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Proceedings of the National Academy of Sciences of the United States of America|August 8, 2023
Reversal of an existing hearing loss by gene activation in <i>Spns2</i> mutant miceElisa Martelletti, Neil J Ingham, Karen P Steel
Frontiers in Cellular Neuroscience|October 26, 2020
Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in MiceElisa Martelletti, Neil J Ingham, Oliver Houston, et al.
Hearing Research|July 11, 2025
Low level of expression of known deafness genes Kcne1, Kcnj10 or Col4a3 is sufficient to maintain hearing in miceDarcey A Kirwin, Nina Treder, Elisa Martelletti, et al.
Hearing Research|September 6, 2024
Two new mouse alleles of Ocm and Slc26a5Marìa Lachgar-Ruiz, Neil J Ingham, Elisa Martelletti, et al.
Cardiovascular Research|November 30, 2017
Reversible Notch1 acetylation tunes proliferative signalling in cardiomyocytesChiara Collesi, Giulia Felician, Ilaria Secco, et al.
Cells|October 27, 2022
The Effect of a <i>Pex3</i> Mutation on Hearing and Lipid Content of the Inner EarRafael M Kochaj, Elisa Martelletti, Neil J Ingham, et al.
Disease Models & Mechanisms|May 11, 2023
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variantsMaría Lachgar-Ruiz, Matías Morín, Elisa Martelletti, et al.
Human Molecular Genetics|September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cellsEva L Morozko, Ayako Nishio, Neil J Ingham, 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.
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