Artículos Científicos en Ingles

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Fibroblast Growth Factor 23 Regulation by Systemic and Local Osteoblast-Synthesized 1,25-Dihydroxyvitamin D

Circulating levels of fibroblast growth factor 23 (FGF23...

Suppressor of Cytokine Signaling-1 Peptidomimetic Limits Progression of Diabetic Nephropathy

Diabetes is the main cause of CKD and ESRD worldwide....

The Genetic Landscape of Renal Complications in Type 1 Diabetes

Diabetes is the leading cause of ESRD. Despite evidence...

Stress Response Gene Nupr1 Alleviates Cyclosporin A Nephrotoxicity In Vivo

Acute tubular damage is a major cause of renal failure,...

MicroRNA-146a in Human and Experimental Ischemic AKI: CXCL8-Dependent Mechanism of Action

AKI leads to tubular injury and interstitial...

Transcription Factor Trps1 Promotes Tubular Cell Proliferation after Ischemia-Reperfusion Injury through cAMP-Specific 3',5'-Cyclic Phosphodiesterase 4D and AKT

Trichorhinophalangeal 1 (Trps1) is a transcription...

An Investigational RNAi Therapeutic Targeting Glycolate Oxidase Reduces Oxalate Production in Models of Primary Hyperoxaluria

Primary hyperoxaluria type 1 (PH1), an inherited rare...

Inhibition of Bromodomain and Extraterminal Domain Family Proteins Ameliorates Experimental Renal Damage

Renal inflammation has a key role in the onset and...

Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII

Amyloidosis is characterized by extracellular deposition...

An Indirect Immunofluorescence Method Facilitates Detection of Thrombospondin Type 1 Domain-Containing 7A-Specific Antibodies in Membranous Nephropathy

Thrombospondin type 1 domain–containing 7A (THSD7A) is a...

A Proposal for a Serology-Based Approach to Membranous Nephropathy

Primary membranous nephropathy (MN) is an autoimmune...

The Emerging Importance of Non-HLA Autoantibodies in Kidney Transplant Complications

Antibodies that are specific to organ donor HLA have...

Changing Paradigms in Contrast Nephropathy

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Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype

Lysozyme amyloidosis (ALys) is a rare form of hereditary...

Vascular Access for Hemodialysis and Value-Based Purchasing for ESRD

Este artículo no posee resumen

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