Review Article
Potential of Gene and Cell Therapy for Inner Ear Hair Cells
Table 1
Animal studies using gene therapies for genetic hearing loss model.
| Year | Country | Vector | Gene | Animal | Reference |
| 2012 | US | AAV | VGLUT3 | mouse (premature) | Akil et al. | 2014 | US | AAV | Gjb2 | mouse (mature) | Yu et al. | 2015 | Japan | AAV | Gjb2 | mouse (mature and premature) | Iizuka et al. | 2015 | US | AAV | TMC1 | mouse (premature) | Askew et al. | 2016 | South Korea | AAV | MsrB3 | mouse (in utero) | Kim et al. | 2017 | US | AAV | USH3 | mouse (premature) | Geng et al. | 2017 | US | AAV | USH1C | Mouse (premature) | Pan et al. |
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AAV: adenoassociated virus; VGLUT3: vesicular glutamate transporter 3; MsrB3: methionine sulfoxide reductase B3; TMC1: transmembrane channel like 1; USH3: Usher syndrome type III; USH1C: Usher syndrome type Ic.
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