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Summary Expression Gene Literature (127) GO Terms (22) Nucleotides (144) Proteins (46) Interactants (359) Wiki
XB--986934

Papers associated with slc4a1 (and Disease Ontology)

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Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases., Vilas GL, Loganathan SK, Liu J, Riau AK, Young JD, Mehta JS, Vithana EN, Casey JR., Hum Mol Genet. November 15, 2013; 22 (22): 4579-90.                    


Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome., Flatt JF, Guizouarn H, Burton NM, Borgese F, Tomlinson RJ, Forsyth RJ, Baldwin SA, Levinson BE, Quittet P, Aguilar-Martinez P, Delaunay J, Stewart GW, Bruce LJ., Blood. November 10, 2011; 118 (19): 5267-77.


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


Coupling modes and stoichiometry of Cl-/HCO3- exchange by slc26a3 and slc26a6., Shcheynikov N, Wang Y, Park M, Ko SB, Dorwart M, Naruse S, Thomas PJ, Muallem S., 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, Devonald MA, Cuthbert AW, Reimann F, Akkarapatumwong V, Yenchitsomanus PT, Bennett WM, Karet FE., J Biol Chem. April 2, 2004; 279 (14): 13833-8.

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