Emerging approaches for restoration of hearing and vision

S Kleinlogel, C Vogl, M Jeschke, J Neef… - Physiological …, 2020 - journals.physiology.org
Impairments of vision and hearing are highly prevalent conditions limiting the quality of life
and presenting a major socioeconomic burden. For a long time, retinal and cochlear …

Towards the clinical application of gene therapy for genetic inner ear diseases

G Lahlou, C Calvet, M Giorgi, MJ Lecomte… - Journal of Clinical …, 2023 - mdpi.com
Hearing loss, the most common human sensory defect worldwide, is a major public health
problem. About 70% of congenital forms and 25% of adult-onset forms of deafness are of …

Robust generation of new hair cells in the mature mammalian inner ear by adenoviral expression of Hath1

J Shou, JL Zheng, WQ Gao - Molecular and Cellular Neuroscience, 2003 - Elsevier
Although hair cells regenerate spontaneously in birds and lower vertebrates following injury,
there is yet no effective way to stimulate hair cell regeneration in mature mammalian inner …

[HTML][HTML] Gene therapy restores hair cell stereocilia morphology in inner ears of deaf whirler mice

WW Chien, K Isgrig, S Roy, IA Belyantseva… - Molecular Therapy, 2016 - cell.com
Hereditary deafness is one of the most common disabilities affecting newborns. Many forms
of hereditary deafness are caused by morphological defects of the stereocilia bundles on the …

Effects of localized neurotrophin gene expression on spiral ganglion neuron resprouting in the deafened cochlea

AK Wise, CR Hume, BO Flynn, YS Jeelall, CL Suhr… - Molecular Therapy, 2010 - cell.com
A cochlear implant may be used to electrically stimulate spiral ganglion neurons (SGNs) in
people with severe sensorineural hearing loss (SNHL). However, these neurons …

The functional and structural outcome of inner ear gene transfer via the vestibular and cochlear fluids in mice

K Kawamoto, SH Oh, S Kanzaki, N Brown, Y Raphael - Molecular Therapy, 2001 - cell.com
Mice present an ideal model for inner ear gene therapy because their genome is being
rapidly sequenced, their generation time is relatively short, and they serve as a valuable …

Adeno-associated virus-mediated gene delivery into the scala media of the normal and deafened adult mouse ear

LA Kilpatrick, Q Li, J Yang, JC Goddard, DM Fekete… - Gene therapy, 2011 - nature.com
Murine models are ideal for studying cochlear gene transfer, as many hearing loss-related
mutations have been discovered and mapped within the mouse genome. However, because …

Gene transfer into supporting cells of the organ of Corti

S Ishimoto, K Kawamoto, S Kanzaki, Y Raphael - Hearing research, 2002 - Elsevier
To utilize the rapidly accumulating genetic information for developing new therapeutic
technologies for inner ear disease, it is necessary to design technologies for expressing …

Cochlear gene transfer mediated by adeno‐associated virus: Comparison of two surgical approaches

WW Chien, DS McDougald, S Roy… - The …, 2015 - Wiley Online Library
Objectives/Hypothesis Gene therapy offers the possibility of delivering corrective genetic
materials to the cochlea, potentially improving hearing. In animals, the most commonly used …

Specific and efficient transduction of Cochlear inner hair cells with recombinant adeno-associated virus type 3 vector

Y Liu, T Okada, K Sheykholeslami, K Shimazaki… - Molecular therapy, 2005 - cell.com
Recombinant adeno-associated virus (AAV) vectors are of interest for cochlear gene therapy
because of their ability to mediate the efficient transfer and long-term stable expression of …