ROGELIO JESÚS
PALOMINO MORALES
PROFESOR TITULAR DE UNIVERSIDAD
MIGUEL
BURGOS POYATOS
CATEDRÁTICO DE UNIVERSIDAD
MIGUEL BURGOS POYATOS-rekin lankidetzan egindako argitalpenak (11)
2022
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Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome
Journal of Personalized Medicine, Vol. 12, Núm. 6
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Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility
Andrology, Vol. 10, Núm. 7, pp. 1339-1350
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Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
Frontiers in Cell and Developmental Biology, Vol. 10
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Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility
Communications Biology, Vol. 5, Núm. 1
2021
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Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort
Andrology, Vol. 9, Núm. 4, pp. 1151-1165
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Evaluation of male fertility-associated loci in a european population of patients with severe spermatogenic impairment
Journal of Personalized Medicine, Vol. 11, Núm. 1, pp. 1-19
2020
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Deficiency of the onco-miRNA cluster, miR-106b∼25, causes oligozoospermia and the cooperative action of miR-106b∼25 and miR-17∼92 is required to maintain male fertility
Molecular Human Reproduction, Vol. 26, Núm. 6, pp. 389-401
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Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment
Fertility and Sterility, Vol. 114, Núm. 2, pp. 398-406
2019
2018
2017
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Enhanced vulnerability of human proteins towards disease-associated inactivation through divergent evolution
Human Molecular Genetics, Vol. 26, Núm. 18, pp. 3531-3544