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DNA microarray-based characterization and antimicrobial resistance phenotypes of clinical MRSA strains from animal hosts
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s10096-011-1330-yopenalex-snapshot
Comparison of Staphylococcus aureus isolates associated with food intoxication with isolates from human nasal carriers and human infections
inferredcites →https://doi.org/10.1007/s40588-018-0094-xopenalex-snapshot
Staphylococcus aureus as a Foodborne Pathogen
inferredcites →https://doi.org/10.1016/j.ijmm.2013.02.006openalex-snapshot
The diversity of antimicrobial resistance genes among staphylococci of animal origin
inferredcites →https://doi.org/10.1016/j.ijmm.2013.02.010openalex-snapshot
Livestock associated MRSA (LA-MRSA) and its relevance for humans in Germany
inferredcites →https://doi.org/10.1016/j.meegid.2013.02.013openalex-snapshot
Livestock-associated Staphylococcus aureus CC398: Animal reservoirs and human infections
inferredcites →https://doi.org/10.1016/j.onehlt.2015.11.004openalex-snapshot
Methicillin-resistant Staphylococcus aureus from infections in horses in Germany are frequent colonizers of veterinarians but rare among MRSA from infections in humans
inferredcites →https://doi.org/10.1016/j.tim.2012.01.006openalex-snapshot
Livestock-associated Staphylococcus aureus: origin, evolution and public health threat
inferredcites →https://doi.org/10.1016/j.vetmic.2013.11.022openalex-snapshot
Identification and characterization of methicillin-resistant Staphylococcus aureus (MRSA) from Austrian companion animals and horses
inferredcites →https://doi.org/10.1016/j.vetmic.2013.12.024openalex-snapshot
Prevalence of methicillin-resistant Staphylococcus aureus carrying mecA or mecC in dairy cattle
inferredcites →https://doi.org/10.1016/j.vetmic.2016.05.022openalex-snapshot
Antimicrobial resistances and virulence markers in Methicillin-resistant Staphylococcus aureus from broiler and turkey: A molecular view from farm to fork
inferredcites →https://doi.org/10.1016/s0140-6736(15)00730-8openalex-snapshot
Animal production and antimicrobial resistance in the clinic
inferredcites →https://doi.org/10.1089/mdr.2008.0845openalex-snapshot
Clusters of Infections in Horses with MRSA ST1, ST254, and ST398 in a Veterinary Hospital
inferredcites →https://doi.org/10.1093/jac/49.2.289openalex-snapshot
Multicentre evaluation of the VITEK 2 Advanced Expert System for interpretive reading of antimicrobial resistance tests
inferredcites →https://doi.org/10.1093/jac/dkn527openalex-snapshot
Comparison of three phenotypic techniques for detection of methicillin resistance in Staphylococcus spp. reveals a species-dependent performance
inferredcites →https://doi.org/10.1093/jac/dkq037openalex-snapshot
Editorial: Assessing the antimicrobial susceptibility of bacteria obtained from animals
inferredcites →https://doi.org/10.1093/jac/dkr115openalex-snapshot
Molecular characterization of spa type t127, sequence type 1 methicillin-resistant Staphylococcus aureus from pigs
inferredcites →https://doi.org/10.1111/j.1365-3164.2012.01046.xopenalex-snapshot
Staphylococcus pseudintermediusin the dog: taxonomy, diagnostics, ecology, epidemiology and pathogenicity
inferredcites →https://doi.org/10.1111/j.1365-3164.2012.01072.xopenalex-snapshot
Are all meticillin‐resistantStaphylococcus aureus(MRSA) equal in all hosts? Epidemiological and genetic comparison between animal and human MRSA
inferredcites →https://doi.org/10.1111/j.1439-0450.1972.tb00439.xopenalex-snapshot
Methicillin (Cloxacillin)-Resistant Staphylococcus aureus strains Isolated from Bovine Mastitis Cases
inferredcites →https://doi.org/10.1111/j.1574-695x.2008.00426.xopenalex-snapshot
Assignment ofStaphylococcus aureusisolates to clonal complexes based on microarray analysis and pattern recognition
inferredcites →https://doi.org/10.1111/j.1863-2378.2010.01353.xopenalex-snapshot
Genotypes, Antibiotic Resistance Profiles and Microarray‐Based Characterization of Methicillin‐Resistant Staphylococcus aureus Strains Isolated from Livestock and Veterinarians in Switzerland
inferredcites →https://doi.org/10.1128/aem.01865-19openalex-snapshot
Methicillin-Resistant Staphylococcus aureus Strains in Swiss Pigs and Their Relation to Isolates from Farmers and Veterinarians
inferredcites →https://doi.org/10.1128/aem.02260-10openalex-snapshot
Virulence and Resistance Determinants of German Staphylococcus aureus ST398 Isolates from Nonhuman Sources
inferredcites →https://doi.org/10.1128/jcm.02864-15openalex-snapshot
Evaluation of Oxacillin and Cefoxitin Disk and MIC Breakpoints for Prediction of Methicillin Resistance in Human and Veterinary Isolates of Staphylococcus intermedius Group
inferredcites →https://doi.org/10.1128/jcm.42.12.5881-5884.2004openalex-snapshot
Clinical Isolates ofStaphylococcus intermediusMasquerading as Methicillin-ResistantStaphylococcus aureus
