Advances in gene therapy hold promise for treating hereditary hearing loss
L Jiang, D Wang, Y He, Y Shu - Molecular Therapy, 2023 - cell.com
Gene therapy focuses on genetic modification to produce therapeutic effects or treat
diseases by repairing or reconstructing genetic material, thus being expected to be the most …
diseases by repairing or reconstructing genetic material, thus being expected to be the most …
Gene therapy for hearing loss
R Omichi, SB Shibata, CC Morton… - Human molecular …, 2019 - academic.oup.com
Sensorineural hearing loss (SNHL) is the most common sensory disorder. Its underlying
etiologies include a broad spectrum of genetic and environmental factors that can lead to …
etiologies include a broad spectrum of genetic and environmental factors that can lead to …
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 …
Gene therapy restores balance and auditory functions in a mouse model of Usher syndrome
K Isgrig, JW Shteamer, IA Belyantseva, MC Drummond… - Molecular therapy, 2017 - cell.com
Dizziness and hearing loss are among the most common disabilities. Many forms of
hereditary balance and hearing disorders are caused by abnormal development of …
hereditary balance and hearing disorders are caused by abnormal development of …
Emerging approaches for restoration of hearing and vision
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 …
and presenting a major socioeconomic burden. For a long time, retinal and cochlear …
Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation
Cochlear gene therapy holds promise for the treatment of genetic deafness. Assessing its
impact in adult murine models of hearing loss, however, has been hampered by technical …
impact in adult murine models of hearing loss, however, has been hampered by technical …
New molecular therapies for the treatment of hearing loss
An estimated 466 million people suffer from hearing loss worldwide. Sensorineural hearing
loss is characterized by degeneration of key structures of the sensory pathway in the …
loss is characterized by degeneration of key structures of the sensory pathway in the …
Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice
Q Yu, Y Wang, Q Chang, J Wang, S Gong, H Li, X Lin - Gene therapy, 2014 - nature.com
Mutations in GJB2, which codes for the gap junction (GJ) protein connexin26 (Cx26), are the
most common causes of human nonsyndromic hereditary deafness. We inoculated modified …
most common causes of human nonsyndromic hereditary deafness. We inoculated modified …
Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange‐Nielsen deafness …
Q Chang, J Wang, Q Li, Y Kim, B Zhou… - EMBO molecular …, 2015 - embopress.org
Mutations in the potassium channel subunit KCNQ 1 cause the human severe congenital
deafness Jervell and Lange‐Nielsen (JLN) syndrome. We applied a gene therapy approach …
deafness Jervell and Lange‐Nielsen (JLN) syndrome. We applied a gene therapy approach …
Delivery of adeno-associated virus vectors in adult mammalian inner-ear cell subtypes without auditory dysfunction
Y Tao, M Huang, Y Shu, A Ruprecht, H Wang… - Human gene …, 2018 - liebertpub.com
Hearing loss, including genetic hearing loss, is one of the most common forms of sensory
deficits in humans with limited options of treatment. Adeno-associated virus (AAV)-mediated …
deficits in humans with limited options of treatment. Adeno-associated virus (AAV)-mediated …