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Current Trends in Antimicrobial Resistance of Escherichia coli
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s10096-015-2356-3openalex-snapshot
Molecular epidemiology of carbapenemase-producing Escherichia coli and the prevalence of ST131 subclone H30 in Shanghai, China
inferredcites →https://doi.org/10.1007/s10096-015-2550-3openalex-snapshot
Characterization of carbapenem-resistant Escherichia coli and Klebsiella pneumoniae from a healthcare region in Hong Kong
inferredcites →https://doi.org/10.1016/bs.aambs.2014.09.002openalex-snapshot
Escherichia coli ST131: The Quintessential Example of an International Multiresistant High-Risk Clone
inferredcites →https://doi.org/10.1016/j.cmi.2014.10.008openalex-snapshot
A multicenter study of the clonal structure and resistance mechanism of KPC-producing Escherichia coli isolates in Israel
inferredcites →https://doi.org/10.1016/j.cmi.2016.03.009openalex-snapshot
Plasmid-mediated colistin resistance: an additional antibiotic resistance menace
inferredcites →https://doi.org/10.1016/j.cmi.2017.09.001openalex-snapshot
New agents for the treatment of infections with Gram-negative bacteria: restoring the miracle or false dawn?
inferredcites →https://doi.org/10.1016/j.diagmicrobio.2013.08.029openalex-snapshot
Carbapenemase-producing Enterobacteriaceae during 2011-12 in the Bolzano area (Northern Italy): increasing diversity in a low-endemicity setting
inferredcites →https://doi.org/10.1016/j.diagmicrobio.2013.11.011openalex-snapshot
Prevalence of antibiotic resistance in US hospitals
inferredcites →https://doi.org/10.1016/j.ijantimicag.2009.11.003openalex-snapshot
Molecular epidemiology of Escherichia coli producing CTX-M β-lactamases: the worldwide emergence of clone ST131 O25:H4
inferredcites →https://doi.org/10.1016/j.ijantimicag.2012.05.011openalex-snapshot
Emergence of the IMP-8 metallo-β-lactamase in the Escherichia coli ST131 clone in Taiwan
inferredcites →https://doi.org/10.1016/j.ijantimicag.2012.08.015openalex-snapshot
Occurrence of OXA-48 and VIM-1 carbapenemase-producing Enterobacteriaceae in Egypt
inferredcites →https://doi.org/10.1016/j.ijantimicag.2014.02.016openalex-snapshot
Colistin resistance in Klebsiella pneumoniae
inferredcites →https://doi.org/10.1016/j.ijantimicag.2014.02.019openalex-snapshot
Chromosomal location of blaCTX-M genes in clinical isolates of Escherichia coli from Germany, The Netherlands and the UK
inferredcites →https://doi.org/10.1016/j.ijantimicag.2015.08.011openalex-snapshot
A resurgence of β-lactamase inhibitor combinations effective against multidrug-resistant Gram-negative pathogens
inferredcites →https://doi.org/10.1016/j.ijantimicag.2016.09.025openalex-snapshot
Epidemiology of infections caused by polymyxin-resistant pathogens
inferredcites →https://doi.org/10.1016/j.ijantimicag.2016.10.003openalex-snapshot
Detection of the high-risk clone ST131 of Escherichia coli carrying the colistin resistance gene mcr-1 and causing acute peritonitis
inferredcites →https://doi.org/10.1016/j.ijantimicag.2017.09.005openalex-snapshot
Discovery and characterisation of an escherichia coli ST206 strain producing NDM-5 and MCR-1 from a patient with acute diarrhoea in China
inferredcites →https://doi.org/10.1016/j.ijid.2016.07.007openalex-snapshot
Plasmid-mediated colistin resistance in Escherichia coli from the Arabian Peninsula
inferredcites →https://doi.org/10.1016/j.ijmm.2005.07.007openalex-snapshot
Virulence factors of septicemic Escherichia coli strains
inferredcites →https://doi.org/10.1016/j.jen.2015.01.006openalex-snapshot
Health Care–Associated Infections (HAIs)
inferredcites →https://doi.org/10.1016/j.jiac.2016.12.013openalex-snapshot
Molecular epidemiology of carbapenemase-producing Enterobacteriaceae in a primary care hospital in Japan, 2010–2013
inferredcites →https://doi.org/10.1016/j.jinf.2015.09.009openalex-snapshot
Extra-intestinal pathogenic Escherichia coli (ExPEC): Disease, carriage and clones
inferredcites →https://doi.org/10.1016/j.mib.2005.12.001openalex-snapshot
Host specificity of septicemic Escherichia coli: human and avian pathogens
inferredcites →https://doi.org/10.1016/j.tim.2011.09.005openalex-snapshot
The emerging NDM carbapenemases
inferredcites →https://doi.org/10.1016/s0140-6736(05)75604-xopenalex-snapshot
Carbapenem-hydrolysing IMP-1 β-lactamase in Klebsiella pneumoniae from Singapore
inferredcites →https://doi.org/10.1016/s0140-6736(98)05954-6openalex-snapshot
