Search Results - Philine Wangemann

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  1. 1
    Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

    Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential by Philine Wangemann

    Published 2006
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  2. 2
    Free radical stress-mediated loss of<i>Kcnj10</i>protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model

    Free radical stress-mediated loss of<i>Kcnj10</i>protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model by Ruchira Singh, Philine Wangemann

    Published 2007
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  3. 3
    Hearing loss associated with enlargement of the vestibular aqueduct: Mechanistic insights from clinical phenotypes, genotypes, and mouse models

    Hearing loss associated with enlargement of the vestibular aqueduct: Mechanistic insights from clinical phenotypes, genotypes, and mouse models by Andrew J. Griffith, Philine Wangemann

    Published 2011
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  4. 4
    Epithelial Cell Stretching and Luminal Acidification Lead to a Retarded Development of Stria Vascularis and Deafness in Mice Lacking Pendrin

    Epithelial Cell Stretching and Luminal Acidification Lead to a Retarded Development of Stria Vascularis and Deafness in Mice Lacking Pendrin by Hyoung‐Mi Kim, Philine Wangemann

    Published 2011
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  5. 5
    Failure of Fluid Absorption in the Endolymphatic Sac Initiates Cochlear Enlargement that Leads to Deafness in Mice Lacking Pendrin Expression

    Failure of Fluid Absorption in the Endolymphatic Sac Initiates Cochlear Enlargement that Leads to Deafness in Mice Lacking Pendrin Expression by Hyoung‐Mi Kim, Philine Wangemann

    Published 2010
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  6. 6
    Potassium Ion Movement in the Inner Ear: Insights from Genetic Disease and Mouse Models

    Potassium Ion Movement in the Inner Ear: Insights from Genetic Disease and Mouse Models by Anselm A. Zdebik, Philine Wangemann, Thomas J. Jentsch

    Published 2009
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  7. 7
    Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

    Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction by Taku Ito, Xiangming Li, Kiyoto Kurima, Byung Yoon Choi, Philine Wangemann, Andrew J. Griffith

    Published 2014
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  8. 8
    Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome

    Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome by Tao Yang, José Gurrola, Hao Wu, Sui Mei Chiu, Philine Wangemann, Peter M. Snyder, Richard J. Smith

    Published 2009
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  9. 9
    Expression of epithelial calcium transport system in rat cochlea and vestibular labyrinth

    Expression of epithelial calcium transport system in rat cochlea and vestibular labyrinth by Daisuke Yamauchi, Kazuhiro Nakaya, Nithya N. Raveendran, Donald G. Harbidge, Ruchira Singh, Philine Wangemann, Daniel C. Marcus

    Published 2010
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  10. 10
    Lack of pendrin HCO<sub>3</sub><sup>−</sup>transport elevates vestibular endolymphatic [Ca<sup>2+</sup>] by inhibition of acid-sensitive TRPV5 and TRPV6 channels

    Lack of pendrin HCO<sub>3</sub><sup>−</sup>transport elevates vestibular endolymphatic [Ca<sup>2+</sup>] by inhibition of acid-sensitive TRPV5 and TRPV6 channels by Kazuhiro Nakaya, Donald G. Harbidge, Philine Wangemann, Bruce D. Schultz, Eric D. Green, Susan M. Wall, Daniel C. Marcus

    Published 2007
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  11. 11
    Microarray-based comparison of three amplification methods for nanogram amounts of total RNA

    Microarray-based comparison of three amplification methods for nanogram amounts of total RNA by Ruchira Singh, Rajanikanth J Maganti, Sairam V. Jabba, Martin Wang, Glenn Deng, Joe Don Heath, Nurith Kurn, Philine Wangemann

    Published 2004
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  12. 12
    Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking <i>Slc26a4</i>/pendrin expression

    Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking <i>Slc26a4</i>/pendrin expression by Philine Wangemann, Hyoung-Mi Kim, Sara Billings, Kazuhiro Nakaya, Xiangming Li, Ruchira Singh, David S. Sharlin, Douglas Forrest, Daniel C. Marcus, Peying Fong

