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CERID Bibliography
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Author [ Title] Type Year Filters: Keyword is Antigens, Protozoan [Clear All Filters]
Genetic and antigenic characterization of Babesia bovis merozoite spherical body protein Bb-1. Mol Biochem Parasitol. 1995 ;69(2):149-59.
. Identification of Babesia bigemina and Babesia bovis merozoite proteins with isolate- and species-common epitopes recognized by antibodies in bovine immune sera. Infect Immun. 1988 ;56(6):1658-60.
. Identification of Babesia bovis merozoite surface antigens by using immune bovine sera and monoclonal antibodies. Infect Immun. 1988 ;56(9):2363-8.
. Immunization with Babesia bigemina rhoptry-associated protein 1 induces a type 1 cytokine response. J Interferon Cytokine Res. 1997 ;17(1):45-54.
Immunodominant T-cell antigens and epitopes of Babesia bovis and Babesia bigemina. Ann Trop Med Parasitol. 1998 ;92(4):473-82.
. Immunogenic B-cell epitopes of Babesia bovis rhoptry-associated protein 1 are distinct from sequences conserved between species. Infect Immun. 1993 ;61(8):3511-7.
. Interstrain conservation of babesial RAP-1 surface-exposed B-cell epitopes despite rap-1 genomic polymorphism. Infect Immun. 1994 ;62(8):3576-9.
. The major 85-kD surface antigen of the mammalian form of Trypanosoma cruzi is encoded by a large heterogeneous family of simultaneously expressed genes. J Exp Med. 1990 ;172(2):589-97.
. Molecular basis for vaccine development against anaplasmosis and babesiosis. Vet Parasitol. 1995 ;57(1-3):233-53.
. Molecular basis for variable expression of merozoite surface antigen gp45 among American isolates of Babesia bigemina. Infect Immun. 2001 ;69(6):3782-90.
. Molecular mimicry by Trypanosoma cruzi: the F1-160 epitope that mimics mammalian nerve can be mapped to a 12-amino acid peptide. Proc Natl Acad Sci U S A. 1991 ;88(14):5993-7.
. Neutralization-sensitive merozoite surface antigens of Babesia bovis encoded by members of a polymorphic gene family. Mol Biochem Parasitol. 1992 ;55(1-2):85-94.
. Persistently infected horses are reservoirs for intrastadial tick-borne transmission of the apicomplexan parasite Babesia equi. Infect Immun. 2008 ;76(8):3525-9.
. Plasmacytoid dendritic cells are activated by Toxoplasma gondii to present antigen and produce cytokines. J Immunol. 2008 ;180(9):6229-36.
. Presentation of Toxoplasma gondii antigens via the endogenous major histocompatibility complex class I pathway in nonprofessional and professional antigen-presenting cells. Infect Immun. 2007 ;75(11):5200-9.
. Prospects for subunit vaccines against tick-borne diseases. Br Vet J. 1996 ;152(6):621-39.
. Sequence conservation among merozoite apical complex proteins of Babesia bovis, Babesia bigemina and other apicomplexa. Mol Biochem Parasitol. 1991 ;49(2):329-32.
. Stimulation of T-helper cell gamma interferon and immunoglobulin G responses specific for Babesia bovis rhoptry-associated protein 1 (RAP-1) or a RAP-1 protein lacking the carboxy-terminal repeat region is insufficient to provide protective immunity again. Infect Immun. 2003 ;71(9):5021-32.
. Strain variation of Babesia bovis merozoite surface-exposed epitopes. Infect Immun. 1991 ;59(9):3340-2.
. Structure, sequence, and transcriptional analysis of the Babesia bovis rap-1 multigene locus. Mol Biochem Parasitol. 1998 ;93(2):215-24.
. Tracking antigen-specific CD4+ T cells throughout the course of chronic Leishmania major infection in resistant mice. Eur J Immunol. 2013 ;43(2):427-38.
. Treatment of cattle with DNA-encoded Flt3L and GM-CSF prior to immunization with Theileria parva candidate vaccine antigens induces CD4 and CD8 T cell IFN-γ responses but not CTL responses. Vet Immunol Immunopathol. 2011 ;140(3-4):244-51.
Trypanosoma cruzi-infected macrophages are defective in major histocompatibility complex class II antigen presentation. Eur J Immunol. 1997 ;27(12):3085-94.
. Use of monoclonal antibodies to identify, characterize, and purify a 96,000-dalton surface antigen of pathogenic Entamoeba histolytica. J Infect Dis. 1987 ;156(2):334-43.
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