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Citations to this article

Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.
M M Kleppel, … , A J Fish, A F Michael
M M Kleppel, … , A J Fish, A F Michael
Published July 1, 1987
Citation Information: J Clin Invest. 1987;80(1):263-266. https://doi.org/10.1172/JCI113057.
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Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.

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Abstract

Alport-type familial nephritis (FN), a genetic disorder, results in progressive renal insufficiency and sensorineural hearing loss. Immunochemical and biochemical analyses of the non-collagenous (NC1) domain of type IV collagen isolated from the glomerular basement membranes (GBM) of three males with this disease demonstrate absence of the normally occurring 28-kilodalton (kD) NC1 monomers, but persistence of the 26- and 24-kD monomeric subunits derived from alpha 1 and 2 (both type IV) collagen chains, respectively.

Authors

M M Kleppel, C E Kashtan, R J Butkowski, A J Fish, A F Michael

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Total citations by year

Year: 2024 2023 2022 2021 2020 2005 2002 2001 1999 1998 1997 1996 1995 1994 1993 1992 1991 1990 1989 1988 1981 Total
Citations: 1 1 1 1 1 1 1 1 4 2 4 4 2 9 4 11 16 15 9 3 1 92
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Citations to this article (92)

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2021
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D Charytan, B MacDonald, H Sugimoto, S Pastan, G Staton, R Hennigar, R Kalluri
American Journal of Kidney Diseases 2005
Genetics of Auditory Disorders
BJ Keats, RR Fay, AN Popper
2002
Quantitative immunoelectron microscopy of type VI collagen in glomeruli in type I diabetic patients
T Moriya, TJ Groppoli, Y Kim, M Mauer
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