Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

פריטים דומים

• Localization and Functional Studies of Pendrin in the Mouse Inner Ear Provide Insight About the Etiology of Deafness in Pendred Syndrome
  מאת: Royaux, Ines E., et al.
  יצא לאור: (2003)
• Expression pattern of the mouse ortholog of the Pendred’s syndrome gene (Pds) suggests a key role for pendrin in the inner ear
  מאת: Everett, Lorraine A., et al.
  יצא לאור: (1999)
• The Renal Physiology of Pendrin-Positive Intercalated Cells
  מאת: Wall, Susan M., et al.
  יצא לאור: (2020)
• The chloride–bicarbonate exchanger pendrin is increased in the kidney of the pregnant rat
  מאת: West, Crystal A., et al.
  יצא לאור: (2015)
• Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model
  מאת: Wangemann, Philine, et al.
  יצא לאור: (2004)