Beatriz Diaz-Garcia
Malaga, AN, Spain
Last Updated: 09/26/2026
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Found 12 publications
Oligodendroctyes: the forgotten players of diabetes pathophysiology.
Journal: Neural regeneration research
Published: October 24, 2023
Tunable hydrogel-based micropillar arrays for myelination studies.
Journal: Nature methods
Published: August 28, 2023
The dorsal root ganglion as a target for neurorestoration in neuropathic pain.
Journal: Neural regeneration research
Published: July 25, 2023
Comparing RNA extraction methods to face the variations in RNA quality using two human biological matrices.
Journal: Molecular biology reports
Published: December 27, 2022
Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency.
Journal: Annals of neurology
Published: November 22, 2016
Lack of aprataxin impairs mitochondrial functions via downregulation of the APE1/NRF1/NRF2 pathway.
Journal: Human molecular genetics
Published: March 13, 2015
Fhl1 W122S causes loss of protein function and late-onset mild myopathy.
Journal: Human molecular genetics
Published: October 03, 2014
Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency.
Journal: EMBO molecular medicine
Published: June 28, 2014
Loss of lysophosphatidic acid receptor LPA1 alters oligodendrocyte differentiation and myelination in the mouse cerebral cortex.
Journal: Brain structure & function
Published: May 27, 2014
Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathy.
Journal: Brain : a journal of neurology
Published: April 15, 2014
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9.
Journal: JAMA neurology
Published: July 10, 2013
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation.
Journal: American journal of human genetics
Published: June 09, 2012
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Last Updated: 09/26/2026