Publication:
Loop-mediated isothermal amplification-integrated CRISPR methods for infectious disease diagnosis at point of care

dc.contributor.coauthorYetisen, Ali K.
dc.contributor.departmentDepartment of Mechanical Engineering
dc.contributor.kuauthorYığcı, Defne
dc.contributor.kuauthorAtçeken, Nazente
dc.contributor.kuauthorTaşoğlu, Savaş
dc.contributor.otherDepartment of Mechanical Engineering
dc.contributor.researchcenterN/A
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.researchcenterKU Arçelik Research Center for Creative Industries (KUAR) / KU Arçelik Yaratıcı Endüstriler Uygulama ve Araştırma Merkezi (KUAR)
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.date.accessioned2024-12-29T09:41:07Z
dc.date.issued2023
dc.description.abstractInfectious diseases continue to pose an imminent threat to global public health, leading to high numbers of deaths every year and disproportionately impacting developing countries where access to healthcare is limited. Biological, environmental, and social phenomena, including climate change, globalization, increased population density, and social inequity, contribute to the emergence of novel communicable diseases. Rapid and accurate diagnoses of infectious diseases are essential to preventing the transmission of infectious diseases. Although some commonly used diagnostic technologies provide highly sensitive and specific measurements, limitations including the requirement for complex equipment/infrastructure and refrigeration, the need for trained personnel, long sample processing times, and high cost remain unresolved. To ensure global access to affordable diagnostic methods, loop-mediated isothermal amplification (LAMP) integrated clustered regularly interspaced short palindromic repeat (CRISPR) based pathogen detection has emerged as a promising technology. Here, LAMP-integrated CRISPR-based nucleic acid detection methods are discussed in point-of-care (PoC) pathogen detection platforms, and current limitations and future directions are also identified.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue46
dc.description.openaccessAll Open Access
dc.description.openaccessGold Open Access
dc.description.openaccessGreen Open Access
dc.description.publisherscopeInternational
dc.description.sponsorsS.T. acknowledges the Tubitak 2232 International Fellowship for Outstanding Researchers Award (118C391), Alexander von Humboldt Research Fellowship for Experienced Researchers, Marie Skłodowska-Curie Individual Fellowship (101003361), and Royal Academy Newton- Katip Çelebi Transforming Systems Through Partnership award (120N019) for financial support of this research. Opinions, interpretations, conclusions, and recommendations are those of the author and are not necessarily endorsed by the TÜBITAK. This work was partially supported by the Science Academy’s Young Scientist Awards Program (BAGEP), Outstanding Young Scientists Awards (GEBIP), and the Bilim Kahramanlari Dernegi Young Scientist Award. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
dc.description.volume8
dc.identifier.doi10.1021/acsomega.3c04422
dc.identifier.issn2470-1343
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85178355486
dc.identifier.urihttps://doi.org/10.1021/acsomega.3c04422
dc.identifier.urihttps://hdl.handle.net/20.500.14288/23541
dc.identifier.wos1141162500001
dc.keywordsMedicine
dc.languageen
dc.publisherAmerican Chemical Society
dc.relation.grantnoRoyal Academy Newton, (120N019)
dc.relation.grantnoAlexander von Humboldt-Stiftung, AvH, (101003361)
dc.relation.grantnoBilim Akademisi
dc.sourceACS Omega
dc.subjectChemistry
dc.subjectMultidisciplinary
dc.titleLoop-mediated isothermal amplification-integrated CRISPR methods for infectious disease diagnosis at point of care
dc.typeReview
dspace.entity.typePublication
local.contributor.kuauthorYığcı, Defne
local.contributor.kuauthorAtçeken, Nazente
local.contributor.kuauthorTaşoğlu, Savaş
relation.isOrgUnitOfPublicationba2836f3-206d-4724-918c-f598f0086a36
relation.isOrgUnitOfPublication.latestForDiscoveryba2836f3-206d-4724-918c-f598f0086a36

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