Guay-Woodford, L M; Wright, C J; Walz, G et al. (2000) Quantitative trait loci modulate renal cystic disease severity in the mouse bpk model. J Am Soc Nephrol 11:1253-60
|
Guay-Woodford, L M; Green, W J; Lindsey, J R et al. (2000) Germline and somatic loss of function of the mouse cpk gene causes biliary ductal pathology that is genetically modulated. Hum Mol Genet 9:769-78
|
Nauta, J; Goedbloed, M A; Herck, H V et al. (2000) New rat model that phenotypically resembles autosomal recessive polycystic kidney disease. J Am Soc Nephrol 11:2272-84
|
Mrug, M; Stockwin, J; Wuthrich, R P et al. (2000) Mapping of mouse alpha 1(XIII) collagen to chromosome 10 and its exclusion as a kd candidate gene. Biochem Genet 38:337-40
|
Guay-Woodford, L M (1999) Overview: the genetics of renal disease. Semin Nephrol 19:312-8
|
Guay-Woodford, L M (1999) Phenotypic variability in PKD1: the family as a starting point. Kidney Int 56:344-6
|
Zerres, K; Mucher, G; Becker, J et al. (1998) Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology. Am J Med Genet 76:137-44
|
Guay-Woodford, L M; Galliani, C A; Musulman-Mroczek, E et al. (1998) Diffuse renal cystic disease in children: morphologic and genetic correlations. Pediatr Nephrol 12:173-82
|
Sharp, C K; Bergman, S M; Stockwin, J M et al. (1997) Dominantly transmitted glomerulocystic kidney disease: a distinct genetic entity. J Am Soc Nephrol 8:77-84
|
Guay-Woodford, L M; Bryda, E C; Christine, B et al. (1996) Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Kidney Int 50:1158-65
|