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Summary Anatomy Item Literature (18809) Expression Attributions Wiki
XB-ANAT-476

Papers associated with cell (and fxyd2)

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HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes., Grand K., J Am Soc Nephrol. March 1, 2023; 34 (3): 412-432.                          

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome., Mann N., J Am Soc Nephrol. March 1, 2021; 32 (3): 580-596.    

Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel., Sha Q., Am J Physiol Renal Physiol. July 1, 2008; 295 (1): F91-9.

Impaired routing of wild type FXYD2 after oligomerisation with FXYD2-G41R might explain the dominant nature of renal hypomagnesemia., Cairo ER., Biochim Biophys Acta. February 1, 2008; 1778 (2): 398-404.

The prepattern transcription factor Irx3 directs nephron segment identity., Reggiani L., Genes Dev. September 15, 2007; 21 (18): 2358-70.                

FXYD7, mapping of functional sites involved in endoplasmic reticulum export, association with and regulation of Na,K-ATPase., Crambert G., J Biol Chem. July 16, 2004; 279 (29): 30888-95.

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