Cerebral cortex development: an outside‐in perspective von Agirman, Gulistan, Broix, Loïc, Nguyen, Laurent

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Coordination between Transport and Local Translation in Neurons von Broix, Loïc, Turchetto, Silvia, Nguyen, Laurent

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ATP-citrate lyase promotes axonal transport across species von Even, Aviel, Morelli, Giovanni, Turchetto, Silvia, Shilian, Michal, Bail, Romain Le, Laguesse, Sophie, Krusy, Nathalie, Brisker, Ariel, Brandis, Alexander, Inbar, Shani, Chariot, Alain, Saudou, Frédéric, Dietrich, Paula, Dragatsis, Ioannis, Brone, Bert, Broix, Loïc, Rigo, Jean-Michel, Weil, Miguel, Nguyen, Laurent

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The centrosome protein AKNA regulates neurogenesis via microtubule organization von Camargo Ortega, Germán, Falk, Sven, Johansson, Pia A., Peyre, Elise, Broix, Loïc, Sahu, Sanjeeb Kumar, Hirst, William, Schlichthaerle, Thomas, De Juan Romero, Camino, Draganova, Kalina, Vinopal, Stanislav, Chinnappa, Kaviya, Gavranovic, Anna, Karakaya, Tugay, Steininger, Thomas, Merl-Pham, Juliane, Feederle, Regina, Shao, Wei, Shi, Song-Hai, Hauck, Stefanie M., Jungmann, Ralf, Bradke, Frank, Borrell, Victor, Geerlof, Arie, Reber, Simone, Tiwari, Vijay K., Huttner, Wieland B., Wilsch-Bräuninger, Michaela, Nguyen, Laurent, Götz, Magdalena

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Publisher Correction: ATP-citrate lyase promotes axonal transport across species von Even, Aviel, Morelli, Giovanni, Turchetto, Silvia, Shilian, Michal, Bail, Romain Le, Laguesse, Sophie, Krusy, Nathalie, Brisker, Ariel, Brandis, Alexander, Inbar, Shani, Chariot, Alain, Saudou, Frédéric, Dietrich, Paula, Dragatsis, Ioannis, Brone, Bert, Broix, Loïc, Rigo, Jean-Michel, Weil, Miguel, Nguyen, Laurent

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Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development von Broix, Loïc, Asselin, Laure, Silva, Carla G, Ivanova, Ekaterina L, Tilly, Peggy, Gilet, Johan G, Lebrun, Nicolas, Jagline, Hélène, Muraca, Giuseppe, Saillour, Yoann, Drouot, Nathalie, Reilly, Madeline Louise, Francis, Fiona, Benmerah, Alexandre, Bahi-Buisson, Nadia, Belvindrah, Richard, Nguyen, Laurent, Godin, Juliette D, Chelly, Jamel, Hinckelmann, Maria-Victoria

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Ex Vivo Recording of Axonal Transport Dynamics on Postnatal Organotypic Cortical Slices von Turchetto, Silvia, Broix, Loic, Nguyen, Laurent

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Mutations in the HECT domain of NEDD4L lead to AKT–mTOR pathway deregulation and cause periventricular nodular heterotopia von Broix, Loïc, Jagline, Hélène, L Ivanova, Ekaterina, Schmucker, Stéphane, Drouot, Nathalie, Clayton-Smith, Jill, Pagnamenta, Alistair T, Metcalfe, Kay A, Isidor, Bertrand, Louvier, Ulrike Walther, Poduri, Annapurna, Taylor, Jenny C, Tilly, Peggy, Poirier, Karine, Saillour, Yoann, Lebrun, Nicolas, Stemmelen, Tristan, Rudolf, Gabrielle, Muraca, Giuseppe, Saintpierre, Benjamin, Elmorjani, Adrienne, Moïse, Martin, Weirauch, Nathalie Bednarek, Guerrini, Renzo, Boland, Anne, Olaso, Robert, Masson, Cecile, Tripathy, Ratna, Keays, David, Beldjord, Cherif, Nguyen, Laurent, Godin, Juliette, Kini, Usha, Nischké, Patrick, Deleuze, Jean-François, Bahi-Buisson, Nadia, Sumara, Izabela, Hinckelmann, Maria-Victoria, Chelly, Jamel

