TY  - JOUR
AU  - Cervan-Martin, Miriam
AU  - Bossini-Castillo, Lara
AU  - Guzman-Jimenez, Andrea
AU  - Rivera-Egea, Rocio
AU  - Garrido, Nicolas
AU  - Lujan, Saturnino
AU  - Romeu, Gema
AU  - Santos-Ribeiro, Samuel
AU  - Lisbon Clinical Group,
AU  - Castilla, Jose A
AU  - Gonzalvo, M Carmen
AU  - Clavero, Ana
AU  - Vicente, F Javier
AU  - Maldonado, Vicente
AU  - Gonzalez-Muñoz, Sara
AU  - Rodriguez-Martin, Inmaculada
AU  - Burgos, Miguel
AU  - Jimenez, Rafael
AU  - Pinto, Maria Graça
AU  - Pereira, Isabel
AU  - Nunes, Joaquim
AU  - Sanchez-Curbelo, Josvany
AU  - Lopez-Rodrigo, Olga
AU  - Pereira-Caetano, Iris
AU  - Marques, Patricia Isabel
AU  - Carvalho, Filipa
AU  - Barros, Alberto
AU  - Bassas, Lluis
AU  - Seixas, Susana
AU  - Gonçalves, João
AU  - Larriba, Sara
AU  - Lopes, Alexandra M
AU  - Carmona, F David
AU  - Palomino-Morales, Rogelio J
PY  - 2022
DO  - 10.3390/jpm12060932
SN  - 2075-4426
UR  - http://hdl.handle.net/10668/21383
T2  - Journal of personalized medicine
AB  - 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...
LA  - en
PB  - MDPI AG
KW  - PIN1
KW  - Sertoli cell-only syndrome
KW  - male infertility
KW  - severe spermatogenic failure
KW  - single-nucleotide polymorphism
KW  - Cell Proliferation
KW  - Stem Cells
KW  - Protein Isoforms
KW  - Gene Expression
KW  - Sertoli Cell-Only Syndrome
KW  - Infertility, Male
KW  - Genotype
KW  - Polymorphism, Single Nucleotide
KW  - Blood-Testis Barrier
KW  - Logistic Models
KW  - Sertoli Cells
KW  - Oligospermia
KW  - Alleles
KW  - Peptidylprolyl Isomerase
KW  - Transcription Factors
KW  - Azoospermia
TI  - Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.
TY  - research article
VL  - 12
ER  -