Works matching AU Simon, Michelle M.

Results: 16
    1

    Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout.

    Published in:
    FASEB Journal, 2023, v. 37, n. 11, p. 1, doi. 10.1096/fj.202201918R
    By:
    • Bai, Ying;
    • Bentley, Liz;
    • Ma, Chao;
    • Naveenan, Navaratnam;
    • Cleak, James;
    • Wu, Yixing;
    • Simon, Michelle M.;
    • Westerberg, Henrik;
    • Cañas, Ramón Casero;
    • Horner, Neil;
    • Pandey, Rajesh;
    • Paphiti, Keanu;
    • Schulze, Ulrike;
    • Mianné, Joffrey;
    • Hough, Tertius;
    • Teboul, Lydia;
    • de Baaij, Jeroen H. F.;
    • Cox, Roger D.
    Publication type:
    Article
    2
    3

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

    Published in:
    BMC Biology, 2018, v. 16, n. 1, p. 1, doi. 10.1186/s12915-018-0530-7
    By:
    • Codner, Gemma F.;
    • Mianné, Joffrey;
    • Caulder, Adam;
    • Loeffler, Jorik;
    • Fell, Rachel;
    • King, Ruairidh;
    • Allan, Alasdair J.;
    • Mackenzie, Matthew;
    • Pike, Fran J.;
    • McCabe, Christopher V.;
    • Christou, Skevoulla;
    • Joynson, Sam;
    • Hutchison, Marie;
    • Stewart, Michelle E.;
    • Kumar, Saumya;
    • Simon, Michelle M.;
    • Agius, Loranne;
    • Anstee, Quentin M.;
    • Volynski, Kirill E.;
    • Kullmann, Dimitri M.
    Publication type:
    Article
    4

    Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003219
    By:
    • Bull, Katherine R.;
    • Rimmer, Andrew J.;
    • Siggs, Owen M.;
    • Miosge, Lisa A.;
    • Roots, Carla M.;
    • Enders, Anselm;
    • Bertram, Edward M.;
    • Crockford, Tanya L.;
    • Whittle, Belinda;
    • Potter, Paul K.;
    • Simon, Michelle M.;
    • Mallon, Ann-Marie;
    • Brown, Steve D. M.;
    • Beutler, Bruce;
    • Goodnow, Christopher C.;
    • Lunter, Gerton;
    • Cornall, Richard J.
    Publication type:
    Article
    5

    Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function.

    Published in:
    EMBO Molecular Medicine, 2019, v. 11, n. 9, p. N.PAG, doi. 10.15252/emmm.201910288
    By:
    • Dunbar, Lucy A;
    • Patni, Pranav;
    • Aguilar, Carlos;
    • Mburu, Philomena;
    • Corns, Laura;
    • Wells, Helena RR;
    • Delmaghani, Sedigheh;
    • Parker, Andrew;
    • Johnson, Stuart;
    • Williams, Debbie;
    • Esapa, Christopher T;
    • Simon, Michelle M;
    • Chessum, Lauren;
    • Newton, Sherylanne;
    • Dorning, Joanne;
    • Jeyarajan, Prashanthini;
    • Morse, Susan;
    • Lelli, Andrea;
    • Codner, Gemma F;
    • Peineau, Thibault
    Publication type:
    Article
    6

    Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

    Published in:
    Nature Communications, 2016, v. 7, n. 8, p. 12444, doi. 10.1038/ncomms12444
    By:
    • Potter, Paul K.;
    • Bowl, Michael R.;
    • Jeyarajan, Prashanthini;
    • Wisby, Laura;
    • Blease, Andrew;
    • Goldsworthy, Michelle E.;
    • Simon, Michelle M.;
    • Greenaway, Simon;
    • Michel, Vincent;
    • Barnard, Alun;
    • Aguilar, Carlos;
    • Agnew, Thomas;
    • Banks, Gareth;
    • Blake, Andrew;
    • Chessum, Lauren;
    • Dorning, Joanne;
    • Falcone, Sara;
    • Goosey, Laurence;
    • Harris, Shelley;
    • Haynes, Andy
    Publication type:
    Article
    7

    A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

    Published in:
    Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00595-4
    By:
    • 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.;
    • Xiang Gao;
    • Bradley, Allan;
    • Skarnes, William C.
    Publication type:
    Article
    8

    A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.

