Works by Williams, Debbie


Results: 34
    1
    2
    3

    Clinical characteristics and outcomes of HIV-associated immune complex kidney disease.

    Published in:
    Nephrology Dialysis Transplantation, 2016, v. 31, n. 12, p. 2099, doi. 10.1093/ndt/gfv436
    By:
    • Booth, John W.;
    • Hamzah, Lisa;
    • Jose, Sophie;
    • Horsfield, Catherine;
    • O'Donnell, Patrick;
    • McAdoo, Stephen;
    • Kumar, Emil A.;
    • Turner-Stokes, Tabitha;
    • Khatib, Nadia;
    • Das, Partha;
    • Naftalin, Claire;
    • Mackie, Nicola;
    • Kingdon, Ed;
    • Williams, Debbie;
    • Hendry, Bruce M.;
    • Sabin, Caroline;
    • Jones, Rachael;
    • Levy, Jeremy;
    • Hilton, Rachel;
    • Connolly, John
    Publication type:
    Article
    4
    5

    Crafts: A Criminal Offence?

    Published in:
    1987
    By:
    • Williams, Debbie;
    • Harrison, Jane;
    • Newell, Catherine;
    • Holt, Jo;
    • Rees, Colin
    Publication type:
    Journal Article
    6

    Crafts: A Criminal Offence?

    Published in:
    British Journal of Occupational Therapy, 1987, v. 50, n. 1, p. 12, doi. 10.1177/030802268705000107
    By:
    • Williams, Debbie;
    • Harrison, Jane;
    • Newell, Catherine;
    • Holt, Jo;
    • Rees, Colin
    Publication type:
    Article
    7

    REMAP.

    Published in:
    1986
    By:
    • Williams, Debbie
    Publication type:
    Journal Article
    8

    REMAP.

    Published in:
    British Journal of Occupational Therapy, 1986, v. 49, n. 1, p. 22
    By:
    • Williams, Debbie
    Publication type:
    Article
    9
    10
    11

    HIF--VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants.

    Published in:
    PLoS Genetics, 2011, v. 7, n. 10, p. 1, doi. 10.1371/journal.pgen.1002336
    By:
    • Cheeseman, Michael T.;
    • Tyrer, Hayley E.;
    • Williams, Debbie;
    • Hough, Tertius A.;
    • Pathak, Paras;
    • Romero, Maria R.;
    • Hilton, Helen;
    • Bali, Sulzhan;
    • Parker, Andrew;
    • Vizor, Lucie;
    • Purnell, Tom;
    • Vowell, Kate;
    • Wells, Sara;
    • Bhutta, Mahmood F.;
    • Potter, Paul K.;
    • Brown, Steve D. M.
    Publication type:
    Article
    12

    A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy.

    Published in:
    PLoS Genetics, 2010, v. 6, n. 6, p. 1, doi. 10.1371/journal.pgen.1001000
    By:
    • Ashrafian, Houman;
    • Docherty, Louise;
    • Leo, Vincenzo;
    • Towlson, Christopher;
    • Neilan, Monica;
    • Steeples, Violetta;
    • Lygate, Craig A.;
    • Hough, Tertius;
    • Townsend, Stuart;
    • Williams, Debbie;
    • Wells, Sara;
    • Norris, Dominic;
    • Glyn-Jones, Sarah;
    • Land, John;
    • Barbaric, Ivana;
    • Lalanne, Zuzanne;
    • Denny, Paul;
    • Szumska, Dorota;
    • Bhattacharya, Shoumo;
    • Griffin, Julian L.
    Publication type:
    Article
    13
    14

    Understanding Educators' Experiences in the 2018 Oklahoma Walkouts.

    Published in:
    Critical Education, 2022, v. 13, n. 2, p. 77
    By:
    • Dyke, Erin;
    • Anderson, Heather;
    • Brown, Autumn;
    • El Sabbagh, Jinan;
    • Fernandez, Hannah;
    • Goodwin, Stacey;
    • Hickey, Mark;
    • Lowther, Jennie;
    • Price, Stephanie;
    • Ruby, Megan;
    • Self, Kristy;
    • Williams, Debbie;
    • Williams, Jennifer;
    • Worth, Angel
    Publication type:
    Article
    15
    16
    17
    18

    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
    19
    20
    21
    22
    23
    24

    Book Review.

    Published in:
    2000
    By:
    • Williams, Debbie
    Publication type:
    Book Review
    25
    26
    27
    28

    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
    29

    A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.

    Published in:
    Human Molecular Genetics, 2018, v. 27, n. 10, p. 1723, doi. 10.1093/hmg/ddy077
    By:
    • Corrochano, Silvia;
    • Blanco, Gonzalo;
    • Williams, Debbie;
    • Wettstein, Jessica;
    • Simon, Michelle;
    • Kumar, Saumya;
    • Moir, Lee;
    • Agnew, Thomas;
    • Stewart, Michelle;
    • Landman, Allison;
    • Kotiadis, Vassilios N.;
    • Duchen, Michael R.;
    • Wackerhage, Henning;
    • Rubinsztein, David C.;
    • Brown, Steve D. M.;
    • Acevedo-Arozena, Abraham
    Publication type:
    Article
    30

    Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 8, p. 1706, doi. 10.1093/hmg/ddr605
    By:
    • Kurapati, Ramakrishna;
    • McKenna, Caoimhe;
    • Lindqvist, Johan;
    • Williams, Debbie;
    • Simon, Michelle;
    • LeProust, Emily;
    • Baker, Jane;
    • Cheeseman, Michael;
    • Carroll, Natalie;
    • Denny, Paul;
    • Laval, Steve;
    • Lochmüller, Hanns;
    • Ochala, Julien;
    • Blanco, Gonzalo
    Publication type:
    Article
    31

    Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 19, p. 3553, doi. 10.1093/hmg/ddp304
    By:
    • Mackenzie, Francesca E.;
    • Romero, Rosario;
    • Williams, Debbie;
    • Gillingwater, Thomas;
    • Hilton, Helen;
    • Dick, Jim;
    • Riddoch-Contreras, Joanna;
    • Wong, Frances;
    • Ireson, Lisa;
    • Powles-Glover, Nicola;
    • Riley, Genna;
    • Underhill, Peter;
    • Hough, Tertius;
    • Arkell, Ruth;
    • Greensmith, Linda;
    • Ribchester, Richard R.;
    • Blanco, Gonzalo
    Publication type:
    Article
    32
    33
    34