نتائج البحث

Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss – A Common Hereditary Deafness حسب Jeffrey C. Wingard, Hong-Bo Zhao

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Development of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing loss حسب Heiko Locher, John C. M. J. de Groot, Liesbeth van Iperen, Margriet A. Huisman, Johan H. M. Frijns, Susana M. Chuva de Sousa Lopes

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Effects of Furosemide Applied Chronically to the Round Window: A Model of Metabolic Presbyacusis حسب Richard A. Schmiedt, Hainan Lang, Hiro-oki Okamura, Bradley A. Schulte

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Fast motility of isolated mammalian auditory sensory cells حسب H. P. Zenner, Ulrike Zimmermann, Alfred H. Gitter

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Alterations in cochlear function during induced acute hyperinsulinemia in an animal model حسب Roberto Dihl Angeli, Luíz Lavinsky, Alexandre Dolganov

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Mechanism Generating Endocochlear Potential: Role Played by Intermediate Cells in Stria Vascularis حسب Shunji Takeuchi, Motonori Ando, Akinobu Kakigi

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Deafness and Permanently Reduced Potassium Channel Gene Expression and Function in Hypothyroid<i>Pit1</i>^dwMutants حسب Mirna Mustapha, Qing Fang, Tzy-Wen Gong, David F. Dolan, Yehoash Raphael, Sally A. Camper, Robert Duncan

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Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders حسب Jin Chen, Jing Chen, Yan Zhu, Chun Liang, Hong-Bo Zhao

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The role of an inwardly rectifying K+ channel (Kir4.1) in the inner ear and hearing loss حسب Jin Chen, Hongbo Zhao

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Perivascular-resident macrophage-like melanocytes in the inner ear are essential for the integrity of the intrastrial fluid–blood barrier حسب Wenjing Zhang, Min Dai, Anders Fridberger, Ahmed M. Hassan, Jacqueline M. DeGagne, Lingling Neng, Fei Zhang, Wenxuan He, Tianying Ren, Dennis R. Trune, Manfred Auer, Xiaorui Shi

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The nature of the negative endocochlear potentials produced by anoxia and ethacrynic acid in the rat and guinea‐pig. حسب S. K. Bosher

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BAAV Mediated GJB2 Gene Transfer Restores Gap Junction Coupling in Cochlear Organotypic Cultures from Deaf Cx26Sox10Cre Mice حسب Giulia Crispino, Giovanni Di Pasquale, Pietro Scimemi, Laura Rodríguez, Fabián Galindo Ramírez, Romolo Daniele De Siati, Rosa Maria Santarelli, Edoardo Arslan, Mario Bortolozzi, John A. Chiorini, Fabio Mammano

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Nuclear Factor κB Deficiency Is Associated with Auditory Nerve Degeneration and Increased Noise-Induced Hearing Loss حسب Hainan Lang, Bradley A. Schulte, Daohong Zhou, Nancy Smythe, Samuel S. Spicer, Richard A. Schmiedt

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Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall حسب Ying-Peng Liu, Hong-Bo Zhao

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Vanilloid Receptors in Hearing: Altered Cochlear Sensitivity by Vanilloids and Expression of TRPV1 in the Organ of Corti حسب Jiefu Zheng, Chunfu Dai, Peter S. Steyger, Young‐Ki Kim, Zoltán Vass, Tianying Ren, Alfred L. Nuttall

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The relation between the endocochlear potential and spontaneous activity in auditory nerve fibres of the cat. حسب William F. Sewell

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Mechanism of endocochlear potential generation by stria vascularis حسب Alec N. Salt, Ivo Melichar, Ruediger Thalmann

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Chronic Reduction of Endocochlear Potential Reduces Auditory Nerve Activity: Further Confirmation of an Animal Model of Metabolic Presbyacusis حسب Hainan Lang, Vinu Jyothi, Nancy Smythe, Judy R. Dubno, Bradley A. Schulte, Richard A. Schmiedt

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The Novel PMCA2 Pump Mutation Tommy Impairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice حسب Mario Bortolozzi, Marisa Brini, Nick Parkinson, Giulia Crispino, Pietro Scimemi, Romolo Daniele De Siati, Francesca Di Leva, Andrew Parker, Saida Ortolano, Edoardo Arslan, Steve D. M. Brown, Ernesto Carafoli, Fabio Mammano

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

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