    Published in:
    Genome Biology, 2013, v. 14, n. 7, p. R82, doi. 10.1186/gb-2013-14-7-r82
    By:
    • Simon, Michelle M;
    • Greenaway, Simon;
    • White, Jacqueline K;
    • Fuchs, Helmut;
    • Gailus-Durner, Valérie;
    • Wells, Sara;
    • Sorg, Tania;
    • Kim Wong;
    • Bedu, Elodie;
    • Cartwright, Elizabeth J;
    • Dacquin, Romain;
    • Djebali, Sophia;
    • Estabel, Jeanne;
    • Graw, Jochen;
    • Ingham, Neil J;
    • Jackson, Ian J;
    • Lengeling, Andreas;
    • Mandillo, Silvia;
    • Marvel, Jacqueline;
    • Meziane, Hamid
    Publication type:
    Article
    9
    10

    Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.

    Published in:
    Journal of Bone & Mineral Research, 2019, v. 34, n. 7, p. 1324, doi. 10.1002/jbmr.3695
    By:
    • Gorvin, Caroline M;
    • Loh, Nellie Y;
    • Stechman, Michael J;
    • Falcone, Sara;
    • Hannan, Fadil M;
    • Ahmad, Bushra N;
    • Piret, Sian E;
    • Reed, Anita AC;
    • Jeyabalan, Jeshmi;
    • Leo, Paul;
    • Marshall, Mhairi;
    • Sethi, Siddharth;
    • Bass, Paul;
    • Roberts, Ian;
    • Sanderson, Jeremy;
    • Wells, Sara;
    • Hough, Tertius A;
    • Bentley, Liz;
    • Christie, Paul T;
    • Simon, Michelle M
    Publication type:
    Article
    11

    An N‐Ethyl‐N‐Nitrosourea (ENU)‐Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.

    Published in:
    Journal of Bone & Mineral Research, 2019, v. 34, n. 3, p. 497, doi. 10.1002/jbmr.3624
    By:
    • Gorvin, Caroline M;
    • Ahmad, Bushra N;
    • Stechman, Michael J;
    • Loh, Nellie Y;
    • Hough, Tertius A;
    • Leo, Paul;
    • Marshall, Mhairi;
    • Sethi, Siddharth;
    • Bentley, Liz;
    • Piret, Sian E;
    • Reed, Anita;
    • Jeyabalan, Jeshmi;
    • Christie, Paul T;
    • Wells, Sara;
    • Simon, Michelle M;
    • Mallon, Ann‐Marie;
    • Schulz, Herbert;
    • Huebner, Norbert;
    • Brown, Matthew A;
    • Cox, Roger D
    Publication type:
    Article
    12
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    14
    15

    A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.

    Published in:
    PLoS Genetics, 2017, v. 13, n. 8, p. 1, doi. 10.1371/journal.pgen.1006969
    By:
    • Crompton, Michael;
    • Purnell, Tom;
    • Tyrer, Hayley E.;
    • Parker, Andrew;
    • Ball, Greg;
    • Hardisty-Hughes, Rachel E.;
    • Gale, Richard;
    • Williams, Debbie;
    • Dean, Charlotte H.;
    • Simon, Michelle M.;
    • Mallon, Ann-Marie;
    • Wells, Sara;
    • Bhutta, Mahmood F.;
    • Burton, Martin J.;
    • Tateossian, Hilda;
    • Brown, Steve D. M.
    Publication type:
    Article
    16

    Mouse genomic and cellular annotations.

    Published in:
    Mammalian Genome, 2022, v. 33, n. 1, p. 19, doi. 10.1007/s00335-021-09936-7
    By:
    • Long, Helen;
    • Reeves, Richard;
    • Simon, Michelle M.
    Publication type:
    Article