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

類似資料

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