Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome

We aimed to analyze the role of the common genetic variants located in the PIN1 locus, a relevant prolyl isomerase required to control the proliferation of spermatogonial stem cells and the integrity of the blood–testis barrier, in the genetic risk of developing male infertility due to a severe sper...

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Detalles Bibliográficos
Autores principales: Cerván-Martín, Miriam, Bossini-Castillo, Lara, Guzmán-Jimenez, Andrea, Rivera-Egea, Rocío, Garrido, Nicolás, Luján, Saturnino, Romeu, Gema, Santos-Ribeiro, Samuel, Castilla, José A., Gonzalvo, M. Carmen, Clavero, Ana, Vicente, F. Javier, Maldonado, Vicente, González-Muñoz, Sara, Rodríguez-Martín, Inmaculada, Burgos, Miguel, Jiménez, Rafael, Pinto, Maria Graça, Pereira, Isabel, Nunes, Joaquim, Sánchez-Curbelo, Josvany, López-Rodrigo, Olga, Pereira-Caetano, Iris, Marques, Patricia Isabel, Carvalho, Filipa, Barros, Alberto, Bassas, Lluís, Seixas, Susana, Gonçalves, João, Larriba, Sara, Lopes, Alexandra M., Carmona, F. David, Palomino-Morales, Rogelio J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225465/
https://www.ncbi.nlm.nih.gov/pubmed/35743717
http://dx.doi.org/10.3390/jpm12060932

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225465/
https://www.ncbi.nlm.nih.gov/pubmed/35743717
http://dx.doi.org/10.3390/jpm12060932

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