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Distribution and frequency of VKORC1 sequence variants conferring resistance to anticoagulants in Mus musculus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ps.2780430111openalex-snapshot
Anticoagulant resistance in Europe: Appraisal of the data from the 1992 EPPO questionnaire
inferredcites →https://doi.org/10.1007/s00436-008-1054-9openalex-snapshot
Network “Rodent-borne pathogens” in Germany: longitudinal studies on the geographical distribution and prevalence of hantavirus infections
inferredcites →https://doi.org/10.1016/j.artres.2008.09.002openalex-snapshot
A cardiovascular phenotype in warfarin-resistantVkorc1mutant rats☆
inferredcites →https://doi.org/10.1016/s0021-9258(18)41669-9openalex-snapshot
Identification of a glycine-rich sequence as an NAD(P)H-binding site and tyrosine 128 as a dicumarol-binding site in rat liver NAD(P)H:quinone oxidoreductase by site-directed mutagenesis.
inferredcites →https://doi.org/10.1017/s0022172400040109openalex-snapshot
The toxicity of 0·025% warfarin to wild house-mice (Mus musculus L.)
inferredcites →https://doi.org/10.1017/s0022172400046957openalex-snapshot
Laboratory evaluation of difenacoum as a rodenticide
inferredcites →https://doi.org/10.1017/s0022172400055078openalex-snapshot
A major gene controlling warfarin-resistance in the house mouse
inferredcites →https://doi.org/10.1017/s0022172400055819openalex-snapshot
Trials of the anticoagulant rodenticide WBA 8119 against confined colonies of warfarin-resistant house mice (Mus musculus L.)
inferredcites →https://doi.org/10.1017/s0022172400060721openalex-snapshot
Pen and field trials of a new anticoagulant rodenticide flocoumafen against the house mouse (Mus musculus L.)
inferredcites →https://doi.org/10.1017/s0022172400069370openalex-snapshot
Trials of the anticoagulant rodenticides bromadiolone and difenacoum against the house mouse (Mus musculus L.)
inferredcites →https://doi.org/10.1038/nature02214openalex-snapshot
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
inferredcites →https://doi.org/10.1038/nature08720openalex-snapshot
Structure of a bacterial homologue of vitamin K epoxide reductase
inferredcites →https://doi.org/10.1074/jbc.m500765200openalex-snapshot
Membrane Topology Mapping of Vitamin K Epoxide Reductase by in Vitro Translation/Cotranslocation
inferredcites →https://doi.org/10.1079/9781845938178.0000openalex-snapshot
Rodent pests and their control
inferredcites →https://doi.org/10.1080/09670870701245215openalex-snapshot
DNA-based field monitoring of warfarin resistance in rats (Rattus norvegicus)
inferredcites →https://doi.org/10.1111/j.1365-2338.1995.tb01122.xopenalex-snapshot
GUIDELINE ON GOOD PLANT PROTECTION PRACTICE DIRECTIVE SUR LA BONNE PRATIQUE PHYTOSANITAIRE
inferredcites →https://doi.org/10.1186/1471-2156-10-4openalex-snapshot
Novel mutations in the VKORC1 gene of wild rats and mice – a response to 50 years of selection pressure by warfarin?
inferredcites →https://doi.org/10.1534/genetics.104.040360openalex-snapshot
The Genetic Basis of Resistance to Anticoagulants in Rodents
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.4820673openalex-extracted
First Wide-Ranging Survey of Vkorc1 Missense Mutations in the Mediterranean Islands Reveals Widespread Rodenticide Resistance in House Mice
inferred← citeshttps://doi.org/10.1002/ece3.2829openalex-snapshot
Adaptative evolution of theVkorc1gene inMus musculus domesticusis influenced by the selective pressure of anticoagulant rodenticides
inferred← citeshttps://doi.org/10.1002/ps.3352openalex-snapshot
Brodifacoum is effective against Norway rats (Rattus norvegicus) in a tyrosine139cysteine focus of anticoagulant resistance in Westphalia, Germany
inferred← citeshttps://doi.org/10.1002/ps.4020openalex-snapshot
Evidence of a target resistance to antivitamin K rodenticides in the roof rat Rattus rattus: identification and characterisation of a novel Y25F mutation in the Vkorc1 gene
inferred← citeshttps://doi.org/10.1002/ps.4027openalex-snapshot
VKOR variant and sex are the main influencing factors on bromadiolone tolerance of the house mouse (Mus musculus L.)
