BIOTECMED
Institut d' investigació
Instituto de Investigación Sanitaria Fundación para la Investigación del Hospital Clínico de Valencia
Valencia, EspañaPublicacións en colaboración con investigadores/as de Instituto de Investigación Sanitaria Fundación para la Investigación del Hospital Clínico de Valencia (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