Appearance of IMP-1 metallo-β-lactamase in Europe
inferredcites →https://doi.org/10.1016/s1286-4579(03)00049-2openalex-snapshot
Medical and economic impact of extraintestinal infections due to Escherichia coli: focus on an increasingly important endemic problem
inferredcites →https://doi.org/10.1016/s1473-3099(08)70041-0openalex-snapshot
Extended-spectrum β-lactamase-producing Enterobacteriaceae: an emerging public-health concern
inferredcites →https://doi.org/10.1016/s1473-3099(09)70054-4openalex-snapshot
The real threat of Klebsiella pneumoniae carbapenemase-producing bacteria
inferredcites →https://doi.org/10.1016/s1473-3099(10)70143-2openalex-snapshot
Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: a molecular, biological, and epidemiological study
inferredcites →https://doi.org/10.1016/s1473-3099(10)70277-2openalex-snapshot
Global spread of New Delhi metallo-β-lactamase 1
inferredcites →https://doi.org/10.1016/s1473-3099(10)70279-6openalex-snapshot
Global spread of New Delhi metallo-β-lactamase 1
inferredcites →https://doi.org/10.1016/s1473-3099(11)70059-7openalex-snapshot
Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: an environmental point prevalence study
inferredcites →https://doi.org/10.1016/s1473-3099(13)70318-9openalex-snapshot
Antibiotic resistance—the need for global solutions
inferredcites →https://doi.org/10.1016/s1473-3099(15)00424-7openalex-snapshot
Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: a microbiological and molecular biological study
inferredcites →https://doi.org/10.1016/s1473-3099(16)00007-4openalex-snapshot
Co-occurrence of extended spectrum β lactamase and MCR-1 encoding genes on plasmids
inferredcites →https://doi.org/10.1016/s1473-3099(16)00056-6openalex-snapshot
Emergence of the mcr-1 colistin resistance gene in carbapenem-resistant Enterobacteriaceae
inferredcites →https://doi.org/10.1016/s1473-3099(16)00057-8openalex-snapshot
Carbapenem-resistant and colistin-resistant Escherichia coli co-producing NDM-9 and MCR-1
inferredcites →https://doi.org/10.1016/s1473-3099(16)00061-xopenalex-snapshot
Early emergence of mcr-1 in Escherichia coli from food-producing animals
inferredcites →https://doi.org/10.1016/s1473-3099(16)30527-8openalex-snapshot
Prevalence, risk factors, outcomes, and molecular epidemiology of mcr-1-positive Enterobacteriaceae in patients and healthy adults from China: an epidemiological and clinical study
inferredcites →https://doi.org/10.1038/146837a0openalex-snapshot
An Enzyme from Bacteria able to Destroy Penicillin
inferredcites →https://doi.org/10.1038/nrmicro2319openalex-snapshot
Antibiotic resistance and its cost: is it possible to reverse resistance?
inferredcites →https://doi.org/10.1038/srep15082openalex-snapshot
Stepwise evolution of pandrug-resistance in Klebsiella pneumoniae
inferredcites →https://doi.org/10.1073/pnas.1322678111openalex-snapshot
Global dissemination of a multidrug resistant Escherichia coli clone
inferredcites →https://doi.org/10.1086/497831openalex-snapshot
Dissemination of the Metallo- -Lactamase Gene blaIMP-4 among Gram-Negative Pathogens in a Clinical Setting in Australia
inferredcites →https://doi.org/10.1086/514732openalex-snapshot
Intravenous Colistin as Therapy for Nosocomial Infections Caused by Multidrug‐Resistant Pseudomonas aeruginosa and Acinetobacter baumannii
inferredcites →https://doi.org/10.1086/595011openalex-snapshot
Bad Bugs, No Drugs: No ESKAPE! An Update from the Infectious Diseases Society of America
inferredcites →https://doi.org/10.1086/653932openalex-snapshot
Escherichia coliSequence Type ST131 as the Major Cause of Serious Multidrug‐ResistantE. coliInfections in the United States
inferredcites →https://doi.org/10.1089/mdr.2010.0132openalex-snapshot
The CTX-M Conundrum: Dissemination of Plasmids and Escherichia coli Clones
inferredcites →https://doi.org/10.1093/cid/cis387openalex-snapshot
Features of Infections Due to Klebsiella pneumoniae Carbapenemase–Producing Escherichia coli: Emergence of Sequence Type 131
inferredcites →https://doi.org/10.1093/cid/cis588openalex-snapshot
Predictors of Mortality in Bloodstream Infections Caused by Klebsiella pneumoniae Carbapenemase-Producing K. pneumoniae: Importance of Combination Therapy
inferredcites →https://doi.org/10.1093/jac/dkl562openalex-snapshot
Colistin-resistant isolates of Klebsiella pneumoniae emerging in intensive care unit patients: first report of a multiclonal cluster
inferredcites →https://doi.org/10.1093/jac/dkm464openalex-snapshot
