about
A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner earGene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c.The molecules that mediate sensory transduction in the mammalian inner ear.Transgenic Tmc2 expression preserves inner ear hair cells and vestibular function in mice lacking Tmc1Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 functionImproved TMC1 gene therapy restores hearing and balance in mice with genetic inner ear disordersPublisher Correction: Improved TMC1 gene therapy restores hearing and balance in mice with genetic inner ear disordersAllele-specific gene editing prevents deafness in a model of dominant progressive hearing loss
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description
onderzoeker
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researcher ORCID ID = 0000-0001-9746-3420
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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Bifeng Pan
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0000-0001-9746-3420