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XB-GENEPAGE-483048
Papers associated with fxyd2
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HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes., Grand K, Stoltz M, Rizzo L, Röck R, Kaminski MM, Salinas G, Getwan M, Naert T, Pichler R, Lienkamp SS., J Am Soc Nephrol. March 1, 2023; 34 (3): 412-432.  |
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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome., Mann N, Mzoughi S, Schneider R, Kühl SJ, Schanze D, Klämbt V, Lovric S, Mao Y, Shi S, Tan W, Kühl M, Onuchic-Whitford AC, Treimer E, Kitzler TM, Kause F, Schumann S, Nakayama M, Buerger F, Shril S, van der Ven AT, Majmundar AJ, Holton KM, Kolb A, Braun DA, Rao J, Jobst-Schwan T, Mildenberger E, Lennert T, Kuechler A, Wieczorek D, Gross O, Ermisch-Omran B, Werberger A, Skalej M, Janecke AR, Soliman NA, Mane SM, Lifton RP, Kadlec J, Guccione E, Schmeisser MJ, Zenker M, Hildebrandt F., J Am Soc Nephrol. March 1, 2021; 32 (3): 580-596.  |
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The Wnt/JNK signaling target gene alcam is required for embryonic kidney development., Cizelsky W, Tata A, Kühl M, Kühl SJ., Development. May 1, 2014; 141 (10): 2064-74.  |
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Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel., Sha Q, Pearson W, Burcea LC, Wigfall DA, Schlesinger PH, Nichols CG, Mercer RW., Am J Physiol Renal Physiol. July 1, 2008; 295 (1): F91-9. |
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Impaired routing of wild type FXYD2 after oligomerisation with FXYD2-G41R might explain the dominant nature of renal hypomagnesemia., Cairo ER, Friedrich T, Swarts HG, Knoers NV, Bindels RJ, Monnens LA, Willems PH, De Pont JJ, Koenderink JB., Biochim Biophys Acta. February 1, 2008; 1778 (2): 398-404. |
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The prepattern transcription factor Irx3 directs nephron segment identity., Reggiani L, Raciti D, Airik R, Kispert A, Brändli AW., Genes Dev. September 15, 2007; 21 (18): 2358-70.  |
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Structural and functional interaction sites between Na,K-ATPase and FXYD proteins., Li C, Grosdidier A, Crambert G, Horisberger JD, Michielin O, Geering K., J Biol Chem. September 10, 2004; 279 (37): 38895-902. |
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FXYD7, mapping of functional sites involved in endoplasmic reticulum export, association with and regulation of Na,K-ATPase., Crambert G, Li C, Swee LK, Geering K., J Biol Chem. July 16, 2004; 279 (29): 30888-95. |
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Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K+-ATPase gamma-subunit., Meij IC, Koenderink JB, De Jong JC, De Pont JJ, Monnens LA, Van Den Heuvel LP, Knoers NV., Ann N Y Acad Sci. April 1, 2003; 986 437-43. |
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Xenopus Na,K-ATPase: primary sequence of the beta2 subunit and in situ localization of alpha1, beta1, and gamma expression during pronephric kidney development., Eid SR, Brändli AW., Differentiation. September 1, 2001; 68 (2-3): 115-25.  |
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