Works matching David Humphreys


Results: 256
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    DAVID HUMPHREYS.

    Published in:
    Notes & Queries, 1920, v. 6, n. 112, p. 281-d
    By:
    • SANBORN, M. RAY
    Publication type:
    Article
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    DAVID HUMPHREYS.

    Published in:
    Notes & Queries, 1920, v. 6, n. 109, p. 217
    By:
    • HUMPHREYS, A. L.
    Publication type:
    Article
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    DAVID HUMPHREYS.

    Published in:
    Notes & Queries, 1920, v. 6, n. 109, p. 217
    By:
    • HILL, N. W.
    Publication type:
    Article
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    DAVID HUMPHREYS.

    Published in:
    Notes & Queries, 1920, v. 6, n. 108, p. 198
    By:
    • MAYCOCK, WILLOUGHBY
    Publication type:
    Article
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    David Humphreys, D.D.

    Published in:
    Notes & Queries, 1858, v. 6, n. 156, p. 529-a
    By:
    • LEE, ALFRED T.
    Publication type:
    Article
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    Evaluation of the humphrey A.D.E. system.

    Published in:
    Canadian Journal of Anaesthesia / Journal Canadien d'Anesthésie, 1988, v. 35, n. 3, p. 323, doi. 10.1007/BF03010643
    By:
    • Humphrey, David;
    • Artru, Alan
    Publication type:
    Article
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    Engineered hexavalent Fc proteins with enhanced Fc-gamma receptor avidity provide insights into immune-complex interactions.

    Published in:
    Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0149-9
    By:
    • Rowley, Tania F.;
    • Peters, Shirley J.;
    • Aylott, Mike;
    • Griffin, Robert;
    • Davies, Nicola L.;
    • Healy, Louise J.;
    • Cutler, Rona M.;
    • Eddleston, Alison;
    • Pither, Thomas L.;
    • Sopp, Joshua M.;
    • Zaccheo, Oliver;
    • Fossati, Gianluca;
    • Cain, Katharine;
    • Ventom, Andrew M.;
    • Hailu, Hanna;
    • Ward, Eleanor J.;
    • Sherington, John;
    • Brennan, Frank R.;
    • Fallah-Arani, Farnaz;
    • Humphreys, David P.
    Publication type:
    Article
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    Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line.

    Published in:
    eLife, 2023, p. 1, doi. 10.7554/eLife.83606
    By:
    • Marjaneh, Mahdi Moradi;
    • Kirk, Edwin P.;
    • Patrick, Ralph;
    • Alankarage, Dimuthu;
    • Humphreys, David T.;
    • Monte-Nieto, Gonzalo Del;
    • Cornejo-Paramo, Paola;
    • Janbandhu, Vaibhao;
    • Doan, Tram B.;
    • Dunwoodie, Sally L.;
    • Wong, Emily S.;
    • Moran, Chris;
    • Martin, Ian CA;
    • Thomson, Peter C.;
    • Harvey, Richard P.
    Publication type:
    Article
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    Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.

    Published in:
    Human Molecular Genetics, 2020, v. 29, n. 22, p. 3662, doi. 10.1093/hmg/ddaa258
    By:
    • Martin, Ella M M A;
    • Enriquez, Annabelle;
    • Sparrow, Duncan B;
    • Humphreys, David T;
    • McInerney-Leo, Aideen M;
    • Leo, Paul J;
    • Duncan, Emma L;
    • Iyer, Kavitha R;
    • Greasby, Joelene A;
    • Ip, Eddie;
    • Giannoulatou, Eleni;
    • Sheng, Delicia;
    • Wohler, Elizabeth;
    • Dimartino, Clémantine;
    • Amiel, Jeanne;
    • Capri, Yline;
    • Lehalle, Daphné;
    • Mory, Adi;
    • Wilnai, Yael;
    • Lebenthal, Yael
    Publication type:
    Article
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