Departamento
BIOQUÍMICA Y BIOLOGÍA MOLECULAR I
Publicaciones (54) Publicaciones en las que ha participado algún/a investigador/a
2022
-
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
-
A polygenic risk score for multiple myeloma risk prediction
European Journal of Human Genetics, Vol. 30, Núm. 4, pp. 474-479
-
Acceleration of the DNA methylation clock among lynch syndrome-associated mutation carriers
BMC medical genomics, Vol. 15, Núm. 1, pp. 45
-
Age and Chronodisruption in Mouse Heart: Effect of the NLRP3 Inflammasome and Melatonin Therapy
International Journal of Molecular Sciences, Vol. 23, Núm. 12
-
Allosteric Communication in the Multifunctional and Redox NQO1 Protein Studied by Cavity‐Making Mutations
Antioxidants, Vol. 11, Núm. 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
-
Autophagy in Hematological Malignancies
Cancers, Vol. 14, Núm. 20
-
Biological Evaluation of New Thienopyridinium and Thienopyrimidinium Derivatives as Human Choline Kinase Inhibitors
Pharmaceutics, Vol. 14, Núm. 4
-
Characterization of Genetic Variants of Uncertain Significance for the ALPL Gene in Patients With Adult Hypophosphatasia
Frontiers in Endocrinology, Vol. 13
-
Combined Magnetic Hyperthermia and Photothermia with Polyelectrolyte/Gold-Coated Magnetic Nanorods
Polymers, Vol. 14, Núm. 22
-
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
-
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
-
Comparison of Metagenomics and Metatranscriptomics Tools: A Guide to Making the Right Choice
Genes, Vol. 13, Núm. 12
-
Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
Frontiers in Cell and Developmental Biology, Vol. 10
-
Corrigendum: Transcriptional and epigenetic response to sedentary behavior and physical activity in children and adolescents: A systematic review, (Front. Pediatr, (2022), 10, (917152), 10.3389/fped.2022.917152)
Frontiers in Pediatrics
-
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
-
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
-
ESHRE guideline: endometriosis
Human Reproduction Open, Vol. 2022, Núm. 2
-
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
-
Editorial: Molecular and cellular aspects of regulatory and subjacent mechanisms in host/microbiota association and its involvement in cancer
Frontiers in Cell and Developmental Biology