Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies

por Agudelo, William A., Gil-Quiñones, Sebastian Ramiro, Fonseca, Alejandra, Arenas, Alvaro, Castro, Laura, Sierra-Díaz, Diana Carolina, Patarroyo, Manuel A., Laissue, Paul, Suárez, Carlos F., Cabrera, Rodrigo
Publicado 2021

FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

por Quintero-Ronderos, Paula, Jiménez, Karen Marcela, Esteban-Pérez, Clara, Ojeda, Diego A., Bello, Sandra, Fonseca, Dora Janeth, Coronel, María Alejandra, Moreno-Ortiz, Harold, Sierra-Díaz, Diana Carolina, Lucena, Elkin, Barbaux, Sandrine, Vaiman, Daniel, Laissue, Paul
Publicado 2019

Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

por Laissue, Paul, Lakhal, Besma, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Gris, Jean-Christophe, Cocquet, Julie, Vaiman, Daniel
Publicado 2016