Publicacións en colaboración con investigadores/as de Universidad de Salamanca (32)

2024

  1. A Missense Variant in TP53 Could Be a Genetic Biomarker Associated with Bone Tissue Alterations

    International Journal of Molecular Sciences, Vol. 25, Núm. 3

  2. Stress and sleep deprivation-related biomarkers in saliva in patients with retinitis pigmentosa

    PLoS ONE, Vol. 19, Núm. 6 June

2023

  1. Endothelial nitric oxide synthase rs1799983 gene polymorphism is associated with the risk of developing intracranial aneurysm

    Acta Neurochirurgica, Vol. 165, Núm. 5, pp. 1261-1267

  2. Predominantly Pro-Inflammatory Phenotype with Mixed M1/M2 Polarization of Peripheral Blood Classical Monocytes and Monocyte-Derived Macrophages among Patients with Excessive Ethanol Intake

    Antioxidants, Vol. 12, Núm. 9

  3. Short-Wavelength Light–Blocking Filters and Oral Melatonin Administration in Patients With Retinitis Pigmentosa: Protocol for a Randomized Controlled Trial

    JMIR Research Protocols, Vol. 12, Núm. 1

2022

  1. Association between genetic variants in oxidative stress-related genes and osteoporotic bone fracture. The Hortega follow-up study

    Gene, Vol. 809

  2. Complications associated with the use of silicone oil in vitreoretinal surgery: A systemic review and meta-analysis

    Acta Ophthalmologica, Vol. 100, Núm. 4, pp. e864-e880

  3. Genetic variants in obesity-related genes and the risk of osteoporotic fracture. The Hortega Follow-up Study

    Frontiers in bioscience (Landmark edition), Vol. 27, Núm. 1, pp. 32

  4. Hair cortisol level as a molecular biomarker in retinitis pigmentosa patients

    Experimental Eye Research, Vol. 219

  5. PPAR-γ Gene Expression in Human Adipose Tissue Is Associated with Weight Loss After Sleeve Gastrectomy

    Journal of Gastrointestinal Surgery, Vol. 26, Núm. 2, pp. 286-297

  6. Programmed Cell Death and Autophagy in an in vitro Model of Spontaneous Neuroretinal Degeneration

    Frontiers in Neuroanatomy, Vol. 16

  7. Retinal Neuroprotective Effect of Mesenchymal Stem Cells Secretome Through Modulation of Oxidative Stress, Autophagy, and Programmed Cell Death

    Investigative ophthalmology & visual science, Vol. 63, Núm. 4, pp. 27

2021

  1. Analysis of Lymphotoxin Alpha Expression in Human Retina and Generation of Expression Vectors to Functional Characterization of Polymorphisms in the Tumor Necrosis Factor Locus

    Methods in Molecular Biology (Humana Press Inc.), pp. 243-250

  2. Dopamine receptors and the kidney: An overview of health-and pharmacological-targeted implications

    Biomolecules, Vol. 11, Núm. 2, pp. 1-16

  3. Rho-Kinase Inhibitors for the Treatment of Refractory Diabetic Macular Oedema

    Cells, Vol. 10, Núm. 7

2020

  1. A mutation in p62 protein (p. R321C), associated to Paget's disease of bone, causes a blockade of autophagy and an activation of NF-kB pathway

    Bone, Vol. 133

  2. Association between genetic variants in CYP2E1 and CTRC genes and susceptibility to alcoholic pancreatitis: A systematic review and meta-analysis

    Drug and Alcohol Dependence, Vol. 209

  3. Human Mesenchymal Stem Cell Secretome Exhibits a Neuroprotective Effect over In Vitro Retinal Photoreceptor Degeneration

    Molecular Therapy - Methods and Clinical Development, Vol. 17, pp. 1155-1166

  4. Matrix metalloproteinases in age-related macular degeneration (Amd)

    International Journal of Molecular Sciences, Vol. 21, Núm. 16, pp. 1-32

  5. Polymorphisms in genes involved in inflammation, the NF-kB pathway and the renin-angiotensin-aldosterone system are associated with the risk of osteoporotic fracture. The Hortega Follow-up Study

    Bone, Vol. 138