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Rattiyaporn Kanlaya

Researcher at Mahidol University

Publications -  41
Citations -  1623

Rattiyaporn Kanlaya is an academic researcher from Mahidol University. The author has contributed to research in topics: Dengue virus & Vimentin. The author has an hindex of 18, co-authored 36 publications receiving 1364 citations.

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Systematic Evaluation of Sample Preparation Methods for Gel-Based Human Urinary Proteomics: Quantity, Quality, and Variability

TL;DR: Recovery yield and pattern of resolved protein spots were compared among different methods and intra-/inter-individual variabilities were examined, and male urine had greater amount of total protein but provided smaller number of protein spots compared to female urine.
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Alterations in actin cytoskeletal assembly and junctional protein complexes in human endothelial cells induced by dengue virus infection and mimicry of leukocyte transendothelial migration.

TL;DR: Functional analyses of alterations in actin cytoskeletal assembly and endothelial integrity focusing on adherens junction, tight junction and adhesive molecule after 24-h of DEN-2 infection and simulation of transendothelial migration by PECAM-1 cross-linking suggest alterations may potentially be a molecular basis explaining increased endothelial permeability or vascular leakage in DSS.
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Protective effect of epigallocatechin-3-gallate (EGCG) via Nrf2 pathway against oxalate-induced epithelial mesenchymal transition (EMT) of renal tubular cells.

TL;DR: The data indicate that oxalate turned on EMT of renal tubular cells that could be prevented by EGCG via Nrf2 pathway, and shed light onto development of novel therapeutics or preventive strategies of renal fibrosis in the future.
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The Ubiquitin−Proteasome Pathway Is Important for Dengue Virus Infection in Primary Human Endothelial Cells

TL;DR: Host responses as determined by changes in the cellular proteome of primary human endothelial cells upon infection with dengue virus serotype 2 at a multiplicity of infection (MOI) of 10 for 24 h suggest that various biological processes were triggered in response to d Dengue infection, particularly antiviral IFN and ubiquitin-proteasome pathways.