RICARDO
USATEGUI MARTÍN
Investigador en el periodo 2013-2014
Hospital Universitario de Salamanca
Salamanca, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario de Salamanca (21)
2024
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A Missense Variant in TP53 Could Be a Genetic Biomarker Associated with Bone Tissue Alterations
International Journal of Molecular Sciences, Vol. 25, Núm. 3
2023
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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
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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
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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
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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
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Polymorphisms in CYP1B1 gene and the risk of suffering Primary Open-Angle Glaucoma: Systematic review and meta-analysis
European Journal of Ophthalmology, Vol. 32, Núm. 4, pp. 1841-1849
2021
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Dopamine receptors and the kidney: An overview of health-and pharmacological-targeted implications
Biomolecules, Vol. 11, Núm. 2, pp. 1-16
2020
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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
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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
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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
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Meta-analysis of the rs243865 MMP-2 polymorphism and age-related macular degeneration risk
PLoS ONE, Vol. 14, Núm. 3
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VEGFR2 and OPG genes modify the risk of subclinical coronary atherosclerosis in patients with familial hypercholesterolemia
Atherosclerosis, Vol. 285, pp. 17-22
2018
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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
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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
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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
2016
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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
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VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone
Genetic Testing and Molecular Biomarkers, Vol. 20, Núm. 6, pp. 335-337
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Varón de 40 años con dolor súbito dorsal intenso
Medicine (Spain), Vol. 12, Núm. 16, pp. 934.e-934.e
2015
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Manifestaciones trombóticas en el síndrome SAPHO. Revisión de la literatura
Reumatologia Clinica
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Polymorphisms in autophagy genes are associated with paget disease of bone
PLoS ONE, Vol. 10, Núm. 6