Development of gene therapy for inner ear disease: Using bilateral vestibular hypofunction as a vehicle for translational research

Hearing Research

Volumn 276, Issue 1-2, 2011, Pages 44-51

  Staecker, Hinrich ^a   Praetorius, Mark ^b   Brough, Douglas E ^c  

^a UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c GENVEC INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; PARVOVIRUS VECTOR; PROTEIN ATOH1; PROTEIN MATH1; UNCLASSIFIED DRUG;

CELL REGENERATION; DISEASE MODEL; GENE TARGETING; GENE THERAPY; GENE VECTOR; HAIR CELL; HUMAN; IMMUNE RESPONSE; INNER EAR DISEASE; MOLECULARLY TARGETED THERAPY; NONHUMAN; PRIORITY JOURNAL; REVIEW; VESTIBULAR DISORDER; VIRAL GENE DELIVERY SYSTEM; VIRAL GENE THERAPY;

ADENOVIRIDAE; ANIMALS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; EAR, INNER; GENE TARGETING; GENE THERAPY; GENE TRANSFER TECHNIQUES; GENETIC VECTORS; HAIR CELLS, AUDITORY; HUMANS; LABYRINTH DISEASES; MODELS, ANIMAL; REGENERATION; TRANSLATIONAL RESEARCH; VESTIBULAR DISEASES;

EID: 79957942610     PISSN: 03785955     EISSN: 18785891     Source Type: Journal    
DOI: 10.1016/j.heares.2011.01.006     Document Type: Review

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