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1 tes, using the upstream regulatory region of cottontail rabbit papillomavirus.
2 l (hepatitis B virus, rhesus papillomavirus, cottontail rabbit papillomavirus) but also many without
3 expressing the major capsid protein (L1) of cottontail rabbit papillomavirus (CRPV) and tested the e
4 ection patterns similar to those found after cottontail rabbit papillomavirus (CRPV) challenge when c
8 viously showed that DNA vaccination with the cottontail rabbit papillomavirus (CRPV) E6 gene induced
9 developed a model using chimeric HPV capsid/cottontail rabbit papillomavirus (CRPV) genome particles
13 ies have identified two different strains of cottontail rabbit papillomavirus (CRPV) that differ by a
14 irus-produced virus-like particles (VLPs) of cottontail rabbit papillomavirus (CRPV) to determine whe
16 rus (Ad) vector expressing the E2 protein of cottontail rabbit papillomavirus (CRPV) was tested for t
17 V16, bovine papillomavirus type 1 (BPV1), or cottontail rabbit papillomavirus (CRPV) were produced in
18 omavirus, rabbit oral papillomavirus (ROPV), cottontail rabbit papillomavirus (CRPV), bovine papillom
20 e used to elicit therapeutic immunity in the cottontail rabbit papillomavirus (CRPV)-rabbit model of
22 re protected against infection with a mutant cottontail rabbit papillomavirus DNA containing an embed
23 DNA vaccine based on epitope selection from cottontail rabbit papillomavirus E1 using MHC class I ep
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