檢索結果 - Neil V. Morgan

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  1. 1
    Venous Thrombosis Unchained: Pandora's Box of Non-Inflammatory Mechanisms

    Venous Thrombosis Unchained: Pandora's Box of Non-Inflammatory Mechanisms 由 Samuel Smith, Neil V. Morgan, Alexander Brill

    出版 2025
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  2. 2
    Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan

    Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan 由 Ben Johnson, Sarah J. Fletcher, Neil V. Morgan

    出版 2016
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  3. 3
    Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding

    Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding 由 Ibrahim Almazni, Rachel J. Stapley, Neil V. Morgan

    出版 2019
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  4. 4
    Genotyping and phenotyping of platelet function disorders

    Genotyping and phenotyping of platelet function disorders 由 Steve P. Watson, Gillian Lowe, Marie Lordkipanidzé, Neil V. Morgan

    出版 2013
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  5. 5
    High Frequency of Large Intragenic Deletions in the Fanconi Anemia Group A Gene

    High Frequency of Large Intragenic Deletions in the Fanconi Anemia Group A Gene 由 Neil V. Morgan, Alex J. Tipping, Hans Joenje, Christopher G. Mathew

    出版 1999
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  6. 6
    Comparison of multiple electrode aggregometry with lumi‐aggregometry for the diagnosis of patients with mild bleeding disorders

    Comparison of multiple electrode aggregometry with lumi‐aggregometry for the diagnosis of patients with mild bleeding disorders 由 Rashid Al Ghaithi, Sian Drake, Steve P. Watson, Neil V. Morgan, Paul Harrison

    出版 2017
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  7. 7
    Potential genetic causes of miscarriage in euploid pregnancies: a systematic review

    Potential genetic causes of miscarriage in euploid pregnancies: a systematic review 由 Emily Colley, Susan Hamilton, Paul Smith, Neil V. Morgan, Arri Coomarasamy, Stephanie Allen

    出版 2019
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  8. 8
    CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution

    CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution 由 Abdullah O. Khan, Victoria A. Simms, Jeremy A. Pike, Steven G. Thomas, Neil V. Morgan

    出版 2017
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  9. 9
    Germline mutation in DOK7 associated with fetal akinesia deformation sequence

    Germline mutation in DOK7 associated with fetal akinesia deformation sequence 由 Julie Vogt, Neil V. Morgan, Tamás Marton, Susan Maxwell, Benjamin J. Harrison, David Beeson, Eamonn R. Maher

    出版 2009
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  10. 10
    Paraneoplastic erythrocytosis associated with an inactivating point mutation of the von Hippel-Lindau gene in a renal cell carcinoma

    Paraneoplastic erythrocytosis associated with an inactivating point mutation of the von Hippel-Lindau gene in a renal cell carcinoma 由 Michael S. Wiesener, Melchior Seyfarth, Christina Warnecke, Jan Steffen Jürgensen, Christian Rosenberger, Neil V. Morgan, Eamonn R. Maher, Ulrich Frei, Kai‐Uwe Eckardt

    出版 2002
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  11. 11
    Mutation in GNE is associated with severe congenital thrombocytopenia

    Mutation in GNE is associated with severe congenital thrombocytopenia 由 Jane Wong Fütterer, Amanda Dalby, Gillian Lowe, Ben Johnson, Michael A. Simpson, Jayashree Motwani, Mike Williams, Steve P. Watson, Neil V. Morgan

    出版 2018
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  12. 12
    Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple Pterygium Syndrome/Fetal Akinesia Patients

    Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple Pterygium Syndrome/Fetal Akinesia Patients 由 Julie Vogt, Benjamin J. Harrison, Hayley Spearman, Judy Cossins, Sascha Vermeer, Lambert Naudin ten Cate, Neil V. Morgan, David Beeson, Eamonn R. Maher

    出版 2008
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  13. 13
    Schlafen 14 (SLFN14) is a novel antiviral factor involved in the control of viral replication

    Schlafen 14 (SLFN14) is a novel antiviral factor involved in the control of viral replication 由 Rak-Kyun Seong, Seong-Wook Seo, Ji-Ae Kim, Sarah J. Fletcher, Neil V. Morgan, Mukesh Kumar, Young Ki Choi, Ok Sarah Shin

    出版 2017
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  14. 14
    Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa

    Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa 由 A. J. Tipping, Tommy Pearson, Neil V. Morgan, Rachel A. Gibson, L. P. Kuyt, Charmaine Havenga, Éliane Gluckman, Hans Joenje, Thomy de Ravel, S Jansen, Christopher G. Mathew

    出版 2001
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  15. 15
    Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

    Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders 由 Vincenzo Leo, Neil V. Morgan, Danai Bem, Matthew L. Jones, Gillian Lowe, Marie Lordkipanidzé, Sian Drake, Michael A. Simpson, Paul Gissen, Andrew Mumford, Steve P. Watson, Mary E. Daly

    出版 2014
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  16. 16
    STAT2 deficiency and susceptibility to viral illness in humans

    STAT2 deficiency and susceptibility to viral illness in humans 由 Sophie Hambleton, Stephen Goodbourn, D. F. Young, Paul Dickinson, Siti Mardhiana Mohamad, Manoj Valappil, Naomi McGovern, Andrew J. Cant, Scott Hackett, Peter Ghazal, Neil V. Morgan, Richard E. Randall

    出版 2013
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  17. 17
    The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity

    The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity 由 Rune Busk Damgaard, Jennifer A. Walker, Paola Marco‐Casanova, Neil V. Morgan, Hannah Titheradge, P.R. Elliott, Duncan McHale, Eamonn R. Maher, Andrew N. J. McKenzie, David Komander

    出版 2016
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  18. 18
    HIF activation identifies early lesions in VHL kidneys

    HIF activation identifies early lesions in VHL kidneys 由 Stefano J. Mandriota, Kevin Turner, David R. Davies, Paul G. Murray, Neil V. Morgan, Heidi Sowter, Charles C. Wykoff, Eamonn R. Maher, Adrian L. Harris, Peter J. Ratcliffe, Patrick H. Maxwell

    出版 2002
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  19. 19
    Complementation Analysis in Fanconi Anemia: Assignment of the Reference FA-H Patient to Group A

    Complementation Analysis in Fanconi Anemia: Assignment of the Reference FA-H Patient to Group A 由 Hans Joenje, Marieke Levitus, Quinten Waisfisz, Alan D. D’Andrea, Irene García-Higuera, Tommy Pearson, Carola G.M. van Berkel, Martin A. Rooimans, Neil V. Morgan, Christopher G. Mathew, Fré Arwert

    出版 2000
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  20. 20
    A novel ESR2 frameshift mutation predisposes to medullary thyroid carcinoma and causes inappropriate RET expression

    A novel ESR2 frameshift mutation predisposes to medullary thyroid carcinoma and causes inappropriate RET expression 由 Martin L. Read, Joel Smith, Jon Hoffman, Vicki E. Smith, Neil V. Morgan, Christopher Campbell, N. Wake, John Watkinson, Yvonne Wallis, Eamonn R. Maher, Christopher J. McCabe, Emma R. Woodward

    出版 2017
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