Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness. - Wikidata - wikimedia - TriplyDB

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

http://www.wikidata.org/entity/Q42153064

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Reduced Connexin26 in the Mature Cochlea Increases Susceptibility to Noise-Induced Hearing Lossin Mice ACEMg Diet Supplement Modifies Progression of Hereditary Deafness.Pilot study of large-scale production of mutant pigs by ENU mutagenesis Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea.Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea-a super-resolution structured illumination microscopy (SR-SIM) study.Cochlear hair cell regeneration after noise-induced hearing loss: Does regeneration follow development?Emerging Gene Therapies for Genetic Hearing Loss.In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors.Recent Advancements in the Regeneration of Auditory Hair Cells and Hearing Restoration Engraftment of Human Pluripotent Stem Cell-derived Progenitors in the Inner Ear of Prenatal Mice.Inner ear manifestations in CHARGE: Abnormalities, treatments, animal models, and progress toward treatments in auditory and vestibular structures.Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation.Cochlear Gene Therapy for Sensorineural Hearing Loss: Current Status and Major Remaining Hurdles for Translational Success.

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Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

http://www.wikidata.org/entity/Q42153064

description

2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

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2015年學術文章

@zh-hant

name

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

@en

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

@nl

type

label

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

@en

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

@nl

prefLabel

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

@en

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

@nl

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P1433

Human Molecular Genetics

P1476

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.

@en

P2093

Katsuhisa Ikeda

http://www.w3.org/2001/XMLSchema#string

Kazusaku Kamiya

http://www.w3.org/2001/XMLSchema#string

Masaaki Suzuki

http://www.w3.org/2001/XMLSchema#string

Osamu Minowa

http://www.w3.org/2001/XMLSchema#string

Satoru Gotoh

http://www.w3.org/2001/XMLSchema#string

Takashi Iizuka

http://www.w3.org/2001/XMLSchema#string

Tetsuo Noda

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Yoshinobu Sugitani

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P2860

Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice

The endocochlear potential depends on two K+ diffusion potentials and an electrical barrier in the stria vascularis of the inner ear

Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

K+ cycling and the endocochlear potential

Human connexin26 and connexin30 form functional heteromeric and heterotypic channels

Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea

Hearing is normal without connexin30

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

Assembly of the cochlear gap junction macromolecular complex requires connexin 26.

Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals

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3651-3661

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scholarly article

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10.1093/HMG/DDV109

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13

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24

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2015-03-23T00:00:00Z

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25801282

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