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For: Yu Q, Wang Y, Chang Q, Wang J, Gong S, Li H, Lin X. Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice. Gene Ther 2014;21:71-80. [PMID: 24225640 DOI: 10.1038/gt.2013.59] [Cited by in Crossref: 71] [Cited by in F6Publishing: 63] [Article Influence: 8.9] [Reference Citation Analysis]
Number Citing Articles
1 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: 3.5] [Reference Citation Analysis]
2 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: 27.0] [Reference Citation Analysis]
3 Shibata SB, Ranum PT, Moteki H, Pan B, Goodwin AT, Goodman SS, Abbas PJ, Holt JR, Smith RJH. RNA Interference Prevents Autosomal-Dominant Hearing Loss. Am J Hum Genet 2016;98:1101-13. [PMID: 27236922 DOI: 10.1016/j.ajhg.2016.03.028] [Cited by in Crossref: 60] [Cited by in F6Publishing: 51] [Article Influence: 12.0] [Reference Citation Analysis]
4 Bankoti K, Generotti C, Hwa T, Wang L, O'Malley BW Jr, Li D. Advances and challenges in adeno-associated viral inner-ear gene therapy for sensorineural hearing loss. Mol Ther Methods Clin Dev 2021;21:209-36. [PMID: 33850952 DOI: 10.1016/j.omtm.2021.03.005] [Reference Citation Analysis]
5 Xie L, Chen S, Xu K, Cao HY, Du AN, Bai X, Sun Y, Kong WJ. Reduced postnatal expression of cochlear Connexin26 induces hearing loss and affects the developmental status of pillar cells in a dose-dependent manner. Neurochem Int 2019;128:196-205. [PMID: 31034913 DOI: 10.1016/j.neuint.2019.04.012] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
6 Lan Y, Tao Y, Wang Y, Ke J, Yang Q, Liu X, Su B, Wu Y, Lin CP, Zhong G. Recent development of AAV-based gene therapies for inner ear disorders. Gene Ther 2020;27:329-37. [PMID: 32424232 DOI: 10.1038/s41434-020-0155-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
7 Huang SN, Zhou YP, Jiang X, Yang B, Cheng H, Luo MH. Hearing Loss Caused by HCMV Infection through Regulating the Wnt and Notch Signaling Pathways. Viruses 2021;13:623. [PMID: 33917368 DOI: 10.3390/v13040623] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Choo DI, Tawfik KO, Martin DM, Raphael Y. Inner ear manifestations in CHARGE: Abnormalities, treatments, animal models, and progress toward treatments in auditory and vestibular structures. Am J Med Genet C Semin Med Genet 2017;175:439-49. [PMID: 29082607 DOI: 10.1002/ajmg.c.31587] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
9 Askew C, Chien WW. Adeno-associated virus gene replacement for recessive inner ear dysfunction: Progress and challenges. Hear Res 2020;394:107947. [PMID: 32247629 DOI: 10.1016/j.heares.2020.107947] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 6.0] [Reference Citation Analysis]
10 Crane R, Conley SM, Al-Ubaidi MR, Naash MI. Gene Therapy to the Retina and the Cochlea. Front Neurosci 2021;15:652215. [PMID: 33815052 DOI: 10.3389/fnins.2021.652215] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Jimenez JE, Nourbakhsh A, Colbert B, Mittal R, Yan D, Green CL, Nisenbaum E, Liu G, Bencie N, Rudman J, Blanton SH, Zhong Liu X. Diagnostic and therapeutic applications of genomic medicine in progressive, late-onset, nonsyndromic sensorineural hearing loss. Gene 2020;747:144677. [PMID: 32304785 DOI: 10.1016/j.gene.2020.144677] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
12 Ahmed H, Shubina-Oleinik O, Holt JR. Emerging Gene Therapies for Genetic Hearing Loss. J Assoc Res Otolaryngol 2017;18:649-70. [PMID: 28815315 DOI: 10.1007/s10162-017-0634-8] [Cited by in Crossref: 46] [Cited by in F6Publishing: 40] [Article Influence: 11.5] [Reference Citation Analysis]
