scholarly article | Q13442814 |
P50 | author | Bradley W Kesser | Q70426433 |
P2093 | author name string | Jeffrey R Holt | |
George T Hashisaki | |||
P2860 | cites work | KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness | Q22008780 |
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C | Q24290185 | ||
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin | Q24294773 | ||
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23 | Q24298183 | ||
Defective myosin VIIA gene responsible for Usher syndrome type 1B | Q24314638 | ||
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome | Q24318498 | ||
Mutations of MYO6 are associated with recessive deafness, DFNB37 | Q24532041 | ||
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 | Q24535604 | ||
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss | Q24535864 | ||
A simplified system for generating recombinant adenoviruses | Q24682328 | ||
Math1 gene transfer generates new cochlear hair cells in mature guinea pigs in vivo | Q28178896 | ||
KCNE1 mutations cause jervell and Lange-Nielsen syndrome | Q28253362 | ||
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells | Q28509764 | ||
Math1: an essential gene for the generation of inner ear hair cells | Q28513764 | ||
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D | Q28589238 | ||
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene | Q28589565 | ||
TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells | Q28591781 | ||
Complementary roles of BDNF and NT-3 in vestibular and auditory development | Q28594015 | ||
Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness | Q28594332 | ||
Viral-mediated gene transfer to study the molecular physiology of the Mammalian inner ear. | Q30309437 | ||
An in vitro model system to study gene therapy in the human inner ear. | Q30438620 | ||
Dominant-negative inhibition of M-like potassium conductances in hair cells of the mouse inner ear | Q30440196 | ||
Spiral ganglion neurons are protected from degeneration by GDNF gene therapy. | Q30473538 | ||
Morphology of auditory hair cells in guinea pig cochlea after transgene expression | Q33200503 | ||
Structural recovery from sound and aminoglycoside damage in the avian cochlea. | Q33749308 | ||
Vestibular hair cell regeneration and restoration of balance function induced by math1 gene transfer | Q46713382 | ||
Cochlear gene transfer: round window versus cochleostomy inoculation | Q48097614 | ||
NT-3 and/or BDNF therapy prevents loss of auditory neurons following loss of hair cells | Q49052948 | ||
Glutathione limits noise-induced hearing loss. | Q50495238 | ||
Cracking the auditory genetic code: nonsyndromic hereditary hearing impairment. | Q50502591 | ||
Hair cells and supporting cells share a common progenitor in the avian inner ear. | Q50504230 | ||
Adenoviral-mediated gene transfer into guinea pig cochlear cells in vivo. | Q50515400 | ||
New hair cells arise from supporting cell conversion in the acoustically damaged chick inner ear. | Q50515888 | ||
Transgene expression in mature guinea pig cochlear cells in vitro | Q64378275 | ||
Functional expression of exogenous proteins in mammalian sensory hair cells infected with adenoviral vectors | Q64381584 | ||
Transfection of neonatal rat cochlear cells in vitro with an adenovirus vector | Q64382380 | ||
Cochlear gene therapy | Q73818064 | ||
A novel vestibular approach for gene transfer into the inner ear | Q78604396 | ||
Progress with retroviral gene vectors | Q33920752 | ||
Auditory hair cell replacement and hearing improvement by Atoh1 gene therapy in deaf mammals | Q34394494 | ||
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. | Q34469642 | ||
HIV-1-derived lentiviral vectors | Q34561994 | ||
Neuronal survival and cell death signaling pathways. | Q35063052 | ||
KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway. | Q35682356 | ||
Utilization of adenovirus vectors for multiple gene transfer applications | Q35762017 | ||
Drug delivery to the inner ear using gene therapy. | Q35912971 | ||
Hearing and hair cells are protected by adenoviral gene therapy with TGF-β1 and GDNF | Q40650824 | ||
Glial cell line-derived neurotrophic factor and chronic electrical stimulation prevent VIII cranial nerve degeneration following denervation | Q40688618 | ||
Gene expression in the mammalian cochlea: a study of multiple vector systems. | Q40708362 | ||
A surgical approach appropriate for targeted cochlear gene therapy in the mouse | Q40734130 | ||
Differential protective effects of neurotrophins in the attenuation of noise-induced hair cell loss | Q40865835 | ||
Effect of transgenic GDNF expression on gentamicin-induced cochlear and vestibular toxicity | Q40871245 | ||
Green fluorescent protein as a reporter for gene transfer studies in the cochlea | Q40871576 | ||
