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Noninvasive Detection of Equid Herpesviruses in Fecal Samples
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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/zoo.21380openalex-snapshot
Equine behavioral enrichment toys as tools for non‐invasive recovery of viral and host DNA
inferredcites →https://doi.org/10.1007/978-4-431-77134-0openalex-snapshot
Management of Disease in Wild Mammals
inferredcites →https://doi.org/10.1007/978-4-431-77134-0_10openalex-snapshot
Wildlife Disease Surveillance and Monitoring
inferredcites →https://doi.org/10.1007/bf01320781openalex-snapshot
Variation in cellular tropism between isolates of Equine herpesvirus-1 in Foals
inferredcites →https://doi.org/10.1007/s00705-015-2614-9openalex-snapshot
High prevalence and diversity of viruses of the subfamily Gammaherpesvirinae, family Herpesviridae, in fecal specimens from bats of different species in southern China
inferredcites →https://doi.org/10.1016/0168-1591(88)90099-8openalex-snapshot
Time budgets of adult Przewalski horses: Effects of sex, reproductive status and enclosure
inferredcites →https://doi.org/10.1016/j.biocon.2010.02.032openalex-snapshot
Stress: An inevitable component of animal translocation
inferredcites →https://doi.org/10.1016/j.cbpa.2011.07.005openalex-snapshot
Is there an influence of body mass on digesta mean retention time in herbivores? A comparative study on ungulates
inferredcites →https://doi.org/10.1016/j.cub.2012.07.035openalex-snapshot
A Potentially Fatal Mix of Herpes in Zoos
inferredcites →https://doi.org/10.1016/j.rvsc.2008.06.001openalex-snapshot
Prevalence of equine herpesvirus-1 and equine herpesvirus-4 infections in equidae species in Turkey as determined by ELISA and multiplex nested PCR
inferredcites →https://doi.org/10.1016/j.tvjl.2009.08.017openalex-snapshot
Equine gammaherpesviruses: Pathogenesis, epidemiology and diagnosis
inferredcites →https://doi.org/10.1016/j.vetmic.2007.12.013openalex-snapshot
Isolation of a gammaherpesvirus similar to asinine herpesvirus-2 (AHV-2) from a mule and a survey of mules and donkeys for AHV-2 infection by real-time PCR
inferredcites →https://doi.org/10.1016/j.vetmic.2010.11.024openalex-snapshot
Fatal epizootic equine herpesvirus 1 infections in new and unnatural hosts
inferredcites →https://doi.org/10.1016/j.vetmic.2011.04.017openalex-snapshot
Kinetics of Equid herpesvirus type 2 infections in a group of Thoroughbred foals
inferredcites →https://doi.org/10.1016/j.vetmic.2013.05.031openalex-snapshot
Equine gammaherpesviruses: Perfect parasites?
inferredcites →https://doi.org/10.1016/j.vetmic.2013.06.018openalex-snapshot
Equine herpesviruses type 1 (EHV-1) and 4 (EHV-4)—Masters of co-evolution and a constant threat to equids and beyond
inferredcites →https://doi.org/10.1016/j.vetmic.2013.12.011openalex-snapshot
Zebra-borne equine herpesvirus type 1 (EHV-1) infection in non-African captive mammals
inferredcites →https://doi.org/10.1016/j.yhbeh.2018.04.005openalex-snapshot
Plains zebra (Equus quagga) adrenocortical activity increases during times of large aggregations in the Serengeti ecosystem
inferredcites →https://doi.org/10.1023/a:1008064118057openalex-snapshot
Detection of New DNA Polymerase Genes of Known and Potentially Novel Herpesviruses by PCR with Degenerate and Deoxyinosine-Substituted Primers
inferredcites →https://doi.org/10.1038/s41598-018-28688-0openalex-snapshot
Physiological costs of infection: herpesvirus replication is linked to blood oxidative stress in equids
inferredcites →https://doi.org/10.1038/srep46559openalex-snapshot
Long term stability and infectivity of herpesviruses in water
inferredcites →https://doi.org/10.1080/00480169.2014.899945openalex-snapshot
A review of equid herpesvirus 1 for the veterinary practitioner. Part A: clinical presentation, diagnosis and treatment
inferredcites →https://doi.org/10.1080/00480169.2014.899946openalex-snapshot
A review of equid herpesvirus 1 for the veterinary practitioner. Part B: pathogenesis and epidemiology
inferredcites →https://doi.org/10.1111/j.1600-065x.2011.01074.xopenalex-snapshot
Immune modulation during latent herpesvirus infection
inferredcites →https://doi.org/10.1111/j.1751-0813.2001.tb10674.xopenalex-snapshot
Identification of equine herpesvirus 3 (equine coital exanthema virus), equine gammaherpesviruses 2 and 5, equine adenoviruses 1 and 2, equine arteritis virus and equine rhinitis A virus by polymerase chain reaction
inferredcites →https://doi.org/10.1111/j.1939-1676.2009.0304.xopenalex-snapshot
Equine Herpesvirus-1 Consensus Statement
inferredcites →https://doi.org/10.1111/j.2042-3306.1985.tb02030.xopenalex-snapshot