inferred← citeshttps://doi.org/10.1002/ps.4304openalex-snapshot
Vkorc1 sequencing suggests anticoagulant resistance in rats in New Zealand
inferred← citeshttps://doi.org/10.1002/ps.4319openalex-snapshot
Study of the efficiency of anticoagulant rodenticides to control Mus musculus domesticus introgressed with Mus spretus Vkorc1
inferred← citeshttps://doi.org/10.1002/ps.4797openalex-snapshot
Elevated difenacoum metabolism is involved in the difenacoum‐resistant phenotype observed in Berkshire rats homozygous for the L120Q mutation in the vitamin K epoxide reductase complex subunit 1 ( Vkorc1 ) gene
inferred← citeshttps://doi.org/10.1002/ps.5040openalex-snapshot
Low warfarin resistance frequency in Norway rats in two cities in China after 30 years of usage of anticoagulant rodenticides
inferred← citeshttps://doi.org/10.1002/ps.6012openalex-snapshot
A VKORC1 ‐based SNP survey of anticoagulant rodenticide resistance in the house mouse, Norway rat and roof rat in the USA
inferred← citeshttps://doi.org/10.1002/ps.6905openalex-snapshot
Accelerated evolution of Vkorc1 in desert rodent species reveals genetic preadaptation to anticoagulant rodenticides
inferred← citeshttps://doi.org/10.1002/ps.70480openalex-snapshot
Rapid population expansion drives the widespread spread of a dominant anticoagulant‐resistance Vkorc1 allele in Asian house rats ( Rattus tanezumi ) across China
inferred← citeshttps://doi.org/10.1002/ps.7066openalex-snapshot
Anticoagulant rodenticide blood‐clotting dose‐responses and resistance factors for Tyrosine139Cysteine ( Y139C ) heterozygous‐ and homozygous‐resistant house mice (Mus musculus)
inferred← citeshttps://doi.org/10.1002/ps.70833openalex-snapshot
Distribution and frequency of Vkorc1 polymorphisms in house mice and Norway rats in the northeastern United States
inferred← citeshttps://doi.org/10.1002/ps.7261openalex-snapshot
Large‐scale identification of rodenticide resistance in Rattus norvegicus and Mus musculus in the Netherlands based on Vkorc1 codon 139 mutations
inferred← citeshttps://doi.org/10.1007/978-3-319-64377-9_10openalex-snapshot
Development of Resistance to Anticoagulant Rodenticides in Rodents
inferred← citeshttps://doi.org/10.1007/978-3-319-64377-9_11openalex-snapshot
An International Perspective on the Regulation of Rodenticides
inferred← citeshttps://doi.org/10.1007/s00103-013-1930-zopenalex-snapshot
Rodentizidresistenz und Konsequenzen
inferred← citeshttps://doi.org/10.1007/s10340-020-01299-3openalex-snapshot
Sublethal dose of warfarin induction promotes the accumulation of warfarin resistance in susceptible Norway rats
inferred← citeshttps://doi.org/10.1007/s11030-026-11611-5openalex-snapshot
Structural disruption of VKORC1 by resistance mutations reveals a conserved hydrophobic pattern essential for warfarin binding: insights from molecular dynamics analyses
inferred← citeshttps://doi.org/10.1016/b978-0-12-811410-0.00046-5openalex-snapshot
Anticoagulant Rodenticides
inferred← citeshttps://doi.org/10.1016/b978-0-443-29007-7.00024-8openalex-snapshot
Anticoagulant rodenticides
inferred← citeshttps://doi.org/10.1016/j.jspr.2020.101688openalex-snapshot
Anticoagulant rodenticides and resistance development in rodent pest species – A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.pestbp.2018.02.004openalex-snapshot
Thrombin generation test: A reliable tool to evaluate the pharmacodynamics of vitamin K antagonist rodenticides in rats
inferred← citeshttps://doi.org/10.1016/j.pestbp.2022.105052openalex-snapshot
Distribution of non-synonymous Vkorc1 mutations in roof rats (Rattus rattus) in France and in Spain - consequences for management
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.157192openalex-snapshot
Widespread resistance to anticoagulant rodenticides in Mus musculus domesticus in the city of Barcelona
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.166290openalex-snapshot
Widespread distribution of rodenticide resistance-conferring mutations in the Vkorc1 gene among house mouse populations in Portuguese Macaronesian islands and Iberian Atlantic areas
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.176090openalex-snapshot
A survey of VKORC1 missense mutations in eleven Italian islands reveals widespread rodenticide resistance in house mice
inferred← citeshttps://doi.org/10.1016/j.tox.2016.02.002openalex-snapshot
Origin of the gender differences of the natural resistance to antivitamin K anticoagulants in rats
inferred← citeshttps://doi.org/10.1038/s41598-018-22815-7openalex-snapshot
VKORC1 sequence variants associated with resistance to anticoagulant rodenticides in Irish populations of Rattus norvegicus and Mus musculus domesticus
inferred← citeshttps://doi.org/10.1038/s41598-022-16550-3openalex-snapshot
The screening for anticoagulant rodenticide gene VKORC1 polymorphism in the rat Rattus norvegicus, Rattus tanezumi and Rattus losea in Hong Kong
inferred← citeshttps://doi.org/10.1038/s41598-022-26638-5openalex-snapshot
