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Scandinavian Journal of Immunology|February 1, 1987
Loss of antigen recognition and impaired cytolytic function in most hybrids between cytotoxic T cells and BW5147D Woodland, D L Janković, H U Weltzien, et al.
Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.
The Clinical Investigator|November 1, 1992
On the potential of simple repetitive DNA for fingerprinting in clinical, forensic, and evolutionary dynamic studiesJ T Epplen, G Melmer, P Schmidt, et al.
Nature|March 19, 1987
Dominance of one T-cell receptor in the H-2Kb/TNP responseU Hochgeschwender, H G Simon, H U Weltzien, et al.
Human Molecular Genetics|June 1, 1995
Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patientsL Schöls, A M Vieira-Saecker, S Schöls, et al.
Genes and Immunity|June 12, 2002
Inhibitors in the NFkappaB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinationsB Miterski, S Böhringer, W Klein, et al.
Clinical and Experimental Immunology|August 12, 1999
Immunogenetic risk factors for anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitisM Gencik, S Borgmann, R Zahn, et al.
International Journal of Immunogenetics|September 17, 2005
A case-control study of tyrosine phosphatase (PTPN22) confirms the lack of association with Crohn's diseaseS E N Wagenleiter, W Klein, T Griga, et al.
Human Genetics|October 13, 2000
Genetic background of apparently idiopathic sporadic cerebellar ataxiaL Schöls, S Szymanski, S Peters, et al.
Molecular Biology and Evolution|March 1, 1994
Interdependent MHC-DRB exon-plus-intron evolution in artiodactylsF W Schwaiger, E Weyers, J Buitkamp, et al.
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