Maica Hurtado-Llavero
Edinburgh, SCT, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver Disease.
Journal: Cellular and molecular gastroenterology and hepatology
Published: May 04, 2020
UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophy.
Journal: Brain : a journal of neurology
Published: February 08, 2018
Cellular and Molecular Anatomy of the Human Neuromuscular Junction.
Journal: Cell reports
Published: June 14, 2017
Molecular analysis of axonal-intrinsic and glial-associated co-regulation of axon degeneration.
Journal: Cell death & disease
Published: April 13, 2017
Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation.
Journal: Expert review of proteomics
Published: June 23, 2016
Proteomic Profiling of Cranial (Superior) Cervical Ganglia Reveals Beta-Amyloid and Ubiquitin Proteasome System Perturbations in an Equine Multiple System Neuropathy.
Journal: Molecular & cellular proteomics : MCP
Published: August 20, 2015
Label-free quantitative proteomic profiling identifies disruption of ubiquitin homeostasis as a key driver of Schwann cell defects in spinal muscular atrophy.
Journal: Journal of proteome research
Published: August 26, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026