Mitochondrial dysfunction as a central actor in intellectual disability-related diseases: an overview of Down syndrome, autism, Fragile X and Rett syndrome von Valenti, Daniela, de Bari, Lidia, De Filippis, Bianca, Henrion-Caude, Alexandra, Vacca, Rosa Anna

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Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome: Extremely Variable Liver Disease Severity From Claudin-1 Deficiency von Paganelli, Massimiliano, Stephenne, Xavier, Gilis, Allison, Jacquemin, Emmanuel, Caude, Alexandra Henrion, Girard, Muriel, Gonzales, Emmanuel, Revencu, Nicole, Reding, Raymond, Wanty, Catherine, Smets, Françoise, Sokal, Etienne M

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Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy von Cartault, François, Munier, Patrick, Benko, Edgar, Desguerre, Isabelle, Hanein, Sylvain, Boddaert, Nathalie, Bandiera, Simonetta, Vellayoudom, Jeanine, Krejbich-Trotot, Pascale, Bintner, Marc, Hoarau, Jean-Jacques, Girard, Muriel, Génin, Emmanuelle, de Lonlay, Pascale, Fourmaintraux, Alain, Naville, Magali, Rodriguez, Diana, Feingold, Josué, Renouil, Michel, Munnich, Arnold, Westhof, Eric, Fähling, Michael, Lyonnet, Stanislas, Henrion-Caude, Alexandra

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miR-122, a paradigm for the role of microRNAs in the liver von Girard, Muriel, Jacquemin, Emmanuel, Munnich, Arnold, Lyonnet, Stanislas, Henrion-Caude, Alexandra

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Mitochondria as pharmacological targets in Down syndrome von Valenti, Daniela, Braidy, Nady, De Rasmo, Domenico, Signorile, Anna, Rossi, Leonardo, Atanasov, A.G., Volpicella, Mariateresa, Henrion-Caude, Alexandra, Nabavi, S.M., Vacca, R.A.

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Nuclear outsourcing of RNA interference components to human mitochondria von Bandiera, Simonetta, Rüberg, Silvia, Girard, Muriel, Cagnard, Nicolas, Hanein, Sylvain, Chrétien, Dominique, Munnich, Arnold, Lyonnet, Stanislas, Henrion-Caude, Alexandra

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Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans von de Pontual, Loïc, Yao, Evelyn, Callier, Patrick, Faivre, Laurence, Drouin, Valérie, Cariou, Sandra, Van Haeringen, Arie, Geneviève, David, Goldenberg, Alice, Oufadem, Myriam, Manouvrier, Sylvie, Munnich, Arnold, Vidigal, Joana Alves, Vekemans, Michel, Lyonnet, Stanislas, Henrion-Caude, Alexandra, Ventura, Andrea, Amiel, Jeanne

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Footprints of a Singular 22-Nucleotide RNA Ring at the Origin of Life von Demongeot, Jacques, Henrion-Caude, Alexandra

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MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease von Girard, Muriel, Lacaille, Florence, Verkarre, Virginie, Mategot, Raphael, Feldmann, Gerard, Grodet, Alain, Sauvat, Frédérique, Irtan, Sabine, Davit‐Spraul, Anne, Jacquemin, Emmanuel, Ruemmele, Frank, Rainteau, Dominique, Goulet, Olivier, Colomb, Virginie, Chardot, Christophe, Henrion‐Caude, Alexandra, Debray, Dominique

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DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis von Girard, Muriel, Bizet, Albane A., Lachaux, Alain, Gonzales, Emmanuel, Filhol, Emilie, Collardeau-Frachon, Sophie, Jeanpierre, Cécile, Henry, Charline, Fabre, Monique, Viremouneix, Loic, Galmiche, Louise, Debray, Dominique, Bole-Feysot, Christine, Nitschke, Patrick, Pariente, Danièle, Guettier, Catherine, Lyonnet, Stanislas, Heidet, Laurence, Bertholet, Aurelia, Jacquemin, Emmanuel, Henrion-Caude, Alexandra, Saunier, Sophie

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Biliary atresia: Clinical advances and perspectives von Nizery, Laure, Chardot, Christophe, Sissaoui, Samira, Capito, Carmen, Henrion-Caude, Alexandra, Debray, Dominique, Girard, Muriel