13 Zhang W, Kim SM, Wang W, Cai C, Feng Y, Kong W, Lin X. Cochlear Gene Therapy for Sensorineural Hearing Loss: Current Status and Major Remaining Hurdles for Translational Success. Front Mol Neurosci 2018;11:221. [PMID: 29997477 DOI: 10.3389/fnmol.2018.00221] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 7.3] [Reference Citation Analysis]
14 Wu X, Zhang W, Li Y, Lin X. Structure and Function of Cochlear Gap Junctions and Implications for the Translation of Cochlear Gene Therapies. Front Cell Neurosci 2019;13:529. [PMID: 31827424 DOI: 10.3389/fncel.2019.00529] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
15 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: 3.0] [Reference Citation Analysis]
16 György B, Sage C, Indzhykulian AA, Scheffer DI, Brisson AR, Tan S, Wu X, Volak A, Mu D, Tamvakologos PI, Li Y, Fitzpatrick Z, Ericsson M, Breakefield XO, Corey DP, Maguire CA. Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV. Mol Ther 2017;25:379-91. [PMID: 28082074 DOI: 10.1016/j.ymthe.2016.12.010] [Cited by in Crossref: 108] [Cited by in F6Publishing: 101] [Article Influence: 27.0] [Reference Citation Analysis]
17 Hosoya M, Fujioka M, Nara K, Morimoto N, Masuda S, Sugiuchi T, Katsunuma S, Takagi A, Morita N, Ogawa K, Kaga K, Matsunaga T. Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers. Int J Pediatr Otorhinolaryngol 2021;149:110840. [PMID: 34293626 DOI: 10.1016/j.ijporl.2021.110840] [Reference Citation Analysis]
18 Delmaghani S, El-Amraoui A. Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges. J Clin Med 2020;9:E2309. [PMID: 32708116 DOI: 10.3390/jcm9072309] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 14.0] [Reference Citation Analysis]
19 Lee MY, Park YH. Potential of Gene and Cell Therapy for Inner Ear Hair Cells. Biomed Res Int. 2018;2018:8137614. [PMID: 30009175 DOI: 10.1155/2018/8137614] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
20 Lin J, Huang H, Lv G, Xu X, Lin W, Xu X, Cheng J, Zheng M. Chronic prenatal hypoxia impairs cochlear development, a mechanism involving connexin26 expression and promoter methylation. Int J Mol Med 2018;41:852-8. [PMID: 29207085 DOI: 10.3892/ijmm.2017.3303] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
21 Kelly KM, Lalwani AK. On the Distant Horizon--Medical Therapy for Sensorineural Hearing Loss. Otolaryngol Clin North Am 2015;48:1149-65. [PMID: 26409822 DOI: 10.1016/j.otc.2015.07.012] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
22 Wingard JC, Zhao HB. Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness. Front Cell Neurosci 2015;9:202. [PMID: 26074771 DOI: 10.3389/fncel.2015.00202] [Cited by in Crossref: 73] [Cited by in F6Publishing: 70] [Article Influence: 12.2] [Reference Citation Analysis]
23 Rudman JR, Mei C, Bressler SE, Blanton SH, Liu XZ. Precision medicine in hearing loss. J Genet Genomics 2018;45:99-109. [PMID: 29500086 DOI: 10.1016/j.jgg.2018.02.004] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
24 Zhang L, Wu X, Lin X. Gene therapy for genetic mutations affecting non-sensory cells in the cochlea. Hear Res 2020;394:107858. [PMID: 31791650 DOI: 10.1016/j.heares.2019.107858] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
25 Chen S, Sun Y, Lin X, Kong W. Down regulated connexin26 at different postnatal stage displayed different types of cellular degeneration and formation of organ of Corti. Biochem Biophys Res Commun 2014;445:71-7. [PMID: 24491564 DOI: 10.1016/j.bbrc.2014.01.154] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 2.6] [Reference Citation Analysis]
