Search Results - Ingham, Neil
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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 2012Text -
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Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype by Norgett, Elizabeth E., Golder, Zoe J., Lorente-Cánovas, Beatriz, Ingham, Neil, Steel, Karen P., Karet Frankl, Fiona E.
Published 2012Text -
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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 2013Text -
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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 2011Text -
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Presynaptic maturation in auditory hair cells requires a critical period of sensory-independent spiking activity by Johnson, Stuart L., Kuhn, Stephanie, Franz, Christoph, Ingham, Neil, Furness, David N., Knipper, Marlies, Steel, Karen P., Adelman, John P., Holley, Matthew C., Marcotti, Walter
Published 2013Text -
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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 2016Text -
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The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss by Spiden, Sarah L., Bortolozzi, Mario, Di Leva, Francesca, de Angelis, Martin Hrabé, Fuchs, Helmut, Lim, Dmitry, Ortolano, Saida, Ingham, Neil J., Brini, Marisa, Carafoli, Ernesto, Mammano, Fabio, Steel, Karen P.
Published 2008Text -
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The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice by Schütz, Melanie, Scimemi, Pietro, Majumder, Paromita, De Siati, Romolo Daniele, Crispino, Giulia, Rodriguez, Laura, Bortolozzi, Mario, Santarelli, Rosamaria, Seydel, Anke, Sonntag, Stephan, Ingham, Neil, Steel, Karen P., Willecke, Klaus, Mammano, Fabio
Published 2010Text -
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Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss by Chen, Jing, Ingham, Neil, Kelly, John, Jadeja, Shalini, Goulding, David, Pass, Johanna, Mahajan, Vinit B., Tsang, Stephen H., Nijnik, Anastasia, Jackson, Ian J., White, Jacqueline K., Forge, Andrew, Jagger, Daniel, Steel, Karen P.
Published 2014Text -
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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 2013Text -
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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 2013Text -
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miR-96 regulates the progression of differentiation in mammalian cochlear inner and outer hair cells by Kuhn, Stephanie, Johnson, Stuart L., Furness, David N., Chen, Jing, Ingham, Neil, Hilton, Jennifer M., Steffes, Georg, Lewis, Morag A., Zampini, Valeria, Hackney, Carole M., Masetto, Sergio, Holley, Matthew C., Steel, Karen P., Marcotti, Walter
Published 2011Text