Intercontinental emergence of Escherichia coli clone O25:H4-ST131 producing CTX-M-15
inferredcites →https://doi.org/10.1093/jac/dkm508openalex-snapshot
Linkage of acquired quinolone resistance (qnrS1) and metallo- -lactamase (blaVIM-1) genes in multiple species of Enterobacteriaceae from Bolzano, Italy
inferredcites →https://doi.org/10.1093/jac/dkq269openalex-snapshot
Complete nucleotide sequence of the IncN plasmid pKOX105 encoding VIM-1, QnrS1 and SHV-12 proteins in Enterobacteriaceae from Bolzano, Italy compared with IncN plasmids encoding KPC enzymes in the USA
inferredcites →https://doi.org/10.1093/jac/dkq415openalex-snapshot
Escherichia coli O25b-ST131: a pandemic, multiresistant, community-associated strain
inferredcites →https://doi.org/10.1093/jac/dkr081openalex-snapshot
Trends in carbapenemase-producing Escherichia coli and Klebsiella spp. from Europe and the Americas: report from the SENTRY antimicrobial surveillance programme (2007–09)
inferredcites →https://doi.org/10.1093/jac/dkr180openalex-snapshot
Dissemination of the New Delhi metallo-β-lactamase-1 (NDM-1) among Enterobacteriaceae in a tertiary referral hospital in north India
inferredcites →https://doi.org/10.1093/jac/dkr240openalex-snapshot
Increasing prevalence and dissemination of NDM-1 metallo- -lactamase in India: data from the SMART study (2009)
inferredcites →https://doi.org/10.1093/jac/dkr299openalex-snapshot
Prevalence of faecal carriage of Enterobacteriaceae with NDM-1 carbapenemase at military hospitals in Pakistan, and evaluation of two chromogenic media
inferredcites →https://doi.org/10.1093/jac/dkr317openalex-snapshot
Temocillin use in England: clinical and microbiological efficacies in infections caused by extended-spectrum and/or derepressed AmpC β-lactamase-producing Enterobacteriaceae
inferredcites →https://doi.org/10.1093/jac/dks121openalex-snapshot
OXA-48-like carbapenemases: the phantom menace
inferredcites →https://doi.org/10.1093/jac/dks124openalex-snapshot
Characterization of Enterobacteriaceae producing OXA-48-like carbapenemases in the UK
inferredcites →https://doi.org/10.1093/jac/dkt051openalex-snapshot
Chromosome-mediated OXA-48 carbapenemase in highly virulent Escherichia coli
inferredcites →https://doi.org/10.1093/jac/dkt519openalex-snapshot
Prevalence of day-care centre children (France) with faecal CTX-M-producing Escherichia coli comprising O25b:H4 and O16:H5 ST131 strains
inferredcites →https://doi.org/10.1093/jac/dku132openalex-snapshot
Emergence of Escherichia coli ST131 sub-clone H30 producing VIM-1 and KPC-3 carbapenemases, Italy
inferredcites →https://doi.org/10.1093/jac/dku168openalex-snapshot
Combination therapy for carbapenem-resistant Gram-negative bacteria
inferredcites →https://doi.org/10.1093/jac/dkv017openalex-snapshot
CTX-M-27- and CTX-M-14-producing, ciprofloxacin-resistant Escherichia coli of the H 30 subclonal group within ST131 drive a Japanese regional ESBL epidemic
inferredcites →https://doi.org/10.1093/jac/dkw122openalex-snapshot
Colistin resistance genemcr-1 inEscherichia coliisolates from humans and retail meats, Taiwan
inferredcites →https://doi.org/10.1093/jac/dkw148openalex-snapshot
Carbapenemase-producingEscherichia coliis becoming more prevalent in Spain mainly because of the polyclonal dissemination of OXA-48
inferredcites →https://doi.org/10.1093/jac/dkx355openalex-snapshot
Emergence of mcr-1 and carbapenemase genes in hospital sewage water in Beijing, China
inferredcites →https://doi.org/10.1096/fj.12-224014openalex-snapshot
NDM‐1, the ultimate promiscuous enzyme: substrate recognition and catalytic mechanism
inferredcites →https://doi.org/10.1111/1469-0691.12719openalex-snapshot
The difficult-to-control spread of carbapenemase producers among Enterobacteriaceae worldwide
inferredcites →https://doi.org/10.1111/apm.12034openalex-snapshot
First report of a K lebsiella pneumoniae strain coproducing NDM ‐1, VIM ‐1 and OXA ‐48 carbapenemases isolated in M orocco
inferredcites →https://doi.org/10.1111/j.1198-743x.2010.03225.xopenalex-snapshot
Metallo-β-lactamases among Enterobacteriaceae from routine samples in an Italian tertiary care hospital and long-term care facilities during 2008
inferredcites →https://doi.org/10.1111/j.1469-0691.2011.03514.xopenalex-snapshot
Predictors of mortality in patients with bloodstream infections caused by KPC-producing Klebsiella pneumoniae and impact of appropriate antimicrobial treatment
inferredcites →https://doi.org/10.1111/j.1469-0691.2011.03649.xopenalex-snapshot
