- Institut de Recerca Biomèdica de Lleida (IRB-Lleida)
Instituto de investigación
![Foto de Josep E.](/img/nophoto.png)
Josep E.
Esquerda Colell
Publicaciones en las que colabora con Josep E. Esquerda Colell (51)
2023
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NOD mouse dorsal root ganglia display morphological and gene expression defects before and during autoimmune diabetes development
Frontiers in Endocrinology, Vol. 14
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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
2021
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Beneficial effects of dietary supplementation with green tea catechins and cocoa flavanols on aging-related regressive changes in the mouse neuromuscular system
Aging, Vol. 13, Núm. 14, pp. 18051-18093
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Microglial recruitment and mechanisms involved in the disruption of afferent synaptic terminals on spinal cord motor neurons after acute peripheral nerve injury
GLIA, Vol. 69, Núm. 5, pp. 1216-1240
2020
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Motoneuron deafferentation and gliosis occur in association with neuromuscular regressive changes during ageing in mice
Journal of Cachexia, Sarcopenia and Muscle, Vol. 11, Núm. 6, pp. 1628-1660
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The Y172 Monoclonal Antibody Against p-c-Jun (Ser63) Is a Marker of the Postsynaptic Compartment of C-Type Cholinergic Afferent Synapses on Motoneurons
Frontiers in Cellular Neuroscience, Vol. 13
2019
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Localization and dynamic changes of neuregulin-1 at C-type synaptic boutons in association with motor neuron injury and repair
FASEB Journal, Vol. 33, Núm. 7, pp. 7833-7851
2018
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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
2016
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Chronic Treatment with the AMPK Agonist AICAR Prevents Skeletal Muscle Pathology but Fails to Improve Clinical Outcome in a Mouse Model of Severe Spinal Muscular Atrophy
Neurotherapeutics, Vol. 13, Núm. 1, pp. 198-216
2015
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Adverse effects of a SOD1-peptide immunotherapy on SOD1G93A mouse slow model of amyotrophic lateral sclerosis
Neuroscience, Vol. 310, pp. 38-50
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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Mechanisms involved in spinal cord central synapse loss in a mouse model of spinal muscular atrophy
Journal of Neuropathology and Experimental Neurology, Vol. 73, Núm. 6, pp. 519-535
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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
2013
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Chronic treatment with lithium does not improve neuromuscular phenotype in a mouse model of severe spinal muscular atrophy
Neuroscience, Vol. 250, pp. 417-433
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Immunodetection of disease-associated conformers of mutant Cu/Zn superoxide dismutase 1 selectively expressed in degenerating neurons in amyotrophic lateral sclerosis
Journal of Neuropathology and Experimental Neurology, Vol. 72, Núm. 7, pp. 646-661
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
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Sera from amyotrophic lateral sclerosis patients induce the non-canonical activation of NMDA receptors "in vitro"
Neurochemistry International, Vol. 59, Núm. 6, pp. 954-964
2010
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Increased intramuscular nerve branching and inhibition of programmed cell death of chick embryo motoneurons by immunoglobulins from patients with motoneuron disease
Journal of Neuroimmunology, Vol. 229, Núm. 1-2, pp. 157-168