Sat1 is dispensable for active oxalate secretion in mouse duodenum

American Journal of Physiology - Cell Physiology

Volumn 303, Issue 1, 2012, Pages

  Ko, Narae ^a   Knauf, Felix ^a   Jiang, Zhirong ^a   Markovich, Daniel ^b   Aronson, Peter S ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Basolateral membrane; Bicarbonate; SLC26A1; SLC26A6; Sulfate

Indexed keywords

ACETAZOLAMIDE; BICARBONATE; OXALIC ACID; PROTEIN; PROTEIN SULFATE ANION TRANSPORTER 1; STILBENEDISULFONIC ACID; SULFATE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANION EXCHANGE; ARTICLE; BASOLATERAL MEMBRANE; CALCIUM OXALATE STONE; CONTROLLED STUDY; DUODENUM; HYPEROXALURIA; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

4,4'-DIISOTHIOCYANOSTILBENE-2,2'-DISULFONIC ACID; ACETAZOLAMIDE; ANIMALS; ANION TRANSPORT PROTEINS; ANTIPORTERS; BIOLOGICAL TRANSPORT, ACTIVE; DUODENUM; MICE; MICE, KNOCKOUT; OXALATES;

MUS;

EID: 84863533203     PISSN: 03636143     EISSN: 15221563     Source Type: Journal    
DOI: 10.1152/ajpcell.00385.2011     Document Type: Article

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