Grötzinger, Joachim

Treatment of type 2 diabetes with the designer cytokine IC7Fc

Findeisen, M., Allen, T. L., Henstridge, D. C., Kammoun, H., Brandon, A. E., Baggio, L. L., Watt, K. I., Pal, M., Cron, L., Estevez, E., et al. (2019) · Nature

Cytokine Signaling Pathways and InteractionsAdipokines, Inflammation, and Metabolic Diseases

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Disulphide-reduced psoriasin is a human apoptosis-inducing broad-spectrum fungicide

Hein, K. Z., Takahashi, H., Tsumori, T., Yasui, Y., Nanjoh, Y., Toga, T., Wu, Z., Grötzinger, J., Jung, S., Wehkamp, J., et al. (2015) · Proceedings of the National Academy of Sciences

Nail Diseases and TreatmentsS100 Proteins and Annexins

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A novel entity of clinically isolated adrenal insufficiency caused by a partially inactivating mutation of the gene encoding for P450 side chain cleavage enzyme (CYP11A1)

Parajes, S., Kamrath, C., Rose, I. T., Taylor, A. E., Mooij, C. F., Dhir, V., Grötzinger, J., Arlt, W., & Krone, N. (2011) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersSexual Differentiation and Disorders

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Congenital Adrenal Hyperplasia due to 11-Hydroxylase Deficiency – Insights from Two Novel CYP11B1 Mutations (p.M92X, p.R453Q)

Krone, N., Grötzinger, J., Holterhus, P.-M., Sippell, W. G., Schwarz, H.-P., & Riepe, F. G. (2009) · Hormone Research in Paediatrics

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

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Functional characterization of three CYP21A2 sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co-expression system: Functional Characterization of CYP21A2 Variants

Bleicken, C., Loidi, L., Dhir, V., Parajes, S., Quinteiro, C., Dominguez, F., Grötzinger, J., Sippell, W. G., Riepe, F. G., Arlt, W., et al. (2009) · Human Mutation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

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