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Yohannes Hagos

Researcher at University of Göttingen

Publications -  60
Citations -  2544

Yohannes Hagos is an academic researcher from University of Göttingen. The author has contributed to research in topics: Organic anion transporter 1 & Organic cation transport proteins. The author has an hindex of 23, co-authored 57 publications receiving 2206 citations.

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Epithelial-to-mesenchymal transition induces cell cycle arrest and parenchymal damage in renal fibrosis

TL;DR: In mouse models of experimentally induced renal fibrosis, conditional deletion of Twist1 or Snai1 in proximal TECs resulted in inhibition of the EMT program and the maintenance of TEC integrity, while also restoring cell proliferation, dedifferentiation-associated repair and regeneration of the kidney parenchyma and attenuating interstitial fibrosis.
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Human Renal Organic Anion Transporter 4 Operates as an Asymmetric Urate Transporter

TL;DR: In this article, the authors evaluated the physiologic role, transport mode, and driving forces of human organic anion transporter 4 (hOAT4) and showed that it facilitates substantial uptake of [(14)C]urate, which was elevated 2.6-fold by intracellular HCTZ.
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Identification of a New Urate and High Affinity Nicotinate Transporter, hOAT10 (SLC22A13) *

TL;DR: Surprisingly, urate–/glutathione exchange by hOAT10 is detected, consistent with an involvement of hO AT10 in the renal glutathione cycle, and the first molecular evidence for cyclosporine A-induced hyperuricemia is provided.
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Rat renal cortical OAT1 and OAT3 exhibit gender differences determined by both androgen stimulation and estrogen inhibition.

TL;DR: Gender differences in the rat renal cortical OAT1 and OAT3 (M > F) appear after puberty and are determined by both a stimulatory effect of androgens (and progesterone in the case of OAT2) and an inhibitory effect of estrogens.
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Murine renal organic anion transporters mOAT1 and mOAT3 facilitate the transport of neuroactive tryptophan metabolites

TL;DR: Six tryptophan metabolites, including the bioactive substances KYNA, XA, and the serotonin metabolite 5-hydroxyindol acetate inhibited [(3)H]p-aminohippurate (PAH) or 6-carboxyfluorescein (6-CF) uptake by 50-85%, demonstrating that these compounds interact with OAT1 as well as with Oat3.