Hasil Pencarian - Michelle M. Simon

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  1. 1
    Genic constraint against nonsynonymous variation across the mouse genome

    Genic constraint against nonsynonymous variation across the mouse genome oleh George Powell, Michelle M. Simon, Sara Pulit, Ann-Marie Mallon, Cecilia M. Lindgren

    Diterbitkan 2023-09-01
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  2. 2
    Interactions between the otitis media gene, Fbxo11, and p53 in the mouse embryonic lung

    Interactions between the otitis media gene, Fbxo11, and p53 in the mouse embryonic lung oleh Hilda Tateossian, Susan Morse, Michelle M. Simon, Charlotte H. Dean, Steve D. M. Brown

    Diterbitkan 2015-12-01
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  3. 3
    Making sense of the linear genome, gene function and TADs

    Making sense of the linear genome, gene function and TADs oleh Helen S. Long, Simon Greenaway, George Powell, Ann-Marie Mallon, Cecilia M. Lindgren, Michelle M. Simon

    Diterbitkan 2022-01-01
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  4. 4
    A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease

    A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease oleh Siddharth Sethi, Ilya E. Vorontsov, Ivan V. Kulakovskiy, Simon Greenaway, John Williams, Vsevolod J. Makeev, Steve D. M. Brown, Michelle M. Simon, Ann-Marie Mallon

    Diterbitkan 2020-11-01
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  5. 5
    Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function

    Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function oleh Amy S. Findlay, Roderick N. Carter, Becky Starbuck, Lisa McKie, Klára Nováková, Peter S. Budd, Margaret A. Keighren, Joseph A. Marsh, Sally H. Cross, Michelle M. Simon, Paul K. Potter, Nicholas M. Morton, Ian J. Jackson

    Diterbitkan 2018-12-01
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  6. 6
    A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.

    A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways. oleh Michael Crompton, Tom Purnell, Hayley E Tyrer, Andrew Parker, Greg Ball, Rachel E Hardisty-Hughes, Richard Gale, Debbie Williams, Charlotte H Dean, Michelle M Simon, Ann-Marie Mallon, Sara Wells, Mahmood F Bhutta, Martin J Burton, Hilda Tateossian, Steve D M Brown

    Diterbitkan 2017-08-01
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  7. 7
    Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations.

    Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations. oleh Katherine R Bull, Andrew J Rimmer, Owen M Siggs, Lisa A Miosge, Carla M Roots, Anselm Enders, Edward M Bertram, Tanya L Crockford, Belinda Whittle, Paul K Potter, Michelle M Simon, Ann-Marie Mallon, Steve D M Brown, Bruce Beutler, Christopher C Goodnow, Gerton Lunter, Richard J Cornall

    Diterbitkan 2013-01-01
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  8. 8
    Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants

    Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants oleh Gemma F. Codner, Joffrey Mianné, Adam Caulder, Jorik Loeffler, Rachel Fell, Ruairidh King, Alasdair J. Allan, Matthew Mackenzie, Fran J. Pike, Christopher V. McCabe, Skevoulla Christou, Sam Joynson, Marie Hutchison, Michelle E. Stewart, Saumya Kumar, Michelle M. Simon, Loranne Agius, Quentin M. Anstee, Kirill E. Volynski, Dimitri M. Kullmann, Sara Wells, Lydia Teboul

    Diterbitkan 2018-06-01
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  9. 9
    Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function

    Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function oleh Lucy A Dunbar, Pranav Patni, Carlos Aguilar, Philomena Mburu, Laura Corns, Helena RR Wells, Sedigheh Delmaghani, Andrew Parker, Stuart Johnson, Debbie Williams, Christopher T Esapa, Michelle M Simon, Lauren Chessum, Sherylanne Newton, Joanne Dorning, Prashanthini Jeyarajan, Susan Morse, Andrea Lelli, Gemma F Codner, Thibault Peineau, Suhasini R Gopal, Kumar N Alagramam, Ronna Hertzano, Didier Dulon, Sara Wells, Frances M Williams, Christine Petit, Sally J Dawson, Steve DM Brown, Walter Marcotti, Aziz El‐Amraoui, Michael R Bowl

    Diterbitkan 2019-09-01
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  10. 10
    Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

    Novel gene function revealed by mouse mutagenesis screens for models of age-related disease oleh Paul K. Potter, Michael R. Bowl, Prashanthini Jeyarajan, Laura Wisby, Andrew Blease, Michelle E. Goldsworthy, Michelle M. Simon, Simon Greenaway, Vincent Michel, Alun Barnard, Carlos Aguilar, Thomas Agnew, Gareth Banks, Andrew Blake, Lauren Chessum, Joanne Dorning, Sara Falcone, Laurence Goosey, Shelley Harris, Andy Haynes, Ines Heise, Rosie Hillier, Tertius Hough, Angela Hoslin, Marie Hutchison, Ruairidh King, Saumya Kumar, Heena V. Lad, Gemma Law, Robert E. MacLaren, Susan Morse, Thomas Nicol, Andrew Parker, Karen Pickford, Siddharth Sethi, Becky Starbuck, Femke Stelma, Michael Cheeseman, Sally H. Cross, Russell G. Foster, Ian J. Jackson, Stuart N. Peirson, Rajesh V. Thakker, Tonia Vincent, Cheryl Scudamore, Sara Wells, Aziz El-Amraoui, Christine Petit, Abraham Acevedo-Arozena, Patrick M. Nolan, Roger Cox, Anne-Marie Mallon, Steve D. M. Brown

    Diterbitkan 2016-08-01
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  11. 11
    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
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