Viability of Long-Term Gene Therapy in the Cochlea
Spiral ganglion
Neurotrophin-3
DOI:
10.1038/srep04733
Publication Date:
2014-04-22T09:09:54Z
AUTHORS (5)
ABSTRACT
Gene therapy has been investigated as a way to introduce variety of genes treat neurological disorders. An important clinical consideration is its long-term effectiveness. This research aims study the expression and effectiveness gene in promoting spiral ganglion neuron survival after deafness. Adenoviral vectors modified express brain derived neurotrophic factor or neurotrophin-3 were unilaterally injected into guinea pig cochlea one week post ototoxic deafening. After six months, persistence significantly greater neuronal neurotrophin-treated cochleae compared contralateral observed. The observed indicates that potentially viable; however degeneration transduced cells result original insult may limit With further aimed at transducing stable cochlear cells, be an efficacious neurotrophins promote hearing loss.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (29)
CITATIONS (13)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....