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  • Title: The glomerular basement membrane defect in Alport-type hereditary nephritis: absence of cationic antigenic components.
    Author: van den Heuvel LP, Savage CO, Wong M, Price RG, Noel L, Grunfeld JP, Lockwood CM.
    Journal: Nephrol Dial Transplant; 1989; 4(9):770-5. PubMed ID: 2483255.
    Abstract:
    Alport-type hereditary nephritis is a familial disorder which results in progressive renal insufficiency and sensorineural hearing loss. It is thought to result from a biochemical defect affecting basement membranes. To study this further, non-collagenous components of type IV collagen were prepared from the glomerular basement membrane (GBM) by collagenase digestion from three male patients with hereditary nephritis. The normal Goodpasture antigenicity of the 28 and 26 kD monomers and 54 and 50 kD dimers which may be isolated from the GBM was absent on one-dimensional immunoblots. Two-dimensional electrophoresis and immunoblotting studies showed absence of Goodpasture antigenicity of these molecular weight components as well as all cationic monomeric and dimeric spots. It is concluded that the expression of the Goodpasture antigen is altered in basement membranes of hereditary nephritis patients. The altered antigenicity thus acts as a marker for the underlying abnormality.
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