Footprints of a Singular 22-Nucleotide RNA Ring at the Origin of Life

Por Demongeot, Jacques, Henrion-Caude, Alexandra
Publicado no Biology (Basel) (2020)

Mitochondria as Novel Players of the Cellular RNA Interference

Por Bandiera, S., Hanein, S., Lyonnet, S., Henrion-Caude, Alexandra
Publicado em 2011

Identification and Characterization of a Tissue-Specific Coactivator, GT198, That Interacts with the DNA-Binding Domains of Nuclear Receptors

Por Ko, Lan, Cardona, Guemalli R., Henrion-Caude, Alexandra, Chin, William W.
Publicado em 2002

Intracellular colocalization and interaction of IGF-binding protein-2 with the cyclin-dependent kinase inhibitor p21(CIP1/WAF1) during growth inhibition

Por Terrien, Xavier, Bonvin, Elise, Corroyer, Sophie, Tabary, Olivier, Clement, Annick, Henrion Caude, Alexandra
Publicado em 2005

Novel Mutation and Structural RNA Analysis of the Noncoding RNase MRP Gene in Cartilage-Hair Hypoplasia

Por Cherkaoui Jaouad, Imane, Laarabi, Fatima Z., Chafai Elalaoui, Siham, Lyonnet, Stanislas, Henrion-Caude, Alexandra, Sefiani, Abdelaziz
Publicado no Mol Syndromol (2015)

Regulation of WNK1 Expression by miR-192 and Aldosterone

Por Elvira-Matelot, Emilie, Zhou, Xiao-ou, Farman, Nicolette, Beaurain, Geneviève, Henrion-Caude, Alexandra, Hadchouel, Juliette, Jeunemaitre, Xavier
Publicado em 2010

Deficiency in type 1 insulin-like growth factor receptor in mice protects against oxygen-induced lung injury

Por Ahamed, Karmene, Epaud, Ralph, Holzenberger, Martin, Bonora, Monique, Flejou, Jean-François, Puard, Julien, Clement, Annick, Henrion-Caude, Alexandra
Publicado em 2005

Nuclear Outsourcing of RNA Interference Components to Human Mitochondria

Por Bandiera, Simonetta, Rüberg, Silvia, Girard, Muriel, Cagnard, Nicolas, Hanein, Sylvain, Chrétien, Dominique, Munnich, Arnold, Lyonnet, Stanislas, Henrion-Caude, Alexandra
Publicado em 2011

Cystic Fibrosis Transmembrane Conductance Regulator Controls Lung Proteasomal Degradation and Nuclear Factor-κB Activity in Conditions of Oxidative Stress

Por Boncoeur, Emilie, Roque, Telma, Bonvin, Elise, Saint-Criq, Vinciane, Bonora, Monique, Clement, Annick, Tabary, Olivier, Henrion-Caude, Alexandra, Jacquot, Jacky
Publicado em 2008

Genetic Variations Creating MicroRNA Target Sites in the FXN 3′-UTR Affect Frataxin Expression in Friedreich Ataxia

Por Bandiera, Simonetta, Cartault, François, Jannot, Anne-Sophie, Hatem, Elie, Girard, Muriel, Rifai, Laila, Loiseau, Clemence, Munnich, Arnold, Lyonnet, Stanislas, Henrion-Caude, Alexandra
Publicado em 2013

Role of Secondary Structure in Discrimination between Constitutive and Inducible Activators

Por Parker, David, Rivera, Morris, Zor, Tsaffir, Henrion-Caude, Alexandra, Radhakrishnan, Ishwar, Kumar, Alok, Shapiro, Linda H., Wright, Peter E., Montminy, Marc, Brindle, Paul K.
Publicado em 1999

Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis

Por Corvol, Harriet, Nathan, Nadia, Charlier, Celine, Chadelat, Katarina, Le Rouzic, Philippe, Tabary, Olivier, Fauroux, Brigitte, Henrion-Caude, Alexandra, Feingold, Josue, Boelle, Pierre-Yves, Clement, Annick
Publicado em 2007

Knockout of Insulin-Like Growth Factor-1 Receptor Impairs Distal Lung Morphogenesis

Por 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
Publicado em 2012

Chromosome 21 Scan in Down Syndrome Reveals DSCAM as a Predisposing Locus in Hirschsprung Disease

Por 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
Publicado em 2013

Germline deletion of the miR-17-92 cluster causes growth and skeletal defects in humans

Por 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
Publicado em 2011

Hypoxia-induced gene expression results from selective mRNA partitioning to the endoplasmic reticulum

Por Staudacher, Jonas J., Naarmann-de Vries, Isabel S., Ujvari, Stefanie J., Klinger, Bertram, Kasim, Mumtaz, Benko, Edgar, Ostareck-Lederer, Antje, Ostareck, Dirk H., Bondke Persson, Anja, Lorenzen, Stephan, Meier, Jochen C., Blüthgen, Nils, Persson, Pontus B., Henrion-Caude, Alexandra, Mrowka, Ralf, Fähling, Michael
Publicado no Nucleic Acids Res (2015)

Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy

Por 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
Publicado em 2012

Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability

Por Emison, Eileen Sproat, Garcia-Barcelo, Merce, Grice, Elizabeth A., Lantieri, Francesca, Amiel, Jeanne, Burzynski, Grzegorz, Fernandez, Raquel M., Hao, Li, Kashuk, Carl, West, Kristen, Miao, Xiaoping, Tam, Paul K.H., Griseri, Paola, Ceccherini, Isabella, Pelet, Anna, Jannot, Anne-Sophie, de Pontual, Loic, Henrion-Caude, Alexandra, Lyonnet, Stanislas, Verheij, Joke B.G.M., Hofstra, Robert M.W., Antiñolo, Guillermo, Borrego, Salud, McCallion, Andrew S., Chakravarti, Aravinda
Publicado em 2010

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly

Por Lahrouchi, Najim, George, Aman, Ratbi, Ilham, Schneider, Ronen, Elalaoui, Siham C., Moosa, Shahida, Bharti, Sanita, Sharma, Ruchi, Abu-Asab, Mones, Onojafe, Felix, Adadi, Najlae, Lodder, Elisabeth M., Laarabi, Fatima-Zahra, Lamsyah, Yassine, Elorch, Hamza, Chebbar, Imane, Postma, Alex V., Lougaris, Vassilios, Plebani, Alessandro, Altmueller, Janine, Kyrieleis, Henriette, Meiner, Vardiella, McNeill, Helen, Bharti, Kapil, Lyonnet, Stanislas, Wollnik, Bernd, Henrion-Caude, Alexandra, Berraho, Amina, Hildebrandt, Friedhelm, Bezzina, Connie R., Brooks, Brian P., Sefiani, Abdelaziz
Publicado no Nat Commun (2019)