Results 61 to 70 of about 8,883 (209)
Natural History of Chronic Kidney Disease in Sickle Cell Disease
ABSTRACT Kidney complications, referred to as nephropathy, develop early in sickle cell disease (SCD). In addition to its known morbidity, abundant data show that chronic kidney disease (CKD) is associated with an increased mortality risk in SCD. Increasing evidence suggests that the natural history of SCD nephropathy is progressive. Initial glomerular
Kenneth I. Ataga
wiley +1 more source
The Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome. [PDF]
The pathogenesis of proteinuria in Alport syndrome (AS) remains unclear. Vascular endothelial growth factor A (VEGFA) is a key regulator of the glomerular filtration barrier (GFB).
Haiyan Wang +6 more
doaj +1 more source
Podocyte mPGES‐2 Determines Renal Aging and Contributes to Senile Osteoporosis
Podocyte mPGES‐2 drives renal aging through PGE2/EP1‐dependent senescence and disrupts renal endocrine support for bone homeostasis. Genetic deletion or pharmacological inhibition of mPGES‐2 protects aged mice from kidney dysfunction and osteoporosis. ABSTRACT Renal aging shortens healthspan and propagates organ dysfunction beyond the kidney, yet its ...
Dandan Zhong +16 more
wiley +1 more source
Conditional deletion of nephrin in podocytes.
(A) Schematic of the targeting vector containing a neomycin cassette, Frt sites and loxP sites were engineered to flank exon 5 of mouse nephrin. Successful recombination was verified using Southern blot with probes 1 and 2 flanking the nephrin gene.
Rakesh Verma (151646) +8 more
core +1 more source
GR‐A knockin mice were generated that express the classic full‐length glucocorticoid receptor (GR‐A) but lack the highly conserved translational isoforms GR‐B, GR‐C1, GR‐C2, GR‐C3, GR‐D1, GR‐D2, and GR‐D3 that have progressively shorter N‐terminal transactivation domains (NTDs).
Robert H. Oakley +8 more
wiley +1 more source
Reduced nephrin tyrosine phosphorylation with A419T and C623F mutations.
(A) HEK293T cells were transfected with Myc-tagged nephrin variants, alone or in combination, and lysates were immunoblotted (IB) as indicated with antibodies to nephrin, total phosphotyrosine (pY) or site-specific phosphorylated nephrin (pY1176 or ...
Claire E. Martin (5746709) +5 more
core +1 more source
Nephrin as a biomarker of sickle cell glomerulopathy in Malawi [PDF]
AbstractBackgroundGlomerulopathy is an increasingly identified complication in young patients with sickle cell disease (SCD). Hyperfiltration and albuminuria followed by declining glomerular filtration rates and eventual end‐stage renal disease (ESRD) is assumed to be the typical progression of glomerular disease.
J. Brett Heimlich +12 more
openaire +2 more sources
Figure 1 visually summarizes the core biological functions and therapeutic potential of the HGF/c‐Met signaling axis. Abstract Hepatocyte growth factor (HGF) is a multifunctional cytokine that activates the tyrosine kinase activity of its specific receptor, c‐Met (mesenchymal–epithelial transition factor).
Hongqin Sun +7 more
wiley +1 more source
Deletion of nephrin in adult mature glomerulus.
(A) Immunofluorescence images showing nephrin and synaptopodin staining at 2 weeks following Cre-induction with tamoxifen. There is abrogation of peri-nuclear nephrin staining following induction (arrowheads).
Rakesh Verma (151646) +8 more
core +1 more source
Background: Idiopathic nephrotic syndrome (INS) is a glomerular disorder characterized by podocyte injury and proteinuria. Emerging evidence suggests that anti-nephrin autoantibodies (Abs) may contribute to disease pathogenesis in a subset of INS ...
Sonia Spinelli +18 more
doaj +1 more source

