نتائج البحث - Mark A. Rutherford
- يعرض 1 - 15 نتائج من 15
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GluA3 subunits are required for appropriate assembly of AMPAR GluA2 and GluA4 subunits on cochlear afferent synapses and for presynaptic ribbon modiolar–pillar morphology حسب Mark A. Rutherford, Atri Bhattacharyya, Maolei Xiao, Hou-Ming Cai, Indra Pal, María E. Rubio
منشور في 2023Artigo -
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Disruption of the Presynaptic Cytomatrix Protein Bassoon Degrades Ribbon Anchorage, Multiquantal Release, and Sound Encoding at the Hair Cell Afferent Synapse حسب Zhizi Jing, Mark A. Rutherford, Hideki Takago, Thomas Frank, Anna Fejtová, Darina Khimich, Tobias Moser, Nicola Strenzke
منشور في 2013Artigo -
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Developmental refinement of hair cell synapses tightens the coupling of Ca<sup>2</sup><sup>+</sup>influx to exocytosis حسب Aaron B. Wong, Mark A. Rutherford, Mantas Gabrielaitis, Tina Pangršič, Fabian Göttfert, Thomas Frank, Susann Michanski, Stefan W. Hell, Fred Wolf, Carolin Wichmann, Tobias Moser
منشور في 2014Artigo -
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Hair cells use active zones with different voltage dependence of Ca <sup>2+</sup> influx to decompose sounds into complementary neural codes حسب Tzu‐Lun Ohn, Mark A. Rutherford, Zhizi Jing, Sangyong Jung, Carlos J. Duque-Afonso, Gerhard Hoch, Maria Magdalena Picher, Anja Scharinger, Nicola Strenzke, Tobias Moser
منشور في 2016Artigo -
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Bassoon and the Synaptic Ribbon Organize Ca2+ Channels and Vesicles to Add Release Sites and Promote Refilling حسب Thomas Frank, Mark A. Rutherford, Nicola Strenzke, Andreas Neef, Tina Pangršič, Darina Khimich, Anna Fejtová, Eckart D. Gundelfinger, M. Charles Liberman, Benjamin Harke, Keith E. Bryan, Amy Lee, Alexander Egner, Dietmar Riedel, Tobias Moser
منشور في 2010Artigo -
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Vesicular Glutamatergic Transmission in Noise-Induced Loss and Repair of Cochlear Ribbon Synapses حسب Kyunghee X. Kim, Shelby Payne, Aizhen Yang-Hood, Song-Zhe Li, Bethany Davis, Jason Carlquist, Babak V-Ghaffari, Jay A. Gantz, Dorina Kallogjeri, James A. J. Fitzpatrick, Kevin K. Ohlemiller, Keiko Hirose, Mark A. Rutherford
منشور في 2019Artigo -
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A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss حسب Simon von Ameln, Geng Wang, Redouane Boulouiz, Mark A. Rutherford, Geoffrey Smith, Yun Li, Hans‐Martin Pogoda, Gudrun Nürnberg, Barbara Stiller, Alexander E. Volk, Guntram Borck, Jason Hong, Richard J. Goodyear, Omar Abidi, Peter Nürnberg, Kay Hofmann, Guy P. Richardson, Matthias Hammerschmidt, Tobias Moser, Bernd Wollnik, Carla M. Koehler, Michael A. Teitell, Abdelhamid Barakat, Christian Kubisch
منشور في 2012Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Biochemistry
Neuroscience
Chemistry
Cochlea
Receptor
Biophysics
Membrane
Cell biology
Ribbon synapse
Synaptic vesicle
Vesicle
Spiral ganglion
Neurotransmission
Synapse
AMPA receptor
Genetics
Glutamate receptor
Hair cell
Excitatory postsynaptic potential
Medicine
Postsynaptic potential
Exocytosis
Inhibitory postsynaptic potential
Inner ear
Active zone
Afferent
Anatomy
Brainstem
Cochlear nucleus