Now showing items 1-3 of 3

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

      Laissue, Paul; Lakha, Besma; Vatin, Magalie; Batista, Frank; Burgio, Gaetan; Mercier, Eric; Dos Santos, Esther; Buffat, Christophe; Sierra Diaz, Diana Carolina; Renault, Gilles; Montagutelli, Xavier; Salmon, Jane; Monget, Philippe; Veitia, Reiner; Meháts, Céline; Fellous, Marc; Gris, Jean-Christophe; Cocquet, Julie; Vaiman, Daniel
      Recurrent spontaneous abortion (RSA) is a common cause of infertility, but previous attempts at identifying RSA causative genes have been relatively unsuccessful. Such failure to describe RSA aetiological genes might be ...
       Artículo. 2016
    • Novel genes and mutations in patients affected by recurrent pregnancy loss 

      Quintero-Ronderos, Paula; Mercier, Eric; Fukuda, Michiko; González, Ronald; Suárez, Carlos Fernando; Alfonso Patarroyo, Manuel; Vaiman, Daniel; Gris, Jean-Christophe; Laissue, Paul
      Recurrent pregnancy loss is a frequently occurring human infertility-related disease affecting ~1% of women. It has been estimated that the cause remains unexplained in >50% cases which strongly suggests that genetic ...
       Artículo. 2017
    • THBD sequence variants potentially related to recurrent pregnancy loss 

      Quintero-Ronderos, Paula; Mercier, Eric; Gris, Jean-Christophe; Esteban-Perez, Clara; Moreno-Ortiz, Harold; Fonseca, Dora Janeth; Lucena, Elkin; Vaiman, Daniel; Laissue, Paul
      "Recurrent pregnancy loss (RPL) is a frequently occurring disease, which is classified as idiopathic in more than 50% of cases. THBD, the endothelial cell receptor for thrombin, has been associated with distinct biological ...
       Artículo. 2017