Colonization and infection by colistin-resistant Gram-negative bacteria in a cohort of critically ill patients
inferredcites →https://doi.org/10.1111/j.1469-0691.2012.03815.xopenalex-snapshot
Identification and screening of carbapenemase-producing Enterobacteriaceae
inferredcites →https://doi.org/10.1128/aac.00017-09openalex-snapshot
Novel VIM Metallo-β-Lactamase Variant from Clinical Isolates of Enterobacteriaceae from Algeria
inferredcites →https://doi.org/10.1128/aac.00022-11openalex-snapshot
OXA-163, an OXA-48-Related Class D β-Lactamase with Extended Activity Toward Expanded-Spectrum Cephalosporins
inferredcites →https://doi.org/10.1128/aac.00035-12openalex-snapshot
Escherichia coli from Italy Producing OXA-48 Carbapenemase Encoded by a Novel Tn 1999 Transposon Derivative
inferredcites →https://doi.org/10.1128/aac.00086-15openalex-snapshot
Prospective Multicenter Study of Carbapenemase-Producing Enterobacteriaceae from 83 Hospitals in Spain Reveals High In Vitro Susceptibility to Colistin and Meropenem
inferredcites →https://doi.org/10.1128/aac.00270-15openalex-snapshot
Clinical Epidemiology and Molecular Analysis of Extended-Spectrum-β-Lactamase-Producing Escherichia coli in Nepal: Characteristics of Sequence Types 131 and 648
inferredcites →https://doi.org/10.1128/aac.00638-12openalex-snapshot
Detection of OXA-48 Carbapenemase in the Pandemic Clone Escherichia coli O25b:H4-ST131 in the Course of Investigation of an Outbreak of OXA-48-Producing Klebsiella pneumoniae
inferredcites →https://doi.org/10.1128/aac.00663-06openalex-snapshot
Emergence of Multidrug-Resistant Klebsiella pneumoniae Isolates Producing VIM-4 Metallo-β-Lactamase, CTX-M-15 Extended-Spectrum β-Lactamase, and CMY-4 AmpC β-Lactamase in a Tunisian University Hospital
inferredcites →https://doi.org/10.1128/aac.00719-11openalex-snapshot
When Carbapenem-Hydrolyzing β-Lactamase KPC Meets Escherichia coli ST131 in France
inferredcites →https://doi.org/10.1128/aac.00731-16openalex-snapshot
Travelers Can Import Colistin-Resistant Enterobacteriaceae, Including Those Possessing the Plasmid-Mediated mcr-1 Gene
inferredcites →https://doi.org/10.1128/aac.00774-09openalex-snapshot
Characterization of a New Metallo-β-Lactamase Gene, bla NDM-1 , and a Novel Erythromycin Esterase Gene Carried on a Unique Genetic Structure in Klebsiella pneumoniae Sequence Type 14 from India
inferredcites →https://doi.org/10.1128/aac.00834-10openalex-snapshot
Colistin Resistance in Acinetobacter baumannii Is Mediated by Complete Loss of Lipopolysaccharide Production
inferredcites →https://doi.org/10.1128/aac.00865-13openalex-snapshot
Unique Structural Modifications Are Present in the Lipopolysaccharide from Colistin-Resistant Strains of Acinetobacter baumannii
inferredcites →https://doi.org/10.1128/aac.00877-17openalex-snapshot
First Report of Klebsiella oxytoca Strain Simultaneously Producing NDM-1, IMP-4, and KPC-2 Carbapenemases
inferredcites →https://doi.org/10.1128/aac.00912-13openalex-snapshot
Emergence of Escherichia coli Sequence Type 131 Isolates Producing KPC-2 Carbapenemase in China
inferredcites →https://doi.org/10.1128/aac.01019-15openalex-snapshot
Carbapenemase-Producing Klebsiella pneumoniae, a Key Pathogen Set for Global Nosocomial Dominance
inferredcites →https://doi.org/10.1128/aac.01081-12openalex-snapshot
Complete Sequence of pJIE186-2, a Plasmid Carrying Multiple Virulence Factors from a Sequence Type 131 Escherichia coli O25 Strain
inferredcites →https://doi.org/10.1128/aac.01103-16openalex-snapshot
Escherichia coli Harboring mcr-1 and bla CTX-M on a Novel IncF Plasmid: First Report of mcr-1 in the United States
inferredcites →https://doi.org/10.1128/aac.01277-13openalex-snapshot
The FDA Reboot of Antibiotic Development
inferredcites →https://doi.org/10.1128/aac.01319-16openalex-snapshot
Coexistence of mcr-1 and bla NDM-1 in Escherichia coli from Venezuela
inferredcites →https://doi.org/10.1128/aac.01363-15openalex-snapshot
Emergence of Raoultella ornithinolytica Coproducing IMP-4 and KPC-2 Carbapenemases in China
inferredcites →https://doi.org/10.1128/aac.01365-16openalex-snapshot
Emergence of NDM-5- and MCR-1-Producing Escherichia coli Clones ST648 and ST156 from a Single Muscovy Duck (Cairina moschata)
inferredcites →https://doi.org/10.1128/aac.01451-07openalex-snapshot
Genetic Structures at the Origin of Acquisition of the β-Lactamase bla KPC Gene
inferredcites →https://doi.org/10.1128/aac.01486-16openalex-snapshot
Acquisition of mcr-1 Plasmid-Mediated Colistin Resistance in Escherichia coli and Klebsiella pneumoniae during Hajj 2013 and 2014
