Publicacións (44) Publicacións de AURORA GOMEZ DURAN

2024

  1. 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

  2. Mitophagy curtails cytosolic mtDNA-dependent activation of cGAS/STING inflammation during aging

    Nature Communications, Vol. 15, Núm. 1

2022

  1. Editorial: Molecular and cellular pathways leading to mitochondrial dysfunction and neurodegeneration: Lessons from in vivo models

    Frontiers in Neuroscience

  2. p38 MAPK priming boosts VSMC proliferation and arteriogenesis by promoting PGC1α-dependent mitochondrial dynamics

    Scientific Reports, Vol. 12, Núm. 1

2021

  1. An atlas of mitochondrial DNA genotype–phenotype associations in the UK Biobank

    Nature Genetics, Vol. 53, Núm. 7, pp. 982-993

  2. Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases

    Nature Medicine, Vol. 27, Núm. 9, pp. 1564-1575

  3. Oxygen tension modulates the mitochondrial genetic bottleneck and influences the segregation of a heteroplasmic mtDNA variant in vitro

    Communications Biology, Vol. 4, Núm. 1

  4. 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

  1. Metabolic effects of bezafibrate in mitochondrial disease

    EMBO Molecular Medicine, Vol. 12, Núm. 3

  2. Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency

    EMBO Journal, Vol. 39, Núm. 23

  3. Methods for the identification of mitochondrial DNA variants

    The Human Mitochondrial Genome: From Basic Biology to Disease (Elsevier), pp. 243-275

2019

  1. Mitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in Drosophila

    Nature Communications, Vol. 10, Núm. 1

2018

  1. Erratum: Correction: Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations (PLoS genetics (2017) 13 12 (e1007126))

    PLoS genetics

  2. Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant Defenses

    Frontiers in Immunology, Vol. 9

  3. 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

  4. Oldies but goldies mtDNA population variants and neurodegenerative diseases

    Frontiers in Neuroscience, Vol. 12, Núm. OCT

2017

  1. Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations

    PLoS Genetics, Vol. 13, Núm. 12

  2. 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

  3. Mutations in mitochondrial DNA causing tubulointerstitial kidney disease

    PLoS Genetics, Vol. 13, Núm. 3

2016

  1. 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