Metabuscador

Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA

por Laissue, Paul, Vaiman, Daniel
Publicado 2020

Interspecific resources: A major tool for quantitative trait locus cloning and speciation research

por L'Hôte, David, Laissue, Paul, Serres, Catherine, Montagutelli, Xavier, Veitia, Reiner A., Vaiman, Daniel
Publicado 2010

Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death

por Vatin, Magalie, Burgio, Gaetan, Renault, Gilles, Laissue, Paul, Firlej, Virginie, Mondon, Françoise, Montagutelli, Xavier, Vaiman, Daniel, Serres, Catherine, Ziyyat, Ahmed
Publicado 2012

Novel genes and mutations in patients affected by recurrent pregnancy loss

por Quintero-Ronderos, Paula, Mercier, Eric, Fukuda, Michiko, González, Ronald, Suarez Martinez, Carlos Fernando, Alfonso Patarroyo, Manuel, Vaiman, Daniel, Gris, Jean-Christophe, Laissue, Paul
Publicado 2017

THBD sequence variants potentially related to recurrent pregnancy loss

por Quintero-Ronderos, Paula, Mercier, Eric, Gris, Jean-Christophe, Esteban-Perez, Clara, Moreno-Ortiz, Harold, Lucena, Elkin, Vaiman, Daniel, Fonseca-Mendoza, Dora Janeth, Laissue, Paul
Publicado 2017

Polymorphisms of human placental alkaline phosphatase are associated with in vitro fertilization success and recurrent pregnancy loss

por Vatin, Magalie, Bouvier, Sylvie, Bellazi, Linda, Montagutelli, Xavier, Laissue, Paul, Ziyyat, Ahmed, Serres, Catherine, De Mazancourt, Philippe, Dieudonné, Marie-Noelle, Mornet, Etienne, Vaiman, Daniel, Gris, Jean-Christophe
Publicado 2014

Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure

por Caburet, Sandrine, Zavadakova, Petra, Ben-Neriah, Ziva, Bouhali, Kamal, Dipietromaria, Aurélie, Charon, Céline, Besse, Céline, Laissue, Paul, Chalifa-Caspi, Vered, Christin-Maitre, Sophie, Vaiman, Daniel, Levi, Giovanni, Veitia, Reiner, Fellous, Marc
Publicado 2012

Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

por Ducat, Aurélien, Doridot, Ludivine, Calicchio, Rosamaria, Méhats, Celine, Vilotte, Jean-Luc, Castille, Johann, Barbaux, Sandrine, Couderc, Betty, Jacques, Sébastien, Letourneur, Franck, Buffat, Christophe, Le Grand, Fabien, Laissue, Paul, Miralles, Francisco, Vaiman, Daniel
Publicado 2016

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, Coronel, María Alejandra, Moreno-Ortiz, Harold, Sierra-Díaz, Diana Carolina, Lucena, Elkin, Barbaux, Sandrine, Vaiman, Daniel, Fonseca-Mendoza, Dora Janeth, Laissue, Paul
Publicado 2019

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

por 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
Publicado 2016