inferredcites →https://doi.org/10.1128/aac.01497-10openalex-snapshot
Early Dissemination of NDM-1- and OXA-181-Producing Enterobacteriaceae in Indian Hospitals: Report from the SENTRY Antimicrobial Surveillance Program, 2006-2007
inferredcites →https://doi.org/10.1128/aac.01763-10openalex-snapshot
Characteristics of NDM-1-Producing Escherichia coli Isolates That Belong to the Successful and Virulent Clone ST131
inferredcites →https://doi.org/10.1128/aac.02379-15openalex-snapshot
Multiyear, Multinational Survey of the Incidence and Global Distribution of Metallo-β-Lactamase-Producing Enterobacteriaceae and Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/aac.02399-12openalex-snapshot
Effectiveness of a Double-Carbapenem Regimen for Infections in Humans Due to Carbapenemase-Producing Pandrug-Resistant Klebsiella pneumoniae
inferredcites →https://doi.org/10.1128/aac.02669-14openalex-snapshot
IS 1R -Mediated Plasticity of IncL/M Plasmids Leads to the Insertion of bla OXA-48 into the Escherichia coli Chromosome
inferredcites →https://doi.org/10.1128/aac.02824-14openalex-snapshot
A New Clone Sweeps Clean: the Enigmatic Emergence of Escherichia coli Sequence Type 131
inferredcites →https://doi.org/10.1128/aac.03938-14openalex-snapshot
Dissemination of NDM Metallo-β-Lactamase Genes among Clinical Isolates of Enterobacteriaceae Collected during the SMART Global Surveillance Study from 2008 to 2012
inferredcites →https://doi.org/10.1128/aac.04378-14openalex-snapshot
Dominance of IMP-4-Producing Enterobacter cloacae among Carbapenemase-Producing Enterobacteriaceae in Australia
inferredcites →https://doi.org/10.1128/aac.05127-11openalex-snapshot
Production of KPC-2 Carbapenemase by an Escherichia coli Clinical Isolate Belonging to the International ST131 Clone
inferredcites →https://doi.org/10.1128/aac.05289-11openalex-snapshot
Genetic Features of the Widespread Plasmid Coding for the Carbapenemase OXA-48
inferredcites →https://doi.org/10.1128/aac.38.1.71openalex-snapshot
Molecular characterization of an enterobacterial metallo beta-lactamase found in a clinical isolate of Serratia marcescens that shows imipenem resistance
inferredcites →https://doi.org/10.1128/aac.39.4.824openalex-snapshot
Plasmid-mediated dissemination of the metallo-beta-lactamase gene blaIMP among clinically isolated strains of Serratia marcescens
inferredcites →https://doi.org/10.1128/aac.40.2.349openalex-snapshot
Multifocal outbreaks of metallo-beta-lactamase-producing Pseudomonas aeruginosa resistant to broad-spectrum beta-lactams, including carbapenems
inferredcites →https://doi.org/10.1128/aac.43.7.1584openalex-snapshot
Cloning and Characterization of bla VIM , a New Integron-Borne Metallo-β-Lactamase Gene from a Pseudomonas aeruginosa Clinical Isolate
inferredcites →https://doi.org/10.1128/aac.44.5.1229-1235.2000openalex-snapshot
Characterization of the Metallo-β-Lactamase Determinant of Acinetobacter baumannii AC-54/97 Reveals the Existence of bla IMP Allelic Variants Carried by Gene Cassettes of Different Phylogeny
inferredcites →https://doi.org/10.1128/aac.44.8.2023-2027.2000openalex-snapshot
Amino Acid Substitutions in a Variant of IMP-1 Metallo-β-Lactamase
inferredcites →https://doi.org/10.1128/aac.45.3.710-714.2001openalex-snapshot
IMP-4, a Novel Metallo-β-Lactamase from Nosocomial Acinetobacter spp. Collected in Hong Kong between 1994 and 1998
inferredcites →https://doi.org/10.1128/aac.45.4.1151-1161.2001openalex-snapshot
Novel Carbapenem-Hydrolyzing β-Lactamase, KPC-1, from a Carbapenem-Resistant Strain of Klebsiella pneumoniae
inferredcites →https://doi.org/10.1128/aac.48.1.15-22.2004openalex-snapshot
Emergence of Oxacillinase-Mediated Resistance to Imipenem inKlebsiella pneumoniae
inferredcites →https://doi.org/10.1128/aac.48.11.4438-4440.2004openalex-snapshot
Plasmid-Mediated Carbapenem-Hydrolyzing Enzyme KPC-2 in an Enterobacter sp
inferredcites →https://doi.org/10.1128/aac.48.12.4929-4930.2004openalex-snapshot
First Detection of a Carbapenem-Hydrolyzing Metalloenzyme in an Enterobacteriaceae Isolate in France
inferredcites →https://doi.org/10.1128/aem.00698-13openalex-snapshot
Evidence for Coexistence of Distinct Escherichia coli Populations in Various Aquatic Environments and Their Survival in Estuary Water
inferredcites →https://doi.org/10.1128/cmr.00125-13openalex-snapshot
Escherichia coli ST131, an Intriguing Clonal Group
inferredcites →https://doi.org/10.1128/cmr.05035-11openalex-snapshot
