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CERID Bibliography
Characterization of caprine interleukin-4. Vet Immunol Immunopathol. 2001 ;78(3-4):219-29.
. Molecular basis for variable expression of merozoite surface antigen gp45 among American isolates of Babesia bigemina. Infect Immun. 2001 ;69(6):3782-90.
. Strain composition of the ehrlichia Anaplasma marginale within persistently infected cattle, a mammalian reservoir for tick transmission. J Clin Microbiol. 2001 ;39(2):631-5.
. A unique phospholipid organization in bovine erythrocyte membranes. Proc Natl Acad Sci U S A. 2001 ;98(14):7736-41.
. Characterization of allelic variation in the Babesia bovis merozoite surface antigen 1 (MSA-1) locus and identification of a cross-reactive inhibition-sensitive MSA-1 epitope. Infect Immun. 2000 ;68(12):6865-70.
. Phosphatidylcholine formation is the predominant lipid biosynthetic event in the hemoparasite Babesia bovis. Mol Biochem Parasitol. 2000 ;106(1):147-56.
. Babesia bigemina: immunization with purified rhoptries induces protection against acute parasitemia. Exp Parasitol. 1999 ;93(2):105-8.
. . . B-lymphocyte proliferation during bovine leukemia virus-induced persistent lymphocytosis is enhanced by T-lymphocyte-derived interleukin-2. J Virol. 1998 ;72(4):3169-77.
. CD4(+) T-lymphocyte and immunoglobulin G2 responses in calves immunized with Anaplasma marginale outer membranes and protected against homologous challenge. Infect Immun. 1998 ;66(11):5406-13.
. Conformational dependence of Anaplasma marginale major surface protein 5 surface-exposed B-cell epitopes. Infect Immun. 1998 ;66(6):2619-24.
. Detection of cattle naturally infected with Anaplasma marginale in a region of endemicity by nested PCR and a competitive enzyme-linked immunosorbent assay using recombinant major surface protein 5. J Clin Microbiol. 1998 ;36(3):777-82.
. Expression of Anaplasma marginale major surface protein 2 variants during persistent cyclic rickettsemia. Infect Immun. 1998 ;66(3):1200-7.
. Helper T-cell epitopes encoded by the Babesia bigemina rap-1 gene family in the constant and variant domains are conserved among parasite strains. Infect Immun. 1998 ;66(4):1561-9.
. Immunodominant T-cell antigens and epitopes of Babesia bovis and Babesia bigemina. Ann Trop Med Parasitol. 1998 ;92(4):473-82.
. In vivo binding of immunoglobulin M to the surfaces of Babesia bigemina-infected erythrocytes. Infect Immun. 1998 ;66(6):2922-7.
. Persistence of Anaplasma ovis infection and conservation of the msp-2 and msp-3 multigene families within the genus Anaplasma. Infect Immun. 1998 ;66(12):6035-9.
. Persistence of antibodies against epitopes encoded by a single gene copy of the Babesia bovis merozoite surface antigen 1 (MSA-1). J Parasitol. 1998 ;84(2):449-52.
. Sequence and functional analysis of the intergenic regions separating babesial rhoptry-associated protein-1 (rap-1) genes. Exp Parasitol. 1998 ;90(2):189-94.
. Structure, sequence, and transcriptional analysis of the Babesia bovis rap-1 multigene locus. Mol Biochem Parasitol. 1998 ;93(2):215-24.
. Anaplasma marginale major surface protein 3 is encoded by a polymorphic, multigene family. Infect Immun. 1997 ;65(1):156-63.
. Genetic variation in the dimorphic regions of RAP-1 genes and rap-1 loci of Babesia bigemina. Mol Biochem Parasitol. 1997 ;90(2):479-89.
. Immunization with Babesia bigemina rhoptry-associated protein 1 induces a type 1 cytokine response. J Interferon Cytokine Res. 1997 ;17(1):45-54.
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