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Study of the efficiency of anticoagulant rodenticides to control Mus musculus domesticus introgressed with Mus spretus Vkorc1

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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/jbt.20104openalex-snapshot

Warfarin resistance in a French strain of rats

inferredcites →https://doi.org/10.1002/jbt.20201openalex-snapshot

Characterization of bromadiolone resistance in a danish strain of Norway rats, rattus norvegicus, by hepatic gene expression profiling of genes involved in vitamin k‐dependent γ‐carboxylation

inferredcites →https://doi.org/10.1002/ps.1506openalex-snapshot

Differential expression of cytochrome P450 genes between bromadiolone‐resistant and anticoagulant‐susceptible Norway rats: a possible role for pharmacokinetics in bromadiolone resistance

inferredcites →https://doi.org/10.1002/ps.2254openalex-snapshot

Distribution and frequency of VKORC1 sequence variants conferring resistance to anticoagulants in Mus musculus

inferredcites →https://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

inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot

A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding

inferredcites →https://doi.org/10.1006/bbrc.1995.2042openalex-snapshot

The Flavin-Containing Monooxygenase in Rat Liver: Evidence for the Expression of a Second Form Different from FMO1

inferredcites →https://doi.org/10.1007/bf00484079openalex-snapshot

Evidence for the presence of two sympatric species of mice (genus Mus L.) in southern France based on biochemical genetics

inferredcites →https://doi.org/10.1016/j.abb.2011.08.010openalex-snapshot

Biochemical characterization of spontaneous mutants of rat VKORC1 involved in the resistance to antivitamin K anticoagulants

inferredcites →https://doi.org/10.1016/j.cub.2011.06.043openalex-snapshot

Adaptive Introgression of Anticoagulant Rodent Poison Resistance by Hybridization between Old World Mice

inferredcites →https://doi.org/10.1016/j.phytochem.2015.08.012openalex-snapshot

Comparative inhibitory effect of prenylated coumarins, ferulenol and ferprenin, contained in the ‘poisonous chemotype’ of Ferula communis on mammal liver microsomal VKORC1 activity

inferredcites →https://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

inferredcites →https://doi.org/10.1016/s0083-6729(07)00003-9openalex-snapshot

The Vitamin K Cycle

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/nature02254openalex-snapshot

Identification of the gene for vitamin K epoxide reductase

inferredcites →https://doi.org/10.1073/pnas.1406298111openalex-snapshot

Interspecific introgressive origin of genomic diversity in the house mouse

inferredcites →https://doi.org/10.1080/00498250110060932openalex-snapshot

Suppression of CYP3A2 mRNA expression in the warfarin-resistant roof rat,Rattus rattus: possible involvement of cytochrome P450 in the warfarin resistance mechanism

inferredcites →https://doi.org/10.1097/fpc.0b013e32832ee55bopenalex-snapshot

Consequences of the Y139F Vkorc1 mutation on resistance to AVKs: in-vivo investigation in a 7th generation of congenic Y139F strain of rats

inferredcites →https://doi.org/10.1111/j.1538-7836.2010.04095.xopenalex-snapshot

Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment

inferredcites →https://doi.org/10.1111/jth.12019openalex-snapshot

VKORC1 mutations detected in patients resistant to vitamin K antagonists are not all associated with a resistant VKOR activity

inferredcites →https://doi.org/10.1111/jth.12306openalex-snapshot

Evaluation of warfarin resistance using transcription activator‐like effector nucleases‐mediated vitamin K epoxide reductase knockout HEK293 cells

inferredcites →https://doi.org/10.1124/dmd.106.011775openalex-snapshot

Elevated Warfarin Metabolism in Warfarin-Resistant Roof Rats (Rattus rattus) in Tokyo

inferredcites →https://doi.org/10.1182/blood-2013-05-501692openalex-snapshot

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

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.4483openalex-snapshot

Vertebrate pest management: research for science‐based solutions

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/10.1007/978-1-0716-0199-0_18openalex-snapshot

Population Genomics of the House Mouse and the Brown Rat

inferred← citeshttps://doi.org/10.1007/s10530-019-02189-1openalex-snapshot

Assessment of rodenticide resistance, eradication units, and pathogen prevalence in black rat populations from a Mediterranean biodiversity hotspot (Pontine Archipelago)

inferred← citeshttps://doi.org/10.1016/j.fct.2019.110984openalex-snapshot

Protective effect of Pedro-Ximénez must against p,p'-DDE-induced liver damages in aged Mus spretus mice

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.reprotox.2020.02.003openalex-snapshot

Vitamin K antagonist rodenticides display different teratogenic activity

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/10.1038/s41598-019-49661-5openalex-snapshot

Resistance to anticoagulant rodenticides in Martinique could lead to inefficient rodent control in a context of endemic leptospirosis

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/10.1079/9781800626508.0004openalex-snapshot

Resistance to Anticoagulant Rodenticides

inferred← citeshttps://doi.org/10.1093/gbe/evab288openalex-snapshot

Bidirectional Introgression between Mus musculus domesticus and Mus spretus

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/10.1371/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/10.70675/604d0956zae55z40bez881cz9bd16deba4e6openalex-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/b18e050bz2ad0z4e29z87ddzc8ed910b9f04openalex-snapshot

Etude de la tératogenicité des anticoagulants antivitamine K : nécessité de rechercher de nouvelles cibles anticoagulantes : la piste du partenaire protéique d’activation de VKORC1

inferred← citeshttps://doi.org/10.7287/peerj.9140v0.1/reviews/1openalex-snapshot

Peer Review #1 of "The reproductive inhibitory effects of levonorgestrel, quinestrol, and EP-1 in Brandt’s vole (Lasiopodomys brandtii) (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.9140v0.1/reviews/2openalex-snapshot

Peer Review #2 of "The reproductive inhibitory effects of levonorgestrel, quinestrol, and EP-1 in Brandt’s vole (Lasiopodomys brandtii) (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.9140v0.2/reviews/1openalex-snapshot

Peer Review #1 of "The reproductive inhibitory effects of levonorgestrel, quinestrol, and EP-1 in Brandt’s vole (Lasiopodomys brandtii) (v0.2)"

inferred← citeshttps://doi.org/10.7287/peerj.9140v0.2/reviews/2openalex-snapshot

Peer Review #2 of "The reproductive inhibitory effects of levonorgestrel, quinestrol, and EP-1 in Brandt’s vole (Lasiopodomys brandtii) (v0.2)"

inferred← citeshttps://doi.org/10.7717/peerj.9140openalex-snapshot

The reproductive inhibitory effects of levonorgestrel, quinestrol, and EP-1 in Brandt’s vole ( Lasiopodomys brandtii )

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