about
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesWbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing.ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells.S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.On the role of ephrinA2 in auditory function.Mouse screen reveals multiple new genes underlying mouse and human hearing loss
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-0916-7347
@en
name
Neil J Ingham
@ast
Neil J Ingham
@en
Neil J Ingham
@nl
type
label
Neil J Ingham
@ast
Neil J Ingham
@en
Neil J Ingham
@nl
prefLabel
Neil J Ingham
@ast
Neil J Ingham
@en
Neil J Ingham
@nl
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0000-0002-0916-7347