Gene therapy development in hearing research in China (Q97587562)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

title

Gene therapy development in hearing research in China (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

Jiping Wang

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

Chunyan Li

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

Wenyue Xue

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

publication date

17 July 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

Sound strategies for hearing restoration.

22 July 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Sensorineural hearing loss in children.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Hearing ability with age in northern European women: a new web-based approach to genetic studies

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Genetic component of noise sensitivity

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Understanding speech in modulated interference: cochlear implant users and normal-hearing listeners

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Engineering adeno-associated virus vectors for gene therapy

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Long-term effect of gene therapy on Leber's congenital amaurosis

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Cochlear Gene Therapy for Sensorineural Hearing Loss: Current Status and Major Remaining Hurdles for Translational Success.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Let There Be Light: Gene and Cell Therapy for Blindness

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Immunobiology of the inner ear.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Pharmacodynamics of adenovector distribution within the inner ear tissues of the mouse.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

1 reference

7 January 2021

From placode to polarization: new tunes in inner ear development

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Cell cycle regulation in hair cell development and regeneration in the mouse cochlea

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

The Atoh1-lineage gives rise to hair cells and supporting cells within the mammalian cochlea.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

The chicken RaxL gene plays a role in the initiation of photoreceptor differentiation

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Absence of Atoh1 induced partially different cell fates of cochlear and vestibular sensory epithelial cells in mice

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

In vivo generation of immature inner hair cells in neonatal mouse cochleae by ectopic Atoh1 expression

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Atoh1 gene therapy in the cochlea for hair cell regeneration

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Atoh1 and other related key regulators in the development of auditory sensory epithelium in the mammalian inner ear: function and interplay

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

In Vivo Interplay between p27Kip1, GATA3, ATOH1, and POU4F3 Converts Non-sensory Cells to Hair Cells in Adult Mice.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Selection of cell fate in the organ of Corti involves the integration of Hes/Hey signaling at the Atoh1 promoter

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Generation of sensory hair cells by genetic programming with a combination of transcription factors.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Wnt signaling activates TIGAR and protects against cisplatin-induced spiral ganglion neuron damage in the mouse cochlea.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Loss of ARHGEF6 Causes Hair Cell Stereocilia Deficits and Hearing Loss in Mice

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Autophagy protects auditory hair cells against neomycin-induced damage.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Knockdown of Foxg1 in supporting cells increases the trans-differentiation of supporting cells into hair cells in the neonatal mouse cochlea

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Bmi1 Regulates the Proliferation of Cochlear Supporting Cells Via the Canonical Wnt Signaling Pathway

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Spontaneous hair cell regeneration in the neonatal mouse cochlea in vivo

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Loss of CIB2 Causes Profound Hearing Loss and Abolishes Mechanoelectrical Transduction in Mice

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Adeno-associated virus at 50: a golden anniversary of discovery, research, and gene therapy success--a personal perspective

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Adeno-associated virus serotypes: vector toolkit for human gene therapy

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Transduction of Adeno-Associated Virus Vectors Targeting Hair Cells and Supporting Cells in the Neonatal Mouse Cochlea

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

In vitro and in vivo gene therapy vector evolution via multispecies interbreeding and retargeting of adeno-associated viruses

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

AAV2.7m8 is a powerful viral vector for inner ear gene therapy

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Dual and triple AAV delivery of large therapeutic gene sequences into the inner ear

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Cochlear gene transfer mediated by adeno-associated virus: Comparison of two surgical approaches

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Restoration of hearing in the VGLUT3 knockout mouse using virally mediated gene therapy.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Hyaluronic acid pretreatment for Sendai virus-mediated cochlear gene transfer

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Efficient cochlear gene transfection in guinea-pigs with adeno-associated viral vectors by partial digestion of round window membrane

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Inner ear gene transfection in neonatal mice using adeno-associated viral vector: a comparison of two approaches

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Canalostomy is an ideal surgery route for inner ear gene delivery in big animal model

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

The winged helix transcription factor Fkh10 is required for normal development of the inner ear.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutations of MYO6 are associated with recessive deafness, DFNB37

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Reduced Connexin26 in the Mature Cochlea Increases Susceptibility to Noise-Induced Hearing Lossin Mice

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Toll-like receptor 4 modulates the cochlear immune response to acoustic injury.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Increased Sensitivity to Noise-Induced Hearing Loss by Blockade of Endogenous PI3K/Akt Signaling.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

ERK2 mediates inner hair cell survival and decreases susceptibility to noise-induced hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Noise induced changes in the expression of p38/MAPK signaling proteins in the sensory epithelium of the inner ear.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Activation of JNK in the inner ear following impulse noise exposure

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

JAK2/STAT3 inhibition attenuates noise-induced hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Functional significance of channels and transporters expressed in the inner ear and kidney

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Targeted connexin26 ablation arrests postnatal development of the organ of Corti

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

RNA Interference Prevents Autosomal-Dominant Hearing Loss.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Tmc gene therapy restores auditory function in deaf mice

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Allele-specific gene editing prevents deafness in a model of dominant progressive hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Genetic Variation in POU4F3 and GRHL2 Associated with Noise-Induced Hearing Loss in Chinese Population: A Case-Control Study

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Cochlear protection against cisplatin by viral transfection of X-linked inhibitor of apoptosis protein across round window membrane.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Protection Against Aminoglycoside-induced Ototoxicity by Regulated AAV Vector-mediated GDNF Gene Transfer Into the Cochlea

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Noise-induced Cochlear Synaptopathy and Signal Processing Disorders

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Noise-induced and age-related hearing loss: new perspectives and potential therapies.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Auditory neuropathy--neural and synaptic mechanisms

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

AAV-mediated NT-3 overexpression protects cochleae against noise-induced synaptopathy.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Functional Mutation of SMAC/DIABLO, Encoding a Mitochondrial Proapoptotic Protein, Causes Human Progressive Hearing Loss DFNA64

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

A dominant mutation in the stereocilia-expressing gene TBC1D24 is a probable cause for nonsyndromic hearing impairment

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

A dominant variant in DMXL2 is linked to nonsyndromic hearing loss.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Whole exome sequencing identifies SCD5 as a novel causative gene for autosomal dominant nonsyndromic deafness

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder

1 reference

https://api.crossref.org/works/10.1038%2FS41434-020-0177-1

7 January 2021

10.1038/S41434-020-0177-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json

22 July 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32681137%20AND%20SRC:MED&resulttype=core&format=json