inferredcites →https://doi.org/10.1128/mbio.00305-11openalex-snapshot
Staphylococcus aureus CC398: Host Adaptation and Emergence of Methicillin Resistance in Livestock
inferredcites →https://doi.org/10.1136/vr.91.6.152openalex-snapshot
Bacteriophage types and antibiotic sensitivity of Staphylococcus aureus isolated from swabs of the noses and skins of dogs
inferredcites →https://doi.org/10.1186/1471-2164-11-376openalex-snapshot
Whole genome analysis of a livestock-associated methicillin-resistant Staphylococcus aureus ST398 isolate from a case of human endocarditis
inferredcites →https://doi.org/10.1186/1746-6148-7-30openalex-snapshot
The increase of methicillin-resistant Staphylococcus aureus(MRSA) and the presence of an unusual sequence type ST49 in slaughter pigs in Switzerland
inferredcites →https://doi.org/10.1186/s13756-016-0105-8openalex-snapshot
New dominant spa type t2741 in livestock-associated MRSA (CC398-MRSA-V) in Finnish fattening pigs at slaughter
inferredcites →https://doi.org/10.1371/journal.pone.0028189openalex-snapshot
Clonal Replacement of Epidemic Methicillin-Resistant Staphylococcus aureus Strains in a German University Hospital over a Period of Eleven Years
inferredcites →https://doi.org/10.1371/journal.pone.0085656openalex-snapshot
Alarming Proportions of Methicillin-Resistant Staphylococcus aureus (MRSA) in Wound Samples from Companion Animals, Germany 2010–2012
inferredcites →https://doi.org/10.17236/sat00070openalex-snapshot
Methicillin-resistant Staphylococcus aureus isolated from dogs and cats in Switzerland
inferredcites →https://doi.org/10.2807/ese.15.16.19542-enopenalex-snapshot
Prevalence and characteristics of meticillin-resistant Staphylococcus aureus in humans in contact with farm animals, in livestock, and in food of animal origin, Switzerland, 2009
inferredcites →https://doi.org/10.2903/j.efsa.2017.4694openalex-snapshot
The European Union summary report on antimicrobial resistance in zoonotic and indicator bacteria from humans, animals and food in 2015
inferredcites →https://doi.org/10.4315/0362-028x.jfp-11-192openalex-snapshot
Comparison of Virulence and Antibiotic Resistance Genes of Food Poisoning Outbreak Isolates of Staphylococcus aureus with Isolates Obtained from Bovine Mastitis Milk and Pig Carcasses
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4744037openalex-extracted
Fixed Rolling Circle Amplification Integrating with Crrna Switch for Methicillin-Resistant Staphylococcus Aureus (Mrsa) Analysis
inferred← citeshttps://doi.org/10.1007/978-981-96-3878-9_17openalex-snapshot
Nanobiosensors for Antimicrobial Resistance Surveillance: Possibilities and Challenges
inferred← citeshttps://doi.org/10.1007/s10529-024-03550-8openalex-snapshot
Rolling circle amplification cooperating crRNA switch for direct and sensitive methicillin-resistant Staphylococcus aureus (MRSA) analysis
inferred← citeshttps://doi.org/10.1007/s40495-021-00264-7openalex-snapshot
Molecular Typing and Global Epidemiology of Staphylococcus aureus
inferred← citeshttps://doi.org/10.1007/s40588-021-00170-yopenalex-snapshot
Livestock-Associated Meticillin-Resistant Staphylococcus aureus—Current Situation and Impact From a One Health Perspective
inferred← citeshttps://doi.org/10.1016/j.microc.2026.118953openalex-snapshot
Product accelerated Cas12a/crRNA regulated DNA walker for sensitive and reliable mecA gene analysis in nursing depressive disorder
inferred← citeshttps://doi.org/10.1039/d5an00001gopenalex-snapshot
Dual proximity ligation mediated chain extension and displacement assisted signal cycles for sensitive and accurate methicillin-resistant Staphylococcus aureus (MRSA) detection
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4505973/v1openalex-snapshot
Proximity Ligation Mediated Signal Recycling with Primer Exchange Reaction for Sensitive and Accurate Methicillin-Resistant Staphylococcus Aureus (MRSA) Detection
inferred← citeshttps://doi.org/10.2460/javma.21.04.0180openalex-snapshot
Patterns of bacterial culture and antimicrobial susceptibility test results for dogs with retrobulbar abscesses: 133 cases (2002–2019)
inferred← citeshttps://doi.org/10.2903/j.efsa.2022.7209openalex-snapshot
The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2019–2020
inferred← citeshttps://doi.org/10.2903/j.efsa.2022.7312openalex-snapshot
Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): antimicrobial‐resistant Staphylococcus aureus in cattle and horses
inferred← citeshttps://doi.org/10.3390/pathogens11101110openalex-snapshot
MRSA in Humans, Pets and Livestock in Portugal: Where We Came from and Where We Are Going
inferred← citeshttps://doi.org/10.55705/cmbr.2021.143413.1016openalex-snapshot
Overview of typing techniques as molecular epidemiology tools for bacterial characterization
inferred← citeshttps://doi.org/10.5772/intechopen.98313openalex-snapshot
Bacteriophages as Anti-Methicillin Resistant Staphylococcus aureus Agents
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