ENCARNACIÓN
MEDINA CARMONA
PROGRAMA INVESTIGACION RAMON Y CAJAL
Publicaciones (18) Publicaciones de ENCARNACIÓN MEDINA CARMONA
2023
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Cell Survival Enabled by Leakage of a Labile Metabolic Intermediate
Molecular biology and evolution, Vol. 40, Núm. 3
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Structure-based discovery and in vitro validation of inhibitors of chloride intracellular channel 4 protein
Computational and Structural Biotechnology Journal, Vol. 21, pp. 688-701
2022
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An Updated View of the Trypanosoma cruzi Life Cycle: Intervention Points for an Effective Treatment
ACS infectious diseases, Vol. 8, Núm. 6, pp. 1107-1115
2020
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A quantitative assay to study the lipid selectivity of membrane-associated systems using solution NMR
Chemical Communications, Vol. 56, Núm. 78, pp. 11665-11668
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Chagas Disease: Current View of an Ancient and Global Chemotherapy Challenge
ACS Infectious Diseases, Vol. 6, Núm. 11, pp. 2830-2843
2019
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Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses
Human Molecular Genetics, Vol. 28, Núm. 1, pp. 1-15
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New polyamine drugs as more effective antichagas agents than benznidazole in both the acute and chronic phases
European Journal of Medicinal Chemistry, Vol. 164, pp. 27-46
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Phosphorylation compromises FAD binding and intracellular stability of wild-type and cancer-associated NQO1: Insights into flavo-proteome stability
International Journal of Biological Macromolecules, Vol. 125, pp. 1275-1288
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Synthesis and biological evaluation of new long-chain squaramides as anti-chagasic agents in the BALB/c mouse model
Bioorganic and Medicinal Chemistry, Vol. 27, Núm. 5, pp. 865-879
2018
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Second Generation of Mannich Base-Type Derivatives with in Vivo Activity against Trypanosoma cruzi
Journal of Medicinal Chemistry, Vol. 61, Núm. 13, pp. 5643-5663
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Synthesis and Biological in vitro and in vivo Evaluation of 2-(5-Nitroindazol-1-yl)ethylamines and Related Compounds as Potential Therapeutic Alternatives for Chagas Disease
ChemMedChem, Vol. 13, Núm. 19, pp. 2104-2118
2017
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A mechanism for cancer-associated inactivation of NQO1 due to P187S and its reactivation by the consensus mutation H80R
FEBS Letters, Vol. 591, Núm. 18, pp. 2826-2835
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Enhanced vulnerability of human proteins towards disease-associated inactivation through divergent evolution
Human Molecular Genetics, Vol. 26, Núm. 18, pp. 3531-3544
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Site-to-site interdomain communication may mediate different loss-of-function mechanisms in a cancer-associated NQO1 polymorphism
Scientific Reports, Vol. 7
2016
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Conformational dynamics is key to understanding loss-of-function of NQO1 cancer-associated polymorphisms and its correction by pharmacological ligands
Scientific Reports, Vol. 6
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Erratum: Conformational dynamics is key to understanding loss-of-function of NQO1 cancer-associated polymorphisms and its correction by pharmacological ligands (Scientific Reports (2016) 6 (20331) DOI: 10.1038/srep20331)
Scientific Reports
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Natural small molecules as stabilizers and activators of cancer-associated NQO1 polymorphisms
Current Drug Targets, Vol. 17, Núm. 13, pp. 1506-1514
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The chondroitin sulfate/dermatan sulfate 4-O-endosulfatase from marine bacterium Vibrio sp FC509 is a dimeric species: Biophysical characterization of an endosulfatase
Biochimie, Vol. 131, pp. 85-95