    Published 2009
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  13. 13
    Loss of cochlear HCO<sub>3</sub><sup>−</sup>secretion causes deafness via endolymphatic acidification and inhibition of Ca<sup>2+</sup>reabsorption in a Pendred syndrome mouse model

    Loss of cochlear HCO<sub>3</sub><sup>−</sup>secretion causes deafness via endolymphatic acidification and inhibition of Ca<sup>2+</sup>reabsorption in a Pendred syndrome mouse mode... by Philine Wangemann, Kazuhiro Nakaya, Tao Wu, Rajanikanth J Maganti, Erin M. Itza, Joel D. Sanneman, Donald G. Harbidge, Sara Billings, Daniel C. Marcus

    Published 2007
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  14. 14
    Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

    Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death by Martine Cohen‐Salmon, Thomas Ott, Vincent Michel, Jean-Pierre Hardelin, Isabelle Perfettini, Michel Eybalin, Tao Wu, Daniel C. Marcus, Philine Wangemann, Klaus Willecke, Christine Petit

    Published 2002
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  15. 15
    A Claudin-9–Based Ion Permeability Barrier Is Essential for Hearing

    A Claudin-9–Based Ion Permeability Barrier Is Essential for Hearing by Yoko Nakano, Sung Huhn Kim, Hyoung-Mi Kim, Joel D. Sanneman, Yuzhou Zhang, Richard J. Smith, Daniel C. Marcus, Philine Wangemann, R. Neßler, Botond Bánfi

    Published 2009
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  16. 16
    Inner Ear Defects Induced by Null Mutationof the isk Gene

    Inner Ear Defects Induced by Null Mutationof the isk Gene by Douglas E. Vetter, Jeffrey R. Mann, Philine Wangemann, Jianzhong Liu, K. John McLaughlin, Florian Lesage, Daniel C. Marcus, Michel Lazdunski, Stephen F. Heinemann, Jacques Barhanin

    Published 1996
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  17. 17
    SLC26A4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc26a4 Mutant Mice

    SLC26A4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc26a4 Mutant Mice by Xiangming Li, Joel D. Sanneman, Donald G. Harbidge, Fei Zhou, Taku Ito, Raoul D. Nelson, Nicolas Picard, Régine Chambrey, Dominique Eladari, Tracy Miesner, Andrew J. Griffith, Daniel C. Marcus, Philine Wangemann

    Published 2013
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  18. 18
    Tumor Necrosis Factor-α Enhances Microvascular Tone and Reduces Blood Flow in the Cochlea via Enhanced Sphingosine-1-Phosphate Signaling

    Tumor Necrosis Factor-α Enhances Microvascular Tone and Reduces Blood Flow in the Cochlea via Enhanced Sphingosine-1-Phosphate Signaling by Elias Q. Scherer, Jing Yang, Martin Canis, Katrin Reimann, K. Ivanov, Christian Diehl, Peter H. Backx, W. Gil Wier, Sebastian Strieth, Philine Wangemann, Julia Voigtlaender‐Bolz, Darcy Lidington, Steffen‐Sebastian Bolz

    Published 2010
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  19. 19
    Molecular architecture underlying fluid absorption by the developing inner ear

    Molecular architecture underlying fluid absorption by the developing inner ear by Keiji Honda, Sung Huhn Kim, Michael C. Kelly, J. C. Burns, Laura A. Constance, Xiangming Li, Fei Zhou, Michael Hoa, Matthew W. Kelley, Philine Wangemann, Robert J. Morell, Andrew J. Griffith

    Published 2017
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  20. 20
    Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

    Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing by Mina Kim, Sung Huhn Kim, Nari Ryu, Ji-Hyun Ma, Ye‐Ri Kim, Jinsei Jung, Chuan‐Jen Hsu, Jae Young Choi, Kyu-Yup Lee, Philine Wangemann, Jinwoong Bok, Un‐Kyung Kim

    Published 2019
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