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Missense mutations in Otopetrin 1 affect subcellular localization and inhibition of purinergic signaling in vestibular supporting cells

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Year: 2011
Type: article
Source: Molecular and Cellular Neuroscience
DOI: 10.1016/j.mcn.2011.01.005
Authors: Euysoo Kim, Krzysztof L. Hyrc, Judith Speck, Felipe T. Salles, Yunxia W. Lundberg, Mark P. Goldberg, Bechara Kachar, Mark E. Warchol, David M. Ornitz
Institutions: Washington University in St. Louis, National Institutes of Health, National Institute on Deafness and Other Communication Disorders, Boys Town National Research Hospital, The University of Texas Southwestern Medical Center
Language: English

Topic: Vestibular and auditory disorders
Subfield: Neurology
Field: Neuroscience
Domain: Life Sciences

Open Access status: green

Funders: National Institute on Deafness and Other Communication Disorders, National Institute of Neurological Disorders and Stroke
Awards: Research Core Center for Auditory and Vestibular Studies, Washington University Center for Translational Neuroscience, G3647780438, G4549778172, OTOCONIA DEVELOPMENT AND MAINTENANCE, G5973595807, BIOLOGICAL FUNCTION OF THE OTOPERTRIN GENE FAMILY, OLIGODENDROCYTE DEATH IN CEREBRAL ISCHEMIA, Cell-Cell Interaction and Hypoxic Brain Injury, G822165535
OpenAlex ID: W2061307688
FWCI: 2.118
Cites: 13
Cited by: 32
Related to: 10
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