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The Role of Mustelids in the Transmission of Sarcocystis spp. Using Cattle as Intermediate 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/10.1002/cpmc.32openalex-snapshot
Isolation, Culture and Cryopreservation ofSarcocystisspecies
inferredcites →https://doi.org/10.1007/978-3-030-16501-7_8openalex-snapshot
Human-Mediated Carrion: Effects on Ecological Processes
inferredcites →https://doi.org/10.1007/bf02189692openalex-snapshot
Feeding habits and trophic niche overlap of two sympatric mustelidae, the polecatMustela putorius and the beech martenMartes foina
inferredcites →https://doi.org/10.1007/s00436-014-4251-8openalex-snapshot
Molecular characterisation of Sarcocystis lutrae n. sp. and Toxoplasma gondii from the musculature of two Eurasian otters (Lutra lutra) in Norway
inferredcites →https://doi.org/10.1007/s00436-015-4348-8openalex-snapshot
Molecular identification of Sarcocystis rileyi sporocysts in red foxes (Vulpes vulpes) and raccoon dogs (Nyctereutes procyonoides) in Lithuania
inferredcites →https://doi.org/10.1007/s00436-015-4881-5openalex-snapshot
Molecular characterisation of Sarcocystis bovifelis, Sarcocystis bovini n. sp., Sarcocystis hirsuta and Sarcocystis cruzi from cattle (Bos taurus) and Sarcocystis sinensis from water buffaloes (Bubalus bubalis)
inferredcites →https://doi.org/10.1007/s00436-016-4998-1openalex-snapshot
Molecular differentiation of Sarcocystis buffalonis and Sarcocystis levinei in water buffaloes (Bubalus bubalis) from Sarcocystis hirsuta and Sarcocystis cruzi in cattle (Bos taurus)
inferredcites →https://doi.org/10.1007/s00436-016-5057-7openalex-snapshot
Morphological and molecular characterization of Sarcocystis taeniata and Sarcocystis pilosa n. sp. from the sika deer (Cervus nippon) in Lithuania
inferredcites →https://doi.org/10.1007/s00436-018-5880-0openalex-snapshot
Molecular identification of Sarcocystis lutrae (Apicomplexa: Sarcocystidae) in muscles of five species of the family Mustelidae
inferredcites →https://doi.org/10.1007/s13364-012-0126-5openalex-snapshot
Feeding habits of invasive American mink (Neovison vison) in northern Germany—potential implications for fishery and waterfowl
inferredcites →https://doi.org/10.1016/j.ijpara.2013.02.004openalex-snapshot
Phylogenetic relationships among Sarcocystis species in cervids, cattle and sheep inferred from the mitochondrial cytochrome c oxidase subunit I gene
inferredcites →https://doi.org/10.1016/j.ijppaw.2019.12.001openalex-snapshot
First report of Sarcocystis pilosa sporocysts in feces from red fox, Vulpes vulpes schrencki, in Hokkaido, Japan
inferredcites →https://doi.org/10.1016/j.ijppaw.2020.09.005openalex-snapshot
Sarcocystis infection in red deer (Cervus elaphus) with eosinophilic myositis/fasciitis in Switzerland and involvement of red foxes (Vulpes vulpes) and hunting dogs in the transmission
inferredcites →https://doi.org/10.1016/j.vetpar.2009.12.043openalex-snapshot
Rhinitis and disseminated disease in a ferret (Mustela putorius furo) naturally infected with Sarcocystis neurona
inferredcites →https://doi.org/10.1016/j.vetpar.2015.03.007openalex-snapshot
Sarcocystis cruzi infection in wood bison (Bison bison athabascae)
inferredcites →https://doi.org/10.1016/j.vetpar.2016.02.011openalex-snapshot
Molecular identification of Sarcocystis spp. in foxes (Vulpes vulpes) and raccoon dogs (Nyctereutes procyonoides) from Germany
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1017/s0031182010000399openalex-snapshot
The red fox (Vulpes vulpes) and the arctic fox (Vulpes lagopus) are definitive hosts ofSarcocystis alcesandSarcocystis hjortifrom moose (Alces alces)
inferredcites →https://doi.org/10.1023/a:1006090232343openalex-snapshot
The present state of species-systematics in Sarcocystis Lankester, 1882 (Protista, Sporozoa, Coccidia)
