Mecanismos moleculares da enfermedade
MeMoEn
Newcastle University
Newcastle-upon-Tyne, Reino UnidoPublicacións en colaboración con investigadores/as de Newcastle University (5)
2021
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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
2020
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Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency
EMBO Journal, Vol. 39, Núm. 23
2016
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The mitochondrial protein CHC HD2 primes the differentiation potential of human induced pluripotent stem cells to neuroectodermal lineages
Journal of Cell Biology, Vol. 215, Núm. 2, pp. 187-202
2013
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Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency
Human Molecular Genetics, Vol. 22, Núm. 22, pp. 4602-4615
2009
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Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations
Biogerontology, Vol. 10, Núm. 4, pp. 435-442