Carbapenemases in Klebsiella pneumoniae and Other Enterobacteriaceae: an Evolving Crisis of Global Dimensions
inferredcites →https://doi.org/10.1128/genomea.00272-15openalex-snapshot
Complete Genome Sequence of a Carbapenem-Resistant Extraintestinal Pathogenic Escherichia coli Strain Belonging to the Sequence Type 131 H 30R Subclade
inferredcites →https://doi.org/10.1128/genomea.00863-16openalex-snapshot
Genome Sequence of Avian Escherichia coli Strain IHIT25637, an Extraintestinal Pathogenic E. coli Strain of ST131 Encoding Colistin Resistance Determinant MCR-1
inferredcites →https://doi.org/10.1128/genomea.00983-15openalex-snapshot
Draft Genome Sequences of Two IMP-4-Producing Escherichia coli Sequence Type 131 Isolates in Australia
inferredcites →https://doi.org/10.1128/jb.172.11.6175-6181.1990openalex-snapshot
Phylogenetic distribution of branched RNA-linked multicopy single-stranded DNA among natural isolates of Escherichia coli
inferredcites →https://doi.org/10.1128/jb.183.6.1835-1842.2001openalex-snapshot
The Pleiotropic Two-Component Regulatory System PhoP-PhoQ
inferredcites →https://doi.org/10.1128/jcm.01491-14openalex-snapshot
Interspecies Transfer of bla IMP-4 in a Patient with Prolonged Colonization by IMP-4-Producing Enterobacteriaceae
inferredcites →https://doi.org/10.1128/jcm.03502-13openalex-snapshot
Rapid and Specific Detection, Molecular Epidemiology, and Experimental Virulence of the O16 Subgroup within Escherichia coli Sequence Type 131
inferredcites →https://doi.org/10.1128/jcm.34.12.2909-2913.1996openalex-snapshot
PCR detection of metallo-beta-lactamase gene (blaIMP) in gram-negative rods resistant to broad-spectrum beta-lactams
inferredcites →https://doi.org/10.1128/jcm.41.8.3893-3896.2003openalex-snapshot
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inferredcites →https://doi.org/10.1128/mbio.00347-16openalex-snapshot
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The Epidemic of Extended-Spectrum-β-Lactamase-Producing Escherichia coli ST131 Is Driven by a Single Highly Pathogenic Subclone, H 30-Rx
inferredcites →https://doi.org/10.1128/mbio.02162-15openalex-snapshot
Evolutionary History of the Global Emergence of the Escherichia coli Epidemic Clone ST131
inferredcites →https://doi.org/10.1128/msphere.00121-16openalex-snapshot
Separate F-Type Plasmids Have Shaped the Evolution of the H 30 Subclone of Escherichia coli Sequence Type 131
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Notes from the Field: Verona Integron-Encoded Metallo-Beta-Lactamase–Producing Carbapenem-Resistant Enterobacteriaceae in a Neonatal and Adult Intensive Care Unit — Kentucky, 2015
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inferredcites →https://doi.org/10.1586/14787210.2013.845523openalex-snapshot
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inferredcites →https://doi.org/10.2807/1560-7917.es.2016.21.9.30155openalex-snapshot
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inferredcites →https://doi.org/10.2807/1560-7917.es.2017.22.31.30584openalex-snapshot
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inferredcites →https://doi.org/10.2807/1560-7917.es.2017.22.31.30586openalex-snapshot
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inferredcites →https://doi.org/10.2807/1560-7917.es2013.18.28.20525openalex-snapshot
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inferredcites →https://doi.org/10.2807/1560-7917.es2014.19.9.20723openalex-snapshot
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inferredcites →https://doi.org/10.2807/ese.13.04.08023-enopenalex-snapshot
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inferredcites →https://doi.org/10.3109/00365548.2013.859392openalex-snapshot
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inferredcites →https://doi.org/10.3201/eid1710.110655openalex-snapshot
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inferredcites →https://doi.org/10.3201/eid2011.141388openalex-snapshot
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inferredcites →https://doi.org/10.3201/eid2211.160519openalex-snapshot
GlobalEscherichia coliSequence Type 131 Clade withblaCTX-M-27Gene
inferredcites →https://doi.org/10.3389/fmicb.2012.00009openalex-snapshot
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inferredcites →https://doi.org/10.3389/fmicb.2012.00110openalex-snapshot
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“Down the drain”: carbapenem‐resistant bacteria in intensive care unit patients and handwashing sinks
