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For: Xia L, Yin S, Wang J. Inner ear gene transfection in neonatal mice using adeno-associated viral vector: a comparison of two approaches. PLoS One 2012;7:e43218. [PMID: 22912830 DOI: 10.1371/journal.pone.0043218] [Cited by in Crossref: 23] [Cited by in F6Publishing: 25] [Article Influence: 2.3] [Reference Citation Analysis]
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7 Ding N, Lee S, Lieber-Kotz M, Yang J, Gao X. Advances in genome editing for genetic hearing loss. Adv Drug Deliv Rev 2021;168:118-33. [PMID: 32387678 DOI: 10.1016/j.addr.2020.05.001] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
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9 Leake PA, Rebscher SJ, Dore' C, Akil O. AAV-Mediated Neurotrophin Gene Therapy Promotes Improved Survival of Cochlear Spiral Ganglion Neurons in Neonatally Deafened Cats: Comparison of AAV2-hBDNF and AAV5-hGDNF. J Assoc Res Otolaryngol 2019;20:341-61. [PMID: 31222416 DOI: 10.1007/s10162-019-00723-5] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
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11 Akil O, Lustig L. AAV-Mediated Gene Delivery to the Inner Ear. Methods Mol Biol 2019;1950:271-82. [PMID: 30783980 DOI: 10.1007/978-1-4939-9139-6_16] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
12 Fukui H, Raphael Y. Gene therapy for the inner ear. Hear Res 2013;297:99-105. [PMID: 23265411 DOI: 10.1016/j.heares.2012.11.017] [Cited by in Crossref: 44] [Cited by in F6Publishing: 36] [Article Influence: 4.4] [Reference Citation Analysis]
13 Guo JY, He L, Qu TF, Liu YY, Liu K, Wang GP, Gong SS. Canalostomy As a Surgical Approach to Local Drug Delivery into the Inner Ears of Adult and Neonatal Mice. J Vis Exp 2018. [PMID: 29889202 DOI: 10.3791/57351] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
14 Zhu BZ, Saleh J, Isgrig KT, Cunningham LL, Chien WW. Hearing Loss after Round Window Surgery in Mice Is due to Middle Ear Effusion. Audiol Neurootol 2016;21:356-64. [PMID: 28068659 DOI: 10.1159/000449239] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 1.6] [Reference Citation Analysis]
15 Akil O, Rouse SL, Chan DK, Lustig LR. Surgical method for virally mediated gene delivery to the mouse inner ear through the round window membrane. J Vis Exp 2015. [PMID: 25867531 DOI: 10.3791/52187] [Cited by in Crossref: 12] [Cited by in F6Publishing: 19] [Article Influence: 1.7] [Reference Citation Analysis]
16 Chen X, Zhao X, Hu Y, Lan F, Sun H, Fan G, Sun Y, Wu J, Kong W, Kong W. The spread of adenoviral vectors to central nervous system through pathway of cochlea in mimetic aging and young rats. Gene Ther 2015;22:866-75. [PMID: 26125607 DOI: 10.1038/gt.2015.63] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
17 Zhang Z, Wang J, Li C, Xue W, Xing Y, Liu F. Gene therapy development in hearing research in China. Gene Ther 2020;27:349-59. [PMID: 32681137 DOI: 10.1038/s41434-020-0177-1] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
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19 Omichi R, Shibata SB, Morton CC, Smith RJH. Gene therapy for hearing loss. Hum Mol Genet 2019;28:R65-79. [PMID: 31227837 DOI: 10.1093/hmg/ddz129] [Cited by in Crossref: 27] [Cited by in F6Publishing: 22] [Article Influence: 13.5] [Reference Citation Analysis]
20 Casey G, Askew C, Brimble MA, Samulski RJ, Davidoff AM, Li C, Walters BJ. Self-complementarity in adeno-associated virus enhances transduction and gene expression in mouse cochlear tissues. PLoS One 2020;15:e0242599. [PMID: 33227033 DOI: 10.1371/journal.pone.0242599] [Reference Citation Analysis]
21 Taiber S, Avraham KB. Genetic Therapies for Hearing Loss: Accomplishments and Remaining Challenges. Neurosci Lett 2019;713:134527. [PMID: 31586696 DOI: 10.1016/j.neulet.2019.134527] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
22 Kurihara S, Fujioka M, Hata J, Yoshida T, Hirabayashi M, Yamamoto Y, Ogawa K, Kojima H, Okano HJ. Anatomical and Surgical Evaluation of the Common Marmoset as an Animal Model in Hearing Research. Front Neuroanat 2019;13:60. [PMID: 31244619 DOI: 10.3389/fnana.2019.00060] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
23 Leake PA, Akil O, Lang H. Neurotrophin gene therapy to promote survival of spiral ganglion neurons after deafness. Hear Res 2020;394:107955. [PMID: 32331858 DOI: 10.1016/j.heares.2020.107955] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
24 Chien WW, McDougald DS, Roy S, Fitzgerald TS, Cunningham LL. Cochlear gene transfer mediated by adeno-associated virus: Comparison of two surgical approaches. Laryngoscope 2015;125:2557-64. [PMID: 25891801 DOI: 10.1002/lary.25317] [Cited by in Crossref: 37] [Cited by in F6Publishing: 38] [Article Influence: 5.3] [Reference Citation Analysis]
25 Verdoodt D, Peeleman N, Van Camp G, Van Rompaey V, Ponsaerts P. Transduction Efficiency and Immunogenicity of Viral Vectors for Cochlear Gene Therapy: A Systematic Review of Preclinical Animal Studies. Front Cell Neurosci 2021;15:728610. [PMID: 34526880 DOI: 10.3389/fncel.2021.728610] [Reference Citation Analysis]