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C J Pruchno

Showing results (1-10 of 9) with videos related to

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American Journal of Medical Genetics|January 15, 1993
Molecular heterogeneity in osteogenesis imperfecta type IM C Willing, C J Pruchno, P H Byers
American Journal of Human Genetics|September 1, 1992
Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagenM C Willing, C J Pruchno, M Atkinson, et al.
The American Journal of Physiology|October 1, 1994
Functional and molecular evidence for Shaker-like K+ channels in rabbit renal papillary epithelial cell lineK A Volk, R F Husted, C J Pruchno, et al.
The American Journal of Pathology|January 1, 1993
Glomerular C3c localization indicates ongoing immune deposit formation and complement activation in experimental glomerulonephritisM Schulze, C J Pruchno, M Burns, et al.
Kidney International|July 1, 1989
Urinary excretion of C5b-9 reflects disease activity in passive Heymann nephritisC J Pruchno, M W Burns, M Schulze, et al.
The American Journal of Pathology|January 1, 1991
Urinary excretion of the C5b-9 membrane attack complex of complement is a marker of immune disease activity in autologous immune complex nephritisC J Pruchno, M M Burns, M Schulze, et al.
Human Genetics|May 1, 1991
Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagenC J Pruchno, D H Cohn, G A Wallis, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Kidney International|September 11, 1991
Elevated urinary excretion of the C5b-9 complex in membranous nephropathyM Schulze, J V Donadio, C J Pruchno, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics|January 15, 1993
Molecular heterogeneity in osteogenesis imperfecta type IM C Willing, C J Pruchno, P H Byers
American Journal of Human Genetics|September 1, 1992
Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagenM C Willing, C J Pruchno, M Atkinson, et al.
The American Journal of Physiology|October 1, 1994
Functional and molecular evidence for Shaker-like K+ channels in rabbit renal papillary epithelial cell lineK A Volk, R F Husted, C J Pruchno, et al.
The American Journal of Pathology|January 1, 1993
Glomerular C3c localization indicates ongoing immune deposit formation and complement activation in experimental glomerulonephritisM Schulze, C J Pruchno, M Burns, et al.
Kidney International|July 1, 1989
Urinary excretion of C5b-9 reflects disease activity in passive Heymann nephritisC J Pruchno, M W Burns, M Schulze, et al.
The American Journal of Pathology|January 1, 1991
Urinary excretion of the C5b-9 membrane attack complex of complement is a marker of immune disease activity in autologous immune complex nephritisC J Pruchno, M M Burns, M Schulze, et al.
Human Genetics|May 1, 1991
Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagenC J Pruchno, D H Cohn, G A Wallis, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Kidney International|September 11, 1991
Elevated urinary excretion of the C5b-9 complex in membranous nephropathyM Schulze, J V Donadio, C J Pruchno, et al.
Pageof 1