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

DNA fingerprinting of Candida rugosa via repetitive sequence-based PCR.

Journal of clinical microbiology - 1 Jul 1996

Redkar R J, Dubé M P, McCleskey F K, Rinaldi M G, Del Vecchio V G

Abstract excerpt

A repetitive sequence-based PCR (rep-PCR) technique was developed to characterize the genotypic relatedness among Candida rugosa isolates. Two repetitive sequences, viz., Care-2 and Com29 from Candida albicans, were used to design primers Ca-21, Ca-22, and Com-21, respectively. When used alone or in combination, these primers generated discriminatory fingerprints by amplifying the adjacent variable regions of the...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to DNA, Fungal
Share to DNA Primers

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

Share to Genotype

Share to Molecular Sequence Data

Share to Polymerase Chain Reaction

Share to Repetitive Sequences, Nucleic Acid

Share to Sensitivity and Specificity

Source

Open in PubMed Open full text

Identifiers

PMID: 8784568
DOI: 10.1128/JCM.34.7.1677-1681.1996
PMCID: PMC229093

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

DNA fingerprinting of Candida rugosa via repetitive sequence-based PCR.PMID 8784568Read ↗

Evaluation of the DiversiLab® automated repetitive sequence-based PCR system for the characterization of Candida albicans and Candida glabrata isolates.Semantic proximity Read ↗

Comparison of pulsed-field gel electrophoresis and three rep-PCR methods for evaluating the genetic relatedness of Stenotrophomonas maltophilia isolates.Semantic proximity Read ↗

Applications of the rep‐PCR DNA fingerprinting technique to study microbial diversity, ecology and evolutionSemantic proximity Read ↗

Species identification and strain differentiation of clinical Candida isolates using the DiversiLab system of automated repetitive sequence-based PCRSemantic proximity Read ↗

Identification to the Species Level and Differentiation between Strains of Aspergillus Clinical Isolates by Automated Repetitive-Sequence-Based PCRSemantic proximity Read ↗

Polymerase chain reaction fingerprinting in fungi using single primers specific to minisatellites and simple repetitive DNA sequences: strain variation in Cryptococcus neoformans.Semantic proximity Read ↗

Computer-assisted methods for assessing strain relatedness in Candida albicans by fingerprinting with the moderately repetitive sequence Ca3.Semantic proximity Read ↗

Genotype analysis of Candida albicans isolates obtained from different body locations of patients with superficial candidiasis using PCRs targeting 25S rDNA and ALT repeat sequences of the RPS.Semantic proximity Read ↗

Evaluation of repetitive sequence PCR and PCR-mass spectrometry for the identification of clinically relevantCandidaspeciesSemantic proximity Read ↗

Comparison of four molecular typing methods to assess genetic relatedness of Candida albicans clinical isolates in Taiwan.Semantic proximity Read ↗

Repetitive-Sequence-PCR-Based DNA Fingerprinting Using the DiversiLab System for Identification of Commonly Encountered DermatophytesSemantic proximity Read ↗

Genotyping of Candida albicans on the basis of polymorphisms of ALT repeats in the repetitive sequence (RPS).Semantic proximity Read ↗

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