Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti

by Carlisle, Francesca A., Steel, Karen P., Lewis, Morag A.
Published 2012

Auditory Function in the Tc1 Mouse Model of Down Syndrome Suggests a Limited Region of Human Chromosome 21 Involved in Otitis Media

by Kuhn, Stephanie, Ingham, Neil, Pearson, Selina, Gribble, Susan M., Clayton, Stephen, Steel, Karen P., Marcotti, Walter
Published 2012

A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice

by Calvert, Jennifer A., Dedos, Skarlatos G., Hawker, Kelvin, Fleming, Michelle, Lewis, Morag A., Steel, Karen P.
Published 2011

Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1

by Bosman, Erika A., Estabel, Jeanne, Ismail, Ozama, Podrini, Christine, White, Jacqueline K., Steel, Karen P.
Published 2012

Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function

by Girotto, Giorgia, Vuckovic, Dragana, Buniello, Annalisa, Lorente-Cánovas, Beatriz, Lewis, Morag, Gasparini, Paolo, Steel, Karen P.
Published 2014

Headbobber: A Combined Morphogenetic and Cochleosaccular Mouse Model to Study 10qter Deletions in Human Deafness

by Buniello, Annalisa, Hardisty-Hughes, Rachel E., Pass, Johanna C., Bober, Eva, Smith, Richard J., Steel, Karen P.
Published 2013

A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo

by Chen, Jing, Johnson, Stuart L, Lewis, Morag A, Hilton, Jennifer M, Huma, Andreea, Marcotti, Walter, Steel, Karen P
Published 2014

Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear

by Lorente-Cánovas, Beatriz, Ingham, Neil, Norgett, Elizabeth E., Golder, Zoe J., Karet Frankl, Fiona E., Steel, Karen P.
Published 2013

Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice

by Hilton, Jennifer M, Lewis, Morag A, Grati, M'hamed, Ingham, Neil, Pearson, Selina, Laskowski, Roman A, Adams, David J, Steel, Karen P
Published 2011

The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65

by Lopes, Vanda S., Gibbs, Daniel, Libby, Richard T., Aleman, Tomas S., Welch, Darcy L., Lillo, Concepción, Jacobson, Samuel G., Radu, Roxana A., Steel, Karen P., Williams, David S.
Published 2011

The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss

by Linden Phillips, Luan, Bitner-Glindzicz, Maria, Lench, Nicholas, Steel, Karen P., Langford, Cordelia, Dawson, Sally J., Davis, Adrian, Simpson, Sue, Packer, Claire
Published 2013

Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss

by Girotto, Giorgia, Abdulhadi, Khalid, Buniello, Annalisa, Vozzi, Diego, Licastro, Danilo, d'Eustacchio, Angela, Vuckovic, Dragana, Alkowari, Moza Khalifa, Steel, Karen P., Badii, Ramin, Gasparini, Paolo
Published 2013

Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) Are Two New Mutations of Lmx1a Causing Severe Cochlear and Vestibular Defects

by Steffes, Georg, Lorente-Cánovas, Beatriz, Pearson, Selina, Brooker, Rachael H., Spiden, Sarah, Kiernan, Amy E., Guénet, Jean-Louis, Steel, Karen P.
Published 2012

Mutations and altered expression of SERPINF1 in patients with familial otosclerosis

by Ziff, Joanna L., Crompton, Michael, Powell, Harry R.F., Lavy, Jeremy A., Aldren, Christopher P., Steel, Karen P., Saeed, Shakeel R., Dawson, Sally J.
Published 2016

Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia

by Ebrahim, Seham, Ingham, Neil J., Lewis, Morag A., Rogers, Michael J.C., Cui, Runjia, Kachar, Bechara, Pass, Johanna C., Steel, Karen P.
Published 2016

Exploring regulatory networks of miR-96 in the developing inner ear

by Lewis, Morag A., Buniello, Annalisa, Hilton, Jennifer M., Zhu, Fei, Zhang, William I., Evans, Stephanie, van Dongen, Stijn, Enright, Anton J., Steel, Karen P.
Published 2016

S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse

by Ingham, Neil J., Carlisle, Francesca, Pearson, Selina, Lewis, Morag A., Buniello, Annalisa, Chen, Jing, Isaacson, Rivka L., Pass, Johanna, White, Jacqueline K., Dawson, Sally J., Steel, Karen P.
Published 2016

The acquisition of mechano‐electrical transducer current adaptation in auditory hair cells requires myosin VI

by Marcotti, Walter, Corns, Laura F., Goodyear, Richard J., Rzadzinska, Agnieszka K., Avraham, Karen B., Steel, Karen P., Richardson, Guy P., Kros, Corné J.
Published 2016

Correction: Mcph1-Deficient Mice Reveal a Role for MCPH1 in Otitis Media

by Chen, Jing, Ingham, Neil, Clare, Simon, Raisen, Claire, Vancollie, Valerie E., Ismail, Ozama, McIntyre, Rebecca E., Tsang, Stephen H., Mahajan, Vinit B., Dougan, Gordon, Adams, David J., White, Jacqueline K., Steel, Karen P.
Published 2013

Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study

by Le Quesne Stabej, Polona, Saihan, Zubin, Rangesh, Nell, Steele-Stallard, Heather B, Ambrose, John, Coffey, Alison, Emmerson, Jenny, Haralambous, Elene, Hughes, Yasmin, Steel, Karen P, Luxon, Linda M, Webster, Andrew R, Bitner-Glindzicz, Maria
Published 2011