Expression of SLC26A4/pendrin in ameloblasts

European Journal of Oral Sciences

Volumn 120, Issue 4, 2012, Pages 368-369

  Frische, Sebastian ^a  

^a AARHUS UNIVERSITY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ANION TRANSPORT PROTEIN;

AMELOBLAST; ANIMAL; EDITORIAL; GENETICS; METABOLISM; PHYSIOLOGY; TOOTH DEVELOPMENT; TOOTH FLORA;

AMELOBLASTS; AMELOGENESIS; ANIMALS; ANION TRANSPORT PROTEINS; ENAMEL ORGAN;

EID: 84864064511     PISSN: 09098836     EISSN: 16000722     Source Type: Journal    
DOI: 10.1111/j.1600-0722.2012.00979.x     Document Type: Editorial

References (7)

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2. Kim YH, Kwon TH, Frische S, Kim J, Tisher CC, Madsen KM, Nielsen S. Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney. Am J Physiol Renal Physiol 2002; 283: F744-F754.
3. Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet 1997; 17: 411-422.
4. Everett LA, Morsli H, Wu DK, Green ED. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. Proc Natl Acad Sci U S A 1999; 96: 9727-9732.
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6. Everett LA, Belyantseva IA, Noben-Trauth K, Cantos R, Chen A, Thakkar SI, Hoogstraten-Miller SL, Kachar B, Wu DK, Green ED. Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome. Hum Mol Genet 2001; 10: 153-161.
7. Amlal H, Petrovic S, Xu J, Wang Z, Sun X, Barone S, Soleimani M. Deletion of the anion exchanger Slc26a4 (pendrin) decreases apical Cl(-)/HCO3(-) exchanger activity and impairs bicarbonate secretion in kidney collecting duct. Am J Physiol Cell Physiol 2010; 299: C33-C41.