Søgeresultater - Pearson, Selina

Peptidergic Activation of Locomotor Pattern Generators in the Neonatal Spinal Cord af Pearson, Selina A., Mouihate, Abdeslam, Pittman, Quentin J., Whelan, Patrick J.

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Ecto‐5′‐nucleotidase (CD73) regulates peripheral chemoreceptor activity and cardiorespiratory responses to hypoxia af Holmes, Andrew P., Ray, Clare J., Pearson, Selina A., Coney, Andrew M., Kumar, Prem

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

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Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) Are Two New Mutations of Lmx1a Causing Severe Cochlear and Vestibular Defects af Steffes, Georg, Lorente-Cánovas, Beatriz, Pearson, Selina, Brooker, Rachael H., Spiden, Sarah, Kiernan, Amy E., Guénet, Jean-Louis, Steel, Karen P.

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Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice af Hilton, Jennifer M, Lewis, Morag A, Grati, M'hamed, Ingham, Neil, Pearson, Selina, Laskowski, Roman A, Adams, David J, Steel, Karen P

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AMP-ACTIVATED PROTEIN KINASE MEDIATES CAROTID BODY EXCITATION BY HYPOXIA af Wyatt, Christopher N., Mustard, Kirsty J.W., Pearson, Selina A., Dallas, Mark L, Atkinson, Lucy, Kumar, Prem, Peers, Chris, Hardie, D. Grahame, Evans, A. Mark

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

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Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme af Lewis, Morag A., Ingham, Neil J., Chen, Jing, Pearson, Selina, Di Domenico, Francesca, Rekhi, Sohinder, Allen, Rochelle, Drake, Matthew, Willaert, Annelore, Rook, Victoria, Pass, Johanna, Keane, Thomas, Adams, David J., Tucker, Abigail S., White, Jacqueline K., Steel, Karen P.

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Targeting of Slc25a21 Is Associated with Orofacial Defects and Otitis Media Due to Disrupted Expression of a Neighbouring Gene af Maguire, Simon, Estabel, Jeanne, Ingham, Neil, Pearson, Selina, Ryder, Edward, Carragher, Damian M., Walker, Nicolas, Bussell, James, Chan, Wai-In, Keane, Thomas M., Adams, David J., Scudamore, Cheryl L., Lelliott, Christopher J., Ramírez-Solis, Ramiro, Karp, Natasha A., Steel, Karen P., White, Jacqueline K., Gerdin, Anna-Karin

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Mouse screen reveals multiple new genes underlying mouse and human hearing loss af Ingham, Neil J., Pearson, Selina A., Vancollie, Valerie E., Rook, Victoria, Lewis, Morag A., Chen, Jing, Buniello, Annalisa, Martelletti, Elisa, Preite, Lorenzo, Lam, Chi Chung, Weiss, Felix D., Powis, Zӧe, Suwannarat, Pim, Lelliott, Christopher J., Dawson, Sally J., White, Jacqueline K., Steel, Karen P.

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A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction af Bowl, Michael R., Simon, Michelle M., Ingham, Neil J., Greenaway, Simon, Santos, Luis, Cater, Heather, Taylor, Sarah, Mason, Jeremy, Kurbatova, Natalja, Pearson, Selina, Bower, Lynette R., Clary, Dave A., Meziane, Hamid, Reilly, Patrick, Minowa, Osamu, Kelsey, Lois, Tocchini-Valentini, Glauco P., Gao, Xiang, Bradley, Allan, Skarnes, William C., Moore, Mark, Beaudet, Arthur L., Justice, Monica J., Seavitt, John, Dickinson, Mary E., Wurst, Wolfgang, de Angelis, Martin Hrabe, Herault, Yann, Wakana, Shigeharu, Nutter, Lauryl M. J., Flenniken, Ann M., McKerlie, Colin, Murray, Stephen A., Svenson, Karen L., Braun, Robert E., West, David B., Lloyd, K. C. Kent, Adams, David J., White, Jacqui, Karp, Natasha, Flicek, Paul, Smedley, Damian, Meehan, Terrence F., Parkinson, Helen E., Teboul, Lydia M., Wells, Sara, Steel, Karen P., Mallon, Ann-Marie, Brown, Steve D. M.

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