Items where authors include "Steel, K.P."

Article

Short, E. orcid.org/0000-0001-5050-589X, Adcock, I.M., Al-Sarireh, B. et al. (224 more authors) (2024) Defining an ageing-related pathology, disease or syndrome: international consensus statement. GeroScience. ISSN 2509-2715

Lorente-Cánovas, B., Eckrich, S., Lewis, M.A. et al. (3 more authors) (2022) Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells. PLoS ONE, 17 (3). e0261530. ISSN 1932-6203

Martelletti, E., Ingham, N.J., Houston, O. et al. (4 more authors) (2020) Synaptojanin2 mutation causes progressive high-frequency hearing loss in mice. Frontiers in Cellular Neuroscience, 14. 561857. ISSN 1662-5102

Corns, L.F., Johnson, S.L., Roberts, T. et al. (10 more authors) (2018) Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation. Nature Communications, 9 (1). 4015.

Marcotti, W. orcid.org/0000-0002-8770-7628, Corns, L.F. orcid.org/0000-0003-1139-3527, Goodyear, R.J. et al. (5 more authors) (2016) The acquisition of mechano-electrical transducer current adaptation in auditory hair cells requires myosin VI. Journal of Physiology, 594 (13). pp. 3667-3681. ISSN 0022-3751

Buniello, A., Ingham, N.J., Lewis, M.A. et al. (12 more authors) (2016) Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing. EMBO Molecular Medicine, 8 (3). pp. 191-207. ISSN 1757-4676

Kuhn, S., Ingham, N., Pearson, S. et al. (4 more authors) (2012) Auditory Function in the Tc1 Mouse Model of Down Syndrome Suggests a Limited Region of Human Chromosome 21 Involved in Otitis Media. PLoS One, 7 (2). e31433.

Marcotti, W., Erven, A., Johnson, S.L. et al. (2 more authors) (2006) Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea. The Journal of Physiology, 574 (3). pp. 677-698. ISSN 0022-3751