Publicaciones (45) Publicaciones en las que ha participado algún/a investigador/a

2022

  1. A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels

    The Journal of clinical endocrinology and metabolism, Vol. 107, Núm. 8, pp. 2350-2361

  2. A polygenic risk score for multiple myeloma risk prediction

    European Journal of Human Genetics, Vol. 30, Núm. 4, pp. 474-479

  3. Acceleration of the DNA methylation clock among lynch syndrome-associated mutation carriers

    BMC medical genomics, Vol. 15, Núm. 1, pp. 45

  4. Age and Chronodisruption in Mouse Heart: Effect of the NLRP3 Inflammasome and Melatonin Therapy

    International Journal of Molecular Sciences, Vol. 23, Núm. 12

  5. Allosteric Communication in the Multifunctional and Redox NQO1 Protein Studied by Cavity‐Making Mutations

    Antioxidants, Vol. 11, Núm. 6

  6. Anticancer Activity of the Choline Kinase Inhibitor PL48 Is Due to Selective Disruption of Choline Metabolism and Transport Systems in Cancer Cell Lines

    Pharmaceutics, Vol. 14, Núm. 2

  7. Autophagy in Hematological Malignancies

    Cancers, Vol. 14, Núm. 20

  8. Biological Evaluation of New Thienopyridinium and Thienopyrimidinium Derivatives as Human Choline Kinase Inhibitors

    Pharmaceutics, Vol. 14, Núm. 4

  9. Characterization of Genetic Variants of Uncertain Significance for the ALPL Gene in Patients With Adult Hypophosphatasia

    Frontiers in Endocrinology, Vol. 13

  10. Combined Magnetic Hyperthermia and Photothermia with Polyelectrolyte/Gold-Coated Magnetic Nanorods

    Polymers, Vol. 14, Núm. 22

  11. 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

  12. 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

  13. Comparison of Metagenomics and Metatranscriptomics Tools: A Guide to Making the Right Choice

    Genes, Vol. 13, Núm. 12

  14. Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia

    Frontiers in Cell and Developmental Biology, Vol. 10

  15. Different phenotypic outcome due to site-specific phosphorylation in the cancer-associated NQO1 enzyme studied by phosphomimetic mutations

    Archives of Biochemistry and Biophysics, Vol. 729

  16. Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Patients with Myeloma?

    Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Vol. 31, Núm. 9, pp. 1863-1866

  17. ESHRE guideline: endometriosis

    Human Reproduction Open, Vol. 2022, Núm. 2

  18. EZH2 endorses cell plasticity to non-small cell lung cancer cells facilitating mesenchymal to epithelial transition and tumour colonization

    Oncogene, Vol. 41, Núm. 28, pp. 3611-3624

  19. Effect of Probiotics on Host-Microbiota in Bacterial Infections

    Pathogens, Vol. 11, Núm. 9

  20. Effects of erythrodiol on the antioxidant response and proteome of HepG2 cells

    Antioxidants, Vol. 11, Núm. 1