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European Cells & Materials|September 21, 2017
Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signallingC L Thompson, J C Plant, A K Wann, et al.
Journal of Pediatric Urology|October 25, 2008
Experimental short-term fetal bladder outflow obstruction: I. Morphology and cell biology associated with urinary flow impairmentM-K Farrugia, D A Long, M L Godley, et al.
The American Journal of Pathology|November 14, 2000
Potential biological role of transforming growth factor-beta1 in human congenital kidney malformationsS P Yang, A S Woolf, H T Yuan, et al.
Science (New York, N.Y.)|September 22, 2001
Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorderN Katsanis, S J Ansley, J L Badano, et al.
American Journal of Human Genetics|February 17, 2001
Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other lociP L Beales, N Katsanis, R A Lewis, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 8, 2001
Multicystic dysplastic kidney and Kallmann's syndrome: a new association?A Deeb, A Robertson, G MacColl, et al.
Clinical Genetics|March 12, 2014
Genetic predictors of cardiovascular morbidity in Bardet-Biedl syndromeE Forsythe, K Sparks, B E Hoskins, et al.
The Journal of Cell Biology|January 1, 1995
Roles of hepatocyte growth factor/scatter factor and the met receptor in the early development of the metanephrosA S Woolf, M Kolatsi-Joannou, P Hardman, et al.
Journal of Medical Genetics|October 3, 2009
Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mappingH M Harville, S Held, A Diaz-Font, et al.
American Journal of Human Genetics|November 22, 2000
Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney diseaseC Bingham, M P Bulman, S Ellard, et al.
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