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

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 explained by the fact that reproductive phenotypes should be considered as quant...

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Detalles Bibliográficos
Autores Principales: 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
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: 2016
Materias:
Evolución & genética
Ginecología & otras especialidades médicas
Developmental biology
Genetics
Genomics
FOXD1 protein
Embryo death
Recurrent spontaneous abortion
Interspecific recombinant congenic mice
DNA microarray
Forkhead transcription factor
Chlorocebus aethiops
C57BL mouse
CV-1 cell line
Acceso en línea:https://repository.urosario.edu.co/handle/10336/21963
https://doi.org/10.1098/rsob.160109

Internet

https://repository.urosario.edu.co/handle/10336/21963
https://doi.org/10.1098/rsob.160109

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