Denovo glomerulonephritis associated with IgA anti-GBM alloantibodies after kidney transplantation in Alport syndrome: A case report with diagnostic implications., PMID:39237079
X-linked Alport syndrome presenting in mother and son with the same unique histopathological features., PMID:38668984
PDGF-D Is Dispensable for the Development and Progression of Murine Alport Syndrome., PMID:38309427
A Neutralizing IL-11 Antibody Improves Renal Function and Increases Lifespan in a Mouse Model of Alport Syndrome., PMID:35140116
COL4A3 is degraded in allergic asthma and degradation predicts response to anti-IgE therapy., PMID:34326188
Neutralization of IL-6 inhibits formation of autoreactive TH17 cells but does not prevent loss of renal function in experimental autoimmune glomerulonephritis., PMID:34015360
Laminin-521 is a Novel Target of Autoantibodies Associated with Lung Hemorrhage in Anti-GBM Disease., PMID:33893224
The clinical and immunological features of the post-extracorporeal shock wave lithotripsy anti-glomerular basement membrane disease., PMID:33435789
Epitope Mapping of Human α3(IV)NC1-Induced Membranous Nephropathy in Mice., PMID:31927545
Klotho regulation by albuminuria is dependent on ATF3 and endoplasmic reticulum stress., PMID:31907991
Plasma exchange in anti-glomerular basement membrane disease., PMID:31703956
Osteopontin Promotes Left Ventricular Diastolic Dysfunction Through a Mitochondrial Pathway., PMID:31146816
Type IV collagen turnover is predictive of mortality in COPD: a comparison to fibrinogen in a prospective analysis of the ECLIPSE cohort., PMID:30935391
Inhibitory Anti-Peroxidasin Antibodies in Pulmonary-Renal Syndromes., PMID:30279272
COL4A3 Gene Variants and Diabetic Kidney Disease in MODY., PMID:30012629
Kidney-targeted inhibition of protein kinase C-α ameliorates nephrotoxic nephritis with restoration of mitochondrial dysfunction., PMID:29731111
Routinely used immunoassays do not detect circulating anti-GBM antibodies against native NC1 hexamer and EA epitope of the α3 chain of type IV collagen., PMID:29644627
A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome., PMID:29530752
Rapidly progressive glomerulonephritis due to anti-glomerular basement membrane disease accompanied by IgA nephropathy: An unusual association., PMID:29265054
Atypical antiglomerular basement membranes disease with nephrotic-range proteinuria, mesangial proliferation, and membranoproliferative glomerulonephritis pattern of injury., PMID:29265053
The critical amino acids of a nephritogenic epitope on human Goodpasture autoantigen for binding to HLA-DRB1*1501., PMID:28570922
Antibodies against linear epitopes on Goodpasture autoantigen in patients with anti-neutrophil cytoplasmic antibody-associated vasculitis., PMID:28550388
The pathogenicity of T cell epitopes on human Goodpasture antigen and its critical amino acid motif., PMID:28296059
Neuropilin1 regulates glomerular function and basement membrane composition through pericytes in the mouse kidney., PMID:27988210
Macroscopic hematuria with normal renal biopsy-following the chain to the diagnosis: Answers., PMID:26628280
Formation of vascular network structures within cardiac cell sheets from mouse embryonic stem cells., PMID:31245454
[GOODPASTURE'S SYNDROME--CASE REPORTS]., PMID:26380476
Human anti-α3(IV)NC1 antibody drug conjugates target glomeruli to resolve nephritis., PMID:26290372
Role of platelet-derived growth factor-CC in capillary rarefaction in renal fibrosis., PMID:26216283
TH1 and TH17 cells promote crescent formation in experimental autoimmune glomerulonephritis., PMID:25965582
Identification of critical residues of linear B cell epitope on Goodpasture autoantigen., PMID:25874890
Autoimmunity to the alpha 3 chain of type IV collagen in glomerulonephritis is triggered by 'autoantigen complementarity'., PMID:25841937
Glomerulopathy induced by immunization with a peptide derived from the goodpasture antigen α3IV-NC1., PMID:25769923
A case of subepidermal blistering disease with autoantibodies to multiple laminin subunits who developed later autoantibodies to alpha-5 chain of type IV collagen associated with membranous glomerulonephropathy., PMID:25633161
MMP mediated degradation of type IV collagen alpha 1 and alpha 3 chains reflects basement membrane remodeling in experimental and clinical fibrosis--validation of two novel biomarker assays., PMID:24376856
Neonatal Fc receptor promotes immune complex-mediated glomerular disease., PMID:24357670
In vivo imaging of disease-modified glomerular extracellular matrix in renal disease., PMID:23903419
Quaternary epitopes of α345(IV) collagen initiate Alport post-transplant anti-GBM nephritis., PMID:23620401
A human monoclonal antibody against the collagen type IV α3NC1 domain is a non-invasive optical biomarker for glomerular diseases., PMID:23515049
Prognostic value of glomerular collagen IV immunofluorescence studies in male patients with X-linked Alport syndrome., PMID:23371956
Proteolysis breaks tolerance toward intact α345(IV) collagen, eliciting novel anti-glomerular basement membrane autoantibodies specific for α345NC1 hexamers., PMID:23303673
Precise mapping of the Goodpasture epitope(s) using phage display, site-directed mutagenesis, and surface plasmon resonance., PMID:23254898
Association of epitope spreading of antiglomerular basement membrane antibodies and kidney injury., PMID:23085731
Antibodies against linear epitopes on the Goodpasture autoantigen and kidney injury., PMID:22461538
Genetic susceptibility to experimental autoimmune glomerulonephritis in the Wistar Kyoto rat., PMID:22445570
Characterization of the renal CD4+ T-cell response in experimental autoimmune glomerulonephritis., PMID:22437418
Murine membranous nephropathy: immunization with α3(IV) collagen fragment induces subepithelial immune complexes and FcγR-independent nephrotic syndrome., PMID:22371398
Increased incidence of anti-GBM disease in Fcgamma receptor 2b deficient mice, but not mice with conditional deletion of Fcgr2b on either B cells or myeloid cells alone., PMID:22244885
Analysis of the role of ZEB1 in the pathogenesis of posterior polymorphous corneal dystrophy., PMID:22199242
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