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P J Winyard

Showing results (11-20 of 18) with videos related to

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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.
Molecular and Cellular Endocrinology|April 28, 1995
KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human developmentV M Duke, P J Winyard, P Thorogood, et al.
The Journal of Pediatric Endocrinology|October 1, 1994
The new highly sensitive adrenocorticotropin assay improves detection of patients with partial adrenocorticotropin deficiency in a short-term metyrapone testP S Thornton, C A Alter, L E Katz, et al.
The American Journal of Pathology|May 20, 1998
Short-term urinary flow impairment deregulates PAX2 and PCNA expression and cell survival in fetal sheep kidneysR Attar, F Quinn, P J Winyard, et al.
Kidney International|January 1, 1996
Deregulation of cell survival in cystic and dysplastic renal developmentP J Winyard, J Nauta, D S Lirenman, 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.
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.
Lancet (London, England)|May 11, 1996
Congenital enterocyte heparan sulphate deficiency with massive albumin loss, secretory diarrhoea, and malnutritionS H Murch, P J Winyard, S Koletzko, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
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.
Molecular and Cellular Endocrinology|April 28, 1995
KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human developmentV M Duke, P J Winyard, P Thorogood, et al.
The Journal of Pediatric Endocrinology|October 1, 1994
The new highly sensitive adrenocorticotropin assay improves detection of patients with partial adrenocorticotropin deficiency in a short-term metyrapone testP S Thornton, C A Alter, L E Katz, et al.
The American Journal of Pathology|May 20, 1998
Short-term urinary flow impairment deregulates PAX2 and PCNA expression and cell survival in fetal sheep kidneysR Attar, F Quinn, P J Winyard, et al.
Kidney International|January 1, 1996
Deregulation of cell survival in cystic and dysplastic renal developmentP J Winyard, J Nauta, D S Lirenman, 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.
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.
Lancet (London, England)|May 11, 1996
Congenital enterocyte heparan sulphate deficiency with massive albumin loss, secretory diarrhoea, and malnutritionS H Murch, P J Winyard, S Koletzko, et al.
Pageof 2