JORDI
CALDERO PARDO
CU
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Instituto de Investigación Biomédica de Lleida
Lleida, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Investigación Biomédica de Lleida (12)
2023
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Persistent NRG1 Type III Overexpression in Spinal Motor Neurons Has No Therapeutic Effect on ALS-Related Pathology in SOD1G93A Mice
Neurotherapeutics, Vol. 20, Núm. 6, pp. 1820-1834
2022
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Accumulation of misfolded SOD1 outlines distinct patterns of motor neuron pathology and death during disease progression in a SOD1G93A mouse model of amyotrophic lateral sclerosis
Brain Pathology, Vol. 32, Núm. 6
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SMN Is Physiologically Downregulated at Wild-Type Motor Nerve Terminals but Aggregates Together with Neurofilaments in SMA Mouse Models
Biomolecules, Vol. 12, Núm. 10
2021
2020
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Nusinersen ameliorates motor function and prevents motoneuron Cajal body disassembly and abnormal poly(A) RNA distribution in a SMA mouse model
Scientific Reports, Vol. 10, Núm. 1
2018
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Accumulation of poly(A) RNA in nuclear granules enriched in Sam68 in motor neurons from the SMNΔ7 mouse model of SMA
Scientific Reports, Vol. 8, Núm. 1
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Glial activation and central synapse loss, but not motoneuron degeneration, are prevented by the sigma-1 receptor agonist pre-084 in the SMN2B/ mouse model of spinal muscular atrophy
Journal of Neuropathology and Experimental Neurology, Vol. 77, Núm. 7, pp. 577-597
2017
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Cellular bases of the RNA metabolism dysfunction in motor neurons of a murine model of spinal muscular atrophy: Role of Cajal bodies and the nucleolus
Neurobiology of Disease, Vol. 108, pp. 83-99
2014
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Accumulation of misfolded SOD1 in dorsal root ganglion degenerating proprioceptive sensory neurons of transgenic mice with amyotrophic lateral sclerosis
BioMed Research International, Vol. 2014
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Neuregulin-1 is concentrated in the postsynaptic subsurface cistern of C-bouton inputs to α-motoneurons and altered during motoneuron diseases
FASEB Journal, Vol. 28, Núm. 8, pp. 3618-3632
2011
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Defective neuromuscular junction organization and postnatal myogenesis in mice with severe spinal muscular atrophy
Journal of Neuropathology and Experimental Neurology, Vol. 70, Núm. 6, pp. 444-461