Kết quả tìm kiếm - Pearson, Selina

Peptidergic Activation of Locomotor Pattern Generators in the Neonatal Spinal Cord Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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 Bằng 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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