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ATAT1-enriched vesicles promote microtubule acetylation via axonal transport von Even, Aviel, Morelli, Giovanni, Broix, Loïc, Scaramuzzino, Chiara, Turchetto, Silvia, Gladwyn-Ng, Ivan, Le Bail, Romain, Shilian, Michal, Freeman, Stephen, Magiera, Maria M, Jijumon, A S, Krusy, Nathalie, Malgrange, Brigitte, Brone, Bert, Dietrich, Paula, Dragatsis, Ioannis, Janke, Carsten, Saudou, Frédéric, Weil, Miguel, Nguyen, Laurent

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Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown von Saillour, Yoann, Broix, Loïc, Bruel-Jungerman, Elodie, Lebrun, Nicolas, Muraca, Giuseppe, Rucci, Julien, Poirier, Karine, Belvindrah, Richard, Francis, Fiona, Chelly, Jamel

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Mosaic parental germline mutations causing recurrent forms of malformations of cortical development von Zillhardt, Julia Lauer, Poirier, Karine, Broix, Loïc, Lebrun, Nicolas, Elmorjani, Adrienne, Martinovic, Jelena, Saillour, Yoann, Muraca, Giuseppe, Nectoux, Juliette, Bessieres, Bettina, Fallet-Bianco, Catherine, Lyonnet, Stanislas, Dulac, Olivier, Odent, Sylvie, Rejeb, Imen, Ben Jemaa, Lamia, Rivier, Francois, Pinson, Lucile, Geneviève, David, Musizzano, Yuri, Bigi, Nicole, Leboucq, Nicolas, Giuliano, Fabienne, Philip, Nicole, Vilain, Catheline, Van Bogaert, Patrick, Maurey, Hélène, Beldjord, Cherif, Artiguenave, François, Boland, Anne, Olaso, Robert, Masson, Cécile, Nitschké, Patrick, Deleuze, Jean-François, Bahi-Buisson, Nadia, Chelly, Jamel

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HOXC4 homeoprotein efficiently expands human hematopoietic stem cells and triggers similar molecular alterations as HOXB4 von AUVRAY, Céline, DELAHAYE, Andrée, VIGON, Isabelle, PFLUMIO, Frangoise, HADDAD, Rima, AMSELLEM, Sophie, MIRI-NEZHAD, Ayda, BROIX, Loïc, YACIA, Azzedine, BULLE, Frédérique, FICHELSON, Serge

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Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly von Poirier, Karine, Lebrun, Nicolas, Broix, Loic, Tian, Guoling, Saillour, Yoann, Boscheron, Cécile, Parrini, Elena, Valence, Stephanie, Pierre, Benjamin Saint, Oger, Madison, Lacombe, Didier, Geneviève, David, Fontana, Elena, Darra, Franscesca, Cances, Claude, Barth, Magalie, Bonneau, Dominique, Bernadina, Bernardo Dalla, N'Guyen, Sylvie, Gitiaux, Cyril, Parent, Philippe, des Portes, Vincent, Pedespan, Jean Michel, Legrez, Victoire, Castelnau-Ptakine, Laetitia, Nitschke, Patrick, Hieu, Thierry, Masson, Cecile, Zelenika, Diana, Andrieux, Annie, Francis, Fiona, Guerrini, Renzo, Cowan, Nicholas J, Bahi-Buisson, Nadia, Chelly, Jamel

