Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagen.

por Willing, M C, Pruchno, C J, Atkinson, M, Byers, P H
Publicado 1992

Glomerular C3c localization indicates ongoing immune deposit formation and complement activation in experimental glomerulonephritis.

por Schulze, M., Pruchno, C. J., Burns, M., Baker, P. J., Johnson, R. J., Couser, W. G.
Publicado 1993

Urinary excretion of the C5b-9 membrane attack complex of complement is a marker of immune disease activity in autologous immune complex nephritis.

por Pruchno, C. J., Burns, M. M., Schulze, M., Johnson, R. J., Baker, P. J., Alpers, C. E., Couser, W. G.
Publicado 1991

A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.

por Barker, D. F., Pruchno, C. J., Jiang, X., Atkin, C. L., Stone, E. M., Denison, J. C., Fain, P. R., Gregory, M. C.
Publicado 1996