Simms R - Search Results

1

Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort.

Wong K, Pitcher D, Braddon F, Downward L, Steenkamp R, Annear N, Barratt J, Bingham C, Chrysochou C, Coward RJ, Game D, Griffin S, Hall M, Johnson S, Kanigicherla D, Karet Frankl F, Kavanagh D, Kerecuk L, Maher ER, Moochhala S, Pinney J, Sayer JA, Simms R, Sinha S, Srivastava S, Tam FWK, Turner AN, Walsh SB, Waters A, Wilson P, Wong E, Taylor CM, Nitsch D, Saleem M, Bockenhauer D, Bramham K, Gale DP; RaDaR consortium. Wong K, et al. Among authors: simms r. Lancet. 2024 Mar 30;403(10433):1279-1289. doi: 10.1016/S0140-6736(23)02843-X. Epub 2024 Mar 13. Lancet. 2024. PMID: 38492578 Free article.

2

Nephrocystin-1 interacts directly with Ack1 and is expressed in human collecting duct.

Eley L, Moochhala SH, Simms R, Hildebrandt F, Sayer JA. Eley L, et al. Among authors: simms r. Biochem Biophys Res Commun. 2008 Jul 11;371(4):877-82. doi: 10.1016/j.bbrc.2008.05.016. Epub 2008 May 12. Biochem Biophys Res Commun. 2008. PMID: 18477472

3

Nephronophthisis.

Simms RJ, Eley L, Sayer JA. Simms RJ, et al. Eur J Hum Genet. 2009 Apr;17(4):406-16. doi: 10.1038/ejhg.2008.238. Epub 2008 Dec 10. Eur J Hum Genet. 2009. PMID: 19066617 Free PMC article.

4

Tc99m WCC identifies occult abscess in a polycystic kidney.

Simms RJ, Hawkins T, Sayer JA. Simms RJ, et al. Kidney Int. 2009 Jan;75(2):246. doi: 10.1038/ki.2008.257. Kidney Int. 2009. PMID: 19116646 Free article. No abstract available.

5

Juvenile nephronophthisis on MRI--a potential case of Joubert syndrome?

Simms RJ, Sayer JA. Simms RJ, et al. Pediatr Radiol. 2010 Sep;40(9):1581; author reply 1582. doi: 10.1007/s00247-010-1707-6. Epub 2010 May 21. Pediatr Radiol. 2010. PMID: 20490483 No abstract available.

6

Nephronophthisis: a genetically diverse ciliopathy.

Simms RJ, Hynes AM, Eley L, Sayer JA. Simms RJ, et al. Int J Nephrol. 2011;2011:527137. doi: 10.4061/2011/527137. Epub 2011 May 15. Int J Nephrol. 2011. PMID: 21660307 Free PMC article.

7

Modelling a ciliopathy: Ahi1 knockdown in model systems reveals an essential role in brain, retinal, and renal development.

Simms RJ, Hynes AM, Eley L, Inglis D, Chaudhry B, Dawe HR, Sayer JA. Simms RJ, et al. Cell Mol Life Sci. 2012 Mar;69(6):993-1009. doi: 10.1007/s00018-011-0826-z. Epub 2011 Sep 29. Cell Mol Life Sci. 2012. PMID: 21959375 Free PMC article.

8

Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome.

Cheng YZ, Eley L, Hynes AM, Overman LM, Simms RJ, Barker A, Dawe HR, Lindsay S, Sayer JA. Cheng YZ, et al. Among authors: simms rj. PLoS One. 2012;7(9):e44975. doi: 10.1371/journal.pone.0044975. Epub 2012 Sep 24. PLoS One. 2012. PMID: 23028714 Free PMC article.

9

The challenges and surprises of a definitive molecular genetic diagnosis.

Sayer JA, Simms RJ. Sayer JA, et al. Kidney Int. 2014 Apr;85(4):748-9. doi: 10.1038/ki.2013.432. Kidney Int. 2014. PMID: 24682124 Free article.

10

Epidemiology of patients in England and Wales with autosomal dominant polycystic kidney disease and end-stage renal failure.

Shaw C, Simms RJ, Pitcher D, Sandford R. Shaw C, et al. Among authors: simms rj. Nephrol Dial Transplant. 2014 Oct;29(10):1910-8. doi: 10.1093/ndt/gfu087. Epub 2014 Apr 15. Nephrol Dial Transplant. 2014. PMID: 24737444

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