
MIGUEL
PAYA PERIS
CATEDRÁTICO/A DE UNIVERSIDAD
Publications (110) MIGUEL PAYA PERIS publications
2019
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Defective induction of COX-2 expression by psoriatic fibroblasts promotes pro-inflammatory activation of macrophages
Frontiers in Immunology, Vol. 10, Núm. MAR
2017
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Adenosine A2A and A2B Receptors Differentially Modulate Keratinocyte Proliferation: Possible Deregulation in Psoriatic Epidermis
Journal of Investigative Dermatology, Vol. 137, Núm. 1, pp. 123-131
2016
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Pharmacological Interventions to Ameliorate Neuropathological Symptoms in a Mouse Model of Lafora Disease
Molecular Neurobiology, Vol. 53, Núm. 2, pp. 1296-1309
2013
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NF-κB and STAT3 inhibition as a therapeutic strategy in psoriasis: In vitro and in vivo effects of BTH
Journal of Investigative Dermatology, Vol. 133, Núm. 10, pp. 2362-2371
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Potential antipsoriatic effect of chondroitin sulfate through inhibition of NF-κB and STAT3 in human keratinocytes
Pharmacological Research, Vol. 70, Núm. 1, pp. 20-26
2011
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Papel de la activacion de NF-KB y de la produccion de TNFá en queratinocitos primarios humanos estimulados con TPA: XXXII Congreso Nacional de la SEF: póster premiado
Actualidad en farmacología y terapéutica, Vol. 9, Núm. 2, pp. 144-146
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Perthamides C-F, potent human antipsoriatic cyclopeptides
Tetrahedron, Vol. 67, Núm. 40, pp. 7780-7786
2010
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Anthrax lethal toxin down-regulates type-IIA secreted phospholipase A2 expression through MAPK/NF-κB inactivation
Biochemical Pharmacology, Vol. 79, Núm. 8, pp. 1149-1155
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Toward the discovery of new agents able to inhibit the expression of microsomal prostaglandin e synthase-1 enzyme as promising tools in drug development
Chemical Biology and Drug Design, Vol. 76, Núm. 1, pp. 17-24
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Type-IIA secreted phospholipase A2 is an endogenous antibiotic-like protein of the host
Biochimie, Vol. 92, Núm. 6, pp. 583-587
2009
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Anti-inflammatory and analgesic activity of a novel inhibitor of microsomal prostaglandin E synthase-1 expression
European Journal of Pharmacology, Vol. 620, Núm. 1-3, pp. 112-119
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Coscinolactams A and B: new nitrogen-containing sesterterpenoids from the marine sponge Coscinoderma mathewsi exerting anti-inflammatory properties
Tetrahedron, Vol. 65, Núm. 15, pp. 2905-2909
2008
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Avarol inhibits TNF-α generation and NF-κB activation in human cells and in animal models
Life Sciences, Vol. 82, Núm. 5-6, pp. 256-264
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Development of a second generation of inhibitors of microsomal prostaglandin E synthase 1 expression bearing the γ-hydroxybutenolide scaffold
Bioorganic and Medicinal Chemistry, Vol. 16, Núm. 19, pp. 9056-9064
2007
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Antipsoriatic effects of avarol-3′-thiosalicylate are mediated by inhibition of TNF-α generation and NF-αB activation in mouse skin
British Journal of Pharmacology, Vol. 152, Núm. 3, pp. 353-365
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Synthesis and evaluation of diverse thio avarol derivatives as potential UVB photoprotective candidates
Bioorganic and Medicinal Chemistry Letters, Vol. 17, Núm. 9, pp. 2561-2565
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Synthesis and pharmacological evaluation of a selected library of new potential anti-inflammatory agents bearing the γ-hydroxybutenolide scaffold: A new class of inhibitors of prostanoid production through the selective modulation of microsomal prostaglandin E synthase-1 expression
Journal of Medicinal Chemistry, Vol. 50, Núm. 9, pp. 2176-2184
2006
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Identification of avarol derivatives as potential antipsoriatic drugs using an in vitro model for keratinocyte growth and differentiation
Life Sciences, Vol. 79, Núm. 25, pp. 2395-2404
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Marine sponge metabolites for the control of inflammatory diseases
Current Opinion in Investigational Drugs, Vol. 7, Núm. 11, pp. 974-979
2005
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Búsqueda y evaluación de nuevos agentes naturales con actividad antiinflamatoria y antiartrítica
Revista de fitoterapia, Vol. 5, Núm. 1, pp. 82