TECPR1 promotes aggrephagy by direct recruitment of LC3C autophagosomes to lysosomes von Wetzel, Lisa, Blanchard, Stéphane, Rama, Sowmya, Beier, Viola, Kaufmann, Anna, Wollert, Thomas

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ATG16L1 induces the formation of phagophore-like membrane cups von Mohan, Jagan, Moparthi, Satish B., Girard-Blanc, Christine, Campisi, Daniele, Blanchard, Stéphane, Nugues, Charlotte, Rama, Sowmya, Salles, Audrey, Pénard, Esthel, Vassilopoulos, Stéphane, Wollert, Thomas

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Alsin/Rac1 signaling controls survival and growth of spinal motoneurons von Jacquier, Arnaud, Buhler, Emmanuelle, Schäfer, Michael K. E., Bohl, Delphine, Blanchard, Stephane, Beclin, Christophe, Haase, Georg

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Human polymorphisms in nicotinic receptors: a functional analysis in iPS‐derived dopaminergic neurons von Deflorio, Cristina, Blanchard, Stíephane, Carisì, Maria Carla, Bohl, Delphine, Maskos, Uwe

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Neurofilament accumulations in amyotrophic lateral sclerosis patients’ motor neurons impair axonal initial segment integrity von Lefebvre-Omar, Cynthia, Liu, Elise, Dalle, Carine, d’Incamps, Boris Lamotte, Bigou, Stéphanie, Daube, Clément, Karpf, Léa, Davenne, Marc, Robil, Noémie, Jost Mousseau, Coline, Blanchard, Stéphane, Tournaire, Guillaume, Nicaise, Charles, Salachas, François, Lacomblez, Lucette, Seilhean, Danielle, Lobsiger, Christian S., Millecamps, Stéphanie, Boillée, Séverine, Bohl, Delphine

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Functional maturation of human iPSC-derived pyramidal neurons in vivo is dependent on proximity with the host tissue von Raïs, Célia, Gaspar Santos, Daniela, Sansone, Giulia, Blanchard, Stéphane, Bourgeois, Jean-Pierre, Jagla, Bernd, Saudemont, Baptiste, Schlick, Laurène, Pons, Stéphanie, Maskos, Uwe

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Long-term development of human iPSC-derived pyramidal neurons quantified after transplantation into the neonatal mouse cortex von D’Alessio, Rosa, Koukouli, Fani, Blanchard, Stéphane, Catteau, Julie, Raïs, Célia, Lemonnier, Thomas, Féraud, Olivier, Bennaceur-Griscelli, Annelise, Groszer, Matthias, Maskos, Uwe

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Modeling neuronal defects associated with a lysosomal disorder using patient-derived induced pluripotent stem cells von LEMONNIER, Thomas, BLANCHARD, Stephane, TOLI, Diana, ROY, Elise, BIGOU, Stephanie, FROISSART, Roseline, ROUVET, Isabelle, VITRY, Sandrine, MICHEL HEARD, Jean, BOHL, Delphine

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Modeling amyotrophic lateral sclerosis in pure human iPSc-derived motor neurons isolated by a novel FACS double selection technique von Toli, Diana, Buttigieg, Dorothée, Blanchard, Stéphane, Lemonnier, Thomas, Lamotte d’Incamps, Boris, Bellouze, Sarah, Baillat, Gilbert, Bohl, Delphine, Haase, Georg

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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C von Petit, Christine, Verpy, Elisabeth, Leibovici, Michel, Zwaenepoel, Ingrid, Liu, Xue-Zhong, Gal, Andreas, Salem, Nabiha, Mansour, Ahmad, Blanchard, Stéphane, Kobayashi, Ichiro, Keats, Bronya J.B, Slim, Rima

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Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle von Boëda, Batiste, El-Amraoui, Aziz, Bahloul, Amel, Goodyear, Richard, Daviet, Laurent, Blanchard, Stéphane, Perfettini, Isabelle, Fath, Karl R., Shorte, Spencer, Reiners, Jan, Houdusse, Anne, Legrain, Pierre, Wolfrum, Uwe, Richardson, Guy, Petit, Christine

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Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31 von Brown, Steve D M, Mburu, Philomena, Weil, Dominique, Blanchard, Stéphane, Coimbra, Roney S, El-Amraoui, Aziz, Varela, Anabel, Paige, Adam J, Holme, Ralph H, Hardisty, Rachel E, Rump, Andreas, Clay, Jo, Glenister, Pete, Rosenthal, Andre, Steel, Karen P, Petit, Christine, Mustapha, Mirna, Parkinson, Nick, Blanco, Gonzalo, Mallon, Ann-Marie, Rogers, Mike J, Liu, Xue Zhong, Moir, Lee, Perfettini, Isabelle

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MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes von El-Amraoui, Aziz, Schonn, Jean-Sébastien, Küssel-Andermann, Polonca, Blanchard, Stéphane, Desnos, Claire, Henry, Jean-Pierre, Wolfrum, Uwe, Darchen, François, Petit, Christine

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Combination of hypoglossal-facial nerve surgical reconstruction and neurotrophin-3 gene therapy for facial palsy: Laboratory investigation von Wan, Hong, Zhang, Liwei, Blanchard, Stephane, Bigou, Stephanie, Bohl, Delphine, Wang, Chuncheng, Liu, Song

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Directed Evolution of Motor Neurons from Genetically Engineered Neural Precursors von Bohl, Delphine, Liu, Song, Blanchard, Stéphane, Hocquemiller, Michaël, Haase, Georg, Heard, Jean‐Michel

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Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus von Lainé, Sophie, Masmoudi, Saber, Hutchin, Tim P, Verpy, Elisabeth, Leibovici, Michel, Nouaille, Sylvie, Del Castillo, Ignacio, Blanchard, Stéphane, Petit, Christine, Popot, Jean-Luc, Moreno, Felipe, Mueller, Robert F, Zwaenepoel, Ingrid

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PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa von Etournay, Raphae̊l, El-Amraoui, Aziz, Bahloul, Amel, Blanchard, Stéphane, Roux, Isabelle, Pézeron, Guillaume, Michalski, Nicolas, Daviet, Laurent, Hardelin, Jean-Pierre, Legrain, Pierre, Petit, Christine

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The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene von Ayadi, Hammadi, Lévy, Gallia, Weil, Dominique, Levi-Acobas, Fabienne, Drira, Mohamed, Blanchard, Stéphane, Petit, Christine, Küssel, Polonca

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Combination of hypoglossal-facial nerve surgical reconstruction and neurotrophin-3 gene therapy for facial palsy von Wan, Hong, Zhang, Liwei, Blanchard, Stephane, Bigou, Stephanie, Bohl, Delphine, Wang, Chuncheng, Liu, Song

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Renshaw cell loss in a transgenic mouse model of amyotrophic lateral sclerosis von AlMarsoummi, Sarmad, Blanchard, Stephane, Kulikov, Sergei, Smith, Margaret, Carr, Patrick

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