BIOQUÍMICA Y BIOLOGÍA MOLECULAR III E INMUNOLOGÍA
Departamento
Hospital Universitario Virgen del Rocío
Sevilla, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario Virgen del Rocío (38)
2023
2022
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Assessing the Impact of SARS-CoV-2 Lineages and Mutations on Patient Survival
Viruses, Vol. 14, Núm. 9
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
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Phylogenetic analysis of the 2020 west nile virus (Wnv) outbreak in andalusia (Spain)
Viruses, Vol. 13, Núm. 5
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The current role of the heavy/light chain assay in the diagnosis, prognosis and monitoring of multiple myeloma: An evidence-based approach
Diagnostics, Vol. 11, Núm. 11
2017
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Adipose tissue-derived mesenchymal stromal cells as part of therapy for chronic graft-versus-host disease: A phase I/II study
Cytotherapy, Vol. 19, Núm. 8, pp. 927-936
2016
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Absence of WASp enhances hematopoietic and megakaryocytic differentiation in a human embryonic stem cell model
Molecular Therapy, Vol. 24, Núm. 2, pp. 342-353
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Association between single-nucleotide polymorphisms in DNA double-strand break repair genes and prostate cancer aggressiveness in the Spanish population
Prostate Cancer and Prostatic Diseases, Vol. 19, Núm. 1, pp. 28-34
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Glutathione Is the Resolving Thiol for Thioredoxin Peroxidase Activity of 1-Cys Peroxiredoxin Without Being Consumed during the Catalytic Cycle
Antioxidants and Redox Signaling, Vol. 24, Núm. 3, pp. 115-128
2015
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Genetic variations in genes involved in testosterone metabolism are associated with prostate cancer progression: A Spanish multicenter study
Urologic Oncology: Seminars and Original Investigations, Vol. 33, Núm. 7, pp. 331.e1-331.e7
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Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
Journal of Genetics, Vol. 94, Núm. 2, pp. 335-341
2014
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Single nucleotide polymorphisms in DNA repair genes as risk factors associated to prostate cancer progression
BMC Medical Genetics, Vol. 15, Núm. 1
2013
2012
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Analysis of class II human leucocyte antigens in Italian and Spanish systemic sclerosis
Rheumatology, Vol. 51, Núm. 1, pp. 52-59
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Clinical significance of langerhans cells in squamous cell carcinoma of the larynx
Journal of Oncology
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The TT genotype of the STAT4 rs7574865 polymorphism is associated with high disease activity and disability in patients with early arthritis
PLoS ONE, Vol. 7, Núm. 8
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Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-G
Annals of the Rheumatic Diseases, Vol. 71, Núm. 5, pp. 777-784
2009
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Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus
Human Molecular Genetics, Vol. 18, Núm. 19, pp. 3739-3748
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Investigation of TLR5 and TLR7 as candidate genes for susceptibility to systemic lupus erythematosus
Clinical and Experimental Rheumatology