Hasil Pencarian - Morag A Lewis

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  1. 1
    Investigating the characteristics of genes and variants associated with self-reported hearing difficulty in older adults in the UK Biobank

    Investigating the characteristics of genes and variants associated with self-reported hearing difficulty in older adults in the UK Biobank oleh Morag A. Lewis, Bradley A. Schulte, Judy R. Dubno, Karen P. Steel

    Diterbitkan 2022-06-01
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  2. 2
    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
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  3. 3
    Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells.

    Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells. oleh Beatriz Lorente-Cánovas, Stephanie Eckrich, Morag A Lewis, Stuart L Johnson, Walter Marcotti, Karen P Steel

    Diterbitkan 2022-01-01
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  4. 4
    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
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  5. 5
    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
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  6. 6
    Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

    Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes oleh Morag A. Lewis, Lisa S. Nolan, Barbara A. Cadge, Lois J. Matthews, Bradley A. Schulte, Judy R. Dubno, Karen P. Steel, Sally J. Dawson

    Diterbitkan 2018-09-01
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  7. 7
    In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear.

    In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear. oleh Chiara Chiereghin, Michela Robusto, Morag A Lewis, Susana Caetano, Valentina Massa, Pierangela Castorina, Umberto Ambrosetti, Karen P Steel, Stefano Duga, Rosanna Asselta, Giulia Soldà

    Diterbitkan 2023-01-01
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  8. 8
    Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss.

    Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. oleh Morag A Lewis, Jennifer Schulte, Lois Matthews, Kenneth I Vaden, Claire J Steves, Frances M K Williams, Bradley A Schulte, Judy R Dubno, Karen P Steel

    Diterbitkan 2023-11-01
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  9. 9
    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
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  10. 10
    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
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  11. 11
    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
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  12. 12
    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
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