Adeno-associated virus-mediated gene transfer targeting normal and traumatized mouse utricle
Balance dysfunction is closely associated with loss of vestibular hair cells (HCs). Gene
therapy shows promise when used to protect or regenerate vestibular HCs to preserve or …
therapy shows promise when used to protect or regenerate vestibular HCs to preserve or …
Gene transfer targeting mouse vestibule using adenovirus and adeno-associated virus vectors
H Okada, T Iizuka, H Mochizuki, T Nihira… - Otology & …, 2012 - journals.lww.com
Background Loss of vestibular hair cell is seen in various balance disorder diseases. There
have been some reports concerning gene delivery to the mouse vestibule in recent years …
have been some reports concerning gene delivery to the mouse vestibule in recent years …
[HTML][HTML] Cochlear gene therapy with ancestral AAV in adult mice: complete transduction of inner hair cells without cochlear dysfunction
J Suzuki, K Hashimoto, R Xiao, LH Vandenberghe… - Scientific reports, 2017 - nature.com
The use of viral vectors for inner ear gene therapy is receiving increased attention for
treatment of genetic hearing disorders. Most animal studies to date have injected viral …
treatment of genetic hearing disorders. Most animal studies to date have injected viral …
Optimizing atoh1‐induced vestibular hair cell regeneration
H Staecker, C Schlecker, S Kraft… - The …, 2014 - Wiley Online Library
Objectives/Hypothesis Determine the optimal design characteristics of an adenoviral (Ad)
vector to deliver atoh1 and induce regeneration of vestibular hair cells. Study Design …
vector to deliver atoh1 and induce regeneration of vestibular hair cells. Study Design …
[HTML][HTML] Co-transduction of dual-adeno-associated virus vectors in the neonatal and adult mouse utricles
ZR Chen, JY Guo, L He, S Liu, JY Xu… - Frontiers in Molecular …, 2022 - frontiersin.org
Adeno-associated virus (AAV)-mediated gene transfer is an efficient method of gene over-
expression in the vestibular end organs. However, AAV has limited usefulness for delivering …
expression in the vestibular end organs. However, AAV has limited usefulness for delivering …
Selective atonal gene delivery improves balance function in a mouse model of vestibular disease
C Schlecker, M Praetorius, DE Brough, RG Presler… - Gene therapy, 2011 - nature.com
Loss of balance is often due to loss of vestibular hair cells. In mammals, regeneration of
functional hair cells in the mature sensory epithelium is limited; therefore, loss of sensory …
functional hair cells in the mature sensory epithelium is limited; therefore, loss of sensory …
Vestibular regeneration–experimental models and clinical implications
S Albu, DF Muresanu - Journal of Cellular and Molecular …, 2012 - Wiley Online Library
Therapies aimed at the protection and/or regeneration of inner ear hair cells are of great
interest, given the significant monetary and quality of life impact of balance disorders …
interest, given the significant monetary and quality of life impact of balance disorders …
[HTML][HTML] Rescue of hearing by gene delivery to inner-ear hair cells using exosome-associated AAV
B György, C Sage, AA Indzhykulian, DI Scheffer… - Molecular Therapy, 2017 - cell.com
Adeno-associated virus (AAV) is a safe and effective vector for gene therapy for retinal
disorders. Gene therapy for hearing disorders is not as advanced, in part because gene …
disorders. Gene therapy for hearing disorders is not as advanced, in part because gene …
[HTML][HTML] A single cisterna magna injection of AAV leads to binaural transduction in mice
Viral-mediated gene augmentation, silencing, or editing offers tremendous promise for the
treatment of inherited and acquired deafness. Inner-ear gene therapies often require a safe …
treatment of inherited and acquired deafness. Inner-ear gene therapies often require a safe …
[HTML][HTML] Efficient viral transduction in mouse inner ear hair cells with utricle injection and AAV9-PHP. B
J Lee, C Nist-Lund, P Solanes, H Goldberg, J Wu… - Hearing research, 2020 - Elsevier
Viral delivery of exogenous coding sequences into the inner ear has the potential for
therapeutic benefit for patients suffering genetic or acquired hearing loss. To devise …
therapeutic benefit for patients suffering genetic or acquired hearing loss. To devise …