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Biochimica Et Biophysica Acta|May 8, 2007
TRPM6 and TRPM7--Gatekeepers of human magnesium metabolismKarl P Schlingmann, Siegfried Waldegger, Martin Konrad, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 15, 2011
Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genesTulay Guran, Teoman Akcay, Abdullah Bereket, et al.American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|March 29, 2005
Salt handling in the distal nephron: lessons learned from inherited human disordersNikola Jeck, Karl P Schlingmann, Stephan C Reinalter, et al.The Journal of Biological Chemistry|January 2, 2007
Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6Vladimir Chubanov, Karl P Schlingmann, Janine Wäring, et al.Kidney International|August 13, 2003
Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndromeMelanie Peters, Saskia Ermert, Nikola Jeck, et al.Journal of the American Society of Nephrology : JASN|December 1, 2001
Primary gene structure and expression studies of rodent paracellin-1Stefanie Weber, Karl P Schlingmann, Melanie Peters, et al.Journal of Applied Genetics|May 5, 2017
Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH casesEwa Pronicka, Elżbieta Ciara, Paulina Halat, et al.Kidney International|January 29, 2021
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular DisordersMartin Konrad, Tom Nijenhuis, Gema Ariceta, 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.Plos Genetics|April 5, 2014
CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemiaFrancisco J Arjona, Jeroen H F de Baaij, Karl P Schlingmann, et al.Pageof 4