检索结果 - Françoise Phan Dinh Tuy

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  1. 1
    Decreased microviscosity of membrane lipids in leukemic cells: Two possible mechanisms

    Decreased microviscosity of membrane lipids in leukemic cells: Two possible mechanisms 由 Maurice Petitou, Françoise Phan Dinh Tuy, C. Rosenfeld, Z. Mishal, Isabelle Pignot‐Paintrand, C. Jasnin, G Mathé, Michael Inbar

    出版 1978
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  2. 2
    Human disorders of cortical development: from past to present

    Human disorders of cortical development: from past to present 由 Fiona Francis, Gundela Meyer, Catherine Fallet‐Bianco, Sarah Moreno, Caroline Kappeler, Alfredo Cabrera Socorro, Françoise Phan Dinh Tuy, Chérif Beldjord, Jamel Chelly

    出版 2006
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    Revisão
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  3. 3
    Unusual phenotypes of human inducer T cells as measured by OKT4 and related monoclonal antibodies.

    Unusual phenotypes of human inducer T cells as measured by OKT4 and related monoclonal antibodies. 由 Mark A. Bach, Françoise Phan-Dinh-Tuy, Jean‐François Bach, Donald F. H. Wallach, William E. Biddison, S O Sharrow, Gideon Goldstein, Patrick C. Kung

    出版 1981
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  4. 4
    Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice

    Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice 由 Caroline Kappeler, Yoann Saillour, Jean‐Pierre Baudoin, Françoise Phan Dinh Tuy, Chantal Alvarez, Christophe Houbron, Patrícia Gaspar, Ghislaine Hamard, Jamel Chelly, Christine Métin, Fiona Francis

    出版 2006
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    Artigo
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  5. 5
    Epilepsy in Dcx Knockout Mice Associated with Discrete Lamination Defects and Enhanced Excitability in the Hippocampus

    Epilepsy in Dcx Knockout Mice Associated with Discrete Lamination Defects and Enhanced Excitability in the Hippocampus 由 Marika Nosten‐Bertrand, Caroline Kappeler, Céline Dinocourt, Cécile V. Denis, Johanne Germain, Françoise Phan Dinh Tuy, Soraya Verstraeten, Chantal Alvarez, Christine Métin, Jamel Chelly, Bruno Giros, Richard Miles, Antoine Depaulis, Fiona Francis

    出版 2008
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  6. 6
    Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human

    Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human 由 Michel Kielar, Françoise Phan Dinh Tuy, Sara Bizzotto, Cécile Lebrand, Camino de Juan Romero, Karine Poirier, Renske Oegema, Grazia M.S. Mancini, Nadia Bahi‐Buisson, Robert Olaso, Anne‐Gaëlle Le Moing, Katia Boutourlinsky, Dominique Boucher, Wassila Carpentier, Patrick Berquin, Jean‐François Deleuze, Richard Belvindrah, Vı́ctor Borrell, Egbert Welker, Jamel Chelly, Alexandre Croquelois, Fiona Francis

    出版 2014
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  7. 7
    Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

    Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes 由 Dawn E. Watkins‐Chow, Joanna Cooke, Ruth Pidsley, Andrew Edwards, R. Keith Slotkin, Karen E. Leeds, Raymond Mullen, Laura L. Baxter, Thomas G. Campbell, Marion Claudia Salzer, Laura Biondini, Gretchen Gibney, Françoise Phan Dinh Tuy, Jamel Chelly, H Douglas Morris, Johannes Riegler, Mark F. Lythgoe, Ruth M. Arkell, Fabrizio Loreni, Jonathan Flint, William J. Pavan, David A. Keays

    出版 2013
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    Artigo
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  8. 8
    Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria

    Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria 由 Xavier H. Jaglin, Karine Poirier, Yoann Saillour, Emmanuelle Buhler, Guoling Tian, Nadia Bahi‐Buisson, Catherine Fallet‐Bianco, Françoise Phan-Dinh-Tuy, Xiang‐Peng Kong, Pascale Bomont, Laëtitia Castelnau-Ptakhine, Sylvie Odent, Philippe Loget, Manoëlle Kossorotoff, I. Snoeck, Ghislaine Plessis, Philippe Parent, Chérif Beldjord, Carlos Cardoso, Alfonso Represa, Jonathan Flint, David A. Keays, Nicholas J. Cowan, Jamel Chelly

    出版 2009
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  9. 9
    Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (<i>TUBA1A</i>)

    Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (<i>TUBA1A</i>) 由 Karine Poirier, David A. Keays, Fiona Francis, Yoann Saillour, Nadia Bahi, Sylvie Manouvrier, Catherine Fallet‐Bianco, Laurent Pasquier, Annick Toutain, Françoise Phan Dinh Tuy, Thierry Bienvenu, Sylvie Joriot, Sylvie Odent, Dorothée Ville, Isabelle Desguerre, Alice Goldenberg, Marie‐Laure Moutard, Jean‐Pierre Fryns, Hilde Van Esch, Victoria L. Harvey, Christian Siebold, Jonathan Flint, Chérif Beldjord, Jamel Chelly

    出版 2007
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