Natalia Denisenko, Carmen Cifuentes-Diaz, Theano Irinopoulou, Michèle Carnaud, Evelyne Benoit, Michiko Niwa-Kawakita, Fabrice Chareyre, Marco Giovannini, Jean-Antoine Girault, Laurence Goutebroze J Neurosci. 2008 Oct 15;28(42):10472-81.
Publications of the Francis / Goutebroze Team
CORTICAL DEVELOPMENT AND PATHOLOGY
The location of DCX mutations predicts malformation severity in X-linked lissencephaly.
Pierre-Louis Leger, Isabelle Souville, Nathalie Boddaert, Caroline Elie, Jean Marc Pinard, Perrine Plouin, Marie Laure Moutard, Vincent des Portes, Hilde Van Esch, Sylvie Joriot, Jean Louis Renard, Jamel Chelly, Fiona Francis, Cherif Beldjord, Nadia Bahi-Buisson Neurogenetics. 2008 Oct;9(4):277-85.
Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.
Catherine Fallet-Bianco, Laurence Loeuillet, Karine Poirier, Philippe Loget, Françoise Chapon, Laurent Pasquier, Yoann Saillour, Cherif Beldjord, Jamel Chelly, Fiona Francis Brain. 2008 Sep;131(Pt 9):2304-20.
Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus.
Marika Nosten-Bertrand, Caroline Kappeler, Céline Dinocourt, Cécile Denis, Johanne Germain, Françoise Phan Dinh Tuy, Soraya Verstraeten, Chantal Alvarez, Christine Métin, Jamel Chelly, Bruno Giros, Richard Miles, Antoine Depaulis, Fiona Francis PLoS One. 2008 Jun 25;3(6):e2473.
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).
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, Robert J Harvey, Christian Siebold, Jonathan Flint, Chérif Beldjord, Jamel Chelly Hum Mutat. […]
Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency.
Caroline Kappeler, Marc Dhenain, Françoise Phan Dinh Tuy, Yoann Saillour, Serge Marty, Catherine Fallet-Bianco, Isabelle Souville, Evelyne Souil, Jean-Marc Pinard, Gundela Meyer, Ferechté Encha-Razavi, Andreas Volk, Cherif Beldjord, Jamel Chelly, Fiona Francis J Comp Neurol. 2007 Jan 10;500(2):239-54.
PGY repeats and N-glycans govern the trafficking of paranodin and its selective association with contactin and neurofascin-155.
Carine Bonnon, Christophe Bel, Laurence Goutebroze, Bernard Maigret, Jean-Antoine Girault, Catherine Faivre-Sarrailh Mol Biol Cell. 2007 Jan;18(1):229-41.
