檢索結果 - Bertrand Vernay

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  1. 1
    Otx2 Regulates Subtype Specification and Neurogenesis in the Midbrain

    Otx2 Regulates Subtype Specification and Neurogenesis in the Midbrain 由 Bertrand Vernay, Muriel Koch, Flora M. Vaccarino, James Briscoe, Antonio Simeone, Ryoichiro Kageyama, Siew-Lan Ang

    出版 2005
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  2. 2
    Rho kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure

    Rho kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure 由 Sarah Escuin, Bertrand Vernay, Dawn Savery, Christine B. Gurniak, Walter Witke, Nicholas D. E. Greene, Andrew J. Copp

    出版 2015
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  3. 3
    Human γδ T Lymphocytes Are Licensed for Professional Antigen Presentation by Interaction with Opsonized Target Cells

    Human γδ T Lymphocytes Are Licensed for Professional Antigen Presentation by Interaction with Opsonized Target Cells 由 Nourredine Himoudi, Daniel A. Morgenstern, Mengyong Yan, Bertrand Vernay, Luísa Saraiva, Yin Wu, Cyrille J. Cohen, Kenth Gustafsson, John Anderson

    出版 2012
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  4. 4
    An essential function of the mitogen‐activated protein kinase Erk2 in mouse trophoblast development

    An essential function of the mitogen‐activated protein kinase Erk2 in mouse trophoblast development 由 Marc K. Saba-El-Leil, Francis Vella, Bertrand Vernay, Laure Voisin, Lan Chen, Nathalie Labrecque, Siew‐Lan Ang, Sylvain Meloche

    出版 2003
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  5. 5
    Protein deiminases: New players in the developmentally regulated loss of neural regenerative ability

    Protein deiminases: New players in the developmentally regulated loss of neural regenerative ability 由 Sigrun Lange, Stefanie Gögel, Kit‐Yi Leung, Bertrand Vernay, Anthony P. Nicholas, Corey P. Causey, Paul R. Thompson, Nicholas D. E. Greene, Patrizia Ferretti

    出版 2011
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  6. 6
    Injection of embryonic stem cell derived macrophages ameliorates fibrosis in a murine model of liver injury

    Injection of embryonic stem cell derived macrophages ameliorates fibrosis in a murine model of liver injury 由 Sharmin S. Haideri, Alison C. McKinnon, A. Helen Taylor, Phoebe M. Kirkwood, Philip J. Starkey Lewis, Eoghan O’Duibhir, Bertrand Vernay, Stuart J. Forbes, Lesley M. Forrester

    出版 2017
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  7. 7
    Increased Wingless ( <i>Wnt</i> ) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans

    Increased Wingless ( <i>Wnt</i> ) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans 由 Carles Gaston‐Massuet, Cynthia L. Andoniadou, Massimo Signore, Sujatha A. Jayakody, Nicoletta Charolidi, Roger Kyeyune, Bertrand Vernay, Thomas S. Jacques, Makoto M. Taketo, Paul Le Tissier, Mehul Dattani, Juan Pedro Martı́nez-Barberá

    出版 2011
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  8. 8
    Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling

    Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling 由 Elen Griffith, Sarah Walker, Carol-Anne Martin, Paola Vagnarelli, Tom Stiff, Bertrand Vernay, Nouriya Al Sanna, Anand Saggar, Ben C.J. Hamel, William C. Earnshaw, Penny A. Jeggo, Andrew P. Jackson, Mark O’Driscoll

    出版 2007
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  9. 9
    3D human liver tissue from pluripotent stem cells displays stable phenotype in vitro and supports compromised liver function in vivo

    3D human liver tissue from pluripotent stem cells displays stable phenotype in vitro and supports compromised liver function in vivo 由 Hassan Rashidi, N. Thin Luu, Salamah Mohammad Alwahsh, Maaria Ginai, Sharmin Alhaque, Hua Dong, Rute A. Tomaz, Bertrand Vernay, Vasanthy Vigneswara, John M. Hallett, Anil Chandrashekran, Anil Dhawan, Ludovic Vallier, Mark Bradley, Anthony Callanan, Stuart J. Forbes, Philip N. Newsome, David C. Hay

    出版 2018
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  10. 10
    The kinetochore protein,<i>CENPF</i>, is mutated in human ciliopathy and microcephaly phenotypes

    The kinetochore protein,<i>CENPF</i>, is mutated in human ciliopathy and microcephaly phenotypes 由 Aoife Waters, Rowan Asfahani, Paula Carroll, Louise S. Bicknell, Francesco Lescai, Alison Bright, Estelle Chanudet, Anthony G. Brooks, Sonja Christou-Savina, Guled A. Osman, Patrick R. Walsh, Chiara Bacchelli, Ariane Chapgier, Bertrand Vernay, David M. Bader, Charu Deshpande, Mary O’ Sullivan, Louise Ocaka, Horia Stanescu, Helen Stewart, Friedhelm Hildebrandt, Edgar A. Otto, Colin A. Johnson, Katarzyna Szymańska, Nicholas Katsanis, Erica E. Davis, Robert Kleta, Michael Hubank, Stephen Doxsey, Andrew P. Jackson, Elia Stupka, Mark Winey, Philip L. Beales

    出版 2015
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  11. 11
    Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

    Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome 由 Anna Thomas, Hywel Williams, Núria Setó‐Salvia, Chiara Bacchelli, Dagan Jenkins, Mary E. O’Sullivan, Konstantinos Mengrelis, Miho Ishida, Louise Ocaka, Estelle Chanudet, Chela James, Francesco Lescai, Glenn Anderson, Deborah Morrogh, Mina Ryten, Andrew Duncan, Yun Jin Pai, Jorge Saraiva, Fabiana Ramos, Bernadette Farren, Dawn E. Saunders, Bertrand Vernay, Paul Gissen, Anna Straatmaan-Iwanowska, Frank Baas, Nicholas Wood, Joshua Hersheson, Henry Houlden, Jane A. Hurst, Richard H. Scott, Maria Bitner‐Glindzicz, Gudrun E. Moore, Sérgio B. Sousa, Philip Stanier

    出版 2014
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