Mecanismos moleculares da enfermedade
MeMoEn
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Universidad de Zaragoza
Zaragoza, EspañaPublicacións en colaboración con investigadores/as de Universidad de Zaragoza (19)
2018
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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
2014
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Regulation of mouse retroelement MuERV-L/MERVL expression by REX1 and epigenetic control of stem cell potency
Frontiers in Oncology, Vol. 4 FEB
2013
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Functional analysis of rex1 during preimplantation development
Stem Cells and Development, Vol. 22, Núm. 3, pp. 459-472
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Mitochondrial antibiograms in personalized medicine
Human Molecular Genetics, Vol. 22, Núm. 6, pp. 1132-1139
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Stressed cybrids model demyelinated axons in multiple sclerosis
Metabolic Brain Disease, Vol. 28, Núm. 4, pp. 639-645
2012
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Cybrids for mitochondrial DNA pharmacogenomics
Drug Development Research, Vol. 73, Núm. 8, pp. 453-460
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Expression of endogenous retroviruses is negatively regulated by the pluripotency marker Rex1/Zfp42
Nucleic Acids Research, Vol. 40, Núm. 18, pp. 8993-9007
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Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1822, Núm. 8, pp. 1216-1222
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Read-through therapy for mitochondrial DNA nonsense mutations
Drug Discovery Today
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Soy lecithin interferes with mitochondrial function in frozen-thawed ram spermatozoa
Journal of Andrology, Vol. 33, Núm. 4, pp. 717-725
2011
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'progress' renders detrimental an ancient mitochondrial DNA genetic variant
Human Molecular Genetics, Vol. 20, Núm. 21, pp. 4224-4231
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Association of Rex-1 to target genes supports its interaction with Polycomb function
Stem Cell Research, Vol. 7, Núm. 1, pp. 1-16
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Mitochondrial pharma-Q-genomics: Targeting the OXPHOS cytochrome b
Drug Discovery Today
2010
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Mitochondrial pharmacogenomics: barcode for antibiotic therapy
Drug Discovery Today, Vol. 15, Núm. 1-2, pp. 33-39
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Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups
Human Molecular Genetics, Vol. 19, Núm. 17, pp. 3343-3353
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
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Diseases of the human mitochondrial oxidative phosphorylation system
Advances in Experimental Medicine and Biology
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Moroccan mitochondrial genetic background suggests prehistoric human migrations across the Gibraltar Strait
Mitochondrion, Vol. 9, Núm. 6, pp. 402-407
2008
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Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease
Human Molecular Genetics, Vol. 17, Núm. 24, pp. 4001-4011