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Browsing publications by Dr Florence Burte

Newcastle AuthorsTitleYearFull text
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
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