Woolf AS - Search Results

1

Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bank.

Lambert HJ, Stewart A, Gullett AM, Cordell HJ, Malcolm S, Feather SA, Goodship JA, Goodship TH, Woolf AS; UK VUR Study Group. Lambert HJ, et al. Among authors: woolf as. Clin J Am Soc Nephrol. 2011 Apr;6(4):760-6. doi: 10.2215/CJN.04580510. Epub 2011 Mar 24. Clin J Am Soc Nephrol. 2011. PMID: 21441121 Free PMC article.

2

Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations.

Bingham C, Ellard S, Cole TR, Jones KE, Allen LI, Goodship JA, Goodship TH, Bakalinova-Pugh D, Russell GI, Woolf AS, Nicholls AJ, Hattersley AT. Bingham C, et al. Among authors: woolf as. Kidney Int. 2002 Apr;61(4):1243-51. doi: 10.1046/j.1523-1755.2002.00272.x. Kidney Int. 2002. PMID: 11918730 Free article.

3

Recent insights into kidney diseases associated with glomerular cysts.

Woolf AS, Feather SA, Bingham C. Woolf AS, et al. Pediatr Nephrol. 2002 Apr;17(4):229-35. doi: 10.1007/s00467-001-0819-5. Pediatr Nephrol. 2002. PMID: 11956871 Review.

4

OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells.

Romio L, Wright V, Price K, Winyard PJ, Donnai D, Porteous ME, Franco B, Giorgio G, Malcolm S, Woolf AS, Feather SA. Romio L, et al. Among authors: woolf as. J Am Soc Nephrol. 2003 Mar;14(3):680-9. doi: 10.1097/01.asn.0000054497.48394.d2. J Am Soc Nephrol. 2003. PMID: 12595504

5

Primary vesicoureteric reflux as a predictor of renal damage in children hospitalized with urinary tract infection: a systematic review and meta-analysis.

Gordon I, Barkovics M, Pindoria S, Cole TJ, Woolf AS. Gordon I, et al. Among authors: woolf as. J Am Soc Nephrol. 2003 Mar;14(3):739-44. doi: 10.1097/01.asn.0000053416.93518.63. J Am Soc Nephrol. 2003. PMID: 12595511

6

Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.

Jiang S, Gitlin J, Deng FM, Liang FX, Lee A, Atala A, Bauer SB, Ehrlich GD, Feather SA, Goldberg JD, Goodship JA, Goodship TH, Hermanns M, Hu FZ, Jones KE, Malcolm S, Mendelsohn C, Preston RA, Retik AB, Schneck FX, Wright V, Ye XY, Woolf AS, Wu XR, Ostrer H, Shapiro E, Yu J, Sun TT. Jiang S, et al. Among authors: woolf as. Kidney Int. 2004 Jul;66(1):10-9. doi: 10.1111/j.1523-1755.2004.00703.x. Kidney Int. 2004. PMID: 15200408 Free article.

7

OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis.

Romio L, Fry AM, Winyard PJ, Malcolm S, Woolf AS, Feather SA. Romio L, et al. Among authors: woolf as. J Am Soc Nephrol. 2004 Oct;15(10):2556-68. doi: 10.1097/01.ASN.0000140220.46477.5C. J Am Soc Nephrol. 2004. PMID: 15466260

8

De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.

Jenkins D, Bitner-Glindzicz M, Malcolm S, Hu CC, Allison J, Winyard PJ, Gullett AM, Thomas DF, Belk RA, Feather SA, Sun TT, Woolf AS. Jenkins D, et al. Among authors: woolf as. J Am Soc Nephrol. 2005 Jul;16(7):2141-9. doi: 10.1681/ASN.2004090776. Epub 2005 May 11. J Am Soc Nephrol. 2005. PMID: 15888565

9

Mutation analyses of Uroplakin II in children with renal tract malformations.

Jenkins D, Bitner-Glindzicz M, Malcolm S, Allison J, de Bruyn R, Flanagan S, Thomas DF, Belk RA, Feather SA, Bingham C, Southgate J, Woolf AS. Jenkins D, et al. Among authors: woolf as. Nephrol Dial Transplant. 2006 Dec;21(12):3415-21. doi: 10.1093/ndt/gfl465. Epub 2006 Sep 29. Nephrol Dial Transplant. 2006. PMID: 17012268

10

Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations.

Jenkins D, Bitner-Glindzicz M, Thomasson L, Malcolm S, Warne SA, Feather SA, Flanagan SE, Ellard S, Bingham C, Santos L, Henkemeyer M, Zinn A, Baker LA, Wilcox DT, Woolf AS. Jenkins D, et al. Among authors: woolf as. J Pediatr Urol. 2007 Feb;3(1):2-9. doi: 10.1016/j.jpurol.2006.03.002. J Pediatr Urol. 2007. PMID: 17476318 Free PMC article.

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