MARTA
SECO CERVERA
INVEST CONT VALi+d
Centro de Investigación Príncipe Felipe
Valencia, EspañaCentro de Investigación Príncipe Felipe -ko ikertzaileekin lankidetzan egindako argitalpenak (12)
2020
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Acute depletion of telomerase components DKC1 and NOP10 induces oxidative stress and disrupts ribosomal biogenesis via NPM1 and activation of the P53 pathway
Biochimica et Biophysica Acta - Molecular Cell Research, Vol. 1867, Núm. 12
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Oxidative stress, a crossroad between rare diseases and neurodegeneration
Antioxidants, Vol. 9, Núm. 4
2019
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Corrigendum to “A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration” [Biochim. Biophys. Acta 1863 (2017) 801–809](S0925443917300078)(10.1016/j.bbadis.2017.01.003)
Biochimica et Biophysica Acta - Molecular Basis of Disease
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Epigenetic Regulation in the Pathogenesis of Sjögren Syndrome and Rheumatoid Arthritis
Frontiers in Genetics, Vol. 10
2018
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Oxidative stress and the epigenetics of cell senescence: Insights from progeroid syndromes
Current Pharmaceutical Design, Vol. 24, Núm. 40, pp. 4755-4770
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Small RNA-seq analysis of circulating miRNAs to identify phenotypic variability in Friedreich's ataxia patients
Scientific Data, Vol. 5
2017
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A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1863, Núm. 3, pp. 801-809
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Circulating miR-323-3p is a biomarker for cardiomyopathy and an indicator of phenotypic variability in Friedreich's ataxia patients
Scientific Reports, Vol. 7, Núm. 1
2015
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Increased Oxidative Stress and Impaired Antioxidant Response in Lafora Disease
Molecular Neurobiology, Vol. 51, Núm. 3, pp. 932-946
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Mitochondrial defects and neuromuscular degeneration caused by altered expression of Drosophila Gdap1: Implications for the Charcot-Marie-Tooth neuropathy
Human Molecular Genetics, Vol. 24, Núm. 1, pp. 21-36
2014
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Oxidative stress and antioxidant response in fibroblasts from Werner and Atypical Werner Syndromes
Aging, Vol. 6, Núm. 3, pp. 231-245
2013
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Lafora disease fibroblasts exemplify the molecular interdependence between thioredoxin 1 and the proteasome in mammalian cells
Free Radical Biology and Medicine, Vol. 65, pp. 347-359