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Search results (16)

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Nucleoside supplements as treatments for mitochondrial DNA depletion syndrome.

Dombi E. et al, (2024), Front Cell Dev Biol, 12

MRE11-dependent instability in mitochondrial DNA fork protection activates a cGAS immune signaling pathway.

Luzwick JW. et al, (2021), Sci Adv, 7

Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations.

Liu Y-T. et al, (2020), Hum Mol Genet, 29, 1547 - 1567

Maternal circulating syncytiotrophoblast-derived extracellular vesicles contain biologically active 5'-tRNA halves.

Cooke WR. et al, (2019), Biochem Biophys Res Commun, 518, 107 - 113

In vitro decidualisation of human endometrial stromal cells is enhanced by seminal fluid extracellular vesicles.

Rodriguez-Caro H. et al, (2019), J Extracell Vesicles, 8

De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity.

Ladds E. et al, (2018), Neurol Genet, 4

The Mitochondrion-lysosome Axis in Adaptive and Innate Immunity: Effect of Lupus Regulator Peptide P140 on Mitochondria Autophagy and NETosis.

Bendorius M. et al, (2018), Front Immunol, 9

Validating the RedMIT/GFP-LC3 Mouse Model by Studying Mitophagy in Autosomal Dominant Optic Atrophy Due to the OPA1Q285STOP Mutation.

Diot A. et al, (2018), Front Cell Dev Biol, 6

Modulating Mitophagy in Mitochondrial Disease.

Dombi E. et al, (2018), Curr Med Chem, 25, 5597 - 5612

Acute nutritional stress during pregnancy affects placental efficiency, fetal growth and adult glucose homeostasis.

Malik S. et al, (2017), Oncotarget, 8, 109478 - 109486

In Vitro and In Vivo Detection of Mitophagy in Human Cells, C. Elegans, and Mice.

Fang EF. et al, (2017), J Vis Exp

Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations.

Liao C. et al, (2017), Neurology, 88, 131 - 142

Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers.

White B. et al, (2017), Nanotechnol Sci Appl, 10, 163 - 175

Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children.

Diot A. et al, (2016), Biochem Soc Trans, 44, 1091 - 1100

The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy.

Dombi E. et al, (2016), Neurology, 86, 1921 - 1923

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