Latest papers

Real-time quantitative RT-PCR and PCR assays for a novel European field isolate of equine infectious anaemia virus based on sequence determination of the gag gene.

Standardization and validation of an agar gel immunodiffusion test for the diagnosis of equine infectious anemia using a recombinant p26 antigen.

Envelope-specific T-helper and cytotoxic T-lymphocyte responses associated with protective immunity to equine infectious anemia virus.

Serodiagnosis of equine infectious anemia by agar gel immunodiffusion and ELISA using a recombinant p26 viral protein expressed in Escherichia coli as antigen.

An investigation of equine infectious anaemia infection in the central Anatolia region of Turkey.

Correlation between the induction of Th1 cytokines by an attenuated equine infectious anemia virus vaccine and protection against disease progression.

Immune suppression of challenged vaccinates as a rigorous assessment of sterile protection by lentiviral vaccines.

[Study on the role of cytotoxic T lymphocytes during equine infectious anemia virus infection and its epitope specificity].

Long terminal repeats are not the sole determinants of virulence for equine infectious anemia virus.

Description of the first case of equine infectious anaemia in Northern Ireland.

Equine infectious anaemia in Ireland: characterisation of the virus.

Distribution of equine infectious anemia in horses in the north of Minas Gerais State, Brazil.

Equine infectious anaemia in Ireland.

Steps to prevent outbreaks of swamp fever.

Combined amino acid mutations occurring in the envelope closely correlate with pathogenicity of EIAV.

The S2 accessory gene of equine infectious anemia virus is essential for expression of disease in ponies

Amino acid mutations of the infectious clone from Chinese EIAV attenuated vaccine resulted in reversion of virulence.

Apparent elimination of EIAV ancestral species in a long-term inapparent carrier.

Evaluation of high functional avidity CTL to Gag epitope clusters in EIAV carrier horses.

Endocytosis and a low-pH step are required for productive entry of equine infectious anemia virus.