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Mark E. Cooper

Researcher at University of Queensland

Publications -  1514
Citations -  141899

Mark E. Cooper is an academic researcher from University of Queensland. The author has contributed to research in topics: Diabetes mellitus & Diabetic nephropathy. The author has an hindex of 158, co-authored 1463 publications receiving 124887 citations. Previous affiliations of Mark E. Cooper include University of Cambridge & University of Adelaide.

Papers
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Journal Article

Macrophage and myofibroblast proliferation in remnant kidney: Role of angiotensin II

TL;DR: In conclusion, inhibition of local macrophage and myofibroblast proliferation may be an important mechanism by which Ang II blockade attenuated renal injury following renal ablation.
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AT2R Agonist, Compound 21, Is Reno-Protective Against Type 1 Diabetic Nephropathy

TL;DR: It is demonstrated that monotherapy of Compound 21 is protective against the progression of experimental diabetic nephropathy by inhibiting renal oxidative stress, inflammation, and fibrosis.
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Direct quantification of analyte concentration by resonant acoustic profiling

TL;DR: Resonant Acoustic Profiling detects analytes in a relatively simple receptor-binding assay in <10 min and may lead to simple, label-free, high-sensitivity methodologies for reagent and assay validation in clinical chemistry and, ultimately, for real-time in vitro diagnostics.
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Spectrum of proteinuria in type I and type II diabetes

TL;DR: The phase of intermittent proteinuria detected in this study may represent a reversible stage in the development of diabetic nephropathy, but the factors that trigger the transition to progressing proteinuria remain obscure.
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The Amino-terminal Domains of the Ezrin, Radixin, and Moesin (ERM) Proteins Bind Advanced Glycation End Products, an Interaction That May Play a Role in the Development of Diabetic Complications

TL;DR: The isolation and identification of novel AGE-binding proteins from diabetic rat kidneys represent a novel family of intracellular binding molecules for glycated proteins and provide a potential new target for therapeutic intervention in the prevention or treatment of diabetic complications.