26 Kleinlogel S, Vogl C, Jeschke M, Neef J, Moser T. Emerging approaches for restoration of hearing and vision. Physiological Reviews. [DOI: 10.1152/physrev.00035.2019] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 13.0] [Reference Citation Analysis]
27 Shu Y, Tao Y, Li W, Shen J, Wang Z, Chen ZY. Adenovirus Vectors Target Several Cell Subtypes of Mammalian Inner Ear In Vivo. Neural Plast 2016;2016:9409846. [PMID: 28116172 DOI: 10.1155/2016/9409846] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 3.2] [Reference Citation Analysis]
28 Lee S, Dondzillo A, Gubbels SP, Raphael Y. Practical aspects of inner ear gene delivery for research and clinical applications. Hear Res 2020;394:107934. [PMID: 32204962 DOI: 10.1016/j.heares.2020.107934] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Zheng F, Zuo J. Cochlear hair cell regeneration after noise-induced hearing loss: Does regeneration follow development? Hear Res 2017;349:182-96. [PMID: 28034617 DOI: 10.1016/j.heares.2016.12.011] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 3.0] [Reference Citation Analysis]
30 Pfingst BE, Zhou N, Colesa DJ, Watts MM, Strahl SB, Garadat SN, Schvartz-Leyzac KC, Budenz CL, Raphael Y, Zwolan TA. Importance of cochlear health for implant function. Hear Res 2015;322:77-88. [PMID: 25261772 DOI: 10.1016/j.heares.2014.09.009] [Cited by in Crossref: 67] [Cited by in F6Publishing: 62] [Article Influence: 9.6] [Reference Citation Analysis]
31 Devare J, Gubbels S, Raphael Y. Outlook and future of inner ear therapy. Hear Res 2018;368:127-35. [PMID: 29804723 DOI: 10.1016/j.heares.2018.05.009] [Cited by in Crossref: 22] [Cited by in F6Publishing: 19] [Article Influence: 7.3] [Reference Citation Analysis]
32 Hastings ML, Brigande JV. Fetal gene therapy and pharmacotherapy to treat congenital hearing loss and vestibular dysfunction. Hear Res 2020;394:107931. [PMID: 32173115 DOI: 10.1016/j.heares.2020.107931] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
33 Gu X, Chai R, Guo L, Dong B, Li W, Shu Y, Huang X, Li H. Transduction of Adeno-Associated Virus Vectors Targeting Hair Cells and Supporting Cells in the Neonatal Mouse Cochlea. Front Cell Neurosci 2019;13:8. [PMID: 30733670 DOI: 10.3389/fncel.2019.00008] [Cited by in Crossref: 23] [Cited by in F6Publishing: 22] [Article Influence: 11.5] [Reference Citation Analysis]
34 Tan F, Chu C, Qi J, Li W, You D, Li K, Chen X, Zhao W, Cheng C, Liu X, Qiao Y, Su B, He S, Zhong C, Li H, Chai R, Zhong G. AAV-ie enables safe and efficient gene transfer to inner ear cells. Nat Commun 2019;10:3733. [PMID: 31427575 DOI: 10.1038/s41467-019-11687-8] [Cited by in Crossref: 57] [Cited by in F6Publishing: 62] [Article Influence: 28.5] [Reference Citation Analysis]
35 Lee MY, Kurioka T, Nelson MM, Prieskorn DM, Swiderski DL, Takada Y, Beyer LA, Raphael Y. Viral-mediated Ntf3 overexpression disrupts innervation and hearing in nondeafened guinea pig cochleae. Mol Ther Methods Clin Dev 2016;3:16052. [PMID: 27525291 DOI: 10.1038/mtm.2016.52] [Cited by in Crossref: 21] [Cited by in F6Publishing: 16] [Article Influence: 4.2] [Reference Citation Analysis]
36 Géléoc GS, Holt JR. Sound strategies for hearing restoration. Science 2014;344:1241062. [PMID: 24812404 DOI: 10.1126/science.1241062] [Cited by in Crossref: 125] [Cited by in F6Publishing: 119] [Article Influence: 17.9] [Reference Citation Analysis]
37 Atkinson PJ, Kim GS, Cheng AG. Direct cellular reprogramming and inner ear regeneration. Expert Opin Biol Ther 2019;19:129-39. [PMID: 30584811 DOI: 10.1080/14712598.2019.1564035] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
