Open Access
Med Sci (Paris)
Volume 34, Number 10, Octobre 2018
Page(s) 842 - 848
Section M/S Revues
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]

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