Works matching AU Wells, Sara

Results: 90
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    Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.

    Published in:
    PLoS Biology, 2019, v. 17, n. 10, p. 1, doi. 10.1371/journal.pbio.3000520
    By:
    • Haq, Naila;
    • Schmidt-Hieber, Christoph;
    • Sialana, Fernando J.;
    • Ciani, Lorenza;
    • Heller, Janosch P.;
    • Stewart, Michelle;
    • Bentley, Liz;
    • Wells, Sara;
    • Rodenburg, Richard J.;
    • Nolan, Patrick M.;
    • Forsythe, Elizabeth;
    • Wu, Michael C.;
    • Lubec, Gert;
    • Salinas, Patricia C.;
    • Häusser, Michael;
    • Beales, Philip L.;
    • Christou-Savina, Sofia
    Publication type:
    Article
    13

    Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.

    Published in:
    PLoS Biology, 2019, v. 17, n. 9, p. 1, doi. 10.1371/journal.pbio.3000414
    By:
    • Haq, Naila;
    • Schmidt-Hieber, Christoph;
    • Sialana, Fernando J.;
    • Ciani, Lorenza;
    • Heller, Janosch P.;
    • Stewart, Michelle;
    • Bentley, Liz;
    • Wells, Sara;
    • Rodenburg, Richard J.;
    • Nolan, Patrick M.;
    • Forsythe, Elizabeth;
    • Wu, Michael C.;
    • Lubec, Gert;
    • Salinas, P.;
    • Häusser, Michael;
    • Beales, Philip L.;
    • Christou-Savina, Sofia
    Publication type:
    Article
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    Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons.

    Published in:
    PLoS Biology, 2019, v. 17, n. 8, p. 1, doi. 10.1371/journal.pbio.3000414
    By:
    • Haq, Naila;
    • Schmidt-Hieber, Christoph;
    • Sialana, Fernando J.;
    • Ciani, Lorenza;
    • Heller, Janosch P.;
    • Stewart, Michelle;
    • Bentley, Liz;
    • Wells, Sara;
    • Rodenburg, Richard J.;
    • Nolan, Patrick M.;
    • Forsythe, Elizabeth;
    • Wu, Michael C.;
    • Lubec, Gert;
    • Salinas, P.;
    • Häusser, Michael;
    • Beales, Philip L.;
    • Christou-Savina, Sofia
    Publication type:
    Article
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    Pharmacological Inhibition of FTO.

    Published in:
    PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0121829
    By:
    • McMurray, Fiona;
    • Demetriades, Marina;
    • Aik, WeiShen;
    • Merkestein, Myrte;
    • Kramer, Holger;
    • Andrew, Daniel S.;
    • Scudamore, Cheryl L.;
    • Hough, Tertius A.;
    • Wells, Sara;
    • Ashcroft, Frances M.;
    • McDonough, Michael A.;
    • Schofield, Christopher J.;
    • Cox, Roger D.
    Publication type:
    Article
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    An ultra-conserved poison exon in the Tra2b gene encoding a splicing activator is essential for male fertility and meiotic cell division.

    Published in:
    EMBO Journal, 2025, v. 44, n. 3, p. 877, doi. 10.1038/s44318-024-00344-6
    By:
    • Dalgliesh, Caroline;
    • Aldalaqan, Saad;
    • Atallah, Christian;
    • Best, Andrew;
    • Scott, Emma;
    • Ehrmann, Ingrid;
    • Merces, George;
    • Mannion, Joel;
    • Badurova, Barbora;
    • Sandher, Raveen;
    • Illing, Ylva;
    • Wirth, Brunhilde;
    • Wells, Sara;
    • Codner, Gemma;
    • Teboul, Lydia;
    • Smith, Graham R;
    • Hedley, Ann;
    • Herbert, Mary;
    • de Rooij, Dirk G;
    • Miles, Colin
    Publication type:
    Article
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    Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss.

