Not logged inGeneration of two iPSC lines from patients with Aicardi-Goutie`res syndrome carrying either biallelic ADAR1 mutations (PC138) or a heterozygous IFIH1 mutation (PC139)
Zerad, Lisa; Didry-Barca, Blaise; Banal, Celine; Onteniente, Brigitte; Lefort, Nathalie; Lepelley, Alice; Seabra, Luis; Hully, Marie; Zweier, Christiane; Bondurand, Nadege; Crow, Yanick J.; Fremond, Marie-Louise .png)
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SaveOverexpression of Egr1 Transcription Regulator Contributes to Schwann Cell Differentiation Defects in Neural Crest-Specific Adar1 Knockout MiceZerad, Lisa; Gacem, Nadjet; Gayda, Fanny; Day, Lucie; Sinigaglia, Ketty; Richard, Laurence; Parisot, Melanie; Cagnard, Nicolas; Mathis, Stephane; Bole-Feysot, Christine; O'Connell, Mary A.; Pingault, Veronique; Dambroise, Emilie; Keegan, Liam P.; Vallat, Jean Michel; Bondurand, Nadege Share Save Share Save Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humansLe, Thuy-Linh; Galmiche, Louise; Levy, Jonathan; Suwannarat, Pim; Hellebrekers, Debby Mei; Morarach, Khomgrit; Boismoreau, Franck; Theunissen, Tom E. J.; Lefebvre, Mathilde; Pelet, Anna; Martinovic, Jelena; Gelot, Antoinette; Guimiot, Fabien; Calleroz, Amanda; Gitiaux, Cyril; Hully, Marie; Goulet, Olivier; Chardot, Christophe; Drunat, Severine; Capri, Yline; Bole-Feysot, Christine; Nitschke, Patrick; Whalen, Sandra; Mouthon, Linda; Babcock, Holly E.; Hofstra, Robert; de Coo, Irenaeus F. M.; Tabet, Anne-Claude; Molina, Thierry J.; Keren, Boris; Brooks, Alice; Smeets, Hubert J. M.; Marklund, Ulrika; Gordon, Christopher T.; Lyonnet, Stanislas; Amiel, Jeanne; Bondurand, Nadege Share Save ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell developmentGacem, Nadjet; Kavo, Anthula; Zerad, Lisa; Richard, Laurence; Mathis, Stephane; Kapur, Raj P.; Parisot, Melanie; Amiel, Jeanne; Dufour, Sylvie; de la Grange, Pierre; Pingault, Veronique; Vallat, Jean Michel; Bondurand, Nadege Share Save LKB1 specifies neural crest cell fates through pyruvate-alanine cyclingRadu, Anca G.; Torch, Sakina; Fauvelle, Florence; Pernet-Gallay, Karin; Lucas, Anthony; Blervaque, Renaud; Delmas, Veronique; Schlattner, Uwe; Lafanechere, Laurence; Hainaut, Pierre; Tricaud, Nicolas; Pingault, Veronique; Bondurand, Nadege; Bardeesy, Nabeel; Larue, Lionel; Thibert, Chantal; Bilaud, Marc Share Save Share Save EDNRB mutations causeWaardenburg syndrome type II in the heterozygous stateIssa, Sarah; Bondurand, Nadege; Faubert, Emmanuelle; Poisson, Sylvain; Lecerf, Laure; Nitschke, Patrick; Deggouj, Naima; Loundon, Natalie; Jonard, Laurence; David, Albert; Sznajer, Yves; Blanchet, Patricia; Marlin, Sandrine; Pingault, Veronique Share Save Share Save How Tissue Mechanical Properties Affect Enteric Neural Crest Cell Migration (vol 6, 20927, 2016)Chevalier, N. R.; Gazquez, E.; Bidault, L.; Guilbert, T.; Vias, C.; Vian, E.; Watanabe, Y.; Muller, L.; Germain, S.; Bondurand, N.; Dufour, S.; Fleury, V. Share Save How Tissue Mechanical Properties Affect Enteric Neural Crest Cell MigrationChevalier, N. R.; Gazguez, E.; Bidault, L.; Guilbert, T.; Vias, C.; Vian, E.; Watanabe, Y.; Muller, L.; Germain, S.; Bondurand, N.; Dufour, S.; Fleury, V. Share Save Share Save Share Save Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with DeafnessPingault, Veronique; Bodereau, Virginie; Baral, Viviane; Marcos, Severine; Watanabe, Yuli; Chaoui, Asma; Fouveaut, Corinne; Leroy, Chrystel; Verier-Mine, Odile; Francannet, Christine; Dupin-Deguine, Delphine; Archambeaud, Francoise; Kurtz, Francois-Joseph; Young, Jacques; Bertherat, Jerome; Marlin, Sandrine; Goossens, Michel; Hardelin, Jean-Pierre; Dode, Catherine; Bondurand, Nadege Share Save ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild MowatWilson syndromeGhoumid, Jamal; Drevillon, Loic; Alavi-Naini, Seyedeh Maryam; Bondurand, Nadege; Rio, Marlene; Briand-Suleau, Audrey; Nasser, Mayssa; Goodwin, Linda; Raymond, Patrick; Yanicostas, Constantin; Goossens, Michel; Lyonnet, Stanislas; Mowat, David; Amiel, Jeanne; Soussi-Yanicostas, Nadia; Giurgea, Irina Share Save Share Save Share Save Share Save Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4Bondurand, Nadege; Dastot-Le Moal, Florence; Stanchina, Laure; Collot, Nathalie; Baral, Viviane; Marlin, Sandrine; Attie-Bitach, Tania; Giurgea, Irina; Skopinski, Laurent; Reardon, William; Toutain, Annick; Sarda, Pierre; Echaieb, Anis; Lackmy-Port-Lis, Marilyn; Touraine, Renaud; Amiel, Jeanne; Goossens, Michel; Pingault, Veronique Share Save Share Save 
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