檢索結果 - Dylan J. Murray

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  1. 1
    Ligation of CD38 suppresses human B lymphopoiesis.

    Ligation of CD38 suppresses human B lymphopoiesis. 由 M Kumagai, Elaine Coustan‐Smith, Dylan J. Murray, Olli Silvennoinen, K. Gopal Murti, William E. Evans, Fabio Malavasi, Dario Campana

    出版 1995
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    Artigo
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  2. 2
    The COVID-19 Pandemic and its Impact on Plastic Surgery in Europe – An ESPRAS Survey

    The COVID-19 Pandemic and its Impact on Plastic Surgery in Europe – An ESPRAS Survey 由 Riccardo E. Giunta, Konstantin Frank, Horácio Costa, Cenk Demirdöver, Giovanni Di Benedetto, Anna Elander, Mark Henley, Dylan J. Murray, Dirk J. Schaefer, Stephan Spendel, Olavi Vasar, Rado Žic

    出版 2020
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    Revisão
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  3. 3
    FACE-Q craniofacial module: Part 2 Psychometric properties of newly developed scales for children and young adults with facial conditions

    FACE-Q craniofacial module: Part 2 Psychometric properties of newly developed scales for children and young adults with facial conditions 由 Anne F. Klassen, Charlene Rae, Wong Riff, Rafael Denadai, Dylan J. Murray, Shirley Bracken, Douglas J. Courtemanche, Neil Bulstrode, Justine O’Hara, Daniel Butler, Jesse A. Goldstein, Ali Tassi, M. Hol, David Johnson, Ingrid M. Ganske, Lars Kölby, Susana Benítez, E. Breuning, Claudia Malic, Greg Allen, Andrea L. Pusic, Stefan Cano

    出版 2021
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    Artigo
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  4. 4
    FACE-Q Craniofacial Module: Part 1 validation of CLEFT-Q scales for use in children and young adults with facial conditions

    FACE-Q Craniofacial Module: Part 1 validation of CLEFT-Q scales for use in children and young adults with facial conditions 由 Anne F. Klassen, Charlene Rae, Karen WY Wong Riff, Neil Bulstrode, Rafael Denadai, Jesse A. Goldstein, M. Hol, Dylan J. Murray, Shirley Bracken, Douglas J. Courtemanche, Justine O’Hara, Daniel Butler, Ali Tassi, Claudia Malic, Ingrid M. Ganske, Yun Phua, Damian D. Marucci, David Johnson, Marc C. Swan, E. Breuning, Tim Goodacre, Andrea L. Pusic, Stefan Cano

    出版 2021
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    Artigo
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  5. 5
    Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

    Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis 由 Vikram Sharma, Aimée L Fenwick, Mia Brockop, Simon J. McGowan, Jacqueline A.C. Goos, A. Jeannette M. Hoogeboom, Angela F. Brady, Owase Jeelani, Sally Ann Lynch, John B. Mulliken, Dylan J. Murray, Julie Phipps, Elizabeth Sweeney, Susan Tomkins, Louise C. Wilson, Sophia Bennett, Richard J. Cornall, John Broxholme, Alexander Kanapin, David Johnson, Steven A. Wall, Peter J. van der Spek, Irene M. J. Mathijssen, Robert E. Maxson, Stephen R.F. Twigg, Andrew O.M. Wilkie

    出版 2013
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    Artigo
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