Torthaí cuardaigh - Le Béchec, Antony

AMYPdb: A database dedicated to amyloid precursor proteins de réir Pawlicki, Sandrine, Le Béchec, Antony, Delamarche, Christian

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Predicting missing expression values in gene regulatory networks using a discrete logic modeling optimization guided by network stable states de réir Crespo, Isaac, Krishna, Abhimanyu, Le Béchec, Antony, del Sol, Antonio

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A Novel Network Integrating a miRNA-203/SNAI1 Feedback Loop which Regulates Epithelial to Mesenchymal Transition de réir Moes, Michèle, Le Béchec, Antony, Crespo, Isaac, Laurini, Christina, Halavatyi, Aliaksandr, Vetter, Guillaume, del Sol, Antonio, Friederich, Evelyne

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Regulation of epithelial plasticity by miR-424 and miR-200 in a new prostate cancer metastasis model de réir Banyard, Jacqueline, Chung, Ivy, Wilson, Arianne M., Vetter, Guillaume, Le Béchec, Antony, Bielenberg, Diane R., Zetter, Bruce R.

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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 de réir Vetter, Guillaume, Saumet, Anne, Michèle, Moes, Vallar, Laurent, Le Béchec, Antony, Laurini, Cristina, Sabbah, Michelle, Arar, Khalil, Theillet, Charles, Lecellier, Charles-Henri, Friederich, Evelyne

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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 de réir 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

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FAM111A Mutations Result in Hypoparathyroidism and Impaired Skeletal Development de réir 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

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TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT de réir 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

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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 de réir 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

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