Rezultati - Dan Hanson

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  1. 1
    Exploring the spectrum of 3‐M syndrome, a primordial short stature disorder of disrupted ubiquitination

    Exploring the spectrum of 3‐M syndrome, a primordial short stature disorder of disrupted ubiquitination od Peter Clayton, Dan Hanson, Lucia Magee, Philip Murray, Emma Saunders, Sayeda N. Abu‐Amero, Gudrun E. Moore, Graeme Black

    Izdano 2012
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  2. 2
    Nuclear FAK Promotes Cell Proliferation and Survival through FERM-Enhanced p53 Degradation

    Nuclear FAK Promotes Cell Proliferation and Survival through FERM-Enhanced p53 Degradation od Ssang‐Taek Lim, Xiao Lei Chen, Yangmi Lim, Dan Hanson, Thanh‐Trang Vo, Kyle Howerton, Nicholas Larocque, Susan J. Fisher, David D. Schlaepfer, Duško Ilić

    Izdano 2008
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  3. 3
    The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1

    The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1 od Dan Hanson, Philip Murray, Amit Sud, Samia A. Temtamy, Mona Aglan, Andrea Superti‐Furga, Sue Holder, Jill Urquhart, Emma Hilton, Forbes D.C. Manson, Peter Scambler, Graeme Black, Peter Clayton

    Izdano 2009
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  4. 4
    Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

    Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth od Dan Hanson, Philip Murray, James O’Sullivan, Jill Urquhart, Sarah B. Daly, Sanjeev S. Bhaskar, Leslie G. Biesecker, Mars Skae, Claire E. L. Smith, Trevor Cole, Jeremy Kirk, Kate Chandler, Helen Kingston, Dian Donnai, Peter Clayton, Graeme Black

    Izdano 2011
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  5. 5
    An<i>XRCC4</i>Splice Mutation Associated With Severe Short Stature, Gonadal Failure, and Early-Onset Metabolic Syndrome

    An<i>XRCC4</i>Splice Mutation Associated With Severe Short Stature, Gonadal Failure, and Early-Onset Metabolic Syndrome od Christiaan de Bruin, Verónica Mericq, Shayne F. Andrew, Hermine A. van Duyvenvoorde, Nicole S. Verkaik, Monique Losekoot, Aleksey Porollo, Hernán García, Yi Kuang, Dan Hanson, Peter Clayton, Dik C. van Gent, Jan M. Wit, Vivian Hwa, Andrew Dauber

    Izdano 2015
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  6. 6
    Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling

    Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling od Dan Hanson, Philip Murray, Tessa Coulson, Amit Sud, Ajibola Omokanye, Emily Stratta, Faezeh Sakhinia, C Bonshek, Laura C. Wilson, Emma Wakeling, Samia A. Temtamy, Mona Aglan, Elisabeth Rosser, Sahar Mansour, Atilano Carcavilla, Sheela Nampoothiri, Waqas Khan, Indraneel Banerjee, Kate Chandler, Graeme Black, Peter Clayton

    Izdano 2012
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