inferredcites →https://doi.org/10.1046/j.1365-2907.2000.00068.xopenalex-snapshot
Lessons from lean beasts: conservation biology of the mustelids
inferredcites →https://doi.org/10.1080/02701367.1991.10608733openalex-snapshot
What is Missing inp< .05? Effect Size
inferredcites →https://doi.org/10.1080/13921657.2002.10512525openalex-snapshot
Diet Composition of the Red Fox (Vulpes Vulpes L.), Pine Marten (Martes Martes L.) and Raccoon Dog (Nyctereutes Procyonoides Gray) in Clay Plain Landscape, Lithuania
inferredcites →https://doi.org/10.1186/1742-5573-8-1openalex-snapshot
WINPEPI updated: computer programs for epidemiologists, and their teaching potential
inferredcites →https://doi.org/10.1186/s13071-018-2694-yopenalex-snapshot
Identification and genetic characterization of Sarcocystis arctica and Sarcocystis lutrae in red foxes (Vulpes vulpes) from Baltic States and Spain
inferredcites →https://doi.org/10.1186/s13071-020-04108-zopenalex-snapshot
Molecular identification of Sarcocystis lutrae (Apicomplexa: Sarcocystidae) from the raccoon dog, Nyctereutes procyonoides, and the common raccoon, Procyon lotor, in the Czech Republic
inferredcites →https://doi.org/10.1186/s13071-020-04473-9openalex-snapshot
Molecular identification of four Sarcocystis species in cattle from Lithuania, including S. hominis, and development of a rapid molecular detection method
inferredcites →https://doi.org/10.1214/ss/1009213286openalex-snapshot
Interval Estimation for a Binomial Proportion
inferredcites →https://doi.org/10.1292/jvms.16-0127openalex-snapshot
Domestic cats (Felis catus) are definitive hosts for Sarcocystis sinensis from water buffaloes (Bubalus bubalis)
inferredcites →https://doi.org/10.1645/ge-753r1.1openalex-snapshot
Prevalence of Sarcocystis spp. in Two Subspecies of Caribou (Rangifer tarandus) in Newfoundland and Labrador, and Foxes (Vulpes vulpes), Wolves (Canis lupus), and Husky Dogs (Canis familiaris) as Potential Definitive Hosts
inferredcites →https://doi.org/10.17221/151/2017-vetmedopenalex-snapshot
Prevalence and intensity of Sarcocystis spp. infection in animals slaughtered for food in Lithuania
inferredcites →https://doi.org/10.2478/lynx-2017-0009openalex-snapshot
Diet of Martes foina in Bohemia, Czech Republic (Carnivora: Mustelidae)
inferredcites →https://doi.org/10.25225/fozo.v62.i1.a7.2013openalex-snapshot
Diet of the European polecatMustela putoriusin an agricultural area in Poland
inferredcites →https://doi.org/10.3106/041.036.0401openalex-snapshot
Contrasting Sociality in Two Widespread, Generalist, Mustelid Genera,MelesandMartes
inferredcites →https://doi.org/10.3390/su12229777openalex-snapshot
Citizen Scientists Showed a Four-Fold Increase of Lynx Numbers in Lithuania
inferredcites →https://doi.org/10.5281/zenodo.12612535openalex-snapshot
Feeding Habits Of Sympatric Mustelids In An Agricultural Area Of Hungary
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2023.03.001zenodo-depositor-declared
First report of Sarcocystis spp. (Apicomplexa, Sarcocystidae) in Lagostomus maximus (Desmarest, 1917) (Rodentia, Chinchillidae) in Argentina
inferred← citeshttps://doi.org/10.1007/s00436-021-07180-1openalex-snapshot
Invasive American mink (Neovison vison) as potential definitive host of Sarcocystis elongata, S. entzerothi, S. japonica, S. truncata and S. silva using different cervid species as intermediate hosts
inferred← citeshttps://doi.org/10.1007/s00436-024-08234-wopenalex-snapshot
Diversity of Sarcocystis parasites in southeastern Baltic Sea catchment ecosystems
inferred← citeshttps://doi.org/10.1007/s11686-024-00814-1openalex-snapshot
The Distribution of Sarcocsytis Species Described by Ungulates-Canids Life Cycle in Intestines of Small Predators of the Family Mustelidae
inferred← citeshttps://doi.org/10.1016/b978-0-443-18437-6.00032-8openalex-snapshot
Mustelidae and Mephitidae
inferred← citeshttps://doi.org/10.1016/j.fawpar.2024.e00220openalex-snapshot
