Papers associated with distal (and slc4a1)

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	Mutation conferring apical-targeting motif on AE1 exchanger causes autosomal dominant distal RTA., Fry AC., J Am Soc Nephrol. July 1, 2012; 23 (7): 1238-49.
	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.
	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.
	Southeast Asian AE1 associated renal tubular acidosis: cation leak is a class effect., Walsh S., Biochem Biophys Res Commun. May 15, 2009; 382 (4): 668-72.
	Mouse Ae1 E699Q mediates SO42-i/anion-o exchange with [SO42-]i-dependent reversal of wild-type pHo sensitivity., Chernova MN., Am J Physiol Cell Physiol. August 1, 2008; 295 (2): C302-12.
	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.
	A novel Xenopus laevis larval keratin gene, xlk2: its gene structure and expression during regeneration and metamorphosis of limb and tail., Tazawa I., Biochim Biophys Acta. May 1, 2006; 1759 (5): 216-24.
	Molecular physiology of SLC4 anion exchangers., Alper SL., Exp Physiol. January 1, 2006; 91 (1): 153-61.
	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.
	Deficient HCO3- transport in an AE1 mutant with normal Cl- transport can be rescued by carbonic anhydrase II presented on an adjacent AE1 protomer., Dahl NK., J Biol Chem. November 7, 2003; 278 (45): 44949-58.
	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.

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