Latest papers

Identification of a novel HLA-B60-restricted T cell epitope of the minor histocompatibility antigen HA-1 locus.

Minor H antigens: genes and peptides.

Distinguishing self from nonself: immunogenicity of the murine H47 locus is determined by a single amino acid substitution in an unusual peptide.

Obliterative bronchiolitis develops in miniature swine transplanted across a minor histocompatibility barrier.

Differences that matter: major cytotoxic T cell-stimulating minor histocompatibility antigens.

CD40 ligand blockade induces CD4+ T cell tolerance and linked suppression.

A genome-wide search identifies potential new susceptibility loci for Crohn's disease.

Polyriboinosinic polyribocytidylic acid (poly(I:C)) induces stable maturation of functionally active human dendritic cells.

A locus on chromosome 2 influences the development of acute graft-versus-host disease in a murine model.

Biochemical and immunogenetic analysis of an immunodominant peptide (B6dom1) encoded by the classical H7 minor histocompatibility locus.

Continuous combined hormone replacement therapy compared with tibolone.

Contributions of direct and indirect T cell alloreactivity during allograft rejection in mice.

Linked suppression of skin graft rejection can operate through indirect recognition.

Positional cloning and molecular characterization of an immunodominant cytotoxic determinant of the mouse H3 minor histocompatibility complex.

The molecular and functional characterization of a dominant minor H antigen, H60.

On histocompatibility barriers, Th1 to Th2 immune deviation, and the nature of the allograft responses.

Localization to chromosome 11 of a gene encoding a human minor histocompatibility antigen.

Expression screening of a yeast artificial chromosome contig refines the location of the mouse H3a minor histocompatibility antigen gene.

Minor transplantation antigens: animal models for human host-versus-graft, graft-versus-host, and graft-versus-leukemia reactions.

The minor histocompatibility antigen HA-1: a diallelic gene with a single amino acid polymorphism.