Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Morag A Lewis

Showing results (31-40 of 40) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 40 results.
Science Translational Medicine|July 10, 2024
Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutationWenliang Zhu, Wan Du, Arun Prabhu Rameshbabu, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2011
miR-96 regulates the progression of differentiation in mammalian cochlear inner and outer hair cellsStephanie Kuhn, Stuart L Johnson, David N Furness, et al.
Orphanet Journal of Rare Diseases|March 12, 2015
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)Michaela Thoenes, Ulrike Zimmermann, Inga Ebermann, et al.
Nature Genetics|April 14, 2009
An ENU-induced mutation of miR-96 associated with progressive hearing loss in miceMorag A Lewis, Elizabeth Quint, Anne M Glazier, et al.
BMC Biology|March 17, 2022
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programmeMorag A Lewis, Neil J Ingham, Jing Chen, et al.
EMBO Molecular Medicine|February 17, 2016
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearingAnnalisa Buniello, Neil J Ingham, Morag A Lewis, et al.
Plos Biology|April 12, 2019
Mouse screen reveals multiple new genes underlying mouse and human hearing lossNeil J Ingham, Selina A Pearson, Valerie E Vancollie, et al.
Geroscience|June 28, 2025
International Consortium on Ageing-Related Pathologies (ICCARP) Audiovestibular Group: fostering international consensus to refine International Classification of Diseases (ICD-11) codes for hearing loss across the life courseDialechti Tsimpida, Michael A Akeroyd, Barry L Bentley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 23, 2025
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over timeKezang C Tshering, Marina T DiStefano, Andrea M Oza, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2025
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over timeKezang C Tshering, Marina T DiStefano, Andrea M Oza, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Science Translational Medicine|July 10, 2024
Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutationWenliang Zhu, Wan Du, Arun Prabhu Rameshbabu, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2011
miR-96 regulates the progression of differentiation in mammalian cochlear inner and outer hair cellsStephanie Kuhn, Stuart L Johnson, David N Furness, et al.
Orphanet Journal of Rare Diseases|March 12, 2015
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)Michaela Thoenes, Ulrike Zimmermann, Inga Ebermann, et al.
Nature Genetics|April 14, 2009
An ENU-induced mutation of miR-96 associated with progressive hearing loss in miceMorag A Lewis, Elizabeth Quint, Anne M Glazier, et al.
BMC Biology|March 17, 2022
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programmeMorag A Lewis, Neil J Ingham, Jing Chen, et al.
EMBO Molecular Medicine|February 17, 2016
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearingAnnalisa Buniello, Neil J Ingham, Morag A Lewis, et al.
Plos Biology|April 12, 2019
Mouse screen reveals multiple new genes underlying mouse and human hearing lossNeil J Ingham, Selina A Pearson, Valerie E Vancollie, et al.
Geroscience|June 28, 2025
International Consortium on Ageing-Related Pathologies (ICCARP) Audiovestibular Group: fostering international consensus to refine International Classification of Diseases (ICD-11) codes for hearing loss across the life courseDialechti Tsimpida, Michael A Akeroyd, Barry L Bentley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 23, 2025
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over timeKezang C Tshering, Marina T DiStefano, Andrea M Oza, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2025
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over timeKezang C Tshering, Marina T DiStefano, Andrea M Oza, et al.
Pageof 4