Mutation of the Naâº-Kâº-2Cl&oline; cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.

Title:: Mutation of the Naâº-Kâº-2Cl&oline; cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
Document type:: Zeitschriftenaufsatz
Author(s):: Kemter, E. ; Rathkolb, B. ; Bankir, L. ; Schrewe, A. ; Hans, W. ; Landbrecht, C. ; Klaften, M. ; Ivandic, B. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabé de Angelis, M. ; Wolf, E. ; Wanke, R. ; Aigner, B.
Keywords:: Genetics and Epidemiology
Journal title:: Am. J. Physiol.-Renal Physiol.
Year:: 2010
Journal volume:: 298
Pages contribution:: F1405-F1415
Fulltext / DOI:: doi:10.1152/ajprenal.00522.2009
E-ISSN:: 0002-9513
Impact Factor:: 3,731
Notes:: Research Programmes: Genes and Environment in Common Diseases
TUM Institution:: Institute of Experimental Genetics (IEG)
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Mutation of the Naâº-Kâº-2Cl&oline; cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.