Urinary excretion of C5b-9 reflects disease activity in passive Heymann nephritis. Passive Heymann nephritis (PHN) is a model of membranous nephropathy in rats in which glomerular injury is mediated by the terminal C5b-9 membrane attack complex of complement. This model has been shown to be associated with markedly elevated urinary excretion of C5b-9, compared to other experimental models of glomerulonephritis. To determine if urinary C5b-9 excretion could serve as an index of disease activity by correlating with the formation and quantity of glomerular subepithelial immune deposits in PHN, we measured urinary excretion of C5b-9 in PHN under several experimental conditions. In the heterologous phase a direct correlation was demonstrated bet...
Urinary C3dg and C5b-9 indicate active immune disease in human membranous nephropathy. We have measu...
<p>(A).At day 1, 7, 14, 21, and 28 after antiserum injection, rats were sacrificed and the renal cor...
Anti-Fx1A produces complement-dependent cytotoxicity of glomerular epithelial cells. Glomerular inju...
Urinary excretion of C5b-9 reflects disease activity in passive Heymann nephritis. Passive Heymann n...
Increased urinary excretion of C5b-9 distinguishes passive Heymann nephritis in the rat. Increased u...
Elevated urinary excretion of the C5b-9 complex in membranous nephropathy. In experimental membranou...
Active Heymann nephritis in complement component C6 deficient rats. The mechanisms of renal injury t...
Measurement of SC5b-9 in urine in patients with the nephrotic syndrome. In passive or active Heymann...
Glomerular complement regulation is overwhelmed in passive Heymann nephritis.BackgroundAn injection ...
The Heymann nephritis (HN) models of rat membranous nephropathy are extraordinarily valuable tools t...
Possible involvement of terminal complement complex in active Heymann nephritis. We investigated whe...
Enhanced glomerular prostaglandin formation in experimental membranous nephropathy. To determine whe...
Complement mediates nephrin redistribution and actin dissociation in experimental membranous nephrop...
C5b-9 increases albumin permeability of isolated glomeruli in vitro. Deposition of antibody and acti...
Role of T cells in the mediation of Heymann nephritis. ii. Identification of Thl and cytotoxic cells...
Urinary C3dg and C5b-9 indicate active immune disease in human membranous nephropathy. We have measu...
<p>(A).At day 1, 7, 14, 21, and 28 after antiserum injection, rats were sacrificed and the renal cor...
Anti-Fx1A produces complement-dependent cytotoxicity of glomerular epithelial cells. Glomerular inju...
Urinary excretion of C5b-9 reflects disease activity in passive Heymann nephritis. Passive Heymann n...
Increased urinary excretion of C5b-9 distinguishes passive Heymann nephritis in the rat. Increased u...
Elevated urinary excretion of the C5b-9 complex in membranous nephropathy. In experimental membranou...
Active Heymann nephritis in complement component C6 deficient rats. The mechanisms of renal injury t...
Measurement of SC5b-9 in urine in patients with the nephrotic syndrome. In passive or active Heymann...
Glomerular complement regulation is overwhelmed in passive Heymann nephritis.BackgroundAn injection ...
The Heymann nephritis (HN) models of rat membranous nephropathy are extraordinarily valuable tools t...
Possible involvement of terminal complement complex in active Heymann nephritis. We investigated whe...
Enhanced glomerular prostaglandin formation in experimental membranous nephropathy. To determine whe...
Complement mediates nephrin redistribution and actin dissociation in experimental membranous nephrop...
C5b-9 increases albumin permeability of isolated glomeruli in vitro. Deposition of antibody and acti...
Role of T cells in the mediation of Heymann nephritis. ii. Identification of Thl and cytotoxic cells...
Urinary C3dg and C5b-9 indicate active immune disease in human membranous nephropathy. We have measu...
<p>(A).At day 1, 7, 14, 21, and 28 after antiserum injection, rats were sacrificed and the renal cor...
Anti-Fx1A produces complement-dependent cytotoxicity of glomerular epithelial cells. Glomerular inju...