726(99)00008-4

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

Polymorphisms in the human DNA repair gene XPF.PMID 10479728Read ↗

Association between XPF polymorphisms and cancer risk: a meta-analysis.Semantic proximity Read ↗

XPF -673C>T variation is associated with the susceptibility to breast cancer.Semantic proximity Read ↗

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

Association of XPF Levels and Genetic Polymorphism with Susceptibility to Ischemic Stroke.Semantic proximity Read ↗

Identification of four single nucleotide polymorphisms in DNA repair genes: XPA and XPB (ERCC3) in Polish population.Semantic proximity Read ↗

A novel XPF -357A>C polymorphism predicts risk and recurrence of bladder cancer.Semantic proximity Read ↗

Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein.Semantic proximity Read ↗

Deep intronic founder mutations identified in the ERCC4/XPF gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosum.Semantic proximity Read ↗

Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia.Semantic proximity Read ↗

Genetic polymorphisms of the XPG and XPD nucleotide excision repair genes in sarcoma patients.Semantic proximity Read ↗

Single nucleotide polymorphism analyses of the human proliferating cell nuclear antigen (pCNA) and flap endonuclease (FEN1) genes.Semantic proximity Read ↗

The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms.Semantic proximity Read ↗

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