38 Ivanchenko MV, Hanlon KS, Hathaway DM, Klein AJ, Peters CW, Li Y, Tamvakologos PI, Nammour J, Maguire CA, Corey DP. AAV-S: A versatile capsid variant for transduction of mouse and primate inner ear. Mol Ther Methods Clin Dev 2021;21:382-98. [PMID: 33869656 DOI: 10.1016/j.omtm.2021.03.019] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
39 Crispino G, Galindo Ramirez F, Campioni M, Zorzi V, Praetorius M, Di Pasquale G, Chiorini JA, Mammano F. In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors. Sci Rep 2017;7:6567. [PMID: 28779115 DOI: 10.1038/s41598-017-06759-y] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 3.0] [Reference Citation Analysis]
40 Núñez-Batalla F, Jáudenes-Casaubón C, Sequí-Canet JM, Vivanco-Allende A, Zubicaray-Ugarteche J, Cabanillas-Farpón R. Aetiological diagnosis of child deafness: CODEPEH recommendations. Acta Otorrinolaringol Esp 2017;68:43-55. [PMID: 27644946 DOI: 10.1016/j.otorri.2016.05.002] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 1.6] [Reference Citation Analysis]
41 Chien WW, Isgrig K, Roy S, Belyantseva IA, Drummond MC, May LA, Fitzgerald TS, Friedman TB, Cunningham LL. Gene Therapy Restores Hair Cell Stereocilia Morphology in Inner Ears of Deaf Whirler Mice. Mol Ther 2016;24:17-25. [PMID: 26307667 DOI: 10.1038/mt.2015.150] [Cited by in Crossref: 55] [Cited by in F6Publishing: 47] [Article Influence: 9.2] [Reference Citation Analysis]
42 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: 3.0] [Reference Citation Analysis]
43 Kim MA, Ryu N, Kim HM, Kim YR, Lee B, Kwon TJ, Bok J, Kim UK. Targeted Gene Delivery into the Mammalian Inner Ear Using Synthetic Serotypes of Adeno-Associated Virus Vectors. Mol Ther Methods Clin Dev 2019;13:197-204. [PMID: 30805407 DOI: 10.1016/j.omtm.2019.01.002] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 7.5] [Reference Citation Analysis]
44 Minoda R, Miwa T, Ise M, Takeda H. Potential treatments for genetic hearing loss in humans: current conundrums. Gene Ther 2015;22:603-9. [PMID: 25781649 DOI: 10.1038/gt.2015.27] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 2.3] [Reference Citation Analysis]
45 Hosoya M, Fujioka M, Murayama AY, Ogawa K, Okano H, Ozawa H. Dynamic Spatiotemporal Expression Changes in Connexins of the Developing Primate's Cochlea. Genes (Basel) 2021;12:1082. [PMID: 34356098 DOI: 10.3390/genes12071082] [Reference Citation Analysis]
46 Hu X, Wang J, Yao X, Xiao Q, Xue Y, Wang S, Shi L, Shu Y, Li H, Yang H. Screened AAV variants permit efficient transduction access to supporting cells and hair cells. Cell Discov 2019;5:49. [PMID: 31636961 DOI: 10.1038/s41421-019-0115-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
47 Chang Q, Wang J, Li Q, Kim Y, Zhou B, Wang Y, Li H, Lin X. Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome. EMBO Mol Med 2015;7:1077-86. [PMID: 26084842 DOI: 10.15252/emmm.201404929] [Cited by in Crossref: 59] [Cited by in F6Publishing: 53] [Article Influence: 11.8] [Reference Citation Analysis]
48 Peters CW, Maguire CA, Hanlon KS. Delivering AAV to the Central Nervous and Sensory Systems. Trends Pharmacol Sci 2021;42:461-74. [PMID: 33863599 DOI: 10.1016/j.tips.2021.03.004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
49 Chang Q, Tang W, Kim Y, Lin X. Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing. Neurobiol Dis 2015;73:418-27. [PMID: 25251605 DOI: 10.1016/j.nbd.2014.09.005] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 2.7] [Reference Citation Analysis]
