Artículos Científicos en Ingles

Artículos Científicos RSS JASN

Breast Regression Protein-39/Chitinase 3-Like 1 Promotes Renal Fibrosis after Kidney Injury via Activation of Myofibroblasts

The normal response to kidney injury includes a robust...

Intracellular APOL1 Risk Variants Cause Cytotoxicity Accompanied by Energy Depletion

Population genetic approaches have uncovered a strong...

Haploinsufficiency of the Transcription Factor Ets-1 Is Renoprotective in Dahl Salt-Sensitive Rats

Studies using Dahl salt-sensitive (SS) rats identified...

The Loss of GSTM1 Associates with Kidney Failure and Heart Failure

Glutathione S-transferase mu 1 (GSTM1) encodes an...

Regulation of Nephron Progenitor Cell Self-Renewal by Intermediary Metabolism

Nephron progenitor cells (NPCs) show an age-dependent...

Transplantation of Kidneys from HCV-Positive Donors: How to Best Use a Scarce Resource

Este artículo no posee resumen

Extracellular Vesicles in Preeclampsia: Evolving Contributors to Proteinuria

Este artículo no posee resumen

Association between Endothelin-1 Levels and Kidney Disease among Blacks

Endothelin-1, a marker of endothelial dysfunction, is a...

Ets in the Kidney--Unraveling the Molecular Mechanism Underlying Renal Damage in Salt-Sensitive Hypertension

Este artículo no posee resumen

New Insights into Fuel Choices of Nephron Progenitor Cells

Este artículo no posee resumen

Class II Eplet Mismatch Modulates Tacrolimus Trough Levels Required to Prevent Donor-Specific Antibody Development

Despite more than two decades of use, the optimal...

PGC-1{alpha} Protects from Notch-Induced Kidney Fibrosis Development

Kidney fibrosis is the histologic manifestation of CKD....

Association Analysis of the MHC in Lupus Nephritis

Lupus nephritis (LN) is one of the most prevalent and...

Lysophosphatidic Acid Receptor Antagonism Protects against Diabetic Nephropathy in a Type 2 Diabetic Model

Lysophosphatidic acid (LPA) functions through activation...

A Missense Mutation in the Extracellular Domain of {alpha}ENaC Causes Liddle Syndrome

Liddle syndrome is an autosomal dominant form of...

Páginas