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Knockout of insulin-like growth factor-1 receptor impairs distal lung morphogenesis von Epaud, Ralph, Aubey, Flore, Xu, Jie, Chaker, Zayna, Clemessy, Maud, Dautin, Alexandre, Ahamed, Karmène, Bonora, Monique, Hoyeau, Nadia, Fléjou, Jean-François, Mailleux, Arnaud, Clement, Annick, Henrion-Caude, Alexandra, Holzenberger, Martin

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Regulation of WNK1 Expression by miR-192 and Aldosterone von ELVIRA-MATELOT, Emilie, ZHOU, Xiao-Ou, FARMAN, Nicolette, BEAURAIN, Geneviève, HENRION-CAUDE, Alexandra, HADCHOUEL, Juliette, JEUNEMAITRE, Xavier

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MicroRNAs Establish Robustness and Adaptability of a Critical Gene Network to Regulate Progenitor Fate Decisions during Cortical Neurogenesis von Ghosh, Tanay, Aprea, Julieta, Nardelli, Jeannette, Engel, Hannes, Selinger, Christian, Mombereau, Cedric, Lemonnier, Thomas, Moutkine, Imane, Schwendimann, Leslie, Dori, Martina, Irinopoulou, Theano, Henrion-Caude, Alexandra, Benecke, Arndt G., Arnold, Sebastian J., Gressens, Pierre, Calegari, Federico, Groszer, Matthias

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Genetic variations creating microRNA target sites in the FXN 3'-UTR affect frataxin expression in Friedreich ataxia von Bandiera, Simonetta, Cartault, François, Jannot, Anne-Sophie, Hatem, Elie, Girard, Muriel, Rifai, Laila, Loiseau, Clemence, Munnich, Arnold, Lyonnet, Stanislas, Henrion-Caude, Alexandra

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Chromosome 21 scan in Down syndrome reveals DSCAM as a predisposing locus in Hirschsprung disease von Jannot, Anne-Sophie, Pelet, Anna, Henrion-Caude, Alexandra, Chaoui, Asma, Masse-Morel, Marine, Arnold, Stacey, Sanlaville, Damien, Ceccherini, Isabella, Borrego, Salud, Hofstra, Robert M W, Munnich, Arnold, Bondurand, Nadège, Chakravarti, Aravinda, Clerget-Darpoux, Françoise, Amiel, Jeanne, Lyonnet, Stanislas

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Influence of Interleukin-10 on Aspergillus fumigatus Infection in Patients with Cystic Fibrosis von Brouard, Jacques, Knauer, Nicola, Boelle, Pierre-Yves, Corvol, Harriet, Henrion-Caude, Alexandra, Flamant, Cyril, Bremont, François, Delaisi, Bertrand, Duhamel, Jean-Francois, Marguet, Christophe, Roussey, Michel, Miesch, Marie-Claude, Chadelat, Katarina, Boule, Michele, Fauroux, Brigitte, Ratjen, Felix, Grasemann, Hartmut, Clement, Annick

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Polynesian ecology determines seasonality of biliary atresia von Girard, Muriel, Jannot, Anne‐Sophie, Besnard, MArianne, Leutenegger, Anne‐Louise, Jacquemin, Emmanuel, Lyonnet, Stanislas, Henrion‐Caude, Alexandra

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Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis von Corvol, Harriet, Boelle, Pierre-Yves, Brouard, Jacques, Knauer, Nicola, Chadelat, Katarina, Henrion-Caude, Alexandra, Flamant, Cyril, Muselet-Charlier, Celine, Boule, Michele, Fauroux, Brigitte, Vallet, Christelle, Feingold, Josue, Ratjen, Felix, Grasemann, Hartmut, Clement, Annick

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Novel Mutation and Structural RNA Analysis of the Noncoding RNase MRP Gene in Cartilage-Hair Hypoplasia von Cherkaoui Jaouad, Imane, Laarabi, Fatima Z., Chafai Elalaoui, Siham, Lyonnet, Stanislas, Henrion-Caude, Alexandra, Sefiani, Abdelaziz

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