Terryn S - Search Results

1

CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemia.

Stuiver M, Lainez S, Will C, Terryn S, Günzel D, Debaix H, Sommer K, Kopplin K, Thumfart J, Kampik NB, Querfeld U, Willnow TE, Němec V, Wagner CA, Hoenderop JG, Devuyst O, Knoers NV, Bindels RJ, Meij IC, Müller D. Stuiver M, et al. Among authors: terryn s. Am J Hum Genet. 2011 Mar 11;88(3):333-43. doi: 10.1016/j.ajhg.2011.02.005. Am J Hum Genet. 2011. PMID: 21397062 Free PMC article.

2

Dedifferentiation and aberrations of the endolysosomal compartment characterize the early stage of nephropathic cystinosis.

Raggi C, Luciani A, Nevo N, Antignac C, Terryn S, Devuyst O. Raggi C, et al. Among authors: terryn s. Hum Mol Genet. 2014 May 1;23(9):2266-78. doi: 10.1093/hmg/ddt617. Epub 2013 Dec 6. Hum Mol Genet. 2014. PMID: 24319100 Free article.

3

Fluid transport and cystogenesis in autosomal dominant polycystic kidney disease.

Terryn S, Ho A, Beauwens R, Devuyst O. Terryn S, et al. Biochim Biophys Acta. 2011 Oct;1812(10):1314-21. doi: 10.1016/j.bbadis.2011.01.011. Epub 2011 Jan 19. Biochim Biophys Acta. 2011. PMID: 21255645 Free article. Review.

4

Cell therapy for cystinosis.

Terryn S, Devuyst O, Antignac C. Terryn S, et al. Nephrol Dial Transplant. 2010 Jul;25(7):2103-6. doi: 10.1093/ndt/gfq198. Epub 2010 Apr 15. Nephrol Dial Transplant. 2010. PMID: 20395258

5

The soluble intracellular domain of megalin does not affect renal proximal tubular function in vivo.

Christ A, Terryn S, Schmidt V, Christensen EI, Huska MR, Andrade-Navarro MA, Hübner N, Devuyst O, Hammes A, Willnow TE. Christ A, et al. Among authors: terryn s. Kidney Int. 2010 Sep;78(5):473-7. doi: 10.1038/ki.2010.169. Epub 2010 Jun 9. Kidney Int. 2010. PMID: 20531455 Free article.

6

Decreased renal accumulation of aminoglycoside reflects defective receptor-mediated endocytosis in cystic fibrosis and Dent's disease.

Raggi C, Fujiwara K, Leal T, Jouret F, Devuyst O, Terryn S. Raggi C, et al. Among authors: terryn s. Pflugers Arch. 2011 Dec;462(6):851-60. doi: 10.1007/s00424-011-1026-2. Epub 2011 Sep 17. Pflugers Arch. 2011. PMID: 21927812 Free article.

7

Cystic gene dosage influences kidney lesions after nephron reduction.

Le Corre S, Viau A, Burtin M, El-Karoui K, Cnops Y, Terryn S, Debaix H, Bérissi S, Gubler MC, Devuyst O, Terzi F. Le Corre S, et al. Among authors: terryn s. Nephron. 2015;129(1):42-51. doi: 10.1159/000369312. Epub 2014 Dec 19. Nephron. 2015. PMID: 25531116 Free article.

8

A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway.

Bellavia S, Dahan K, Terryn S, Cosyns JP, Devuyst O, Pirson Y. Bellavia S, et al. Among authors: terryn s. Nephrol Dial Transplant. 2010 Dec;25(12):4097-102. doi: 10.1093/ndt/gfq519. Epub 2010 Aug 26. Nephrol Dial Transplant. 2010. PMID: 20798123

9

The transcription factor HNF1α regulates expression of chloride-proton exchanger ClC-5 in the renal proximal tubule.

Tanaka K, Terryn S, Geffers L, Garbay S, Pontoglio M, Devuyst O. Tanaka K, et al. Among authors: terryn s. Am J Physiol Renal Physiol. 2010 Dec;299(6):F1339-47. doi: 10.1152/ajprenal.00077.2010. Epub 2010 Sep 1. Am J Physiol Renal Physiol. 2010. PMID: 20810608 Free article.

10

PKD1 haploinsufficiency causes a syndrome of inappropriate antidiuresis in mice.

Ahrabi AK, Terryn S, Valenti G, Caron N, Serradeil-Le Gal C, Raufaste D, Nielsen S, Horie S, Verbavatz JM, Devuyst O. Ahrabi AK, et al. Among authors: terryn s. J Am Soc Nephrol. 2007 Jun;18(6):1740-53. doi: 10.1681/ASN.2006010052. Epub 2007 May 2. J Am Soc Nephrol. 2007. PMID: 17475819

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

44 results

Search Page