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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.
European Journal of Oral Sciences|January 17, 2012
Developmental expression of solute carrier family 26A member 4 (SLC26A4/pendrin) during amelogenesis in developing rodent teethAntonius L J J Bronckers, Jing Guo, Behrouz Zandieh-Doulabi, 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.
BMC Medicine|December 26, 2006
Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse modelSairam V Jabba, Alisha Oelke, Ruchira Singh, 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.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 9, 2017
Acute genetic ablation of pendrin lowers blood pressure in miceFrancesco Trepiccione, Christelle Soukaseum, Veronique Baudrie, et al.
Elife|October 11, 2017
Molecular architecture underlying fluid absorption by the developing inner earKeiji Honda, Sung Huhn Kim, Michael C Kelly, et al.
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