    Published in:
    Journal of Neuroscience, 2016, v. 36, n. 1, p. 222, doi. 10.1523/JNEUROSCI.1808-15.2016
    By:
    • Carrott, Leanne;
    • Bowl, Michael R.;
    • Aguilar, Carlos;
    • Johnson, Stuart L.;
    • Chessum, Lauren;
    • West, Melissa;
    • Morse, Susan;
    • Dorning, Joanne;
    • Smart, Elizabeth;
    • Hardisty-Hughes, Rachel;
    • Ball, Greg;
    • Parker, Andrew;
    • Barnard, Alun R.;
    • MacLaren, Robert E.;
    • Wells, Sara;
    • Marcotti, Walter;
    • Brown, Steve D. M.
    Publication type:
    Article
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    Identification of genetic elements in metabolism by high-throughput mouse phenotyping.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-01995-2
    By:
    • Rozman, Jan;
    • Rathkolb, Birgit;
    • Oestereicher, Manuela A.;
    • Schütt, Christine;
    • Ravindranath, Aakash Chavan;
    • Leuchtenberger, Stefanie;
    • Sharma, Sapna;
    • Kistler, Martin;
    • Willershäuser, Monja;
    • Brommage, Robert;
    • Meehan, Terrence F.;
    • Mason, Jeremy;
    • Haselimashhadi, Hamed;
    • Hough, Tertius;
    • Mallon, Ann-Marie;
    • Wells, Sara;
    • Santos, Luis;
    • Lelliott, Christopher J.;
    • White, Jacqueline K.;
    • Sorg, Tania
    Publication type:
    Article
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    Applying the ARRIVE Guidelines to an In Vivo Database.

    Published in:
    PLoS Biology, 2015, v. 13, n. 5, p. 1, doi. 10.1371/journal.pbio.1002151
    By:
    • Karp, Natasha A.;
    • Meehan, Terry F.;
    • Morgan, Hugh;
    • Mason, Jeremy C.;
    • Blake, Andrew;
    • Kurbatova, Natalja;
    • Smedley, Damian;
    • Jacobsen, Julius;
    • Mott, Richard F.;
    • Iyer, Vivek;
    • Matthews, Peter;
    • Melvin, David G.;
    • Wells, Sara;
    • Flenniken, Ann M.;
    • Masuya, Hiroshi;
    • Wakana, Shigeharu;
    • White, Jacqueline K.;
    • Lloyd, K. C. Kent;
    • Reynolds, Corey L.;
    • Paylor, Richard
    Publication type:
    Article
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    Want Sport but Can't Find a Team.

    Published in:
    Palaestra, 2014, v. 28, n. 4, p. 33
    By:
    • PIATT, JENNIFER;
    • BELL, STEVEN A.;
    • ROTHWELL, ERIN;
    • WELLS, MARY SARA
    Publication type:
    Article
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    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
    39

    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
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    The Sex Inclusive Research Framework to address sex bias in preclinical research proposals.

    Published in:
    Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-58560-5
    By:
    • Karp, Natasha A.;
    • Berdoy, Manuel;
    • Gray, Kelly;
    • Hunt, Lilian;
    • Jennings, Maggy;
    • Kerton, Angela;
    • Leach, Matt;
    • Tremoleda, Jordi L.;
    • Gledhill, Jon;
    • Pearl, Esther J.;
    • Percie du Sert, Nathalie;
    • Phillips, Benjamin;
    • Reynolds, Penny S.;
    • Ryder, Kathy;
    • Stanford, S. Clare;
    • Wells, Sara;
    • Whitfield, Lucy
    Publication type:
    Article
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    Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration.

    Published in:
    2018
    By:
    • Watson-Scales, Sheona;
    • Kalmar, Bernadett;
    • Lana-Elola, Eva;
    • Gibbins, Dorota;
    • La Russa, Federica;
    • Wiseman, Frances;
    • Williamson, Matthew;
    • Saccon, Rachele;
    • Slender, Amy;
    • Olerinyova, Anna;
    • Mahmood, Radma;
    • Nye, Emma;
    • Cater, Heather;
    • Wells, Sara;
    • Yu, Y. Eugene;
    • Bennett, David L. H.;
    • Greensmith, Linda;
    • Fisher, Elizabeth M. C.;
    • Tybulewicz, Victor L. J.
    Publication type:
    Abstract
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    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
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