50 Lustig L, Akil O. Cochlear Gene Therapy. Cold Spring Harb Perspect Med 2019;9:a033191. [PMID: 30323014 DOI: 10.1101/cshperspect.a033191] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 2.5] [Reference Citation Analysis]
51 Shu Y, Tao Y, Wang Z, Tang Y, Li H, Dai P, Gao G, Chen ZY. Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes. Hum Gene Ther 2016;27:687-99. [PMID: 27342665 DOI: 10.1089/hum.2016.053] [Cited by in Crossref: 47] [Cited by in F6Publishing: 44] [Article Influence: 9.4] [Reference Citation Analysis]
52 Iizuka T, Kamiya K, Gotoh S, Sugitani Y, Suzuki M, Noda T, Minowa O, Ikeda K. Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness. Hum Mol Genet 2015;24:3651-61. [PMID: 25801282 DOI: 10.1093/hmg/ddv109] [Cited by in Crossref: 47] [Cited by in F6Publishing: 43] [Article Influence: 7.8] [Reference Citation Analysis]
53 Maguire CA, Corey DP. Viral vectors for gene delivery to the inner ear. Hear Res 2020;394:107927. [PMID: 32199720 DOI: 10.1016/j.heares.2020.107927] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
54 Guo J, Ma X, Skidmore JM, Cimerman J, Prieskorn DM, Beyer LA, Swiderski DL, Dolan DF, Martin DM, Raphael Y. GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function. Mol Ther Methods Clin Dev 2021;23:319-33. [PMID: 34729379 DOI: 10.1016/j.omtm.2021.09.009] [Reference Citation Analysis]
55 Kelly JJ, Simek J, Laird DW. Mechanisms linking connexin mutations to human diseases. Cell Tissue Res 2015;360:701-21. [DOI: 10.1007/s00441-014-2024-4] [Cited by in Crossref: 56] [Cited by in F6Publishing: 56] [Article Influence: 8.0] [Reference Citation Analysis]
56 Martin DM, Raphael Y. It's All in the Delivery: Improving AAV Transfection Efficiency with Exosomes. Mol Ther 2017;25:309-11. [PMID: 28126363 DOI: 10.1016/j.ymthe.2017.01.004] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
57 Szarka G, Balogh M, Tengölics ÁJ, Ganczer A, Völgyi B, Kovács-Öller T. The role of gap junctions in cell death and neuromodulation in the retina. Neural Regen Res 2021;16:1911-20. [PMID: 33642359 DOI: 10.4103/1673-5374.308069] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
58 Guo JY, Liu YY, Qu TF, Peng Z, Xie J, Wang GP, Gong SS. Cochleovestibular gene transfer in neonatal mice by canalostomy. Neuroreport 2017;28:682-8. [PMID: 28614181 DOI: 10.1097/WNR.0000000000000827] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
59 Yoshimura H, Shibata SB, Ranum PT, Moteki H, Smith RJH. Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness. Mol Ther 2019;27:681-90. [PMID: 30686588 DOI: 10.1016/j.ymthe.2018.12.014] [Cited by in Crossref: 32] [Cited by in F6Publishing: 26] [Article Influence: 16.0] [Reference Citation Analysis]
60 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]
61 Geng R, Omar A, Gopal SR, Chen DH, Stepanyan R, Basch ML, Dinculescu A, Furness DN, Saperstein D, Hauswirth W, Lustig LR, Alagramam KN. Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III. Sci Rep 2017;7:13480. [PMID: 29044151 DOI: 10.1038/s41598-017-13620-9] [Cited by in Crossref: 35] [Cited by in F6Publishing: 32] [Article Influence: 8.8] [Reference Citation Analysis]
62 Wang L, Kempton JB, Brigande JV. Gene Therapy in Mouse Models of Deafness and Balance Dysfunction. Front Mol Neurosci 2018;11:300. [PMID: 30210291 DOI: 10.3389/fnmol.2018.00300] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 5.0] [Reference Citation Analysis]
63 Huang S, Song J, He C, Cai X, Yuan K, Mei L, Feng Y. Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome. Gene Ther 2021. [PMID: 33633356 DOI: 10.1038/s41434-021-00240-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]