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Browsing publications by Florence Burté

Newcastle AuthorsTitleYearFull text
Florence Burté
OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion2023
Dr Marzena Kurzawa-Akanbi
Florence Burté
Dr Birthe Hilgen
Dr Rachel Queen
Dr Jonathan Coxhead
et al.		Retinal pigment epithelium extracellular vesicles are potent inducers of age-related macular degeneration disease phenotype in the outer retina2022
Florence Burté
Dr Holly Duncan
Professor Patrick Chinnery
WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression2022
George Cairns
Florence Burté
Emily O'Connor
Dr Angela Pyle
Professor John Sayer
et al.		A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delay2021
Dr Marzena Kurzawa-Akanbi
Rachel Heap
Professor Matthias Trost
Dr Preeti Singh
Florence Burté
et al.		Altered ceramide metabolism is a feature in the extracellular vesicle-mediated spread of alpha-synuclein in Lewy body disorders2021
Florence Burté
Depleted circulatory complement-lysis inhibitor (CLI) in childhood cerebral malaria returns to normal with convalescence2021
Florence Burté
Dr Patrick Yu Wai Man
Monoamine oxidase-A promotes protective autophagy in human SH-SY5Y neuroblastoma cells through Bcl-2 phosphorylation2019
Selena Trifunov
Dr Angela Pyle
Dr Patrick Yu Wai Man
Florence Burté
Dr Jennifer Duff
et al.		Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells2018
Florence Burté
Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis2018
Florence Burté
A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria2017
David Moore
Florence Burté
Dr Patrick Yu Wai Man
A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions2017
David Moore
Florence Burté
Dr Patrick Yu Wai Man
Corrigendum: A novel CISD2 mutation associated with a classical wolfram syndrome phenotype alters Ca21 homeostasis and ER-mitochondria interactions. [Human Molecular Genetics (2017)], doi: 10.1093/hmg/ddx0602017
Dr Patrick Yu Wai Man
David Moore
Florence Burté
Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy2017
Florence Burté
Dr Dave Houghton
Hannah Lowes
Dr Angela Pyle
Sarah Nesbitt
et al.		Metabolic profiling of Parkinson's disease and mild cognitive impairment2017
Florence Burté
Dr Patrick Yu Wai Man
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis2016
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