Bernhard Hemmer

发表

Predictable TCR antigen recognition based on peptide scans leads to the identification of agonist ligands with no sequence homology.

R. Houghten, C. Pinilla, B. Hemmer, 1998, Journal of immunology.

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

H. Ullum, T. Werge, H. Hakonarson, 2020, Cell.

Relationships among TCR ligand potency, thresholds for effector function elicitation, and the quality of early signaling events in human T cells.

R. Germain, B. Hemmer, R. Martin, 1998, Journal of immunology.

Probing degeneracy in T-cell recognition using peptide combinatorial libraries.

R. Houghten, C. Pinilla, B. Hemmer, 1998, Immunology today.

Immunogenicity. I. Use of peptide libraries to identify epitopes that activate clonotypic CD4+ T cells and induce T cell responses to native peptide ligands.

R A Houghten, R. Houghten, C. Pinilla, 1999, Journal of immunology.

Modifications of peptide ligands enhancing T cell responsiveness imply large numbers of stimulatory ligands for autoreactive T cells.

J. Coligan, B. Hemmer, H. McFarland, 1997, Journal of immunology.

Human autoreactive CD4+ T cell clones use perforin- or Fas/Fas ligand-mediated pathways for target cell lysis.

B. Hemmer, H. McFarland, R. Martin, 1997, Journal of immunology.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

M. Pirinen, P. Donnelly, C. Spencer, 2013, Nature Genetics.