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TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis von Ivanova, Ekaterina L., Gilet, Johan G., Sulimenko, Vadym, Duchon, Arnaud, Rudolf, Gabrielle, Runge, Karen, Collins, Stephan C., Asselin, Laure, Broix, Loic, Drouot, Nathalie, Tilly, Peggy, Nusbaum, Patrick, Vincent, Alexandre, Magnant, William, Skory, Valerie, Birling, Marie-Christine, Pavlovic, Guillaume, Godin, Juliette D., Yalcin, Binnaz, Hérault, Yann, Dráber, Pavel, Chelly, Jamel, Hinckelmann, Maria-Victoria

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Molecular Analysis of Axonal Transport Dynamics upon Modulation of Microtubule Acetylation von Turchetto, Silvia, Le Bail, Romain, Broix, Loïc, Nguyen, Laurent

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Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development von Broix, Loïc, Asselin, Laure, Silva, Carla, Ivanova, Ekaterina, Tilly, Peggy, Gilet, Johan, Lebrun, Nicolas, Jagline, Hélène, Muraca, Giuseppe, Saillour, Yoann, Drouot, Nathalie, Reilly, Madeline Louise, Francis, Fiona, Benmerah, Alexandre, Bahi-Buisson, Nadia, Belvindrah, Richard, Nguyen, Laurent, Godin, Juliette, Chelly, Jamel, Hinckelmann, Maria-Victoria

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Compréhension des mécanismes physiopathologiques des malformations du développement cortical associées à des mutations dans les gènes KIF2A et NEDD4L von Broix, Loïc

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Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny von Gilet, Johan G, Ivanova, Ekaterina L, Trofimova, Daria, Rudolf, Gabrielle, Meziane, Hamid, Broix, Loic, Drouot, Nathalie, Courraud, Jeremie, Skory, Valerie, Voulleminot, Paul, Osipenko, Maria, Bahi-Buisson, Nadia, Yalcin, Binnaz, Birling, Marie-Christine, Hinckelmann, Maria-Victoria, Kwok, Benjamin H, Allingham, John S, Chelly, Jamel

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Erratum: Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly von Poirier, Karine, Lebrun, Nicolas, Broix, Loic, Tian, Guoling, Saillour, Yoann, Boscheron, Cécile, Parrini, Elena, Valence, Stephanie, Pierre, Benjamin Saint, Oger, Madison, Lacombe, Didier, Geneviève, David, Fontana, Elena, Darra, Franscesca, Cances, Claude, Barth, Magalie, Bonneau, Dominique, Bernadina, Bernardo Dalla, N'Guyen, Sylvie, Gitiaux, Cyril, Parent, Philippe, des Portes, Vincent, Pedespan, Jean Michel, Legrez, Victoire, Castelnau-Ptakine, Laetitia, Nitschke, Patrick, Hieu, Thierry, Masson, Cecile, Zelenika, Diana, Andrieux, Annie, Francis, Fiona, Guerrini, Renzo, Cowan, Nicholas J, Bahi-Buisson, Nadia, Chelly, Jamel

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Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly von Poirier, Karine, Lebrun, Nicolas, Broix, Loic, Tian, Guoling, Saillour, Yoann, Boscheron, Cecile, Parrini, Elena, Valence, Stephanie, Pierre, Benjamin Saint, Oger, Madison, Lacombe, Didier, Genevieve, David, Fontana, Elena, Darra, Franscesca, Cances, Claude, Barth, Magalie, Bonneau, Dominique, Bernadina, Bernardo Dalla, N'Guyen, Sylvie, Gitiaux, Cyril, Parent, Philippe, des Portes, Vincent, Pedespan, Jean Michel, Legrez, Victoire, Castelnau-Ptakine, Laetitia, Nitschke, Patrick, Hieu, Thierry, Masson, Cecile, Zelenika, Diana, Andrieux, Annie, Francis, Fiona, Guerrini, Renzo, Cowan, Nicholas J, Bahi-Buisson, Nadia, Chelly, Jamel

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