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

Electronic microarray technique for detection of nine base substitutions including single-nucleotide polymorphisms in the human OGG1 gene.

Clinical chemistry - 1 Aug 2004

Gong Zhilong, Teixeira Christine, Xing James Z, Yokota Jun, Kohno Takashi, Gabos Stephan, Le X Chris, Li Xing-Fang

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Cell Line, Tumor
Share to DNA Glycosylases
Share to Double-Blind Method
Share to OGG1 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Oligonucleotide Array Sequence Analysis

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 15277357
DOI: 10.1373/clinchem.2004.034009

Genes

OGG1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Electronic microarray technique for detection of nine base substitutions including single-nucleotide polymorphisms in the human OGG1 gene.PMID 15277357Read ↗

Improvement of low-density microelectronic array technology to characterize 14 mutations/single-nucleotide polymorphisms from several human genes on a large scale.Semantic proximity Read ↗

Rapid detection of common Chinese glucose-6-phosphate dehydrogenase (G6PD) mutations by microarray-based assay.Semantic proximity Read ↗

Oligonucleotide microarrays with high discriminating power for the detection of single nucleotide variations in the p53 gene.Semantic proximity Read ↗

Rapid screening of 12 common mutations in Turkish GSD 1a patients using electronic DNA microarray.Semantic proximity Read ↗

Hydrogel microarray for detection of polymorphisms in the UGT1A1, DPYD, GSTP1 and ABCB1 genes.Semantic proximity Read ↗

A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genome.Semantic proximity Read ↗

Time-saving multiplex detection of single nucleotide polymorphisms by ultrasensitive DNA microarray.Semantic proximity Read ↗

Rapid genotype method to distinguish frequent and/or functional polymorphisms in human N-acetyltransferase-1.Semantic proximity Read ↗

Electrochemical DNA array for simultaneous genotyping of single-nucleotide polymorphisms associated with the therapeutic effect of interferon.Semantic proximity Read ↗

High-throughput single-base mismatch detection for genotyping of UDP-glucuronosyltransferase (UGT1A1) with probe capture assay coupled with modified allele-specific primer extension reaction (MASPER).Semantic proximity Read ↗

Microarray with LNA-probes for genotyping of polymorphic variants of Gilbert's syndrome gene UGT1A1(TA)n.Semantic proximity Read ↗

OGG1 gene sequence variation in head and neck cancer patients in Pakistan.Semantic proximity Read ↗

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