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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.
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.
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.
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.
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.
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.
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 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.