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AURORA
GOMEZ DURAN
Investigadora contratada Ramón y Cajal
Publicacións (44) Publicacións de AURORA GOMEZ DURAN
2024
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Correction to: Mitophagy curtails cytosolic mtDNA-dependent activation of cGAS/STING inflammation during aging (Nature Communications, (2024), 15, 1, (830), 10.1038/s41467-024-45044-1)
Nature Communications
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Mitophagy curtails cytosolic mtDNA-dependent activation of cGAS/STING inflammation during aging
Nature Communications, Vol. 15, Núm. 1
2022
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Editorial: Molecular and cellular pathways leading to mitochondrial dysfunction and neurodegeneration: Lessons from in vivo models
Frontiers in Neuroscience
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p38 MAPK priming boosts VSMC proliferation and arteriogenesis by promoting PGC1α-dependent mitochondrial dynamics
Scientific Reports, Vol. 12, Núm. 1
2021
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An atlas of mitochondrial DNA genotype–phenotype associations in the UK Biobank
Nature Genetics, Vol. 53, Núm. 7, pp. 982-993
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Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases
Nature Medicine, Vol. 27, Núm. 9, pp. 1564-1575
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Oxygen tension modulates the mitochondrial genetic bottleneck and influences the segregation of a heteroplasmic mtDNA variant in vitro
Communications Biology, Vol. 4, Núm. 1
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Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissues
Nucleic acids research, Vol. 49, Núm. 22, pp. 12757-12768
2020
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Metabolic effects of bezafibrate in mitochondrial disease
EMBO Molecular Medicine, Vol. 12, Núm. 3
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Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency
EMBO Journal, Vol. 39, Núm. 23
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Methods for the identification of mitochondrial DNA variants
The Human Mitochondrial Genome: From Basic Biology to Disease (Elsevier), pp. 243-275
2019
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Mitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in Drosophila
Nature Communications, Vol. 10, Núm. 1
2018
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Erratum: Correction: Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations (PLoS genetics (2017) 13 12 (e1007126))
PLoS genetics
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Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant Defenses
Frontiers in Immunology, Vol. 9
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Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family
Brain, Vol. 141, Núm. 1, pp. 55-62
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Oldies but goldies mtDNA population variants and neurodegenerative diseases
Frontiers in Neuroscience, Vol. 12, Núm. OCT
2017
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Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations
PLoS Genetics, Vol. 13, Núm. 12
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Mitochondrial DNA depletion induces innate immune dysfunction rescued by IFN-γ
Journal of Allergy and Clinical Immunology, Vol. 140, Núm. 5, pp. 1461-1464.e8
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Mutations in mitochondrial DNA causing tubulointerstitial kidney disease
PLoS Genetics, Vol. 13, Núm. 3
2016
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Altered RNA metabolism due to a homozygous RBM7 mutation in a patient with spinal motor neuropathy
Human Molecular Genetics, Vol. 25, Núm. 14, pp. 2985-2996