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Kidney International|December 5, 2020
Clinical and genetic spectra of kidney disease caused by REN mutationsCéline Schaeffer, Eric OlingerKidney International|January 23, 2026
JAG1 of all trades, master of CKD? The role of JAG1 in autosomal dominant tubulointerstitial kidney diseaseMichael S Wiesener, Eric OlingerKidney International|February 25, 2018
Claudins: a tale of interactions in the thick ascending limbEric Olinger, Pascal Houillier, Olivier DevuystNature Reviews. Nephrology|August 8, 2017
Uromodulin: from physiology to rare and complex kidney disordersOlivier Devuyst, Eric Olinger, Luca RampoldiPflugers Archiv : European Journal of Physiology|July 26, 2022
UMOD and the architecture of kidney diseaseOlivier Devuyst, Murielle Bochud, Eric OlingerNephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 14, 2021
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney diseaseHolly Mabillard, John A Sayer, Eric OlingerJournal of Rare Diseases (Berlin, Germany)|December 26, 2022
UMOD and you! Explaining a rare disease diagnosisHolly Mabillard, Eric Olinger, John A SayerBiochemical Society Transactions|May 7, 2021
Molecular genetics of renal ciliopathiesMiguel Barroso-Gil, Eric Olinger, John A SayerKidney International|October 24, 2018
The excretion of uromodulin is modulated by the calcium-sensing receptorNatsuko Tokonami, Eric Olinger, Huguette Debaix, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 13, 2012
Parvalbumin: calcium and magnesium buffering in the distal nephronEric Olinger, Beat Schwaller, Johannes Loffing, et al.Pageof 6