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Clinical Endocrinology|May 26, 1999
The effects of interleukin-2 treatment on endothelin and the activation of the hypothalamic-pituitary-adrenal axisC Raab, E Weidmann, A Schmidt, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1990
Susceptibility to thyroid autoimmune disease: molecular analysis of HLA-D region genes identifies new markers for goitrous Hashimoto's thyroiditisK Badenhoop, G Schwarz, P G Walfish, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|July 18, 2002
A recently described polymorphism in the CD28 gene on chromosome 2q33 is not associated with susceptibility to type 1 diabetesJ P Wood, M A Pani, K Bieda, et al.
Immunogenetics|September 26, 2000
MHC diversity in Caucasians, investigated using highly heterogeneous noncoding sequence motifs at the DQB1 locus including a retroviral long terminal repeat element, and its comparison to nonhuman primate homologuesH Donner, R R Tönjes, R E Bontrop, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2001
The codon 17 polymorphism of the CTLA4 gene in type 2 diabetes mellitusH Rau, J Braun, H Donner, et al.
Clinical Endocrinology|February 24, 2001
Panhypopituitarism associated with severe retroperitoneal fibrosisJ Braun, H Schuldes, J Berkefeld, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 28, 1999
No association between the deltaF508 cystic fibrosis mutation and type 2 diabetes mellitusJ Braun, J Arnemann, M Lohrey, et al.
Tissue Antigens|July 8, 1999
Intronic sequence motifs of HLA-DQB1 are shared between humans, apes and Old World monkeys, but a retroviral LTR element (DQLTR3) is human specificH Donner, R R Tönjes, R E Bontrop, et al.
Tissue Antigens|February 12, 1998
CTLA4 codon 17 dimorphism in patients with rheumatoid arthritisC Seidl, H Donner, B Fischer, et al.
Tissue Antigens|January 1, 1997
Polymorphisms of TAP1 and TAP2 genes in Graves' diseaseH Rau, A Nicolay, K H Usadel, et al.
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