Mammalian inner ear harbors diverse cell types that are essential for hearing and balance. Adenovirus is one of the major vectors to deliver genes into the inner ear for functional studies and hair cell regeneration. To identify adenovirus vectors that target specific cell subtypes in the inner ear, we studied three adenovirus vectors, carrying a reporter gene encoding green fluorescent protein (GFP) from two vendors or with a genome editing gene Cre recombinase (Cre), by injection into postnatal days 0 (P0) and 4 (P4) mouse cochlea through scala media by cochleostomy in vivo. We found three adenovirus vectors transduced mouse inner ear cells with different specificities and expression levels, depending on the type of adenoviral vectors and...
Adeno-associated virus (AAV) is the preferred vector for gene therapy of hereditary deafness, and di...
Adeno-associated virus (AAV) is the preferred vector for gene therapy of hereditary deafness, and di...
Gene transfer is an exciting new tool in medical therapy and scientific investigation, but only very...
Mammalian inner ear harbors diverse cell types that are essential for hearing and balance. Adenoviru...
Targeting specific cell types in the mammalian inner ear is important for treating genetic hearing l...
Efforts to develop gene therapies for hearing loss have been hampered by the lack of safe, efficient...
Viral delivery of exogenous coding sequences into the inner ear has the potential for therapeutic be...
Gene therapy strategies using adeno-associated virus (AAV) vectors to treat hereditary deafnesses ha...
Adeno-associated virus (AAV) is a safe and effective vector for gene therapy for retinal disorders. ...
<div><p>Local gene transfection is a promising technique for the prevention and/or correction of inn...
The use of viral vectors for inner ear gene therapy is receiving increased attention for treatment o...
Numerous studies have shown the recovery of auditory function in mouse models of genetic hearing los...
Sensorineural hearing loss is one of the most common disabilities worldwide. Such prevalence necessi...
Rova, Cherokee R. L., M.S., Autumn 2006 Pharmaceutical Sciences Adeno-associated virus mediated tran...
Efforts to develop gene therapies for hearing loss have been hampered by the lack of safe, efficient...
Adeno-associated virus (AAV) is the preferred vector for gene therapy of hereditary deafness, and di...
Adeno-associated virus (AAV) is the preferred vector for gene therapy of hereditary deafness, and di...
Gene transfer is an exciting new tool in medical therapy and scientific investigation, but only very...
Mammalian inner ear harbors diverse cell types that are essential for hearing and balance. Adenoviru...
Targeting specific cell types in the mammalian inner ear is important for treating genetic hearing l...
Efforts to develop gene therapies for hearing loss have been hampered by the lack of safe, efficient...
Viral delivery of exogenous coding sequences into the inner ear has the potential for therapeutic be...
Gene therapy strategies using adeno-associated virus (AAV) vectors to treat hereditary deafnesses ha...
Adeno-associated virus (AAV) is a safe and effective vector for gene therapy for retinal disorders. ...
<div><p>Local gene transfection is a promising technique for the prevention and/or correction of inn...
The use of viral vectors for inner ear gene therapy is receiving increased attention for treatment o...
Numerous studies have shown the recovery of auditory function in mouse models of genetic hearing los...
Sensorineural hearing loss is one of the most common disabilities worldwide. Such prevalence necessi...
Rova, Cherokee R. L., M.S., Autumn 2006 Pharmaceutical Sciences Adeno-associated virus mediated tran...
Efforts to develop gene therapies for hearing loss have been hampered by the lack of safe, efficient...
Adeno-associated virus (AAV) is the preferred vector for gene therapy of hereditary deafness, and di...
Adeno-associated virus (AAV) is the preferred vector for gene therapy of hereditary deafness, and di...
Gene transfer is an exciting new tool in medical therapy and scientific investigation, but only very...