Ngā hua rapu - Françoise Phan Dinh Tuy

  • E whakaatu ana i te 1 - 9 hua o te 9
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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 mā Maurice Petitou, Françoise Phan Dinh Tuy, C. Rosenfeld, Z. Mishal, Isabelle Pignot‐Paintrand, C. Jasnin, G Mathé, Michael Inbar

    I whakaputaina 1978
    Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    Human disorders of cortical development: from past to present

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

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    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. mā 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

    I whakaputaina 1981
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2006
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    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 mā 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

    I whakaputaina 2008
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2014
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    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 mā 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

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Artigo
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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>) mā 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

    I whakaputaina 2007
    Whiwhi kuputuhi katoa
    Artigo
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