Papers associated with slc26a2

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	Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans., Satoh H, Susaki M, Shukunami C, Iyama K, Negoro T, Hiraki Y., J Biol Chem. May 15, 1998; 273 (20): 12307-15.
	Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene: correlation between sulfate transport activity and chondrodysplasia phenotype., Karniski LP., Hum Mol Genet. July 1, 2001; 10 (14): 1485-90.
	Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9., Lohi H, Kujala M, Makela S, Lehtonen E, Kestila M, Saarialho-Kere U, Markovich D, Kere J., J Biol Chem. April 19, 2002; 277 (16): 14246-54.
	Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter (DTDST) gene mutations in HEK cells., Karniski LP., Hum Mol Genet. October 1, 2004; 13 (19): 2165-71.
	Regulated transport of sulfate and oxalate by SLC26A2/DTDST., Heneghan JF, Akhavein A, Salas MJ, Shmukler BE, Karniski LP, Vandorpe DH, Alper SL., Am J Physiol Cell Physiol. June 1, 2010; 298 (6): C1363-75.
	Pendrin function and regulation in Xenopus oocytes., Reimold FR, Heneghan JF, Stewart AK, Zelikovic I, Vandorpe DH, Shmukler BE, Alper SL., Cell Physiol Biochem. January 1, 2011; 28 (3): 435-50.
	Solute carrier family 26 member a2 (Slc26a2) protein functions as an electroneutral SOFormula/OH-/Cl- exchanger regulated by extracellular Cl-., Ohana E, Shcheynikov N, Park M, Muallem S., J Biol Chem. February 10, 2012; 287 (7): 5122-32.
	Identification of the Catechin Uptake Transporter Responsible for Intestinal Absorption of Epigallocatechin Gallate in Mice., Ishii S, Kitazawa H, Mori T, Kirino A, Nakamura S, Osaki N, Shimotoyodome A, Tamai I., Sci Rep. July 29, 2019; 9 (1): 11014.

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