Glial cell line-derived neurotrophic factor. Potential for otoprotection | Q40875441 | ||
Glial cell line-derived neurotrophic factor has a dose dependent influence on noise-induced hearing loss in the guinea pig cochlea | Q40889342 | ||
Development of in vivo gene therapy for hearing disorders: introduction of adeno-associated virus into the cochlea of the guinea pig. | Q40934948 | ||
Development of retroviral vectors as safe, targeted gene delivery systems | Q40944251 | ||
Viral vectors in gene therapy | Q40945246 | ||
Attenuation of cochlear damage from noise trauma by an iron chelator, a free radical scavenger and glial cell line-derived neurotrophic factor in vivo | Q40983153 | ||
Guinea pig auditory neurons are protected by glial cell line-derived growth factor from degeneration after noise trauma | Q40993628 | ||
GDNF protects the cochlea against noise damage | Q41019032 | ||
Defective HSV-1 vector expressing BDNF in auditory ganglia elicits neurite outgrowth: model for treatment of neuron loss following cochlear degeneration | Q41237702 | ||
Cationic liposome mediated transgene expression in the guinea pig cochlea | Q41614363 | ||
The protective effect of brain-derived neurotrophic factor after gentamicin ototoxicity. | Q41666663 | ||
Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector | Q41685193 | ||
Overexpression of Math1 induces robust production of extra hair cells in postnatal rat inner ears | Q41736617 | ||
Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain | Q42280576 | ||
Hearing preservation after inner ear gene therapy: the effect of vector and surgical approach. | Q42451504 | ||
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. | Q42455765 | ||
Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice | Q42492876 | ||
In vivo adenoviral transduction of the neonatal rat cochlea and middle ear. | Q42497484 | ||
In vitro and in vivo assessment of the ability of adeno-associated virus-brain-derived neurotrophic factor to enhance spiral ganglion cell survival following ototoxic insult | Q42524699 | ||
Interactions of mammalian cells with lipid dispersions containing novel metabolizable cationic amphiphiles | Q42832960 | ||
Antioxidant gene therapy can protect hearing and hair cells from ototoxicity | Q43169212 | ||
Robust generation of new hair cells in the mature mammalian inner ear by adenoviral expression of Hath1. | Q44042846 | ||
Long-term in vivo cochlear transgene expression mediated by recombinant adeno-associated virus | Q44136141 | ||
A modified adenovirus can transfect cochlear hair cells in vivo without compromising cochlear function | Q44441757 | ||
Ebselen attenuates cochlear damage caused by acoustic trauma | Q44509557 | ||
Gene transfer into supporting cells of the organ of Corti | Q44835605 | ||
The functional and structural outcome of inner ear gene transfer via the vestibular and cochlear fluids in mice | Q45071652 | ||
A novel bovine virus efficiently transduces inner ear neuroepithelial cells | Q45457216 | ||
Adeno-associated virus-mediated gene transfer to hair cells and support cells of the murine cochlea | Q45457280 | ||
Cochlear function and transgene expression in the guinea pig cochlea, using adenovirus- and adeno-associated virus-directed gene transfer. | Q45737477 | ||
Gene transfer into the mammalian inner ear using HSV-1 and vaccinia virus vectors | Q45747744 | ||
Expression of adeno-associated virus integrated transgene within the mammalian vestibular organs. | Q45756022 | ||
The effect of cochleostomy and intracochlear infusion on auditory brain stem response threshold in the guinea pig. | Q45855751 | ||
Inner ear transgene expression after adenoviral vector inoculation in the endolymphatic sac. | Q45857676 | ||
Transduction of the contralateral ear after adenovirus-mediated cochlear gene transfer | Q45865689 | ||
Adenovirus-mediated expression of brain-derived neurotrophic factor protects spiral ganglion neurons from ototoxic damage | Q45874526 | ||
Novel method for homogeneous gene transfer to the inner ear. | Q45876825 | ||
Viral-mediated gene transfer in the cochlea | Q45883103 | ||
Brain-derived neurotrophic factor gene therapy prevents spiral ganglion degeneration after hair cell loss | Q45888449 | ||
Cochlear microinjection and its effects upon auditory function in the guinea pig. | Q46100531 | ||
Ebselen prevents noise-induced excitotoxicity and temporary threshold shift | Q46464961 | ||
Cochlear gene delivery through an intact round window membrane in mouse | Q46630707 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | gene therapy | Q213901 |
P304 | page(s) | 821-831 | |
P577 | publication date | 2008-05-01 | |
P1433 | published in | The Laryngoscope | Q15755068 |
P1476 | title | Gene transfer in human vestibular epithelia and the prospects for inner ear gene therapy | |
P478 | volume | 118 |