Publicaciones en colaboración con investigadores/as de Hospital Universitario de Canarias (16)

2024

  1. TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43

    Neurobiology of Disease, Vol. 193

2022

  1. Pridopidine Promotes Synaptogenesis and Reduces Spatial Memory Deficits in the Alzheimer’s Disease APP/PS1 Mouse Model

    Neurotherapeutics, Vol. 19, Núm. 5, pp. 1566-1587

2021

  1. Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models

    iScience, Vol. 24, Núm. 12

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2019

  1. EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome

    Blood, Vol. 134, Núm. 3, pp. 277-290

  2. Inhibition of the mTOR pathway: A new mechanism of β cell toxicity induced by tacrolimus

    American Journal of Transplantation, Vol. 19, Núm. 12, pp. 3240-3249

  3. Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities

    Disease models & mechanisms, Vol. 12, Núm. 2

  4. Transgenic and physiological mouse models give insights into different aspects of amyotrophic lateral sclerosis

    DMM Disease Models and Mechanisms, Vol. 12, Núm. 1

  5. Uses for humanised mouse models in precision medicine for neurodegenerative disease

    Mammalian Genome, Vol. 30, Núm. 7-8, pp. 173-191

2018

  1. A genetic modifier suggests that endurance exercise exacerbates Huntington's disease

    Human Molecular Genetics, Vol. 27, Núm. 10, pp. 1723-1731

  2. Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

    EMBO Journal, Vol. 37, Núm. 11

  3. Pramipexole reduces soluble mutant huntingtin and protects striatal neurons through dopamine D3 receptors in a genetic model of Huntington's disease

    Experimental Neurology, Vol. 299, pp. 137-147

  4. Skeletal Muscle Modulates Huntington’s Disease Pathogenesis in Mice: Role of Physical Exercise

    Journal of Experimental Neuroscience

  5. TDP-43 mutations increase HNRNP A1-7B through gain of splicing function

    Brain

2003

  1. Effects of dopaminergic cell degeneration on electrophysiological characteristics and GAD65/GAD67 expression in the substantia nigra: Different action on GABA cell subpopulations

    Movement Disorders, Vol. 18, Núm. 3, pp. 254-266

2001

  1. Colocalization of tyrosine hydroxylase and GAD65 mRNA in mesostriatal neurons

    European Journal of Neuroscience, Vol. 13, Núm. 1, pp. 57-67