BIOTECMED
Institut d' investigació
Instituto de Investigación Sanitaria Fundación para la Investigación del Hospital Clínico de Valencia
Valencia, EspañaInstituto de Investigación Sanitaria Fundación para la Investigación del Hospital Clínico de Valencia-ko ikertzaileekin lankidetzan egindako argitalpenak (31)
2024
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Alterations in the volume and shape of the basal ganglia and thalamus in schizophrenia with auditory hallucinations
Progress in Neuro-Psychopharmacology and Biological Psychiatry, Vol. 131
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AntimiR treatment corrects myotonic dystrophy primary cell defects across several CTG repeat expansions with a dual mechanism of action
Science advances, Vol. 10, Núm. 41, pp. eadn6525
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Early chronic fasudil treatment rescues hippocampal alterations in the Ts65Dn model for down syndrome
Neurochemistry International, Vol. 174
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Mesenchymal Stem Cells Cultured in a 3D Microgel Environment Containing Platelet-Rich Plasma Significantly Modify Their Chondrogenesis-Related miRNA Expression
International Journal of Molecular Sciences, Vol. 25, Núm. 2
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Msi2 enhances muscle dysfunction in a myotonic dystrophy type 1 mouse model
Biomedical Journal, Vol. 47, Núm. 4
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Progressive loss of cortical gray matter in first episode psychosis patients with auditory hallucinations
Schizophrenia Research, Vol. 267, pp. 534-545
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Taurine activates the AKT-mTOR axis to restore muscle mass and contractile strength in human 3D in vitro models of steroid myopathy
Disease models & mechanisms, Vol. 17, Núm. 4
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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
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Therapeutic potential of oleic acid supplementation in myotonic dystrophy muscle cell models
Biological Research, Vol. 57, Núm. 1
2023
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BlockmiR AONs as Site-Specific Therapeutic MBNL Modulation in Myotonic Dystrophy 2D and 3D Muscle Cells and HSALR Mice
Pharmaceutics, Vol. 15, Núm. 4
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CRISPR-Cas9 editing of a TNPO3 mutation in a muscle cell model of limb-girdle muscular dystrophy type D2
Molecular Therapy - Nucleic Acids, Vol. 31, pp. 324-338
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Fluoxetine increased adult neurogenesis is mediated by 5-HT3 receptor
Neuroscience Letters, Vol. 795
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Natural Compound Boldine Lessens Myotonic Dystrophy Type 1 Phenotypes in DM1 Drosophila Models, Patient-Derived Cell Lines, and HSALR Mice
International Journal of Molecular Sciences, Vol. 24, Núm. 12
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Neuroprotective properties of queen bee acid by autophagy induction
Cell Biology and Toxicology, Vol. 39, Núm. 3, pp. 751-770
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Peptide-conjugated antimiRs improve myotonic dystrophy type 1 phenotypes by promoting endogenous MBNL1 expression
Molecular Therapy - Nucleic Acids, Vol. 34
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Quantitative magnetic resonance imaging assessment of muscle composition in myotonic dystrophy mice
Scientific Reports, Vol. 13, Núm. 1
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The myotonic dystrophy type 1 drug development pipeline: 2022 edition
Drug Discovery Today, Vol. 28, Núm. 3
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Volume alterations of the hippocampus and amygdala in patients with schizophrenia and persistent auditory hallucinations
Revista de Psiquiatria y Salud Mental
2022
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Deciphering the Complex Molecular Pathogenesis of Myotonic Dystrophy Type 1 through Omics Studies
International Journal of Molecular Sciences, Vol. 23, Núm. 3
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Development of potent tripodal G-quadruplex DNA binders and their efficient delivery to cancer cells by aptamer functionalised liposomes
Organic and Biomolecular Chemistry, Vol. 21, Núm. 5, pp. 1000-1007