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201. Reply

204. Modelling the spatial distribution of Culicoides biting midges at the local scale.

205. Two-Host, Two-Vector Basic Reproduction Ratio (R0) for Bluetongue.

208. Why Did Bluetongue Spread the Way It Did? Environmental Factors Influencing the Velocity of Bluetongue Virus Serotype 8 Epizootic Wave in France.

209. The development of linear regression models using environmental variables to explain the spatial distribution of Fasciola hepatica infection in dairy herds in England and Wales

210. Emergence or improved detection of Japanese encephalitis virus in the Himalayan highlands?

211. Avian malaria affecting penguins in zoological gardens, aquariums and wildlife parks in the UK.

212. Opinion: Climate change and the recent emergence of bluetongue in Europe.

213. Scientists' call to action: Microbes, planetary health, and the Sustainable Development Goals.

214. Correction to: Cardinium symbiosis as a potential confounder of mtDNA based phylogeographic inference in Culicoides imicola (Diptera: Ceratopogonidae), a vector of veterinary viruses.

215. Sero-surveillance and risk factors for avian influenza and Newcastle disease virus in backyard poultry in Oman

216. Bayesian optimisation of restriction zones for bluetongue control.

217. FORTEAN TRAVELLER.

218. Cardinium symbiosis as a potential confounder of mtDNA based phylogeographic inference in Culicoides imicola (Diptera: Ceratopogonidae), a vector of veterinary viruses.

220. The challenges posed by equine arboviruses

221. The challenges posed by equine arboviruses

222. The challenges posed by equine arboviruses

223. The challenges posed by equine arboviruses

224. Field-based assessments of the seasonality of Culexpipiens sensu lato in England: an important enzootic vector of Usutu and West Nile viruses.

225. Sheep breed and shearing influences attraction and blood-feeding behaviour of Culicoides (Diptera: Ceratopogonidae) on a UK farm.

227. Integration of shared-pathogen networks and machine learning reveals the key aspects of zoonoses and predicts mammalian reservoirs.

228. A non-invasive feather-based methodology for the detection of blood parasites (Haemosporida).

229. Validation of fluorescent dust marking of Culicoides biting midges and the design of a self-marking technique

231. Dairy Heifers Naturally Exposed to Fasciola hepaticaDevelop a Type 2 Immune Response and Concomitant Suppression of Leukocyte Proliferation

232. Seroprevalence of Fasciola hepatica in dairy herds.

233. Prioritization of livestock diseases by pastoralists in Oloitoktok Sub County, Kajiado County, Kenya.

234. Development and validation of a protocol to identify and recruit participants into a large scale study on liver fluke in cattle.

235. Spatiotemporal activity of the Ixodes ricinus tick in England

236. Climate change and the recent emergence of bluetongue in Europe.

237. The epidemiology and surveillance of Culicoides-borne diseases of ruminants in the UK

238. Blue Tongue.

240. Immune responses and interactions following simultaneous application of live Newcastle disease, infectious bronchitis and avian metapneumovirus vaccines in specific-pathogen-free chicks.

241. Modelling the continental-scale spread of Schmallenberg virus in Europe: Approaches and challenges.

242. Inferences about the transmission of Schmallenberg virus within and between farms.

243. Assessing the impact of non-pharmaceutical interventions (NPI) on the dynamics of COVID-19: A mathematical modelling study of the case of Ethiopia.

244. Blood-feeding ecology of mosquitoes in two zoological gardens in the United Kingdom.

245. One hundred years of zoonoses research in the Horn of Africa: A scoping review.

246. Determining and modelling the Bluetongue vector landscape

247. Quantifying uncertainty in climate-driven disease risk predictions

248. Assessing the suitability for Aedes albopictus and dengue transmission risk in China with a delay differential equation model.

249. Torix Rickettsia are widespread in arthropods and reflect a neglected symbiosis.

250. Does Fasciola hepatica infection increase the susceptibility of cattle to infection with other pathogens normally controlled by a Th1 or pro-inflammatory response?

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