Agnieszka Swiatecka-Urban

PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator.

Activation of mitochondrial apoptotic pathways in human renal allografts after ischemiareperfusion injury.

Anti-interleukin-2 receptor antibodies for the prevention of rejection in pediatric renal transplant patients: current status.

Myosin VI regulates endocytosis of the cystic fibrosis transmembrane conductance regulator.

The short apical membrane half-life of rescued {Delta}F508-cystic fibrosis transmembrane conductance regulator (CFTR) results from accelerated endocytosis of {Delta}F508-CFTR in polarized human airway epithelial cells.

Pseudomonas aeruginosa inhibits endocytic recycling of CFTR in polarized human airway epithelial cells.

Myosin Vb is required for trafficking of the cystic fibrosis transmembrane conductance regulator in Rab11a-specific apical recycling endosomes in polarized human airway epithelial cells.

The Pseudomonas aeruginosa secreted protein PA2934 decreases apical membrane expression of the cystic fibrosis transmembrane conductance regulator.

Mizoribine corrects defective nephrin biogenesis by restoring intracellular energy balance.

The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability.

c-Cbl facilitates endocytosis and lysosomal degradation of cystic fibrosis transmembrane conductance regulator in human airway epithelial cells.

DAB2 facilitates AP-2 independent recruitment of CFTR to endocytic vesicles in polarized human airway epithelial cells.

Membrane trafficking in podocyte health and disease.

Tissue-specific control of CFTR endocytosis by Dab2: Cargo recruitment as a therapeutic target.

Tgf-β1 inhibits Cftr biogenesis and prevents functional rescue of ΔF508-Cftr in primary differentiated human bronchial epithelial cells.

c-Cbl reduces stability of rescued ∆F508-CFTR in human airway epithelial cells: Implications for cystic fibrosis treatment.

LMTK2-mediated phosphorylation regulates CFTR endocytosis in human airway epithelial cells.

Atypical Hemolytic Uremic Syndrome and Chronic Ulcerative Colitis Treated with Eculizumab.

Tubulointerstitial nephritis: diagnosis, treatment, and monitoring.

Endocytic Trafficking at the Mature Podocyte Slit Diaphragm.

Editorial: Nephrotic Syndrome in Pediatric Patients.

Extra-renal manifestations of atypical hemolytic uremic syndrome.

Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study.

The human nephrin YRSL motif is essential for podocyte foot process organization and slit diaphragm formation during glomerular development.

Identification of a novel functional miR-143-5p recognition element in the Cystic Fibrosis Transmembrane Conductance Regulator 3'UTR.

Transforming Growth Factor-β1 Selectively Recruits microRNAs to the RNA-Induced Silencing Complex and Degrades CFTR mRNA under Permissive Conditions in Human Bronchial Epithelial Cells.

Precise Targeting of miRNA Sites Restores CFTR Activity in CF Bronchial Epithelial Cells.

TGF-β1 Augments the Apical Membrane Abundance of Lemur Tyrosine Kinase 2 to Inhibit CFTR-Mediated Chloride Transport in Human Bronchial Epithelia.

The Role of MicroRNA in the Airway Surface Liquid Homeostasis.