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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 29, 2000
Inflammatory mediators in human renal dysplasiaC M Cale, N J Klein, P J Winyard, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1988
The effect of renal transplantation on plasma atrial natriuretic peptideA S Woolf, K L Simpson, M A Mansell, et al.
Angiogenesis|January 1, 1997
A molecular and genetic analysis of renalglomerular capillary developmentS Loughna, P Hardman, E Landels, et al.
The Journal of Urology|January 16, 2007
Ca2+ regulation in detrusor smooth muscle from ovine fetal bladder after in utero bladder outflow obstructionC Wu, N Thiruchelvam, G Sui, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|August 17, 2001
Expression and potential role of angiopoietins and Tie-2 in early development of the mouse metanephrosM Kolatsi-Joannou, X Z Li, T Suda, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|April 5, 2003
Neurotransmission and viscoelasticity in the ovine fetal bladder after in utero bladder outflow obstructionN Thiruchelvam, C Wu, A David, et al.
The Journal of Clinical Investigation|July 15, 1996
The PAX2 tanscription factor is expressed in cystic and hyperproliferative dysplastic epithelia in human kidney malformationsP J Winyard, R A Risdon, V R Sams, et al.
Nephron|January 1, 1989
Effects of physiological infusion of atrial natriuretic factor on healthy subjects and patients with the nephrotic syndromeA S Woolf, T L Lyon, B I Hoffbrand, et al.
Postgraduate Medical Journal|June 1, 1989
The effects of low dose intravenous 99-126 atrial natriuretic factor infusion in patients with chronic renal failureA S Woolf, M A Mansell, B I Hoffbrand, et al.
American Journal of Human Genetics|December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigreesN Katsanis, R A Lewis, D W Stockton, et al.
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