Výsledky vyhledávání - Le Béchec, Antony
- Zobrazuji výsledky 1 - 9 z 9
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A Novel Network Integrating a miRNA-203/SNAI1 Feedback Loop which Regulates Epithelial to Mesenchymal Transition Autor Moes, Michèle, Le Béchec, Antony, Crespo, Isaac, Laurini, Christina, Halavatyi, Aliaksandr, Vetter, Guillaume, del Sol, Antonio, Friederich, Evelyne
Vydáno 2012Text -
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Regulation of epithelial plasticity by miR-424 and miR-200 in a new prostate cancer metastasis model Autor Banyard, Jacqueline, Chung, Ivy, Wilson, Arianne M., Vetter, Guillaume, Le Béchec, Antony, Bielenberg, Diane R., Zetter, Bruce R.
Vydáno 2013Text -
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miR-661 expression in SNAI1-induced epithelial to mesenchymal transition contributes to breast cancer cell invasion by targeting Nectin-1 and StarD10 messengers Autor Vetter, Guillaume, Saumet, Anne, Michèle, Moes, Vallar, Laurent, Le Béchec, Antony, Laurini, Cristina, Sabbah, Michelle, Arar, Khalil, Theillet, Charles, Lecellier, Charles-Henri, Friederich, Evelyne
Vydáno 2010Text -
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MIR@NT@N: a framework integrating transcription factors, microRNAs and their targets to identify sub-network motifs in a meta-regulation network model Autor Le Béchec, Antony, Portales-Casamar, Elodie, Vetter, Guillaume, Moes, Michèle, Zindy, Pierre-Joachim, Saumet, Anne, Arenillas, David, Theillet, Charles, Wasserman, Wyeth W, Lecellier, Charles-Henri, Friederich, Evelyne
Vydáno 2011Text -
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FAM111A Mutations Result in Hypoparathyroidism and Impaired Skeletal Development Autor Unger, Sheila, Górna, Maria W., Le Béchec, Antony, Do Vale-Pereira, Sonia, Bedeschi, Maria Francesca, Geiberger, Stefan, Grigelioniene, Giedre, Horemuzova, Eva, Lalatta, Faustina, Lausch, Ekkehart, Magnani, Cinzia, Nampoothiri, Sheela, Nishimura, Gen, Petrella, Duccio, Rojas-Ringeling, Francisca, Utsunomiya, Akari, Zabel, Bernhard, Pradervand, Sylvain, Harshman, Keith, Campos-Xavier, Belinda, Bonafé, Luisa, Superti-Furga, Giulio, Stevenson, Brian, Superti-Furga, Andrea
Vydáno 2013Text -
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TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT Autor Devalla, Harsha D, Gélinas, Roselle, Aburawi, Elhadi H, Beqqali, Abdelaziz, Goyette, Philippe, Freund, Christian, Chaix, Marie‐A, Tadros, Rafik, Jiang, Hui, Le Béchec, Antony, Monshouwer‐Kloots, Jantine J, Zwetsloot, Tom, Kosmidis, Georgios, Latour, Frédéric, Alikashani, Azadeh, Hoekstra, Maaike, Schlaepfer, Jurg, Mummery, Christine L, Stevenson, Brian, Kutalik, Zoltan, de Vries, Antoine AF, Rivard, Léna, Wilde, Arthur AM, Talajic, Mario, Verkerk, Arie O, Al‐Gazali, Lihadh, Rioux, John D, Bhuiyan, Zahurul A, Passier, Robert
Vydáno 2016Text -
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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation Autor Balak, Chris, Benard, Marianne, Schaefer, Elise, Iqbal, Sumaiya, Ramsey, Keri, Ernoult-Lange, Michèle, Mattioli, Francesca, Llaci, Lorida, Geoffroy, Véronique, Courel, Maité, Naymik, Marcus, Bachman, Kristine K., Pfundt, Rolph, Rump, Patrick, ter Beest, Johanna, Wentzensen, Ingrid M., Monaghan, Kristin G., McWalter, Kirsty, Richholt, Ryan, Le Béchec, Antony, Jepsen, Wayne, De Both, Matt, Belnap, Newell, Boland, Anne, Piras, Ignazio S., Deleuze, Jean-François, Szelinger, Szabolcs, Dollfus, Hélène, Chelly, Jamel, Muller, Jean, Campbell, Arthur, Lal, Dennis, Rangasamy, Sampathkumar, Mandel, Jean-Louis, Narayanan, Vinodh, Huentelman, Matt, Weil, Dominique, Piton, Amélie
Vydáno 2019Text