1. A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Issue 4 (April 2022) Authors: Issler, Naomi; Afonso, Sara; Weissman, Irith; Jordan, Katrin; Cebrian-Serrano, Alberto; Meindl, Katrin; Dahlke, Eileen; Tziridis, Konstantin; Yan, Guanhua; Robles-López, José M.; Tabernero, Lydia; Patel, Vaksha; Kesselheim, Anne; Klootwijk, Enriko D.; Stanescu, Horia C.; Dumitriu, Simona; Iancu, ... Journal: Journal of the American Society of Nephrology Issue: Volume 33:Issue 4(2022) Page Start: 732 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cathepsin B increases ENaC activity leading to hypertension early in nephrotic syndrome. Issue 10 (31st July 2019) Authors: Larionov, Alexey; Dahlke, Eileen; Kunke, Madlen; Zanon Rodriguez, Luis; Schiessl, Ina M.; Magnin, Jean‐Luc; Kern, Ursula; Alli, Abdel A.; Mollet, Geraldine; Schilling, Oliver; Castrop, Hayo; Theilig, Franziska Journal: Journal of cellular and molecular medicine Issue: Volume 23:Issue 10(2019) Page Start: 6543 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The genetic deletion of the Dual Specificity Phosphatase 3 (DUSP3) attenuates kidney damage and inflammation following ischaemia/reperfusion injury in mouse. (9th November 2021) Authors: Khbouz, Badr; Rowart, Pascal; Poma, Laurence; Dahlke, Eileen; Bottner, Martina; Stokes, Matthew; Bolen, Géraldine; Rahmouni, Souad; Theilig, Franziska; Jouret, François Journal: Acta physiologica Issue: Volume 234:Number 2(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