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The Biochemical Journal|July 6, 2006
Increased protein glycation in fructosamine 3-kinase-deficient miceMaria Veiga da-Cunha, Patrick Jacquemin, Ghislain Delpierre, et al.The Journal of Physiology|April 21, 2010
New autosomal recessive mutations in aquaporin-2 causing nephrogenic diabetes insipidus through deficient targeting display normal expression in Xenopus oocytesAlexandre Leduc-Nadeau, Yoann Lussier, Marie-Françoise Arthus, et al.Journal of the American Society of Nephrology : JASN|April 23, 2021
The Effect of Tolvaptan on BP in Polycystic Kidney Disease: A Post Hoc Analysis of the TEMPO 3:4 TrialJudith E Heida, Ron T Gansevoort, Vicente E Torres, et al.Kidney International|December 1, 2004
Comparison between siblings and twins supports a role for modifier genes in ADPKDAlexandre Persu, Michel Duyme, Yves Pirson, et al.Proceedings of the National Academy of Sciences of the United States of America|June 20, 2003
Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubulesErik I Christensen, Olivier Devuyst, Geneviève Dom, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 17, 2007
Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1Bárbara Tazón-Vega, Mireia Vilardell, Laureano Pérez-Oller, et al.Clinical Journal of the American Society of Nephrology : CJASN|December 30, 2020
Multicenter Study of Long-Term Safety of Tolvaptan in Later-Stage Autosomal Dominant Polycystic Kidney DiseaseVicente E Torres, Arlene B Chapman, Olivier Devuyst, et al.Journal of the American Society of Nephrology : JASN|August 28, 2010
Cubilin is essential for albumin reabsorption in the renal proximal tubuleSabine Amsellem, Jakub Gburek, Ghislaine Hamard, et al.Pflugers Archiv : European Journal of Physiology|July 27, 2013
A primary culture system of mouse thick ascending limb cells with preserved function and uromodulin processingBob Glaudemans, Sara Terryn, Nadine Gölz, et al.Kidney International|March 13, 2003
Altered polarity and expression of H+-ATPase without ultrastructural changes in kidneys of Dent's disease patientsPierre Moulin, Takashi Igarashi, Patrick Van der Smissen, et al.Pageof 39