Publications (13) SARA HERNANDEZ ESTAÑOL publications

2023

  1. 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

2021

  1. 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

  1. 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

  1. Chemotherapeutic agent 5-fluorouracil increases survival of SOD1 mouse model of ALS

    PLoS ONE, Vol. 14, Núm. 1

  2. Exposure of a cryptic Hsp70 binding site determines the cytotoxicity of the ALS-associated SOD1-mutant A4V

    Protein engineering, design & selection : PEDS, Vol. 32, Núm. 10, pp. 443-457

  3. 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

2017

  1. Neuregulin 1-ErbB module in C-bouton synapses on somatic motor neurons: Molecular compartmentation and response to peripheral nerve injury

    Scientific Reports, Vol. 7

2013

  1. 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

  2. Rapamycin increases survival in ALS mice lacking mature lymphocytes

    Molecular Neurodegeneration, Vol. 8, Núm. 1

2011

  1. 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

  1. 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

  2. Neurotoxic species of misfolded SOD1G93A recognized by antibodies against the P2X4 subunit of the ATP receptor accumulate in damaged neurons of transgenic animal models of amyotrophic lateral sclerosis

    Journal of Neuropathology and Experimental Neurology, Vol. 69, Núm. 2, pp. 176-187

2008

  1. Strong P2X4 purinergic receptor-like immunoreactivity is selectively associated with degenerating neurons in transgenic rodent models of amyotrophic lateral sclerosis

    Journal of Comparative Neurology, Vol. 506, Núm. 1, pp. 75-92