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 DNA abnormalities by arbitrarily primed PCR fingerprinting: allelic losses in chromosome 10q in lung cancers.

Biochemical and biophysical research communications - 9 Oct 1998

Kawakami K, Yasuda J, Shiraishi M, Kayama T, Doi K, Perucho M, Sekiya T

Abstract excerpt

DNA fingerprinting using arbitrarily primed PCR (AP-PCR) is useful for detecting cancer-specific DNA aberrations without targeting any particular genes or knowing any nucleotide sequences in advance. AP-PCR fingerprinting is an efficient method for finding loss of anonymous chromosomal regions in cancers. We analyzed DNA from 44 human non-small cell lung cancers by fingerprinting using a single primer and found a...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Chromosome Aberrations

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosome Mapping

Share to DNA Fingerprinting

Share to DNA, Neoplasm

Share to Lung Neoplasms

Share to Microsatellite Repeats

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 9790923
DOI: 10.1006/bbrc.1998.9418

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Detection of DNA abnormalities by arbitrarily primed PCR fingerprinting: allelic losses in chromosome 10q in lung cancers.PMID 9790923Read ↗

Prognostic value of genomic damage in non-small-cell lung cancer.Semantic proximity Read ↗

Distinct regions of allelic imbalance on chromosome 10q22-q26 in squamous cell carcinomas of the lung.Semantic proximity Read ↗

Association of genetic defects in primary resected lung adenocarcinoma revealed by targeted allelic imbalance analysis.Semantic proximity Read ↗

Southern Blotting of genomic DNA from lung and its tumors. Application to analysis of allele loss on chromosome 11p15.5.Semantic proximity Read ↗

Detection of microsatellite instability in cancers by arbitrarily primed-PCR fingerprinting using a fluorescently labeled primer (FAP-PCR).Semantic proximity Read ↗

Enriched SSCP: a highly sensitive method for the detection of unknown mutations. Application to the molecular diagnosis of lung cancer in sputum samples.Semantic proximity Read ↗

Increased prevalence of K-ras oncogene mutations in lung adenocarcinoma.Semantic proximity Read ↗

Identification of novel deletion regions on chromosome arms 2q and 6p in breast carcinomas by amplotype analysisSemantic proximity Read ↗

Mapping of the pulmonary surfactant SP5 (SFTP2) locus to 8p21 and characterization of a microsatellite repeat marker that shows frequent loss of heterozygosity in human carcinomas.Semantic proximity Read ↗

Association of the NAT1*10 genotype with increased chromosome aberrations and higher lung cancer risk in cigarette smokers.Semantic proximity Read ↗

Molecular alterations at 9q33.1 and polyploidy in asbestos-related lung cancer.Semantic proximity Read ↗

Isolation and characterization of allelic losses and gains in colorectal tumors by arbitrarily primed polymerase chain reaction.Semantic proximity Read ↗

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