Detection of Sarcocystis hominis, Sarcocystis bovifelis, Sarcocystis cruzi, Sarcocystis hirsuta and Sarcocystis sigmoideus sp. nov. in carcasses affected by bovine eosinophilic myositis
inferred← citeshttps://doi.org/10.1016/j.ijpara.2022.09.009openalex-snapshot
Bovine sarcocystosis: Sarcocystis species, diagnosis, prevalence, economic and public health considerations, and association of Sarcocystis species with eosinophilic myositis in cattle
inferred← citeshttps://doi.org/10.1016/j.vas.2025.100431openalex-snapshot
Prevalence and molecular analysis of Sarcocystis species infection in slaughtered cattle in Alborz, Iran
inferred← citeshttps://doi.org/10.1017/s003118202300094xopenalex-snapshot
Sarcocystis cruzi (Hasselmann, 1923) Wenyon, 1926: redescription, molecular characterization and deposition of life cycle stages specimens in the Smithsonian Museum
inferred← citeshttps://doi.org/10.1186/s12917-026-05345-7openalex-snapshot
First report of Atriotaenia tapeworms and Sarcocystis protists in invasive raccoons (Procyon lotor) from Lithuania
inferred← citeshttps://doi.org/10.1186/s13071-021-04722-5openalex-snapshot
Molecular detection of cattle Sarcocystis spp. in North-West Italy highlights their association with bovine eosinophilic myositis
inferred← citeshttps://doi.org/10.21521/mw.6838openalex-snapshot
Sarcocystis spp. – an underestimated parasite with zoonotic potential associated with food of animal origin
inferred← citeshttps://doi.org/10.3389/fvets.2024.1392618openalex-snapshot
Red foxes (Vulpes vulpes) and raccoon dogs (Nyctereutes procyonoides) as potential spreaders of Sarcocystis species
inferred← citeshttps://doi.org/10.3390/ani11113258openalex-snapshot
The Role of Birds of the Family Corvidae in Transmitting Sarcocystis Protozoan Parasites
inferred← citeshttps://doi.org/10.3390/ani13030467openalex-snapshot
Molecular Identification of Sarcocystis rileyi and Sarcocystis sp. (Closely Related to Sarcocystis wenzeli) in Intestines of Mustelids from Lithuania
inferred← citeshttps://doi.org/10.3390/ani14162391openalex-snapshot
The Genetic Identification of Numerous Apicomplexan Sarcocystis Species in Intestines of Common Buzzard (Buteo buteo)
inferred← citeshttps://doi.org/10.3390/ani16152285openalex-snapshot
High Diversity of Sarcocystis Species Identified in Intestines of Red Foxes (Vulpes vulpes) from Lithuania
inferred← citeshttps://doi.org/10.3390/biology15080593openalex-snapshot
Microscopic and Molecular Identification of Sarcocystis spp. in Intestines of Canids and Mustelids Associated with Sarcocyst-Forming Species in Rodent Muscles
inferred← citeshttps://doi.org/10.3390/pathogens12060752openalex-snapshot
Molecular Confirmation of Accipiter Birds of Prey as Definitive Hosts of Numerous Sarcocystis Species, including Sarcocystis sp., Closely Related to Pathogenic S. calchasi
inferred← citeshttps://doi.org/10.3390/pathogens14030288openalex-snapshot
Molecular Evidence of Raccoon Dog (Nyctereutes procyonoides) as a Natural Definitive Host for Several Sarcocystis Species
inferred← citeshttps://doi.org/10.3390/vetsci12040379openalex-snapshot
European Pine Marten (Martes martes) as Natural Definitive Host of Sarcocystis Species in Latvia: Microscopic and Molecular Analysis
inferred← citeshttps://doi.org/10.3390/vetsci9080412openalex-snapshot
Molecular Identification of Parasitic Protozoa Sarcocystis in Water Samples
inferred← citeshttps://doi.org/10.53730/ijhs.v6ns6.12473openalex-snapshot
Molecular characterization of Sarcocystis species Isolated from sheep in Al-Qadisiyah Governorate – Iraq
inferred← citeshttps://doi.org/10.6084/m9.figshare.14478662openalex-snapshot
Additional file 1 of Molecular detection of cattle Sarcocystis spp. in North-West Italy highlights their association with bovine eosinophilic myositis
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