The pathogenesis of Alport syndrome involves type IV collagen molecules containing the α3(IV) chain: Evidence from anti-GBM nephritis after renal transplantation

Author:

Hudson Billy G.,Kalluri Raghuram,Gunwar Sripad,Weber Manfred,Ballester Fernando,Hudson Julie K.,Noelken Milton E.,Sarras Michael,Richardson Walter R.,Saus Juan,Abrahamson Dale R.,Glick Alan D.,Haralson Michael A.,Helderman J. Harold,Stone William J.,Jacobson Harry R.

Publisher

Elsevier BV

Subject

Nephrology

Reference40 articles.

1. Alport syndrome;Atkins,1988

2. The clinical spectrum of hereditary nephritis;Grunfeld;Kidney Int,1985

3. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome);Hingalias;Lab Invest,1972

4. Glomerular basement membrane: Identification of the noncollagenous domain (hexamer) of collagen IV and the Goodpasture antigen;Gunwar;J Biol Chem,1991

5. Use of polymerase chain reaction to clone and sequence a cDNA encoding the bovine α3 chain of type IV collagen;Morrison;J Biol Chem,1991

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