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Genetics of kidney diseases in 2017: Unveiling the genetic architecture of kidney disease.
Devuyst O. Devuyst O. Nat Rev Nephrol. 2018 Feb;14(2):80-82. doi: 10.1038/nrneph.2017.177. Epub 2018 Jan 8. Nat Rev Nephrol. 2018. PMID: 29307891 Review. No abstract available.
Water channels in peritoneal dialysis.
Devuyst O. Devuyst O. J Nephrol. 2010 Nov-Dec;23 Suppl 16:S170-4. J Nephrol. 2010. PMID: 21170876 Review.
Soluble klotho and autosomal dominant polycystic kidney disease.
Pavik I, Jaeger P, Ebner L, Poster D, Krauer F, Kistler AD, Rentsch K, Andreisek G, Wagner CA, Devuyst O, Wüthrich RP, Schmid C, Serra AL. Pavik I, et al. Among authors: devuyst o. Clin J Am Soc Nephrol. 2012 Feb;7(2):248-57. doi: 10.2215/CJN.09020911. Epub 2011 Dec 22. Clin J Am Soc Nephrol. 2012. PMID: 22193235 Free PMC article.
Osmoregulation, vasopressin, and cAMP signaling in autosomal dominant polycystic kidney disease.
Devuyst O, Torres VE. Devuyst O, et al. Curr Opin Nephrol Hypertens. 2013 Jul;22(4):459-70. doi: 10.1097/MNH.0b013e3283621510. Curr Opin Nephrol Hypertens. 2013. PMID: 23736843 Review.
Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression.
Trudu M, Janas S, Lanzani C, Debaix H, Schaeffer C, Ikehata M, Citterio L, Demaretz S, Trevisani F, Ristagno G, Glaudemans B, Laghmani K, Dell'Antonio G; SKIPOGH team, Loffing J, Rastaldi MP, Manunta P, Devuyst O, Rampoldi L. Trudu M, et al. Among authors: devuyst o. Nat Med. 2013 Dec;19(12):1655-60. doi: 10.1038/nm.3384. Epub 2013 Nov 3. Nat Med. 2013. PMID: 24185693 Free PMC article.
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.
Olden M, Corre T, Hayward C, Toniolo D, Ulivi S, Gasparini P, Pistis G, Hwang SJ, Bergmann S, Campbell H, Cocca M, Gandin I, Girotto G, Glaudemans B, Hastie ND, Loffing J, Polasek O, Rampoldi L, Rudan I, Sala C, Traglia M, Vollenweider P, Vuckovic D, Youhanna S, Weber J, Wright AF, Kutalik Z, Bochud M, Fox CS, Devuyst O. Olden M, et al. Among authors: devuyst o. J Am Soc Nephrol. 2014 Aug;25(8):1869-82. doi: 10.1681/ASN.2013070781. Epub 2014 Feb 27. J Am Soc Nephrol. 2014. PMID: 24578125 Free PMC article.
The role of the renal ammonia transporter Rhcg in metabolic responses to dietary protein.
Bounoure L, Ruffoni D, Müller R, Kuhn GA, Bourgeois S, Devuyst O, Wagner CA. Bounoure L, et al. Among authors: devuyst o. J Am Soc Nephrol. 2014 Sep;25(9):2040-52. doi: 10.1681/ASN.2013050466. Epub 2014 Mar 20. J Am Soc Nephrol. 2014. PMID: 24652796 Free PMC article.
A protein kinase A-independent pathway controlling aquaporin 2 trafficking as a possible cause for the syndrome of inappropriate antidiuresis associated with polycystic kidney disease 1 haploinsufficiency.
Tamma G, Lasorsa D, Trimpert C, Ranieri M, Di Mise A, Mola MG, Mastrofrancesco L, Devuyst O, Svelto M, Deen PM, Valenti G. Tamma G, et al. Among authors: devuyst o. J Am Soc Nephrol. 2014 Oct;25(10):2241-53. doi: 10.1681/ASN.2013111234. Epub 2014 Apr 3. J Am Soc Nephrol. 2014. PMID: 24700872 Free PMC article.
Rare inherited kidney diseases: challenges, opportunities, and perspectives.
Devuyst O, Knoers NV, Remuzzi G, Schaefer F; Board of the Working Group for Inherited Kidney Diseases of the European Renal Association and European Dialysis and Transplant Association. Devuyst O, et al. Lancet. 2014 May 24;383(9931):1844-59. doi: 10.1016/S0140-6736(14)60659-0. Lancet. 2014. PMID: 24856029 Free PMC article. Review.
Renal transplantation in autosomal dominant polycystic kidney disease.
Kanaan N, Devuyst O, Pirson Y. Kanaan N, et al. Among authors: devuyst o. Nat Rev Nephrol. 2014 Aug;10(8):455-65. doi: 10.1038/nrneph.2014.104. Epub 2014 Jun 17. Nat Rev Nephrol. 2014. PMID: 24935705 Review.
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