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inferred← citeshttps://doi.org/10.3390/antibiotics10010028openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/antibiotics10030278openalex-snapshot
Bacterial Pathogens and Evaluation of a Cut-Off for Defining Early and Late Neonatal Infection
inferred← citeshttps://doi.org/10.3390/antibiotics10040415openalex-snapshot
Mechanisms of Antibiotic Resistance in Important Gram-Positive and Gram-Negative Pathogens and Novel Antibiotic Solutions
inferred← citeshttps://doi.org/10.3390/antibiotics10091068openalex-snapshot
Characterization and Evaluation of Layered Bi2WO6 Nanosheets as a New Antibacterial Agent
inferred← citeshttps://doi.org/10.3390/antibiotics11081064openalex-snapshot
Antimicrobial Resistance Trends of Escherichia coli Isolates: A Three-Year Prospective Study of Poultry Production in Spain
inferred← citeshttps://doi.org/10.3390/antibiotics11101346openalex-snapshot
Synergistic Activity of Tetrandrine and Colistin against mcr-1-Harboring Escherichia coli
inferred← citeshttps://doi.org/10.3390/antibiotics12020376openalex-snapshot
The Pork Food Chain as a Route of Transmission of Antimicrobial Resistant Escherichia coli: A Farm-to-Fork Perspective
inferred← citeshttps://doi.org/10.3390/antibiotics13050379openalex-snapshot
First Insights on Resistance and Virulence Potential of Escherichia coli from Captive Birds of Prey in Portugal
inferred← citeshttps://doi.org/10.3390/antibiotics14090915openalex-snapshot
Postβ-Lactamase-Inhibiting Effect of Sulbactam in Combination with Ceftriaxone on Extended-Spectrum-β-Lactamase-Producing Escherichia coli
inferred← citeshttps://doi.org/10.3390/bioengineering11121278openalex-snapshot
Chitosan-Based Multifunctional Biomaterials as Active Agents or Delivery Systems for Antibacterial Therapy
inferred← citeshttps://doi.org/10.3390/books978-3-0365-4417-5openalex-snapshot
Hospital Acquired Infections, Multidrug Resistant (MDR) Bacteria, Alternative Approaches to Antibiotic Therapy
inferred← citeshttps://doi.org/10.3390/foods14173130openalex-snapshot
Carbon Dots from Dried German Chamomile Flower and Its Residual Biomass: Characteristics, Bioactivities, Cytotoxicity and Its Preservative Effect on the Refrigerated Precooked Baby Clam (Paphia undulata)
inferred← citeshttps://doi.org/10.3390/ijms242417204openalex-snapshot
One Health Determinants of Escherichia coli Antimicrobial Resistance in Humans in the Community: An Umbrella Review
inferred← citeshttps://doi.org/10.3390/ijms252111574openalex-snapshot
Restoring Colistin Sensitivity in Multidrug-Resistant Pathogenic E. coli Using Cinacalcet Hydrochloride
inferred← citeshttps://doi.org/10.3390/jcm13092639openalex-snapshot
Chronic E. Coli Drug-Resistant Cystitis Treated with a Sequence of Modulated Extremely Low-Frequency Electromagnetic Fields: A Randomized Study of 148 Cases
inferred← citeshttps://doi.org/10.3390/microorganisms10061217openalex-snapshot
Occurrence and Characteristics of ESBL- and Carbapenemase- Producing Escherichia coli from Wild and Feral Birds in Greece
inferred← citeshttps://doi.org/10.3390/microorganisms12061076openalex-snapshot
Prevalence of Antibiotic Resistance and Virulence Genes in Escherichia coli Carried by Migratory Birds on the Inner Mongolia Plateau of Northern China from 2018 to 2023
inferred← citeshttps://doi.org/10.3390/microorganisms12091871openalex-snapshot
In Vitro Antimicrobial Synergistic Activity and the Mechanism of the Combination of Naringenin and Amikacin Against Antibiotic-Resistant Escherichia coli
inferred← citeshttps://doi.org/10.3390/microorganisms13040954openalex-snapshot
Genetic Evolution of Antibiotic Resistance and Virulence Genes in Escherichia coli Isolates from a Chinese Hospital over a 12-Year Period
inferred← citeshttps://doi.org/10.3390/molecules26020283openalex-snapshot
The Antimicrobial Activity of Origanum vulgare L. Correlated with the Gastrointestinal Perturbation in Patients with Metabolic Syndrome
inferred← citeshttps://doi.org/10.3390/molecules28135115openalex-snapshot
Zinc Oxide Quantum Dots May Provide a Novel Potential Treatment for Antibiotic-Resistant Streptococcus agalactiae in Lama glama
inferred← citeshttps://doi.org/10.3390/nano10122340openalex-snapshot
Antibacterial Effect of Chitosan–Gold Nanoparticles and Computational Modeling of the Interaction between Chitosan and a Lipid Bilayer Model
inferred← citeshttps://doi.org/10.3390/pathogens11060659openalex-snapshot
