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Alison J. Cox

Researcher at University of Melbourne

Publications -  73
Citations -  5377

Alison J. Cox is an academic researcher from University of Melbourne. The author has contributed to research in topics: Diabetic nephropathy & ACE inhibitor. The author has an hindex of 40, co-authored 73 publications receiving 5148 citations. Previous affiliations of Alison J. Cox include Royal North Shore Hospital & Royal Prince Alfred Hospital.

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Increased renal expression of vascular endothelial growth factor (VEGF) and its receptor VEGFR-2 in experimental diabetes.

TL;DR: Assessment of VEGF, 125I-VEGF binding, and vascular endothelial growth factor receptor-2 (VEGFR-2) in the kidney was performed after 3 and 32 weeks of streptozotocin-induced diabetes to indicate an early and persistent increase in renal V EGF gene expression in association with experimental diabetes.
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The (Pro)Renin Receptor: Site-Specific and Functional Linkage to the Vacuolar H+-ATPase in the Kidney

TL;DR: The predominant expression of the (P)RR at the apex of acid-secreting cells in the collecting duct, along with its colocalization and homology with an accessory protein of the vacuolar H+-ATPase, suggests that the ( P)RR may function primarily in distal nephron H+ transport, recently noted to be, at least in part, an angiotensin II–dependent phenomenon.
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Proteinuria and the expression of the podocyte slit diaphragm protein, nephrin, in diabetic nephropathy: effects of angiotensin converting enzyme inhibition.

TL;DR: Modulation in nephrin expression is related to the extent of proteinuria in diabetic nephropathy and the effects of anti-proteinuric treatment with ACE inhibition, at a molecular level alterations in the glomerulus.
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Transforming growth factor β1 and renal injury following subtotal nephrectomy in the rat: Role of the renin-angiotensin system

TL;DR: An interaction between the intrarenal RAS and TGF-β in the pathogenesis of the glomerular and tubulointerstitial fibrosis that follow a major reduction in renal mass is suggested.
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Vascular hypertrophy in experimental diabetes. Role of advanced glycation end products.

TL;DR: Treatment of diabetic rats with aminoguanidine resulted in significant amelioration of the described pathological changes including overexpression of TGF-beta1 and alpha1 (IV) collagen, which implicate the formation of AGEs in T GF-beta overeexpression and tissue changes which accompany the diabetic state.