檢索結果 - Gillian Carpenter

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  1. 1
    Functional Analysis of Individual Binding Activities of the Scaffold Protein eIF4G

    Functional Analysis of Individual Binding Activities of the Scaffold Protein eIF4G 由 Tracey M. Hinton, Mark J. Coldwell, Gillian Carpenter, Simon Morley, Virginia M. Pain

    出版 2006
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  2. 2
    Disruption of the Interaction of Mammalian Protein Synthesis Eukaryotic Initiation Factor 4B with the Poly(A)-binding Protein by Caspase- and Viral Protease-mediated Cleavages

    Disruption of the Interaction of Mammalian Protein Synthesis Eukaryotic Initiation Factor 4B with the Poly(A)-binding Protein by Caspase- and Viral Protease-mediated Cleavages 由 Martin Bushell, Wendy Wood, Gillian Carpenter, Virginia M. Pain, Simon Morley, Michael J. Clemens

    出版 2001
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  3. 3
    Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism

    Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism 由 Ghayda Mirzaa, Benjamin Vitre, Gillian Carpenter, I Abramowiçz, Joseph G. Gleeson, Alex R. Paciorkowski, Don W. Cleveland, William B. Dobyns, Mark O’Driscoll

    出版 2014
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  4. 4
    Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks

    Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks 由 Claudia Kerzendorfer, Annabel Whibley, Gillian Carpenter, Emily Outwin, Shih‐Chieh Chiang, Gillian Turner, Charles E. Schwartz, Sherif F. El‐Khamisy, F. Lucy Raymond, Mark O’Driscoll

    出版 2010
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  5. 5
    Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome

    Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome 由 Akio Tanaka, Sarah Weinel, Nikoletta Nagy, Mark O’Driscoll, Joey E. Lai‐Cheong, Carol L. Kulp‐Shorten, Alfred L. Knable, Gillian Carpenter, Sheila Fisher, Makiko Hiragun, Yuhki Yanase, Michihiro Hide, Jeffrey P. Callen, John A. McGrath

    出版 2012
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  6. 6
    Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance

    Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance 由 Felicity Payne, Rita Colnaghi, Nuno Rocha, Asha Seth, J. Ieuan Harris, Gillian Carpenter, William Bottomley, Eleanor Wheeler, Stephen Q. Wong, Vladimı́r Saudek, David B. Savage, Stephen O’Rahilly, Jean‐Claude Carel, Inês Barroso, Mark O’Driscoll, Robert K. Semple

    出版 2014
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  7. 7
    Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome

    Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome 由 Tomoo Ogi, Sarah Walker, Tom Stiff, Emma Hobson, Siripan Limsirichaikul, Gillian Carpenter, Katrina Prescott, Mohnish Suri, Philip J. Byrd, Michiko Matsuse, Norisato Mitsutake, Yuka Nakazawa, Pradeep Vasudevan, Margaret Barrow, Grant S. Stewart, A. Malcolm R. Taylor, Mark O’Driscoll, Penny A. Jeggo

    出版 2012
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