Investigation of anticoagulant rodenticide resistance induced by Vkorc1 mutations in rodents in Lebanon
inferred← citeshttps://doi.org/10.1038/s41598-025-85447-8openalex-snapshot
Widespread anticoagulant resistance in house mice (Mus musculus musculus) linked to the Tyr139Phe mutation in the Czech Republic
inferred← citeshttps://doi.org/10.1071/wr19199openalex-snapshot
Small-mammal assemblages in piggeries in a developing country: relationships with management practices and habitat complexity
inferred← citeshttps://doi.org/10.1073/pnas.1406298111openalex-snapshot
Interspecific introgressive origin of genomic diversity in the house mouse
inferred← citeshttps://doi.org/10.1079/9781800626508.0003openalex-snapshot
Characteristics of Rodenticides
inferred← citeshttps://doi.org/10.1080/09670874.2020.1853277openalex-snapshot
Susceptibility of house mouse carriers of Tyr139Cys and Leu128Ser/Tyr139Cys VKOR variants to difenacoum
inferred← citeshttps://doi.org/10.1080/09670874.2023.2234324openalex-snapshot
VKORC1-based resistance to anticoagulant rodenticides widespread in Finnish house mice but not in brown rats
inferred← citeshttps://doi.org/10.1093/jhered/esv054openalex-snapshot
Polymorphism invkorc1Gene of Natal Multimammate Mice,Mastomys natalensis, in Tanzania
inferred← citeshttps://doi.org/10.1111/mec.12415openalex-snapshot
Adaptive introgression in animals: examples and comparison to new mutation and standing variation as sources of adaptive variation
inferred← citeshttps://doi.org/10.1134/s0012496621030029openalex-snapshot
Mutations of the VCORC1 Gene of Resistance to Anticoagulants in Synanthropic Rodents in Urbanized Areas of Russia
inferred← citeshttps://doi.org/10.1134/s2075111722030109openalex-snapshot
Low Level of Resistance to Anticoagulant Rodenticides in the Vkorс1 Gene in House Mice (Mus musculus) and Norway Rats (Rattus norvegicus) in Russia
inferred← citeshttps://doi.org/10.1155/2019/3794876openalex-snapshot
House Mice as a Real Sanitary Threat of Human and Animal Leptospirosis: Proposal for Integrated Management
inferred← citeshttps://doi.org/10.1186/1471-2156-15-17openalex-snapshot
Confirmation of warfarin resistance of naturally occurring VKORC1 variants by coexpression with coagulation factor IX and in silico protein modelling
inferred← citeshttps://doi.org/10.1186/s13028-018-0357-9openalex-snapshot
Quantitative method for analysis of six anticoagulant rodenticides in faeces, applied in a case with repeated samples from a dog
inferred← citeshttps://doi.org/10.1186/s40850-017-0024-zopenalex-snapshot
Indigenous house mice dominate small mammal communities in northern Afghan military bases
inferred← citeshttps://doi.org/10.1371/journal.pone.0088425openalex-snapshot
Mitochondrial DNA Phylogeography of the Norway Rat
inferred← citeshttps://doi.org/10.1371/journal.pone.0221706openalex-snapshot
The potential of VKORC1 polymorphisms in Mustelidae for evolving anticoagulant resistance through selection along the food chain
inferred← citeshttps://doi.org/10.1371/journal.pone.0236234openalex-snapshot
Mus musculus populations in Western Australia lack VKORC1 mutations conferring resistance to first generation anticoagulant rodenticides: Implications for conservation and biosecurity
inferred← citeshttps://doi.org/10.2174/1389450116666150722141906openalex-snapshot
Dicoumarol: A Drug which Hits at Least Two Very Different Targets in Vitamin K Metabolism
inferred← citeshttps://doi.org/10.2478/macvetrev-2019-0010openalex-snapshot
Anticoagulant Resistance in Synanthropic Rodents in the Stara Zagora Region, Bulgaria
inferred← citeshttps://doi.org/10.2779/241180openalex-snapshot
Risk mitigation measures for anticoagulant rodenticides as biocidal products
inferred← citeshttps://doi.org/10.3390/v18010004openalex-snapshot
Lymphocytic Choriomeningitis Virus Seroprevalence in a Cohort of German Forestry Workers
inferred← citeshttps://doi.org/10.35885/1996-1499-15-2-139-141openalex-snapshot
LOW LEVEL OF RESISTANCE TO ANTICOAGULANT RODENTICIDES IN THE VKORC1 GENE IN HOUSE MICE (MUS MUSCULUS) AND NORWAY RATS (RATTUS NORVEGICUS) IN RUSSIA
inferred← citeshttps://doi.org/10.5482/hamo-13-09-0047openalex-snapshot
Comparative genetics of warfarin resistance
inferred← citeshttps://doi.org/10.5772/64204openalex-snapshot
Comparative Biology of the Resistance to Vitamin K Antagonists: An Overview of the Resistance Mechanisms
inferred← citeshttps://doi.org/10.70675/604d0956zae55z40bez881cz9bd16deba4e6openalex-snapshot
Gestion de populations de rongeurs dans un contexte leptospirosique
inferred← citeshttps://doi.org/10.70675/7592cdcbzdd2ez4414z9216zab2377b28261openalex-snapshot
Gestion et maîtrise des risques liés aux rongeurs du Tchad
inferred← citeshttps://doi.org/10.70675/bd9dbe65z0abbz435fzbd7cze3fe41121171openalex-snapshot
Développement d’une nouvelle stratégie efficace et eco-compatible pour une lutte adaptée contre le campagnol terrestre en France.
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