Showing results (31-40 of 39) with videos related to
Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Acta Oto-Laryngologica|May 16, 2012
Na+ absorption by Claudius' cells is regulated by purinergic signaling in the cochleaJae Chul Yoo, Hye-Young Kim, Kyu-Hee Han, et al.Physiological Genomics|November 3, 2005
Glucocorticoid regulation of genes in the amiloride-sensitive sodium transport pathway by semicircular canal duct epithelium of neonatal ratSatyanarayana R Pondugula, Nithya N Raveendran, Zuhal Ergonul, et al.Plos One|May 10, 2014
Slc26a7 chloride channel activity and localization in mouse Reissner's membrane epitheliumKyunghee X Kim, Joel D Sanneman, Hyoung-Mi Kim, et al.American Journal of Physiology. Renal Physiology|February 15, 2007
Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse modelPhiline Wangemann, Kazuhiro Nakaya, Tao Wu, et al.American Journal of Physiology. Renal Physiology|August 21, 2009
Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expressionPhiline Wangemann, Hyoung-Mi Kim, Sara Billings, et al.Current Biology : CB|July 18, 2002
Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell deathMartine Cohen-Salmon, Thomas Ott, Vincent Michel, et al.Plos Genetics|August 22, 2009
A claudin-9-based ion permeability barrier is essential for hearingYoko Nakano, Sung H Kim, Hyoung-Mi Kim, et al.Plos Genetics|July 23, 2013
SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant miceXiangming Li, Joel D Sanneman, Donald G Harbidge, et al.BMC Medicine|August 24, 2004
Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse modelPhiline Wangemann, Erin M Itza, Beatrice Albrecht, et al.Pageof 4