Toggle Main Menu Toggle Search

Open Access padlockePrints

Browsing publications by Dr Florence Burte.

Newcastle AuthorsTitleYearFull text
Dr Florence Burte
Dr Holly Duncan
Professor Patrick Chinnery
WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression2022
George Cairns
Dr Florence Burte
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
Dr Florence Burte
et al.
Altered ceramide metabolism is a feature in the extracellular vesicle-mediated spread of alpha-synuclein in Lewy body disorders2021
Dr Florence Burte
Depleted circulatory complement-lysis inhibitor (CLI) in childhood cerebral malaria returns to normal with convalescence2021
Dr Florence Burte
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
Dr Florence Burte
Dr Jennifer Duff
et al.
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells2018
Dr Florence Burte
Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis2018
Dr Florence Burte
A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria2017
David Moore
Dr Florence Burte
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
Dr Florence Burte
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
Dr Florence Burte
Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy2017
Dr Florence Burte
Dr Dave Houghton
Hannah Lowes
Dr Angela Pyle
Sarah Nesbitt
et al.
Metabolic profiling of Parkinson's disease and mild cognitive impairment2017
Dr Florence Burte
Dr Patrick Yu Wai Man
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis2016
Dr Patrick Yu Wai Man
Dr Florence Burte
A neurodegenerative perspective on mitochondrial optic neuropathies2016
Padraig Flannery
Dr Florence Burte
Professor Robert Taylor
Professor Laurence Bindoff
Dr Patrick Yu Wai Man
et al.
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation2016
Dr Florence Burte
The IL17F and IL17RA Genetic Variants Increase Risk of Cerebral Malaria in Two African Populations2016
Dr Florence Burte
Professor Patrick Chinnery
Dr Patrick Yu Wai Man
Disturbed mitochondrial dynamics and neurodegenerative disorders2015
Dr Florence Burte
Malaria Induces Anemia through CD8+ T Cell-Dependent Parasite Clearance and Erythrocyte Removal in the Spleen2015
Dr Florence Burte
Affinity Proteomics Reveals Elevated Muscle Proteins in Plasma of Children with Cerebral Malaria2014
Dr Florence Burte
Circulatory hepcidin is associated with the anti-inflammatory response but not with iron or anemic status in childhood malaria2013
Dr Florence Burte
Severe childhood malaria syndromes defined by plasma proteome profiles2012
Dr Florence Burte
Alterations in the mitochondrial proteome of neuroblastoma cells in response to complex I inhibition2011