Rogelio González Sarmiento-rekin lankidetzan egindako argitalpenak (22)

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

2022

  1. 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

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

    Frontiers in Neuroanatomy, Vol. 16

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

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

  3. VAV3 rs7528153 and VAV3-AS1 rs1185222 polymorphisms are associated with an increased risk of developing hypertension

    European Journal of Internal Medicine, Vol. 80, pp. 60-65

2019

  1. Meta-analysis of the rs243865 MMP-2 polymorphism and age-related macular degeneration risk

    PLoS ONE, Vol. 14, Núm. 3

2018

  1. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density

    Annals of the rheumatic diseases, Vol. 77, Núm. 3, pp. 378-385

  2. Influence of angiogenic mediators and bone remodelling in paget´s disease of bone

    International Journal of Medical Sciences, Vol. 15, Núm. 11, pp. 1210-1216

  3. Polymorphisms in genes implicated in base excision repair (BER) pathway are associated with susceptibility to Paget's disease of bone

    Bone, Vol. 112, pp. 19-23

2017

  1. Functional characterization of rs2229094 (T>C) Polymorphism in the tumor necrosis factor locus and lymphotoxin alpha expression in human retina: The Retina 4 project

    Clinical Ophthalmology, Vol. 11, pp. 973-981

  2. Proangiogenic gene polymorphisms are associated with susceptibility to Paget's disease of bone and with its clinical features

    Clinical and experimental rheumatology

2016

  1. Association of IL1Β (-511 A/C) and IL6 (-174 G > C) polymorphisms with higher disease activity and clinical pattern of psoriatic arthritis

    Clinical Rheumatology, Vol. 35, Núm. 7, pp. 1789-1794

  2. VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone

    Genetic Testing and Molecular Biomarkers, Vol. 20, Núm. 6, pp. 335-337

2015

  1. BAX and BCL-2 polymorphisms, as predictors of proliferative vitreoretinopathy development in patients suffering retinal detachment: The Retina 4 project

    Acta Ophthalmologica, Vol. 93, Núm. 7, pp. e541-e549