Coprophagy by foals: Effect of age and possible functions
inferredcites →https://doi.org/10.1128/aem.63.10.3741-3751.1997openalex-snapshot
Inhibition and facilitation of nucleic acid amplification
inferredcites →https://doi.org/10.1128/jvi.01865-15openalex-snapshot
Coinfections: Another Variable in the Herpesvirus Latency-Reactivation Dynamic
inferredcites →https://doi.org/10.1128/jvi.02109-09openalex-snapshot
Multiple Diverse Circoviruses Infect Farm Animals and Are Commonly Found in Human and Chimpanzee Feces
inferredcites →https://doi.org/10.1146/annurev-virology-092917-043227openalex-snapshot
How Host Specific Are Herpesviruses? Lessons from Herpesviruses Infecting Wild and Endangered Mammals
inferredcites →https://doi.org/10.1177/104063870601800403openalex-snapshot
Detection and Quantification of Equine Herpesvirus-1 Viremia and Nasal Shedding by Real-Time Polymerase Chain Reaction
inferredcites →https://doi.org/10.1354/vp.09-vp-0007-d-cropenalex-snapshot
Meningoencephalitis in a Polar Bear Caused by Equine Herpesvirus 9 (EHV-9)
inferredcites →https://doi.org/10.1371/journal.pone.0118543openalex-snapshot
Adenovirus and Herpesvirus Diversity in Free-Ranging Great Apes in the Sangha Region of the Republic of Congo
inferredcites →https://doi.org/10.1371/journal.ppat.0030160openalex-snapshot
A Point Mutation in a Herpesvirus Polymerase Determines Neuropathogenicity
inferredcites →https://doi.org/10.2147/vmrr.s39473openalex-snapshot
Gammaherpesvirus infections in equids: a review
inferredcites →https://doi.org/10.2981/0909-6396(2006)12[109:rocmil]2.0.co;2openalex-snapshot
Risk of capture-related mortality in large free-ranging mammals: experiences from Scandinavia
inferredcites →https://doi.org/10.3201/eid1410.080703openalex-snapshot
New Hosts for Equine Herpesvirus 9
inferredcites →https://doi.org/10.7589/0090-3558-46.3.878openalex-snapshot
SURVEILLANCE OF AVIAN INFLUENZA VIRUS IN WILD BIRD FECAL SAMPLES FROM SOUTH KOREA, 2003–2008
inferredcites →https://doi.org/10.7717/peerj.5422openalex-snapshot
Environmental stressors may cause equine herpesvirus reactivation in captive Grévy’s zebras (Equus grevyi)
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.4152868openalex-extracted
Multiplex Real-Time Pcr for the Detection and Differentiation of Equid Gammaherpesvirus 2 and 5
inferred← citeshttps://doi.org/10.1007/s40203-026-00719-zopenalex-snapshot
Computational structure modeling, functional characterization, and identification of potential inhibitors for the cyclic-di-GMP mediated biofilm forming membrane protein in Vibrio cholerae
inferred← citeshttps://doi.org/10.1007/s42991-020-00006-0openalex-snapshot
Immune differences in captive and free-ranging zebras (Equus zebra and E. quagga)
inferred← citeshttps://doi.org/10.1016/b978-0-323-82852-9.00027-7openalex-snapshot
Noninvasive Monitoring of Herpes Viruses
inferred← citeshttps://doi.org/10.1016/j.jviromet.2022.114615openalex-snapshot
Multiplex real-time PCR for the detection and differentiation of equid gammaherpesvirus 2 and 5
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.145446openalex-snapshot
Seasonal host and ecological drivers may promote restricted water as a viral vector
inferred← citeshttps://doi.org/10.1016/j.vetmic.2026.111127openalex-snapshot
Intermittent shedding dynamics of EHV-1 across biological matrices during a natural outbreak linked to international equestrian events
inferred← citeshttps://doi.org/10.1111/1755-0998.13069openalex-snapshot
Terrestrial mammal surveillance using hybridization capture of environmental DNA from African waterholes
inferred← citeshttps://doi.org/10.1111/evj.13512openalex-snapshot
Recent advancements in our understanding of equid gammaherpesvirus infections
inferred← citeshttps://doi.org/10.1111/evj.14007openalex-snapshot
Detection of equine herpesvirus‐1 ( EHV‐1 ) in urine samples during outbreaks of equine herpesvirus myeloencephalopathy
inferred← citeshttps://doi.org/10.2903/j.efsa.2022.7036openalex-snapshot
Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): infection with Equine Herpesvirus‐1
inferred← citeshttps://doi.org/10.3390/pathogens10040423openalex-snapshot
Environmental Detection and Potential Transmission of Equine Herpesviruses
inferred← citeshttps://doi.org/10.3390/pathogens11050574openalex-snapshot
Investigation of the Use of Non-Invasive Samples for the Molecular Detection of EHV-1 in Horses with and without Clinical Infection
inferred← citeshttps://doi.org/10.3390/v17060862openalex-snapshot
First Molecular Evidence of Equine Herpesvirus Type 1 (EHV-1) in Ocular Swabs of Clinically Affected Horses
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