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Rüdiger Göke

Researcher at University of Marburg

Publications -  96
Citations -  7289

Rüdiger Göke is an academic researcher from University of Marburg. The author has contributed to research in topics: Receptor & Insulin. The author has an hindex of 39, co-authored 95 publications receiving 7056 citations. Previous affiliations of Rüdiger Göke include University of Göttingen & University of Michigan.

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Islet amyloid polypeptide (IAPP;amylin) influences the endocrine but not the exocrine rat pancreas.

TL;DR: The data suggest amylin, a secretory product of pancreatic B-cells, as a peptide with approximately strong paracrine effects within the Langerhans islet might be involved in the regulation of glucose homeostasis.
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Signal transduction of the GLP-1-receptor cloned from a human insulinoma.

TL;DR: The understanding of GLP‐1 receptor regulation and signal transduction will aid in the discovery of compounds that act as agonists of the GLP•1 receptor for potential use in the treatment of diabetes and will facilitate the understanding of its expression under normal and pathophysiological conditions.
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Endoproteolysis by isolated membrane peptidases reveal metabolic stability of glucagon-like peptide-1 analogs, exendins-3 and -4.

TL;DR: This in vitro studies aimed to characterize the pattern and the kinetics of endoproteolysis of the insulinotropic hormone glucagon-like peptide-1 (GLP-1) and related peptides by native ectopeptidases and found that exendin-4 is several orders of magnitude more stable than GLP- 1 and Ser-8-GLp-1 is especially noteworthy given this peptide's widely reported insulinotropic potency.
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Identification of specific binding sites for glucagon-like peptide-1 on the posterior lobe of the rat pituitary

TL;DR: Using quantitative in vitro autoradiography, a high density of specific binding sites for GLP-1 was characterized on sections of the posterior pituitary lobe of the rat, revealing high and low affinity binding sites.
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Nuclear survivin is a powerful novel prognostic marker in gastroenteropancreatic neuroendocrine tumor disease.

TL;DR: Nuclear survivin expression appears to be upregulated during progression of gastroenteropancreatic neuroendocrine tumors, which identifies subgroups in metastatic disease with good (survivin–) or with less favorable prognosis (Survivin+).