Worldwide Prevalence of mcr-mediated Colistin-Resistance Escherichia coli in Isolates of Clinical Samples, Healthy Humans, and Livestock—A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.3390/ph17050560openalex-snapshot
Antimicrobial Effect of Honey Phenolic Compounds against E. coli—An In Vitro Study
inferred← citeshttps://doi.org/10.35381/s.v.v5i1.1589openalex-snapshot
Interacción experimental de Escherichia Coli en óxido de grafeno aplicando propiedades de reducción grupo-funcional antibacteriana
inferred← citeshttps://doi.org/10.37762/jgmds.10-3.411openalex-snapshot
Anti-Biofilm Forming Activity of Natural Products Extract Punica Granatum L. and Magnifera Indica L
inferred← citeshttps://doi.org/10.4014/jmb.2306.06030openalex-snapshot
Amygdalin Reverses Macrophage PANoptosis Induced by Drug-Resistant Escherichia coli
inferred← citeshttps://doi.org/10.4014/jmb.2403.03057openalex-snapshot
Bacterial Apoptosis-Like Death through Accumulation of Reactive Oxygen Species by Quercetin in Escherichia coli
inferred← citeshttps://doi.org/10.4236/ojmm.2023.131007openalex-snapshot
Antibiotic Resistance in the Uropathogenic Enterobacteria Isolated from Patients Attending General Reference Hospital (GRH) of Niamey, Niger
inferred← citeshttps://doi.org/10.46496/medula.v10i1.26112openalex-snapshot
Aktivitas Antibakteri dan Skrining Fitokimia Ekstrak Etanol Daun Jambu Mete Anacardium occidentale L. Terhadap Pertumbuhan Escherichia coli Antibacterial Activity and Phytochemical Screening of Ethanol Extract of Cashew Leaves Anacardium occidentale L. Against Escherichia coli
inferred← citeshttps://doi.org/10.47119/ijrp1001241520234900openalex-snapshot
Antimicrobial Susceptibility Test of Mangosteen Fruit Ethanol Extract (Garcinia mangostana Linn) Against Escherichia coli Bacteria
inferred← citeshttps://doi.org/10.48198/njpas/25.a06openalex-snapshot
Antimicrobial activities and phytochemical analyses of Myristica fragrans Seed extracts on Some Clinical Microbial Isolates
inferred← citeshttps://doi.org/10.51412/psnnjp.2025.26openalex-snapshot
Antibacterial Spectrum of Aspartic Acid Complexes
inferred← citeshttps://doi.org/10.51452/kazatuvc.2023.2(002).1416openalex-snapshot
GENOTYPIC RESISTANCE DRUGS OF ESCHERICHIA COLI STRAINS ISOLATED FROM KAZAKHSTANI PRODUCERS’ CHEESES TO ANTIMICROBIAL
inferred← citeshttps://doi.org/10.52673/18570461.22.4-67.04openalex-snapshot
Antimicrobial resistance mechanisms characteristic of clinically important gram-negative baccili
inferred← citeshttps://doi.org/10.5327/z2176-94782175openalex-snapshot
Resistance profile of Escherichia coli strains in micro-basins with different soil use and occupation, in the Northwest of Rio Grande do Sul, Brazil
inferred← citeshttps://doi.org/10.54254/2753-8818/45/20240613openalex-snapshot
Research on novel antibiotics: Bacterial division inhibitors
inferred← citeshttps://doi.org/10.54393/pjhs.v6i5.3085openalex-snapshot
Antibiotic Resistance: Investigating the Prevalence of Antibiotic Resistance in E. Coli Infections among Patients Treated with Ciprofloxacin versus Amoxicillin
inferred← citeshttps://doi.org/10.54751/revistafoco.v16n3-130openalex-snapshot
PERFIL DE RESISTÊNCIA DE STAPHYLOCOCCUS SPP. ISOLADOS DE NASOFARINGE DE CRIANÇAS COM SINTOMAS GRIPAIS EM UNIDADE DE ATENDIMENTO PEDIÁTRICO
inferred← citeshttps://doi.org/10.5772/intechopen.101583openalex-snapshot
Antimicrobial Resistance in Escherichia coli
inferred← citeshttps://doi.org/10.5772/intechopen.108299openalex-snapshot
Antimicrobial Resistance and Virulence of Escherichia coli in the Purview of Public Health Monitoring
inferred← citeshttps://doi.org/10.58837/chula.the.2022.378openalex-snapshot
Transferable r plasmids in Escherichia coli isolated from meat ducks
inferred← citeshttps://doi.org/10.59594/iicqp.2024.v2n1.77openalex-snapshot
Resistencia a antibióticos generada mediante mutaciones cromosómicas en aislados de Escherichia coli provenientes de coprocultivos de niños de una comunidad de Lima, Perú
inferred← citeshttps://doi.org/10.65540/jar.v19i.350openalex-snapshot
التأثير البيولوجي للأسبرين المحضر معمليا على بكتيريا Staphylococcus aureus وبكتريا Escherichia coli
inferred← citeshttps://doi.org/10.70675/947150d2z8a3cz48fez9a28z77c31594ba47openalex-snapshot
Synthesis, antibacterial and cytotoxic evaluation of two natural phthalides and their analogs
inferred← citeshttps://doi.org/10.7759/cureus.52345openalex-snapshot
Susceptibility and Synergistic Effects of Guava Plant Extract and Antimicrobial Drugs on Escherichia coli
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