Hasil Pencarian - Neil J. Ingham

  • Menampilkan 1 - 13 hasil dari 13
Perbaiki Hasil
  1. 1
    Hearing impairment due to Mir183/96/182 mutations suggests both loss-of-function and gain-of-function effects

    Hearing impairment due to Mir183/96/182 mutations suggests both loss-of-function and gain-of-function effects oleh Morag A. Lewis, Francesca Di Domenico, Neil J. Ingham, Haydn M. Prosser, Karen P. Steel

    Diterbitkan 2021-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss.

    Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss. oleh Neil J Ingham, Navid Banafshe, Clarisse Panganiban, Julia L Crunden, Jing Chen, Morag A Lewis, Karen P Steel

    Diterbitkan 2021-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice

    Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice oleh Elisa Martelletti, Neil J. Ingham, Oliver Houston, Johanna C. Pass, Jing Chen, Walter Marcotti, Walter Marcotti, Karen P. Steel

    Diterbitkan 2020-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia

    Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia oleh Seham Ebrahim, Neil J. Ingham, Morag A. Lewis, Michael J.C. Rogers, Runjia Cui, Bechara Kachar, Johanna C. Pass, Karen P. Steel

    Diterbitkan 2016-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    The Effect of a <i>Pex3</i> Mutation on Hearing and Lipid Content of the Inner Ear

    The Effect of a <i>Pex3</i> Mutation on Hearing and Lipid Content of the Inner Ear oleh Rafael M. Kochaj, Elisa Martelletti, Neil J. Ingham, Annalisa Buniello, Bebiana C. Sousa, Michael J. O. Wakelam, Andrea F. Lopez-Clavijo, Karen P. Steel

    Diterbitkan 2022-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants

    Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants oleh María Lachgar-Ruiz, Matías Morín, Elisa Martelletti, Neil J. Ingham, Lorenzo Preite, Morag A. Lewis, Luciana Santos Serrão de Castro, Karen P. Steel, Miguel Ángel Moreno-Pelayo

    Diterbitkan 2023-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease

    Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease oleh Valda Pauzuolyte, Aara Patel, James R Wawrzynski, Neil J Ingham, Yeh Chwan Leong, Rajvinder Karda, Maria Bitner‐Glindzicz, Wolfgang Berger, Simon N Waddington, Karen P Steel, Jane C Sowden

    Diterbitkan 2023-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss.

    The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss. oleh Sarah L Spiden, Mario Bortolozzi, Francesca Di Leva, Martin Hrabé de Angelis, Helmut Fuchs, Dmitry Lim, Saida Ortolano, Neil J Ingham, Marisa Brini, Ernesto Carafoli, Fabio Mammano, Karen P Steel

    Diterbitkan 2008-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme

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

    Diterbitkan 2022-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing

    Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing oleh Annalisa Buniello, Neil J Ingham, Morag A Lewis, Andreea C Huma, Raquel Martinez‐Vega, Isabel Varela‐Nieto, Gema Vizcay‐Barrena, Roland A Fleck, Oliver Houston, Tanaya Bardhan, Stuart L Johnson, Jacqueline K White, Huijun Yuan, Walter Marcotti, Karen P Steel

    Diterbitkan 2016-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    Mouse screen reveals multiple new genes underlying mouse and human hearing loss.

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

    Diterbitkan 2019-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention

    The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention oleh Dale Bryant, Valda Pauzuolyte, Neil J. Ingham, Aara Patel, Waheeda Pagarkar, Lucy A. Anderson, Katie E. Smith, Dale A. Moulding, Yeh C. Leong, Daniyal J. Jafree, David A. Long, Amina Al-Yassin, Karen P. Steel, Daniel J. Jagger, Andrew Forge, Wolfgang Berger, Jane C. Sowden, Maria Bitner-Glindzicz

    Diterbitkan 2022-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction

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

    Diterbitkan 2017-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: