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Current Protocols in Mouse Biology|June 13, 2015
Using the Auditory Brainstem Response (ABR) to Determine Sensitivity of Hearing in Mutant MiceNeil J Ingham, Selina Pearson, Karen P SteelPlos One|February 21, 2012
Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis mediaStephanie Kuhn, Neil Ingham, Selina Pearson, et al.Plos One|December 11, 2012
Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defectsGeorg Steffes, Beatriz Lorente-Cánovas, Selina Pearson, et al.Genome Biology|September 23, 2011
Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch miceJennifer M Hilton, Morag A Lewis, M'hamed Grati, et al.Scientific Reports|July 8, 2016
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouseNeil J Ingham, Francesca Carlisle, Selina Pearson, 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.Plos One|March 20, 2014
Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring geneSimon Maguire, Jeanne Estabel, Neil Ingham, et al.Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.Pageof 1