Search Results - Silvia Martin‐Almedina

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  1. 1
    Human phenotypes caused by <i>PIEZO1</i> mutations; one gene, two overlapping phenotypes?

    Human phenotypes caused by <i>PIEZO1</i> mutations; one gene, two overlapping phenotypes? by Silvia Martin‐Almedina, Sahar Mansour, Pia Østergaard

    Published 2018
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  2. 2
    Development and physiological functions of the lymphatic system: insights from human genetic studies of primary lymphedema

    Development and physiological functions of the lymphatic system: insights from human genetic studies of primary lymphedema by Silvia Martin‐Almedina, Peter Mortimer, Pia Østergaard

    Published 2021
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  3. 3
    Evolutionary perspective on annexin calcium-binding domains

    Evolutionary perspective on annexin calcium-binding domains by Reginald O. Morgan, Silvia Martin‐Almedina, Juan Manuel Iglesias, M.I. Gonzalez-Florez, María P. Fernández

    Published 2004
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  4. 4
    The Transcription Factor Erg Controls Endothelial Cell Quiescence by Repressing Activity of Nuclear Factor (NF)-κB p65

    The Transcription Factor Erg Controls Endothelial Cell Quiescence by Repressing Activity of Nuclear Factor (NF)-κB p65 by Nicola H. Dryden, Andrea Sperone, Silvia Martin‐Almedina, Rebecca Hannah, Graeme M. Birdsey, Samia Khan, Janice A. Layhadi, Justin C. Mason, Dorian O. Haskard, Berthold Göttgens, Anna M. Randi

    Published 2012
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  5. 5
    VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations

    VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations by René Hägerling, Dominik Drees, Aaron Scherzinger, Cathrin Dierkes, Silvia Martin‐Almedina, Stefan Butz, Kristiana Gordon, Michael Schäfers, Klaus Hinrichs, Pia Østergaard, Dietmar Vestweber, Tobias Goerge, Sahar Mansour, Xiaoyi Jiang, Peter Mortimer, Friedemann Kiefer

    Published 2017
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  6. 6
    Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

    Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis by Elisavet Fotiou, Silvia Martin‐Almedina, Michael A. Simpson, Shin Lin, Kristiana Gordon, Glen Brice, Giles Atton, Iona Jeffery, David C. Rees, Cyril Mignot, Julie Vogt, Tessa Homfray, M Snyder, Stanley G. Rockson, Steve Jeffery, Peter Mortimer, Sahar Mansour, Pia Østergaard

    Published 2015
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  7. 7
    EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis

    EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis by Silvia Martin‐Almedina, Inés Martínez‐Corral, Rita Holdhus, Andres Vicente, Elisavet Fotiou, Shin Lin, Kjell Petersen, Michael A. Simpson, Alexander Hoischen, Christian Gilissen, Heather Jeffery, Giles Atton, Christina Karapouliou, Glen Brice, Kristiana Gordon, John Wiseman, Marianne Wedin, Stanley G. Rockson, Steve Jeffery, Peter Mortimer, M Snyder, Siren Berland, Sahar Mansour, Taija Mäkinen, Pia Østergaard

    Published 2016
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