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Pradeep K. Dudeja

Researcher at University of Illinois at Chicago

Publications -  241
Citations -  7127

Pradeep K. Dudeja is an academic researcher from University of Illinois at Chicago. The author has contributed to research in topics: Inflammation & Biology. The author has an hindex of 46, co-authored 209 publications receiving 6209 citations. Previous affiliations of Pradeep K. Dudeja include University of Illinois at Urbana–Champaign & Veterans Health Administration.

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Expression and membrane localization of MCT isoforms along the length of the human intestine

TL;DR: It is speculated that distinct MCT isoforms may be involved in SCFA transport across the apical or basolateral membranes in polarized colonic epithelial cells.
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Mechanism(s) of butyrate transport in Caco-2 cells: role of monocarboxylate transporter 1.

TL;DR: The results suggest that butyrate transport by Caco-2 cells is mediated by a transporter belonging to the monocarboxylate transporter family, and showed that the MCT1 transporter may play a major role in the transport ofbutyrate into Caco -2 cells.
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Modulation of P-glycoprotein-mediated drug transport by alterations in lipid fluidity of rat liver canalicular membrane vesicles

TL;DR: It is demonstrated that while increases in membrane fluidity of CMV are not necessarily required to inhibit P-gp-mediated drug accumulation, they can inhibit these processes, at least in CMV.
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Reversal of Multidrug-Resistance Phenotype by Surfactants: Relationship to Membrane Lipid Fluidity

TL;DR: In this paper, a series of experiments were conducted to examine the role of membrane lipid physical state in MDR reversal by employing a unique class of clinically important lipophilic surfactants and the KB-8-5-11 drug-resistant cell line.
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Toll-like Receptor 4 Mediates Induction of the Bcl10-NFκB-Interleukin-8 Inflammatory Pathway by Carrageenan in Human Intestinal Epithelial Cells

TL;DR: Results indicate that CGN-induced inflammation in human colonocytes proceeds through a pathway of innate immunity, perhaps related to the unusual α-1,3-galactosidic linkage characteristic of CGN, and suggest how dietary CGN intake may contribute to human intestinal inflammation.