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Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|March 27, 2002
Expression of the serine/threonine kinase hSGK1 in chronic viral hepatitisSophie Fillon, Karin Klingel, Simone Wärntges, et al.
Wiener Medizinische Wochenschrift (1946)|March 18, 2026
[Transition and transfer from pediatrics to adult medicine]Valentina Obermayr, Ingrid Pichler, Dorothea Appelt, et al.
Hearing Research|March 22, 2006
Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholdsAndreas Frey, Angelika Lampert, Siegfried Waldegger, et al.
Nature Genetics|May 29, 2002
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene familyKarl P Schlingmann, Stefanie Weber, Melanie Peters, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 2013
TGF-β directs trafficking of the epithelial sodium channel ENaC which has implications for ion and fluid transport in acute lung injuryDorothea M Peters, István Vadász, Lukasz Wujak, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 2020
Twelve-month outcome in juvenile proliferative lupus nephritis: results of the German registry studyAdriana Suhlrie, Imke Hennies, Jutta Gellermann, et al.
Hypertension (Dallas, Tex. : 1979)|May 19, 2004
Activating mutation of the renal epithelial chloride channel ClC-Kb predisposing to hypertensionNikola Jeck, Siegfried Waldegger, Angelika Lampert, et al.
Human Mutation|February 10, 2017
Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcificationsAndreas R Janecke, Ruijuan Xu, Elisabeth Steichen-Gersdorf, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2005
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemiaKarl P Schlingmann, Martin C Sassen, Stefanie Weber, et al.
American Journal of Human Genetics|November 3, 2018
Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual DisabilityKarl P Schlingmann, Sascha Bandulik, Cherry Mammen, et al.
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