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Summary Anatomy Item Literature (3130) Expression Attributions Wiki
XB-ANAT-821

Papers associated with kidney (and slc4a1)

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The role of disease-linked residue glutamine-913 in support of the structure and function of the human electrogenic sodium/bicarbonate cotransporter NBCe1-A., Myers EJ., Sci Rep. February 15, 2018; 8 (1): 3066.                    


Increased water flux induced by an aquaporin-1/carbonic anhydrase II interaction., Vilas G., Mol Biol Cell. March 15, 2015; 26 (6): 1106-18.                    


Molecular cloning and functional characterization of zebrafish Slc4a3/Ae3 anion exchanger., Shmukler BE., Pflugers Arch. August 1, 2014; 466 (8): 1605-18.


Interactions of mouse glycophorin A with the dRTA-related mutant G719D of the mouse Cl-/HCO3- exchanger Ae1., Stewart AK., Biochem Cell Biol. April 1, 2011; 89 (2): 224-35.


Specification of ion transport cells in the Xenopus larval skin., Quigley IK., Development. February 1, 2011; 138 (4): 705-14.                                          


Anion exchanger 1 interacts with nephrin in podocytes., Wu F., J Am Soc Nephrol. September 1, 2010; 21 (9): 1456-67.


Band 3 Edmonton I, a novel mutant of the anion exchanger 1 causing spherocytosis and distal renal tubular acidosis., Chu C., Biochem J. February 24, 2010; 426 (3): 379-88.


Cation transport activity of anion exchanger 1 mutations found in inherited distal renal tubular acidosis., Walsh S., Am J Physiol Renal Physiol. August 1, 2008; 295 (2): F343-50.


Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A., Toye AM., Blood. June 1, 2008; 111 (11): 5380-9.            


Acute regulation of mouse AE2 anion exchanger requires isoform-specific amino acid residues from most of the transmembrane domain., Stewart AK., J Physiol. October 1, 2007; 584 (Pt 1): 59-73.


Coupling modes and stoichiometry of Cl-/HCO3- exchange by slc26a3 and slc26a6., Shcheynikov N., J Gen Physiol. May 1, 2006; 127 (5): 511-24.                  


A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells., Rungroj N., J Biol Chem. April 2, 2004; 279 (14): 13833-8.


Regulation of AE2-mediated Cl- transport by intracellular or by extracellular pH requires highly conserved amino acid residues of the AE2 NH2-terminal cytoplasmic domain., Stewart AK., J Gen Physiol. November 1, 2002; 120 (5): 707-22.                  


Band 3 Walton, a C-terminal deletion associated with distal renal tubular acidosis, is expressed in the red cell membrane but retained internally in kidney cells., Toye AM., Blood. January 1, 2002; 99 (1): 342-7.


Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A., Tanphaichitr VS., J Clin Invest. December 15, 1998; 102 (12): 2173-9.


Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger., Jarolim P., J Biol Chem. March 13, 1998; 273 (11): 6380-8.


The association between familial distal renal tubular acidosis and mutations in the red cell anion exchanger (band 3, AE1) gene., Bruce LJ., Biochem Cell Biol. January 1, 1998; 76 (5): 723-8.


Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene., Bruce LJ., J Clin Invest. October 1, 1997; 100 (7): 1693-707.


NH4Cl activates AE2 anion exchanger in Xenopus oocytes at acidic pHi., Humphreys BD., Am J Physiol. April 1, 1997; 272 (4 Pt 1): C1232-40.


Secondary regulatory volume increase conferred on Xenopus oocytes by expression of AE2 anion exchanger., Jiang L., Am J Physiol. January 1, 1997; 272 (1 Pt 1): C191-202.


The major kidney band 3 gene transcript predicts an amino-terminal truncated band 3 polypeptide., Brosius FC., J Biol Chem. May 15, 1989; 264 (14): 7784-7.

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