MARIA PILAR
GONZALEZ CABO
AJUDANT DOCTOR/A
Instituto de Biomedicina de Valencia
Valencia, EspañaPublications in collaboration with researchers from Instituto de Biomedicina de Valencia (13)
2020
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Cofilin dysregulation alters actin turnover in frataxin-deficient neurons
Scientific Reports, Vol. 10, Núm. 1
2019
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Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich’s Ataxia Mouse Model
Neurotherapeutics, Vol. 16, Núm. 2, pp. 432-449
2017
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Reversible axonal dystrophy by calcium modulation in frataxin-deficient sensory neurons of YG8R mice
Frontiers in Molecular Neuroscience, Vol. 10
2014
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Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolism
Frontiers in Cellular Neuroscience, Vol. 8, Núm. MAY
2013
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Mitochondrial pathophysiology in Friedreich's ataxia
Journal of Neurochemistry, Vol. 126, Núm. SUPPL.1, pp. 53-64
2011
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Differential expression of PGC-1α and metabolic sensors suggest age-dependent induction of mitochondrial biogenesis in friedreich ataxia fibroblasts
PLoS ONE, Vol. 6, Núm. 6
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Disruption of the ATP-binding cassette B7 (ABTM-1/ABCB7) induces oxidative stress and premature cell death in Caenorhabditis elegans
Journal of Biological Chemistry, Vol. 286, Núm. 24, pp. 21304-21314
2010
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Flavin adenine dinucleotide rescues the phenotype of frataxin deficiency
PLoS ONE, Vol. 5, Núm. 1
2009
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Friedreich ataxia: An update on animal models, frataxin function and therapies
Advances in Experimental Medicine and Biology
2007
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The frataxin-encoding operon of Caenorhabditis elegans shows complex structure and regulation
Genomics, Vol. 89, Núm. 3, pp. 392-401
2006
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Reduction of Caenorhabditis elegans frataxin increases sensitivity to oxidative stress, reduces lifespan, and causes lethality in a mitochondrial complex II mutant
FASEB Journal, Vol. 20, Núm. 1, pp. 172-174
2005
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Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology
Revista de Neurologia, Vol. 41, Núm. 7, pp. 409-422
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Frataxin interacts functionally with mitochondrial electron transport chain proteins
Human Molecular Genetics, Vol. 14, Núm. 15, pp. 2091-2098