| scholarly article | Q13442814 |
| P50 | author | Shin-ichi Muramatsu | Q38359179 |
| P2093 | author name string | Takashi Okada | |
| Kianoush Sheykholeslami | |||
| Keiya Ozawa | |||
| Hiroaki Mizukami | |||
| Akihiro Kume | |||
| Yuhe Liu | |||
| Takeharu Kanazawa | |||
| Keiichi Ichimura | |||
| Koichi Takeuchi | |||
| Kuniko Shimazaki | |||
| Tatsuya Nomoto | |||
| Rahim Ajalli | |||
| P2860 | cites work | Transduction of the contralateral ear after adenovirus-mediated cochlear gene transfer | Q45865689 |
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| Distinct patterns of gene transfer to gerbil hippocampus with recombinant adeno-associated virus type 2 and 5. | Q44385521 | ||
| A modified adenovirus can transfect cochlear hair cells in vivo without compromising cochlear function | Q44441757 | ||
| Neurotrophin-3 transduction attenuates cisplatin spiral ganglion neuron ototoxicity in the cochlea | Q44697890 | ||
| Gene transfer into supporting cells of the organ of Corti | Q44835605 | ||
| Ultrastructure of human retroviruses | Q44966201 | ||
| The functional and structural outcome of inner ear gene transfer via the vestibular and cochlear fluids in mice | Q45071652 | ||
| Adeno-associated virus (AAV) vectors achieve prolonged transgene expression in mouse myocardium and arteries in vivo: a comparative study with adenovirus vectors | Q45721934 | ||
| Cochlear function and transgene expression in the guinea pig cochlea, using adenovirus- and adeno-associated virus-directed gene transfer. | Q45737477 | ||
| Adeno-associated virus (AAV)-3-based vectors transduce haematopoietic cells not susceptible to transduction with AAV-2-based vectors | Q45741486 | ||
| Gene transfer into the mammalian inner ear using HSV-1 and vaccinia virus vectors | Q45747744 | ||
| P433 | issue | 4 | |
| P921 | main subject | vector-borne disease | Q2083837 |
| P304 | page(s) | 725-733 | |
| P577 | publication date | 2005-10-01 | |
| P1433 | published in | Molecular Therapy | Q15762400 |
| P1476 | title | Specific and efficient transduction of Cochlear inner hair cells with recombinant adeno-associated virus type 3 vector | |
| P478 | volume | 12 |
| Q60238531 | A dual‐AAV approach restores fast exocytosis and partially rescues auditory function in deaf otoferlin knock‐out mice |
| Q34550656 | A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear |
| Q43427955 | Adeno-associated viral vector-mediated expression of NT4-ADNF-9 fusion gene protects against aminoglycoside-induced auditory hair cell loss in vitro |
| Q30885494 | Adeno-associated viral vectors and their redirection to cell-type specific receptors |
| Q40215583 | Adeno-associated virus transformation into the normal miniature pig and the normal guinea pigs cochlea via scala tympani |
| Q89475407 | Adeno-associated virus vector enables safe and efficient Cas9 activation in neonatal and adult Cas9 knockin murine cochleae |
| Q27026177 | Adeno-associated virus-mediated cancer gene therapy: current status |
| Q30472510 | Adeno-associated virus-mediated gene delivery into the scala media of the normal and deafened adult mouse ear. |
| Q39145475 | Adeno-associated virus-mediated gene transfer targeting normal and traumatized mouse utricle |
| Q37068636 | Advances in molecular and cellular therapies for hearing loss. |
| Q37149675 | Analysis of adeno-associated virus progenitor cell transduction in mouse lung. |
| Q38783334 | Challenges for the application of optical stimulation in the cochlea for the study and treatment of hearing loss |
| Q30359095 | Cochlear gene therapy with ancestral AAV in adult mice: complete transduction of inner hair cells without cochlear dysfunction. |
| Q41309731 | Cochlear gene transfer mediated by adeno-associated virus: Comparison of two surgical approaches |
| Q39062528 | Cochlear hair cell regeneration after noise-induced hearing loss: Does regeneration follow development? |
| Q45874366 | Delivery of Adeno-Associated Viral Vectors in Adult Mammalian Inner Ear Cell Subtypes without Auditory Dysfunction. |
| Q37299072 | Designing heart performance by gene transfer. |
| Q38069585 | Development of Novel Recombinant AAV Vectors and Strategies for the Potential Gene Therapy of Hemophilia |
| Q33386030 | Different tropism of adenoviruses and adeno-associated viruses to corneal cells: implications for corneal gene therapy |
| Q43751966 | Early postnatal virus inoculation into the scala media achieved extensive expression of exogenous green fluorescent protein in the inner ear and preserved auditory brainstem response thresholds |
| Q30454887 | Efficient cochlear gene transfection in guinea-pigs with adeno-associated viral vectors by partial digestion of round window membrane |
| Q98292024 | Efficient in Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65 |
| Q33537349 | Efficient transduction of spiral ganglion cells using adenovirus type 5 vector in the rat. |
| Q30367376 | Electroacoustic stimulation: now and into the future |
| Q40080564 | Emerging Gene Therapies for Genetic Hearing Loss |
| Q50042102 | Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation |
| Q26996322 | Gene therapy for human hearing loss: challenges and promises |
| Q38022141 | Gene transfer in inner ear cells: a challenging race |
| Q41372707 | Hyaluronic acid pretreatment for Sendai virus-mediated cochlear gene transfer |
| Q38848707 | Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes |
| Q34437737 | Improved biolistic transfection of hair cells |
| Q30443547 | Intra-tympanic delivery of short interfering RNA into the adult mouse cochlea |
| Q30498580 | Neurotrophic factors and neural prostheses: potential clinical applications based upon findings in the auditory system. |
| Q58767632 | Novel drug delivery systems for inner ear protection and regeneration after hearing loss |
| Q33863665 | Nuclear entry of hyperbranched polylysine nanoparticles into cochlear cells |
| Q30442172 | Optogenetic stimulation of the auditory pathway. |
| Q38381480 | Potential treatments for genetic hearing loss in humans: current conundrums. |
| Q36779416 | Production and characterization of adeno-associated viral vectors |
| Q40007967 | Protection Against Aminoglycoside-induced Ototoxicity by Regulated AAV Vector-mediated GDNF Gene Transfer Into the Cochlea |
| Q30467210 | Regeneration of Hair Cells: Making Sense of All the Noise |
| Q36545533 | Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice. |
| Q33526697 | Sites in the AAV5 capsid tolerant to deletions and tandem duplications |
| Q37271376 | State-of-the-art mechanisms of intracochlear drug delivery. |
| Q27661320 | The structure of adeno-associated virus serotype 3B (AAV-3B): Insights into receptor binding and immune evasion |
| Q34986477 | Therapeutic effect of adeno-associated virus (AAV)-mediated ADNF-9 expression on cochlea of kanamycin-deafened guinea pigs |
| Q36281581 | Therapeutics of hearing loss: expectations vs reality |
| Q61810234 | Transduction of Adeno-Associated Virus Vectors Targeting Hair Cells and Supporting Cells in the Neonatal Mouse Cochlea |
| Q59353271 | Virally Mediated Overexpression of Glial-Derived Neurotrophic Factor Elicits Age- and Dose-Dependent Neuronal Toxicity and Hearing Loss |
| Q89878841 | rAAV-Mediated Cochlear Gene Therapy: Prospects and Challenges for Clinical Application |
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