Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV. - Wikidata - wikimedia - TriplyDB

Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV.

Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV.

http://www.wikidata.org/entity/Q40383155

about

Emerging Gene Therapies for Genetic Hearing Loss.Extracellular vesicles: nature's nanoparticles for improving gene transfer with adeno-associated virus vectors.Recent Advancements in the Regeneration of Auditory Hair Cells and Hearing Restoration An Essential Role for the Tetraspanin LHFPL4 in the Cell-Type-Specific Targeting and Clustering of Synaptic GABAA Receptors.Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III.Exosomes: Outlook for Future Cell-Free Cardiovascular Disease Therapy.New Technologies for Analysis of Extracellular Vesicles.It's All in the Delivery: Improving AAV Transfection Efficiency with Exosomes.Enhanced Production of Exosome-Associated AAV by Overexpression of the Tetraspanin CD9.CRISPR/Cas9 Mediated Disruption of the Swedish APP Allele as a Therapeutic Approach for Early-Onset Alzheimer's Disease.Cochlear Gene Therapy for Sensorineural Hearing Loss: Current Status and Major Remaining Hurdles for Translational Success.Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

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Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV.

http://www.wikidata.org/entity/Q40383155

description

2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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name

Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV.

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Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV.

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Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV.

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J.YMTHE.2016.12.010

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Molecular Therapy

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Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV.

@en

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Adrienn Volak

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Alain R Brisson

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Bence György

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Casey A Maguire

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Cyrille Sage

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Dakai Mu

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David P Corey

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Deborah I Scheffer

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Maria Ericsson

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Panos I Tamvakologos

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P2860

Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

Exosome-associated AAV vector as a robust and convenient neuroscience tool

Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis

Notch inhibition induces mitotically generated hair cells in mammalian cochleae via activating the Wnt pathway

A type VII myosin encoded by the mouse deafness gene shaker-1

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells

Tmc gene therapy restores auditory function in deaf mice.

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scholarly article

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10.1016/J.YMTHE.2016.12.010

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2

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25

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Artur A Indzhykulian

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2017-01-09T00:00:00Z

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28082074

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