Guillermo López Lluch-rekin lankidetzan egindako argitalpenak (18)

2024

  1. New variants expand the neurological phenotype of COQ7 deficiency

    Journal of Inherited Metabolic Disease

  2. Prenatal and progressive coenzyme Q10 administration to mitigate muscle dysfunction in mitochondrial disease

    Journal of Cachexia, Sarcopenia and Muscle

2022

  1. Calorie Restriction Rescues Mitochondrial Dysfunction in Adck2-Deficient Skeletal Muscle

    Frontiers in Physiology, Vol. 13

2021

  1. Coenzyme q at the hinge of health and metabolic diseases

    Antioxidants, Vol. 10, Núm. 11

  2. Secondary CoQ10 deficiency, bioenergetics unbalance in disease and aging

    BioFactors, Vol. 47, Núm. 4, pp. 551-569

2020

  1. Age-related mitochondrial dysfunction as a key factor in COVID-19 disease

    Experimental Gerontology, Vol. 142

2019

  1. ADCK2 haploinsufficiency reduces mitochondrial lipid oxidation and causes myopathy associated with CoQ deficiency

    Journal of Clinical Medicine, Vol. 8, Núm. 9

  2. Study of the genotype-phenotype correlation in fibroblasts of patients with mutations in COQ4

    Biosaia: Revista de los másteres de Biotecnología Sanitaria y Biotecnología Ambiental, Industrial y Alimentaria, Núm. 8

2018

  1. Mitochondrial dysfunction in metabolism and ageing: shared mechanisms and outcomes?

    Biogerontology, Vol. 19, Núm. 6, pp. 461-480

2016

  1. RNA-binding proteins regulate cell respiration and coenzyme Q biosynthesis by post-transcriptional regulation of COQ7

    RNA Biology, Vol. 13, Núm. 7, pp. 622-634

2015

  1. Mitochondrial responsibility in ageing process: innocent, suspect or guilty

    Biogerontology, Vol. 16, Núm. 5, pp. 599-620

2005

  1. Coenzyme Q distribution in HL-60 human cells depends on the endomembrane system

    Biochimica et Biophysica Acta - Biomembranes, Vol. 1713, Núm. 2, pp. 129-137

  2. Inhibition of COX activity by NSAIDs or ascorbate increases cAMP levels and enhances differentiation in 1α,25-dihydroxyvitamin D3-induced HL-60 cells

    Archives of Biochemistry and Biophysics, Vol. 436, Núm. 1, pp. 32-39

  3. Specificity of coenzyme Q 10 for a balanced function of respiratory chain and endogenous ubiquinone biosynthesis in human cells

    Biochimica et Biophysica Acta - Bioenergetics, Vol. 1706, Núm. 1-2, pp. 174-183

2004

  1. Demethoxy-Q, an intermediate of coenzyme Q biosynthesis, fails to support respiration in Saccharomyces cerevisiae and lacks antioxidant activity

    Journal of Biological Chemistry, Vol. 279, Núm. 25, pp. 25995-26004

2002

  1. Ceramide-dependent caspase 3 activation is prevented by coenzyme Q from plasma membrane in serum-deprived cells

    Free Radical Research, Vol. 36, Núm. 4, pp. 369-374

2000

  1. Coenzyme Q protects cells against serum withdrawal-induced apoptosis by inhibition of ceramide release and caspase-3 activation

    Antioxidants and Redox Signaling, Vol. 2, Núm. 2, pp. 263-275

1999

  1. Role of plasma membrane coenzyme Q on the regulation of apoptosis

    BioFactors, Vol. 9, Núm. 2-4, pp. 171-177