ArticleInfection and drug resistance2021
Design of Rapid Detection System for Five Major Carbapenemase Families (
Article in Infection and drug resistance, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 14 citations in OpenAlex.
- Molecular Insights into Carbapenem Resistance inInternational journal of molecular sciences · 2026Review
- Thermal optimized PCR coupled to CRISPR-Cas12a for rapid detection of blaOXA-1 resistance gene.PloS one · 2026Article
- PathCrisp: an innovative molecular diagnostic tool for early detection of NDM-resistant infections.Scientific reports · 2025Article
- Rapid culture-independent loop-mediated isothermal amplification detection of antimicrobial resistance markers from environmental water samples.Microbial biotechnology · 2023Article
- VIDIIA Hunter diagnostic platform: a low-cost, smartphone connected, artificial intelligence-assisted COVID-19 rapid diagnostics approved for medical use in the UK.Frontiers in molecular biosciences · 2023Article
- Development of a novel loop-mediated isothermal amplification assay for ß-lactamase gene identification using clinical isolates of Gram-negative bacteria.Frontiers in cellular and infection microbiology · 2022Article
- Detection of carbapenemase-producing Enterobacterales by means of matrix-assisted laser desorption ionization time-of-flight mass spectrometry with ertapenem susceptibility-testing disks as source of carbapenem substrate.Frontiers in microbiology · 2022Article
- Development of Loop-Mediated Isothermal Amplification Rapid Diagnostic Assays for the Detection ofFrontiers in molecular biosciences · 2021Article
Corrections and comments
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeCarbapenemase-producing MATERIALS AND
methodsFive sets of LAMP primers were designed, each of which can, respectively, amplify all the carbapenemase subtypes described in this work. Twenty whole genome sequencing-verified-"standard strains", including 1
resultsWith the lowest detection limit of 10 colony forming units (CFU) per reaction for LAMP and 10
conclusionTherefore, LAMP could be used for rapid identification of the five major carbapenemase gene families in routine clinical laboratories.
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Registered trials
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