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Kidney International|October 1, 1996
Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelicL M Guay-Woodford, E C Bryda, B Christine, et al.
Kidney International|October 1, 1996
Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNAB K Yoder, W G Richards, C Sommardahl, et al.
The Journal of Pediatrics|April 1, 1983
Single-dose amoxicillin therapy of uncomplicated pediatric urinary tract infectionsE D Avner, J R Ingelfinger, J T Herrin, et al.
Pediatric Nephrology (Berlin, Germany)|June 18, 1998
Cholelithiasis following Escherichia coli O157:H7-associated hemolytic uremic syndromeJ R Brandt, M W Joseph, L S Fouser, et al.
American Journal of Human Genetics|May 1, 1995
The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counselingL M Guay-Woodford, G Muecher, S D Hopkins, et al.
Science (New York, N.Y.)|May 27, 1994
Candidate gene associated with a mutation causing recessive polycystic kidney disease in miceJ H Moyer, M J Lee-Tischler, H Y Kwon, et al.
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