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Gene therapy in mouse models of deafness and balance dysfunction
Lingyan Wang
, J. Beth Kempton
,
John V. Brigande
Otolaryngology
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Contribution to journal
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Article
›
peer-review
27
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Keyphrases
Mouse Model
100%
Gene Therapy
100%
Balance Dysfunction
100%
Deafness
100%
Hearing Onset
75%
Inner Ear
50%
Knock
50%
Mediated Transfer
50%
Small Molecules
25%
Virus
25%
Small Interfering RNA (siRNA)
25%
Therapeutic Strategies
25%
Antisense Oligonucleotides
25%
Vestibular Disorders
25%
Therapeutic Response
25%
Therapeutic Effect
25%
Second Trimester of Pregnancy
25%
Ribonucleoprotein Complex
25%
Sensory Function
25%
Genetic mutation
25%
Human Fetus
25%
Effective Approach
25%
Gestational Week
25%
Therapeutic Efficacy
25%
Gene Replacement
25%
Neonatal Mice
25%
Drug Administration
25%
Higher Vertebrates
25%
Vertebrate Model
25%
Lipid-mediated
25%
Fetal Hearing
25%
Acoustic Sensitivity
25%
Inner Ear Disease
25%
Early Neonatal
25%
Acoustic Range
25%
Medicine and Dentistry
Hearing Impairment
100%
Gene Therapy
100%
Hearing
100%
Gene Mutation
25%
Small Interfering RNA
25%
Treatment Response
25%
Second Trimester Pregnancy
25%
Ribonucleoprotein
25%
Therapy Effect
25%
Knock Out
25%
Drug Administration
25%
Translating (Language)
25%
Antisense Oligonucleotide
25%
Vestibular Disorder
25%
Lipid
25%
Disease of Inner Ear
25%
Virus
25%