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TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5
Karges, B et al. (2005)
Wissenschaftlicher Artikel
Digenic inheritance of hepatocyte nuclear factor-1 alpha and -1 beta with maturity-onset diabetes of the young, polycystic thyroid, and urogenital malformations
Karges, Beate et al. (2007)
Wissenschaftlicher Artikel
Molecular mechanisms of sulfasalazine-induced T-cell apoptosis
Liptay, S et al. (2002)
Wissenschaftlicher Artikel
Rocaglamide derivatives are potent inhibitors of NF-kappa B activation in T-cells
Baumann, B et al. (2002)
Wissenschaftlicher Artikel
Levothyroxine in euthyroid autoimmune thyroiditis and type 1 diabetes: A randomized, controlled trial
Karges, Beate et al. (2007)
Wissenschaftlicher Artikel
Immunological mechanisms associated with tong-term remission of human type 1 diabetes
Karges, B et al. (2006)
Wissenschaftlicher Artikel
Complete long-term recovery of beta-cell function in autoimmune type 1 diabetes after insulin treatment
Karges, B et al. (2004)
Wissenschaftlicher Artikel
Type II diabetes mellitus and impaired glucose regulation in Caucasian children and adolescents with obesity living in Germany
Wabitsch, Martin et al. (2004)
Wissenschaftlicher Artikel
Compound heterozygous and homozygous mutations of the TSH beta gene as a cause of congenital central hypothyroidism in Europe
Karges, B et al. (2004)
Wissenschaftlicher Artikel
Eradication of a dysfunctional HLA-haploidentical T cell system by a second HLA-identical BMT
Ege, M et al. (2001)
Wissenschaftlicher Artikel