Torthaí cuardaigh - Phil Ancliff

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  1. 1
    Recent advances in the understanding of genetic defects of neutrophil number and function

    Recent advances in the understanding of genetic defects of neutrophil number and function de réir Gerben Bouma, Phil Ancliff, Adrian J. Thrasher, Siobhán O. Burns

    Foilsithe / Cruthaithe 2010
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    Revisão
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  2. 2
    Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease

    Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of... de réir Phil Ancliff, Rosemary E. Gale, Ri Liesner, Ian Hann, David C. Linch

    Foilsithe / Cruthaithe 2001
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    Artigo
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  3. 3
    Notch-1 Mutations Are Secondary Events in Some Patients with T-Cell Acute Lymphoblastic Leukemia

    Notch-1 Mutations Are Secondary Events in Some Patients with T-Cell Acute Lymphoblastic Leukemia de réir Marc R. Mansour, Veronique Duke, Letizia Foroni, Bella Patel, Christopher Allen, Phil Ancliff, Rosemary E. Gale, David C. Linch

    Foilsithe / Cruthaithe 2007
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    Artigo
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  4. 4
    <i><scp>GATA</scp>2</i> mutations in sporadic and familial acute myeloid leukaemia patients with <i><scp>CEBPA</scp></i> mutations

    <i><scp>GATA</scp>2</i> mutations in sporadic and familial acute myeloid leukaemia patients with <i><scp>CEBPA</scp></i> mutations de réir Claire L. Green, Kiran Tawana, Robert K. Hills, Csaba Bödör, Jude Fitzgibbon, Sarah Inglott, Phil Ancliff, Alan K. Burnett, David C. Linch, Rosemary E. Gale

    Foilsithe / Cruthaithe 2013
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    Artigo
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  5. 5
    MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia

    MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia de réir Manuela Germeshausen, Phil Ancliff, Jaime Estrada, Markus Metzler, Eva Ponstingl, Horst Rütschle, Dirk Schwabe, Richard H. Scott, Şule Ünal, Angela Wawer, Bernward Zeller, Matthias Ballmaier

    Foilsithe / Cruthaithe 2018
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    Artigo
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  6. 6
    Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia

    Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia de réir Dale Moulding, Michael P. Blundell, David G. Spiller, Michael White, Giles O. Cory, Yolanda Calle, Helena Kempski, Jo Sinclair, Phil Ancliff, Christine Kinnon, Gareth E. Jones, Adrian J. Thrasher

    Foilsithe / Cruthaithe 2007
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    Artigo
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  7. 7
    Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

    Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia de réir Phil Ancliff, Michael P. Blundell, Giles O. Cory, Yolanda Calle, Austen Worth, Helena Kempski, Siobhán O. Burns, Gareth E. Jones, Jo Sinclair, Christine Kinnon, Ian Hann, Rosemary E. Gale, David C. Linch, Adrian J. Thrasher

    Foilsithe / Cruthaithe 2006
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    Artigo
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  8. 8
    Targeting acute myeloid leukemia by drug-induced c-MYB degradation

    Targeting acute myeloid leukemia by drug-induced c-MYB degradation de réir Vanessa Walf-Vorderwülbecke, Kerra Pearce, Tony Brooks, Michael Hubank, M M van den Heuvel-Eibrink, C. Michel Zwaan, Stuart Adams, Dylan R. Edwards, Jack Bartram, Sujith Samarasinghe, Phil Ancliff, Asim Khwaja, Nicholas Goulden, Gareth Williams, Jasper de Boer, Owen Williams

    Foilsithe / Cruthaithe 2017
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  9. 9
    Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia

    Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia de réir Virginia Turati, José Afonso Guerra‐Assunção, Nicola Potter, Rajeev Gupta, Simone Ecker, Agne Daneviciute, Maxime Tarabichi, Amy P. Webster, Chuling Ding, Gillian May, Chela James, John Brown, Lucía Conde, Lisa J. Russell, Phil Ancliff, Sarah Inglott, Giovanni Cazzaniga, Andrea Biondi, Georgina Hall, Mark Lynch, Michael Hubank, Iain C. Macaulay, Stephan Beck, Peter Van Loo, Sten Eirik W. Jacobsen, Mel Greaves, Javier Herrero, Tariq Enver

    Foilsithe / Cruthaithe 2021
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  10. 10
    Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow Transplantation

    Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow Transplantation de réir Francesca Fioredda, Simona Iacobelli, Anja van Biezen, Bobby Gaspar, Phil Ancliff, Jean Donadieu, Mahmoud Aljurf, Christina Peters, Michaela Calvillo, Susanne Matthes‐Martin, Giuseppe Morreale, Nelleke van ’t Veer-Tazelaar, Liesbeth C. de Wreede, Amal Al Seraihy, Akif Yeşilipek, Alain Fischer, Marc Bierings, Gülyüz Öztürk, Owen Smith, Paul Veys, Per Ljungman, Régis Peffault de Latour, José Sánchez de Toledo Codina, Reuven Or, Arnold Ganser, Boris V. Afanasyev, Robert Wynn, Krzysztof Kałwak, Judith Marsh, Carlo Dufour

    Foilsithe / Cruthaithe 2015
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  11. 11
    Benefits for children with suspected cancer from routine whole-genome sequencing

    Benefits for children with suspected cancer from routine whole-genome sequencing de réir Angus Hodder, Sarah M. Leiter, Jonathan Kennedy, Dilys Addy, Munaza Ahmed, Thankamma Ajithkumar, Kieren Allinson, Phil Ancliff, Shivani Bailey, Gemma Barnard, G.A. Amos Burke, Charlotte Burns, Julian Cano-Flanagan, Jane Chalker, Nicholas Coleman, Danny Cheng, Yasmin Clinch, C Dryden, Sara Ghorashian, Blanche Griffin, Gail Horan, Michael Hubank, Phillippa May, Joanna McDerra, Rajvi Nagrecha, James C. Nicholson, David O’Connor, Vesna Pavasovic, Annelies Quaegebeur, Anupama Rao, Thomas C. Roberts, Sujith Samarasinghe, Iryna Stasevich, John A. Tadross, Claire Trayers, Jamie Trotman, Ajay Vora, James Watkins, Lyn S. Chitty, Sarah Bowdin, Ruth Armstrong, Matthew J. Murray, Catherine Elizabeth Hook, Patrick Tarpey, Aditi Vedi, Jack Bartram, Sam Behjati

    Foilsithe / Cruthaithe 2024
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