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 streptomycin and quinolone resistance in Mycobacterium tuberculosis by a low-density DNA array.

Tuberculosis (Edinburgh, Scotland) - 1 Sept 2013

Moure Raquel, Tudó Griselda, Medina Rebeca, Vicente Eva, Caldito José María, Codina Maria Gemma, Coll Pere, Español Montserrat, Gonzalez-Martin Julian, Rey-Jurado Emma, Salvadó Margarita, Tórtola Maria Teresa, Alcaide Fernando

Abstract excerpt

In cases of multidrug-resistant tuberculosis, it is crucial to rule out resistance to second-line antituberculous (anti-TB) agents. In the present study, a low-cost low-density DNA array including four genetic regions (rrs 530 loop, rrs 1400, rpsL and gyrA) was designed for the rapid detection of the most important mutations related to anti-TB injectable drugs (mainly streptomycin) and fluoroquinolone resistance...

Read the complete abstract on PubMed

Topics

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

Share to Antitubercular Agents
Share to Drug Resistance, Multiple, Bacterial

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

Share to Fluoroquinolones

Share to Microbial Sensitivity Tests

Share to Mycobacterium tuberculosis

Share to Oligonucleotide Array Sequence Analysis

Share to Streptomycin

Share to Tuberculosis, Multidrug-Resistant

Source

Identifiers

PMID: 23906937
DOI: 10.1016/j.tube.2013.07.001

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 streptomycin and quinolone resistance in Mycobacterium tuberculosis by a low-density DNA array.PMID 23906937Read ↗

Simultaneous drug resistance detection and genotyping of Mycobacterium tuberculosis using a low-density hydrogel microarray.Semantic proximity Read ↗

Genotypic assessment of drug-resistant tuberculosis in Baghdad and other Iraqi provinces using low-cost and low-density DNA microarrays.Semantic proximity Read ↗

Detection of second-line drug resistance in Mycobacterium tuberculosis using oligonucleotide microarrays.Semantic proximity Read ↗

Rapid detection of specific gene mutations associated with isoniazid or rifampicin resistance in Mycobacterium tuberculosis clinical isolates using non-fluorescent low-density DNA microarrays.Semantic proximity Read ↗

Detection of mutations in Mycobacterium tuberculosis genome determining resistance to fluoroquinolones by hybridization on biological microchips.Semantic proximity Read ↗

Use of a high-density DNA probe array for detecting mutations involved in rifampicin resistance in Mycobacterium tuberculosis.Semantic proximity Read ↗

Multicenter Evaluation of Genechip for Detection of Multidrug-Resistant Mycobacterium tuberculosisSemantic proximity Read ↗

Rapid detection of resistance in Mycobacterium tuberculosis: a review discussing molecular approaches.Semantic proximity Read ↗

Drug-susceptibility testing in TB: current status and future prospectsSemantic proximity Read ↗

Proficient Detection of Multi-Drug-Resistant Mycobacterium tuberculosis by Padlock Probes and Lateral Flow Nucleic Acid Biosensors.Semantic proximity Read ↗

A minimally instrumented method for the detection of rifampicin resistance-causing mutations in Mycobacterium tuberculosis utilizing lateral flow readout.Semantic proximity Read ↗

Rapid Molecular Detection of Multidrug-Resistant Tuberculosis by PCR-Nucleic Acid Lateral Flow Immunoassay.Semantic proximity Read ↗

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