Fisiología, Anatomía y Biología Celular
Department

Rocío
Ruiz Laza
Publications by the researcher in collaboration with Rocío Ruiz Laza (14)
2025
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HERC1 E3 Ubiquitin Ligase Is Necessary for Autophagy Processes and for the Maintenance and Homeostasis of Vesicles in Motor Nerve Terminals, but Not for Proteasomal Activity
International Journal of Molecular Sciences, Vol. 26, Núm. 2
2023
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ARG1-expressing microglia show a distinct molecular signature and modulate postnatal development and function of the mouse brain
Nature Neuroscience, Vol. 26, Núm. 6, pp. 1008-1020
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Targeting galectin-3 to counteract spike-phase uncoupling of fast-spiking interneurons to gamma oscillations in Alzheimer’s disease
Translational Neurodegeneration, Vol. 12, Núm. 1
2022
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The HERC proteins and the nervous system
Seminars in Cell and Developmental Biology, Vol. 132, pp. 5-15
2021
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Selective deletion of Caspase-3 gene in the dopaminergic system exhibits autistic-like behaviour
Progress in Neuro-Psychopharmacology and Biological Psychiatry, Vol. 104
2020
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HERC1 Ubiquitin Ligase Is Required for Hippocampal Learning and Memory
Frontiers in Neuroanatomy, Vol. 14
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The Ubiquitin Proteasome System in Neuromuscular Disorders: Moving Beyond Movement
International journal of molecular sciences, Vol. 21, Núm. 17
2018
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HERC1 Ubiquitin Ligase Is Required for Normal Axonal Myelination in the Peripheral Nervous System
Molecular Neurobiology, Vol. 55, Núm. 12, pp. 8856-8868
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Mutation of the HERC 1 Ubiquitin Ligase Impairs Associative Learning in the Lateral Amygdala
Molecular Neurobiology, Vol. 55, Núm. 2, pp. 1157-1168
2016
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AMPK function in aging process
Current Drug Targets, Vol. 17, Núm. 8, pp. 932-941
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HERC 1 ubiquitin ligase mutation affects neocortical, CA3 hippocampal and spinal cord projection neurons: An ultrastructural study
Frontiers in Neuroanatomy, Vol. 10, Núm. APR
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The HERC2 ubiquitin ligase is essential for embryonic development and regulates motor coordination
Oncotarget, Vol. 7, Núm. 35, pp. 56083-56106
2015
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The HERC1 E3 Ubiquitin Ligase is essential for normal development and for neurotransmission at the mouse neuromuscular junction
Cellular and Molecular Life Sciences, Vol. 72, Núm. 15, pp. 2961-2971
2013
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Motor learning of mice lacking cerebellar Purkinje cells
Frontiers in Neuroanatomy