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Elias Castanas

Researcher at University of Crete

Publications -  211
Citations -  10660

Elias Castanas is an academic researcher from University of Crete. The author has contributed to research in topics: Receptor & Cancer. The author has an hindex of 45, co-authored 206 publications receiving 9367 citations. Previous affiliations of Elias Castanas include Pierre-and-Marie-Curie University & National and Kapodistrian University of Athens.

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Enhanced OXER1 expression is indispensable for human cancer cell migration.

TL;DR: In this paper, the role of OXER1 and its endogenous ligand in the control of cell migration of human cancer epithelial cells (DU-145, T47D and Hep3B), mimicking the activation/migration phase of healing.
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Comparative thermodynamics of opioid receptor ligand interaction in the bovine adrenal medulla membranes—Evidence of opioid site heterogeneity

TL;DR: A marked dependence on temperature of agonist binding delta, mu and kappa 1-3 opioid sites in the bovine adrenal medulla was observed, suggesting the interaction of opioid agonists with their receptor is exergonic and entropy driven.
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Relation between glucose tolerance and serum insulin levels in man before and after thiopental intravenous administration.

TL;DR: A small but significant decrease in glucose tolerance, not related to serum insulin levels, was seen in healthy volunteers before and after a single dose of intravenous sodium thiopental.
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Original contributionAnti–saccharomyces cerevisiae mannan antibodies and antineutrophil cytoplasmic autoantibodies in Greek patients with inflammatory bowel disease

TL;DR: In this paper, perinuclear antineutrophil cytoplasmic autoantibodies (pANCA) and anti-Saccharomyces cerevisiae mannan antibodies (ASCA) were combined as a valuable diagnostic approach in inflammatory bowel disease (IBD).
Journal Article

[Characterization and modulation of anterior pituitary binding sites for rat corticotropin releasing factor (r-CRF)].

TL;DR: The finding suggests that circulating glucocorticoids may control the anterior pituitary binding sites for CRF, either by a direct action on the anteriorpituitary, or by a modulatory effect on hypothalamic CRF secretion.