BIOTECMED
Institut d' investigació
Centro de Investigación Príncipe Felipe
Valencia, EspañaCentro de Investigación Príncipe Felipe -ko ikertzaileekin lankidetzan egindako argitalpenak (118)
2024
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A renal clearable fluorogenic probe for in vivo β-galactosidase activity detection during aging and senolysis
Nature Communications, Vol. 15, Núm. 1
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SUMOylation modulates eIF5A activities in both yeast and pancreatic ductal adenocarcinoma cells
Cellular and Molecular Biology Letters, Vol. 29, Núm. 1
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The impact of sex on gene expression in the brain of schizophrenic patients: a systematic review and meta-analysis of transcriptomic studies
Biology of Sex Differences, Vol. 15, Núm. 1
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The role of microRNAs in understanding sex-based differences in Alzheimer’s disease
Biology of Sex Differences, Vol. 15, Núm. 1
2023
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Neuroprotective properties of queen bee acid by autophagy induction
Cell Biology and Toxicology, Vol. 39, Núm. 3, pp. 751-770
2022
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Beyond the Brain: MIDS Extends BIDS to Multiple Modalities and Anatomical Regions
Studies in health technology and informatics, Vol. 295, pp. 116-117
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Beyond the Brain: MIDS Extends BIDS to Multiple Modalities and Anatomical Regions
Studies in Health Technology and Informatics
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Metabolic Alterations in a Drosophila Model of Parkinson’s Disease Based on DJ-1 Deficiency
Cells, Vol. 11, Núm. 3
2021
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A High-Throughput Chemical Screen in DJ-1β Mutant Flies Identifies Zaprinast as a Potential Parkinson’s Disease Treatment
Neurotherapeutics, Vol. 18, Núm. 4, pp. 2565-2578
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Bioengineered in vitro 3D model of myotonic dystrophy type 1 human skeletal muscle
Biofabrication, Vol. 13, Núm. 3
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Inhibition of autophagy rescues muscle atrophy in a LGMDD2 Drosophila model
FASEB Journal, Vol. 35, Núm. 10
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Musashi-2 contributes to myotonic dystrophy muscle dysfunction by promoting excessive autophagy through miR-7 biogenesis repression
Molecular Therapy - Nucleic Acids, Vol. 25, pp. 652-667
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Myotonic dystrophy type 1 drug development: A pipeline toward the market
Drug Discovery Today, Vol. 26, Núm. 7, pp. 1765-1772
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Nrg1 haploinsufficiency alters inhibitory cortical circuits
Neurobiology of Disease, Vol. 157
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Rabphilin silencing causes dilated cardiomyopathy in a Drosophila model of nephrocyte damage
Scientific Reports, Vol. 11, Núm. 1
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The hallmarks of myotonic dystrophy type 1 muscle dysfunction
Biological Reviews, Vol. 96, Núm. 2, pp. 716-730
2020
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Cofilin dysregulation alters actin turnover in frataxin-deficient neurons
Scientific Reports, Vol. 10, Núm. 1
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Drosophila SMN2 minigene reporter model identifies moxifloxacin as a candidate therapy for SMA
FASEB Journal, Vol. 34, Núm. 2, pp. 3021-3036
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Erratum: Structures of collagen IV globular domains: Insight into associated pathologies, folding and network assembly (IUCrJ (2018) 5 765-779) DOI: 10.1107/S2052252518012459)
IUCrJ