EDP Sciences logo
Subscriber Authentication Point
Search
Menu
Home All issues Volume 34 / No 10 (Octobre 2018) Med Sci (Paris), 34 10 (2018) 842-848 References
Open Access
Issue
Med Sci (Paris)
Volume 34, Number 10, Octobre 2018
Page(s) 842 - 848
Section M/S Revues
DOI https://doi.org/10.1051/medsci/2018210
Published online 19 November 2018
  1. Iizuka T, Kanzaki S, Mochizuki H, et al. Noninvasive In vivo delivery of transgene via adeno-associated virus into supporting cells of the neonatal mouse cochlea. Hum Gene Ther 2008 ; 19 : 384–390. [Google Scholar]
  2. Emptoz A, Michel V, Lelli A, et al. Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G. Proc Natl Acad Sci USA 2017 ; 114 : 9695–9700. [CrossRef] [Google Scholar]
  3. Pan B, Askew C, Galvin A, et al. Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c. Nat Biotechnol 2017 ; 35 : 264–272. [CrossRef] [PubMed] [Google Scholar]
  4. György B, Sage C, Indzhykulian AA, et al. Rescue of hearing by gene delivery to inner-ear hair cells using exosome-associated AAV. Mol Ther 2017 ; 25 : 379–391. [CrossRef] [PubMed] [Google Scholar]
  5. Guo J, Liu Y, Qu T, et al. Cochleovestibular gene transfer in neonatal mice by canalostomy. Neuroreport 2017 ; 28 : 682–688. [CrossRef] [PubMed] [Google Scholar]
  6. Yoshimura H, Shibata SB, Ranum PT, et al. Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation. Sci Rep 2018 ; 8 : 2980. [CrossRef] [PubMed] [Google Scholar]
  7. Pyykkö I, Zou J, Zhang W, et al. Nanoparticle-based delivery for the treatment of inner ear disorders. Curr Opin Otolaryngol Head Neck Surg 2011 ; 19 : 388–396. [CrossRef] [PubMed] [Google Scholar]
  8. Schlenk F, Grund S, Fischer D. Recent developments and perspectives on gene therapy using synthetic vectors. Ther Deliv 2013 ; 4 : 95–113. [CrossRef] [PubMed] [Google Scholar]
  9. Sacheli R, Delacroix L, Vandenackerveken P, et al. Gene transfer in inner ear cells: a challenging race. Gene Ther 2013 ; 20 : 237–247. [CrossRef] [PubMed] [Google Scholar]
  10. Choi JH, Yu NK, Baek GC, et al. Optimization of AAV expression cassettes to improve packaging capacity and transgene expression in neurons. Mol Brain 2014; 7. [PubMed] [Google Scholar]
  11. Zinn E, Pacouret S, Khaychuk V, et al. In silico reconstruction of the viral evolutionary lineage yields a potent gene therapy vector. Cell Rep 2015 ; 12 : 1056–1068. [CrossRef] [PubMed] [Google Scholar]
  12. Landegger LD, Pan B, Askew C, et al. A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear. Nat Biotechnol 2017 ; 35 : 280–284. [CrossRef] [PubMed] [Google Scholar]
  13. Kimberling WJ, Hildebrand MS, Shearer AE, et al. Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children. Genet Med 2010 ; 12 : 512–516. [CrossRef] [PubMed] [Google Scholar]
  14. Isgrig K, Shteamer JW, Belyantseva IA, et al. Gene therapy restores balance and auditory functions in a mouse model of Usher syndrome. Mol Ther 2017 ; 25 : 780–791. [CrossRef] [PubMed] [Google Scholar]
  15. Caberlotto E, Michel V, Foucher I, et al. Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia. Proc Natl Acad Sci USA 2011 ; 108 : 5825–5830. [CrossRef] [Google Scholar]
  16. Kang WS, Nguyen K, McKenna CE, et al. Intracochlear drug delivery through the oval window in fresh cadaveric human temporal bones. Otol Neurotol 2016 ; 37 : 218–222. [CrossRef] [PubMed] [Google Scholar]
  17. Hanen Khabou H, Dalkara D. La conception de vecteurs adaptés à la thérapie génique oculaire. Med Sci (Paris) 2015; 31 : 529–37. [Google Scholar]
  18. El-Amraoui A, Lefèvre G, Hardelin JP, Petit C. Syndrome de Usher de type 1 et développement de la touffe ciliaire des cellules sensorielles de l’oreille interne. Med Sci (Paris) 2005 ; 21 : 737–740. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  19. Grillet N. Harmonine est un composant de la machinerie de mécanotransduction auditive. Med Sci (Paris) 2009 ; 25 : 903–906. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.