Rasheed Gbadegesin

Hepatocyte Growth Factor Suppresses Renal Interstitial Myofibroblast Activation and Intercepts Smad Signal Transduction

Stressed podocytes—mechanical forces, sensors, signaling and response

Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome

TGF-β: the master regulator of fibrosis

Super-resolution microscopy demystified

Cellular and molecular mechanisms of renal fibrosis

Piezos thrive under pressure: mechanically activated ion channels in health and disease

Insulin Signaling to the Glomerular Podocyte Is Critical for Normal Kidney Function

Causes and pathogenesis of focal segmental glomerulosclerosis

Susceptibility to acute pyelonephritis or asymptomatic bacteriuria: Host–pathogen interaction in urinary tract infections

Akt signalling in health and disease

Focal Segmental Glomerulosclerosis

Diabetic Nephropathy

Differential Diagnosis of Glomerular Disease: A Systematic and Inclusive Approach

Urinary Tract Infection Syndromes

Inflammation in obesity, diabetes, and related disorders

Macrophage Polarization: Different Gene Signatures in M1(LPS+) vs. Classically and M2(LPS–) vs. Alternatively Activated Macrophages

Does the Interdependence between Oxidative Stress and Inflammation Explain the Antioxidant Paradox?

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

Focal segmental glomerulosclerosis in pediatric kidney transplantation: 30 years’ experience

Chronic Kidney Disease Influences Multiple Systems: Describing the Relationship between Oxidative Stress, Inflammation, Kidney Damage, and Concomitant Disease

Congenital and Infantile Nephrotic Syndrome

ARHGAP18: an endogenous inhibitor of angiogenesis, limiting tip formation and stabilizing junctions

Pathobiology of focal segmental glomerulosclerosis

Mechanisms of Diabetic Complications

Pathogenesis and therapy of focal segmental glomerulosclerosis: an update

Therapeutic targets in focal and segmental glomerulosclerosis

Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome

Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

Role of TGF-β1 in renal parenchymal scarring following childhood urinary tract infection

Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2)