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

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

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

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Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus von Nosten-Bertrand, Marika, Kappeler, Caroline, Dinocourt, Céline, Denis, Cécile, Germain, Johanne, Phan Dinh Tuy, Françoise, Verstraeten, Soraya, Alvarez, Chantal, Métin, Christine, Chelly, Jamel, Giros, Bruno, Miles, Richard, Depaulis, Antoine, Francis, Fiona

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Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria von Jaglin, Xavier Hubert, Poirier, Karine, Saillour, Yoann, Buhler, Emmanuelle, Tian, Guoling, Bahi-Buisson, Nadia, Fallet-Bianco, Catherine, Phan-Dinh-Tuy, Françoise, Kong, Xiang Peng, Bomont, Pascale, Castelnau-Ptakhine, Laëtitia, Odent, Sylvie, Loget, Philippe, Kossorotoff, Manoelle, Snoeck, Irina, Plessis, Ghislaine, Parent, Philippe, Beldjord, Cherif, Cardoso, Carlos, Represa, Alfonso, Flint, Jonathan, Keays, David Anthony, Cowan, Nicholas Justin, Chelly, Jamel

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Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes von Watkins-Chow, Dawn E, Cooke, Joanna, Pidsley, Ruth, Edwards, Andrew, Slotkin, Rebecca, Leeds, Karen E, Mullen, Raymond, Baxter, Laura L, Campbell, Thomas G, Salzer, Marion C, Biondini, Laura, Gibney, Gretchen, Phan Dinh Tuy, Françoise, Chelly, Jamel, Morris, H Douglas, Riegler, Johannes, Lythgoe, Mark F, Arkell, Ruth M, Loreni, Fabrizio, Flint, Jonathan, Pavan, William J, Keays, David A

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Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency von Kappeler, Caroline, Dhenain, Marc, Phan Dinh Tuy, Françoise, Saillour, Yoann, Marty, Serge, Fallet-Bianco, Catherine, Souville, Isabelle, Souil, Evelyne, Pinard, Jean-Marc, Meyer, Gundela, Encha-Razavi, Ferechté, Volk, Andreas, Beldjord, Cherif, Chelly, Jamel, Francis, Fiona

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Novel Target Sequences for Pax-6 in the Brain-specific Activating Regions of the Rat Aldolase C Gene von Skala-Rubinson, Henriette, Vinh, Joëlle, Labas, Valérie, Kahn, Axel, Tuy, Françoise Phan Dinh

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Alternative Transcripts of Dclk1 and Dclk2 and Their Expression in Doublecortin Knockout Mice von Phan Dinh Tuy, Françoise, Saillour, Yoann, Kappeler, Caroline, Chelly, Jamel, Francis, Fiona

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Mutations in the [beta]-tubulin gene TUBB2B result in asymmetrical polymicrogyria von Jaglin, Xavier Hubert, Poirier, Karine, Saillour, Yoann, Buhler, Emmanuelle, Tian, Guoling, Bahi-Buisson, Nadia, Fallet-Bianco, Catherine, Phan-Dinh-Tuy, Françoise, Kong, Xiang Peng, Bomont, Pascale, Castelnau-Ptakhine, Laëtitia, Odent, Sylvie, Loget, Philippe, Kossorotoff, Manoelle, Snoeck, Irina, Plessis, Ghislaine, Parent, Philippe, Beldjord, Cherif, Cardoso, Carlos, Represa, Alfonso, Flint, Jonathan, Keays, David Anthony, Cowan, Nicholas Justin, Chelly, Jamel

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

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

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Mutations du gène EML1/Eml1, progéniteurs neuronaux et hétérotopies chez l’homme et la souris von Kielar, Michel, Phan Dinh Tuy, Françoise, Bizzotto, Sara, Belvindrah, Richard, Croquelois, Alexandre, Francis, Fiona

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

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REVIEW ARTICLE: Human disorders of cortical development: from past to present von Francis, Fiona, Meyer, Gundela, Fallet-Bianco, Catherine, Moreno, Sarah, Kappeler, Caroline, Socorro, Alfredo Cabrera, Tuy, Francoise Phan Dinh, Beldjord, Cherif, Chelly, Jamel

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Mutations in Eml1/EML1 lead to ectopic progenitors and neuronal heterotopia in mouse and human von Kielar, Michel, Phan Dinh Tuy, Françoise, Bizzotto, Sara, Belvindrah, Richard, Croquelois, Alexandre, Francis, Fiona

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Metabolism of proline in a human leukemic lymphoblastoid cell line von Lorans, G, Rosenfeld, C, Petitou, M, Phan-Dinh-Tuy, F, Mathé, G

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Bidirectional activity and orientation-dependent specificity of the rat aldolase C promoter in transgenic mice von Phan Dinh Tuy, Françoise, Porteu, Arlette, Kahn, Axel, Skala, Henriette

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High tyrosine kinase activity in normal nonproliferating cells von Dinh Tuy, Francoise Phan, Henry, Joëlle, Rosenfeld, Claude, Kahn, Axel

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DEFICIT OF SUPPRESSOR T CELLS IN ACTIVE MULTIPLE SCLEROSIS von Bach, Marie-Anne, Tournier, Elizabeth, Phan-Dinh-Tuy, Francoise, Chatenoud, Lucienne, Bach, Jean-Francois, Martin, Claude, Degos, Jean-Denis

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