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

Detection of mutations by fill-in ligation reaction with enzyme-linked immunosorbent assay for rapid medical diagnosis.

Bioscience, biotechnology, and biochemistry - 1 Jan 2014

Tang Yi-Tong, Xiao Na, Li Zhi-Shan, Zou Jiu-Ming, Cao Rui, Zhao Xue-Hong, Shao Jin-Hui

Abstract excerpt

Several approaches for parallel genotyping have been developed with increasingly available information on DNA variation. However, these methods require either complex laboratory procedures or expensive instrumentation. None of these procedures is readily performed in local clinical laboratories. In this study, we developed a flexible genotyping method involving fill-in ligation reaction with enzyme-linked...

Read the complete abstract on PubMed

Topics

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

Share to Enzyme-Linked Immunosorbent Assay
Share to ErbB Receptors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gefitinib

Share to Genotyping Techniques

Share to Lung Neoplasms

Share to Molecular Diagnostic Techniques

Share to Plasmids

Share to Quinazolines

Source

Identifiers

PMID: 25036125
DOI: 10.1080/09168451.2014.921555

Genes

EGFR

Variants

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

Detection of mutations by fill-in ligation reaction with enzyme-linked immunosorbent assay for rapid medical diagnosis.PMID 25036125Read ↗

Identification of single-nucleotide polymorphisms by the oligonucleotide ligation reaction: a DNA biosensor for simultaneous visual detection of both alleles.Semantic proximity Read ↗

Genotyping by ligation assays.Semantic proximity Read ↗

Single nucleotide polymorphism genotyping and point mutation detection by ligation on microarrays.Semantic proximity Read ↗

Advances in ligase chain reaction and ligation-based amplifications for genotyping assays: Detection and applications.Semantic proximity Read ↗

Highly multiplex and sensitive SNP genotyping method using a three-color fluorescence-labeled ligase detection reaction coupled with conformation-sensitive CE.Semantic proximity Read ↗

Controllable Mismatched Ligation for Bioluminescence Screening of Known and Unknown Mutations.Semantic proximity Read ↗

Improvement of limit of detection in primer extension-based multiplexed mutation assay using capillary electrophoresis.Semantic proximity Read ↗

Enrichment of low-abundance gene mutation by a combined polymerase and ligase chain reaction.Semantic proximity Read ↗

A multiplex single nucleotide polymorphism genotyping method using ligase-based mismatch discrimination and CE-SSCP.Semantic proximity Read ↗

A mass spectrometry-based multiplex SNP genotyping by utilizing allele-specific ligation and strand displacement amplification.Semantic proximity Read ↗

Dry-reagent disposable biosensor for visual genotyping of single nucleotide polymorphisms by oligonucleotide ligation reaction: application to pharmacogenetic analysis.Semantic proximity Read ↗

Genotyping of single nucleotide polymorphisms by primer extension reaction and a dual-analyte bio/chemiluminometric assay.Semantic proximity Read ↗

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