Terapia Génica para Encefalopatías Congénitas
Centro de Investigación Médica Aplicada
Pamplona, EspañaPublicaciones en colaboración con investigadores/as de Centro de Investigación Médica Aplicada (56)
2024
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Characterization of brain transduction capability of a BBB-penetrant AAV vector in mice, rats and macaques reveals differences in expression profiles
Gene Therapy, Vol. 31, Núm. 9-10, pp. 455-466
2023
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Engineering U1-Based Tetracycline-Inducible Riboswitches to Control Gene Expression in Mammals
ACS Nano, Vol. 17, Núm. 23, pp. 23331-23346
2022
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Galectin-3 inhibition boosts the therapeutic efficacy of Semliki Forest virus in pediatric osteosarcoma
Molecular Therapy - Oncolytics, Vol. 26, pp. 246-264
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High value of 64Cu as a tool to evaluate the restoration of physiological copper excretion after gene therapy in Wilson's disease
Molecular Therapy - Methods and Clinical Development, Vol. 26, pp. 98-106
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Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma
New England Journal of Medicine, Vol. 386, Núm. 26, pp. 2471-2481
2021
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Adenovirus-mediated inducible expression of a pd-l1 blocking antibody in combination with macrophage depletion improves survival in a mouse model of peritoneal carcinomatosis
International Journal of Molecular Sciences, Vol. 22, Núm. 8
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AdrA as a Potential Immunomodulatory Candidate for STING-Mediated Antiviral Therapy That Required Both Type I IFN and TNF-α Production
Journal of immunology (Baltimore, Md. : 1950), Vol. 206, Núm. 2, pp. 376-385
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Local administration of IL-12 with an HC vector results in local and metastatic tumor control in pediatric osteosarcoma
Molecular Therapy - Oncolytics, Vol. 20, pp. 23-33
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Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations
Molecular Therapy - Nucleic Acids, Vol. 25, pp. 585-602
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Understanding the molecular mechanism of mir-877-3p could provide potential biomarkers and therapeutic targets in squamous cell carcinoma of the cervix
Cancers, Vol. 13, Núm. 7
2020
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Alterations of the Hippocampal Neurogenic Niche in a Mouse Model of Dravet Syndrome
Frontiers in Cell and Developmental Biology, Vol. 8
2019
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Danio rerio as model organism for adenoviral vector evaluation
Genes, Vol. 10, Núm. 12
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Influence of interleukin-8 and neutrophil extracellular trap (NET) formation in the tumor microenvironment: Is there a pathogenic role?
Journal of Immunology Research, Vol. 2019
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Liver Expression of a MiniATP7B Gene Results in Long-Term Restoration of Copper Homeostasis in a Wilson Disease Model in Mice
Hepatology, Vol. 70, Núm. 1, pp. 108-126
2018
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Brain copper storage after genetic long-term correction in a mouse model of Wilson disease
Neurology: Genetics, Vol. 4, Núm. 3
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Inhibition of adenovirus infection by mifepristone
Antiviral Research, Vol. 159, pp. 77-83
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Visualization of the therapeutic efficacy of a gene correction approach in Wilson's disease by laser-ablation inductively coupled mass spectrometry
Journal of Hepatology
2017
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Adaptation of vectors and drug-inducible systems for controlled expression of transgenes in the tumor microenvironment
Journal of Controlled Release, Vol. 268, pp. 247-258
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Improvement of Adeno-Associated Virus-Mediated Liver Transduction Efficacy by Regional Administration in Macaca fascicularis
Human Gene Therapy Clinical Development, Vol. 28, Núm. 2, pp. 68-73
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X-box Binding Protein 1 Regulates Unfolded Protein, Acute-Phase, and DNA Damage Responses During Regeneration of Mouse Liver
Gastroenterology, Vol. 152, Núm. 5, pp. 1203-1216.e15