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Plos One
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March 2, 2022
Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells
Beatriz Lorente-Cánovas, Stephanie Eckrich, Morag A Lewis, et al.
The European Journal of Neuroscience
|
January 23, 2014
A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo
Jing Chen, Stuart L Johnson, Morag A Lewis, et al.
Hearing Research
|
July 27, 2024
A new mutation of Sgms1 causes gradual hearing loss associated with a reduced endocochlear potential
Jing Chen, Morag A Lewis, Alisa Wai, et al.
Plos One
|
October 1, 2021
Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss
Neil J Ingham, Navid Banafshe, Clarisse Panganiban, et al.
Communications Biology
|
November 1, 2025
Large-scale audiometric phenotyping identifies distinct genes and pathways involved in hearing loss subtypes
Samah Ahmed, Kenneth I Vaden, Morag A Lewis, et al.
Hearing Research
|
June 18, 2025
A machine-learning-based approach to predict early hallmarks of progressive hearing loss
Federico Ceriani, Joshua Giles, Neil J Ingham, et al.
Hearing Research
|
January 14, 2020
Functional analysis of candidate genes from genome-wide association studies of hearing
Neil J Ingham, Victoria Rook, Francesca Di Domenico, et al.
Hearing Research
|
September 6, 2024
Two new mouse alleles of Ocm and Slc26a5
Marìa Lachgar-Ruiz, Neil J Ingham, Elisa Martelletti, et al.
Genome Biology
|
September 23, 2011
Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice
Jennifer M Hilton, Morag A Lewis, M'hamed Grati, et al.
Cell Reports
|
April 28, 2016
Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia
Seham Ebrahim, Neil J Ingham, Morag A Lewis, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 40) with videos related to
Sort By:
Page
of 4
Plos One
|
March 2, 2022
Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells
Beatriz Lorente-Cánovas, Stephanie Eckrich, Morag A Lewis, et al.
The European Journal of Neuroscience
|
January 23, 2014
A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo
Jing Chen, Stuart L Johnson, Morag A Lewis, et al.
Hearing Research
|
July 27, 2024
A new mutation of Sgms1 causes gradual hearing loss associated with a reduced endocochlear potential
Jing Chen, Morag A Lewis, Alisa Wai, et al.
Plos One
|
October 1, 2021
Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss
Neil J Ingham, Navid Banafshe, Clarisse Panganiban, et al.
Communications Biology
|
November 1, 2025
Large-scale audiometric phenotyping identifies distinct genes and pathways involved in hearing loss subtypes
Samah Ahmed, Kenneth I Vaden, Morag A Lewis, et al.
Hearing Research
|
June 18, 2025
A machine-learning-based approach to predict early hallmarks of progressive hearing loss
Federico Ceriani, Joshua Giles, Neil J Ingham, et al.
Hearing Research
|
January 14, 2020
Functional analysis of candidate genes from genome-wide association studies of hearing
Neil J Ingham, Victoria Rook, Francesca Di Domenico, et al.
Hearing Research
|
September 6, 2024
Two new mouse alleles of Ocm and Slc26a5
Marìa Lachgar-Ruiz, Neil J Ingham, Elisa Martelletti, et al.
Genome Biology
|
September 23, 2011
Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice
Jennifer M Hilton, Morag A Lewis, M'hamed Grati, et al.
Cell Reports
|
April 28, 2016
Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia
Seham Ebrahim, Neil J Ingham, Morag A Lewis, et al.
Page
of 4