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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.Proceedings of the National Academy of Sciences of the United States of America|February 21, 2004
Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemiaVladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler, et al.The Journal of Clinical Investigation|January 12, 2008
Claudin-16 and claudin-19 interact and form a cation-selective tight junction complexJianghui Hou, Aparna Renigunta, Martin Konrad, et al.Pediatric Nephrology (Berlin, Germany)|December 2, 2025
Overcoming anatomical barriers in pediatric kidney transplantationFabian Eibensteiner, Thomas Mueller-Sacherer, Siegfried Waldegger, et al.Kidney International|January 8, 2015
Genetic homogeneity but IgG subclass-dependent clinical variability of alloimmune membranous nephropathy with anti-neutral endopeptidase antibodiesMarina Vivarelli, Francesco Emma, Thimothée Pellé, 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|June 30, 2006
Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporterCarsten A Pressler, Jolanta Heinzinger, Nikola Jeck, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 11, 2005
Influence of standard haemodialysis treatment on transcription of human serum- and glucocorticoid-inducible kinase SGK1 and taurine transporter TAUT in blood leukocytesBjörn Friedrich, Dorothea Alexander, Wilhelm Karl Aicher, et al.Kidney International|October 22, 2004
Regulation of CLC-Ka/barttin by the ubiquitin ligase Nedd4-2 and the serum- and glucocorticoid-dependent kinasesHamdy M Embark, Christoph Böhmer, Monica Palmada, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 3, 2018
Successful management of recurrent focal segmental glomerulosclerosisKatrin Kienzl-Wagner, Alejandra Rosales, Stefan Scheidl, et al.Pageof 5