Items where authors include "Brown, S.D.M."
Article
Jeng, J-Y., Carlton, A.J. orcid.org/0000-0002-1054-3901, Goodyear, R.J. et al. (10 more authors) (2022) AAV-mediated rescue of Eps8 expression in vivo restores hair-cell function in a mouse model of recessive deafness. Molecular Therapy - Methods & Clinical Development, 26. pp. 355-370. ISSN 2329-0501
Newton, S., Kong, F., Carlton, A.J. et al. (8 more authors) (2022) Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing. PLoS Genetics, 18 (1). e1009937. ISSN 1553-7390
Carlton, A.J. orcid.org/0000-0002-1054-3901, Halford, J., Underhill, A. et al. (9 more authors) (2021) Loss of Baiap2l2 destabilizes the transducing stereocilia of cochlear hair cells and leads to deafness. The Journal of Physiology, 599 (4). pp. 1173-1198. ISSN 0022-3751
Jeng, J., Carlton, A.J. orcid.org/0000-0002-1054-3901, Johnson, S.L. et al. (4 more authors) (2021) Biophysical and morphological changes in inner hair cells and their efferent innervation in the ageing mouse cochlea. The Journal of Physiology, 599 (1). pp. 269-287. ISSN 0022-3751
Jeng, J., Ceriani, F. orcid.org/0000-0002-5366-341X, Olt, J. et al. (5 more authors) (2020) Pathophysiological changes in inner hair cell ribbon synapses in the ageing mammalian cochlea. The Journal of Physiology, 598 (19). pp. 4339-4355. ISSN 0022-3751
Jeng, J., Johnson, S.L., Carlton, A.J. orcid.org/0000-0002-1054-3901 et al. (11 more authors) (2020) Age‐related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells. The Journal of Physiology, 598 (18). pp. 3891-3910. ISSN 0022-3751
Dunbar, L.A., Patni, P., Aguilar, C. et al. (29 more authors) (2019) Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function. EMBO Molecular Medicine, 11 (9). ISSN 1757-4676
Chessum, L., Matern, M.S., Kelly, M.C. et al. (20 more authors) (2018) Helios is a key transcriptional regulator of outer hair cell maturation. Nature, 563 (7733). pp. 696-700. ISSN 0028-0836
Esapa, C.T., Piret, S.E., Nesbit, M.A. et al. (13 more authors) (2018) An N -ethyl- N -nitrosourea (ENU) mutagenized mouse model for autosomal dominant non-syndromic kyphoscoliosis due to vertebral fusion. JBMR Plus, 2 (3). pp. 154-163. ISSN 2473-4039
Mulay, A., Hood, D.W., Williams, D. et al. (5 more authors) (2018) Loss of the homeostatic protein BPIFA1, leads to exacerbation of otitis media severity in the Junbo mouse model. Scientific Reports, 8. 3128. ISSN 2045-2322
Loh, N.Y., Bentley, L., Dimke, H. et al. (17 more authors) (2013) Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5. PLoS ONE, 8 (1). e55412. ISSN 1932-6203
Esapa, C.T., Head, R.A., Jeyabalan, J. et al. (11 more authors) (2012) A Mouse with an N-Ethyl-N-Nitrosourea (ENU) Induced Trp589Arg Galnt3 Mutation Represents a Model for Hyperphosphataemic Familial Tumoural Calcinosis. PLoS ONE, 7 (8). e43205. ISSN 1932-6203
Duncan, E.L., Danoy, P., Kemp, J.P. et al. (44 more authors) (2011) Genome-Wide Association Study Using Extreme Truncate Selection Identifies Novel Genes Affecting Bone Mineral Density and Fracture Risk. PLoS Genetics, 7 (4). e1001372. ISSN 1553-7390
Parkinson, N., Hardisty-Hughes, R.E., Tateossian, H. et al. (15 more authors) (2006) Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media. PLoS Genetics, 2 (10). e149. pp. 1556-1564. ISSN 1553-7390