Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c

Defective myosin VIIA gene responsible for Usher syndrome type IB

Dominique Well, Stéphane Blanchard, Josseline Kaplan et al. · Nature · 1995 · 1.1K citations

Life Sciences, Genetics, Molecular Genetics +7

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda Peters, Saima Riazuddin et al. · The American Journal of Human Genetics · 2001 · 557 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Lighting up the Senses: FM1-43 Loading of Sensory Cells through Nonselective Ion Channels

Jason R. Meyers, Richard B. MacDonald, Anne Duggan et al. · Journal of Neuroscience · 2003 · 533 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

Circular Intermediates of Recombinant Adeno-Associated Virus Have Defined Structural Characteristics Responsible for Long-Term Episomal Persistence in Muscle Tissue

Dongsheng Duan, Prerna Sharma, Jusan Yang et al. · Journal of Virology · 1998 · 518 citations · Full text

Life Sciences, Biology, Molecular Biology +17

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

Hanno J. Bolz, Benigna von Brederlow, Alfredo Ramı́rez et al. · Nature Genetics · 2001 · 497 citations

Life Sciences, Genetics, Molecular Genetics +6