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Florence Burté
Florence Burté
Research Associate, Newcastle University
Bestätigte E-Mail-Adresse bei ncl.ac.uk
Titel
Zitiert von
Zitiert von
Jahr
Disturbed mitochondrial dynamics and neurodegenerative disorders
F Burté, V Carelli, PF Chinnery, P Yu-Wai-Man
Nature reviews neurology 11 (1), 11-24, 2015
6832015
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis
EC Genin, M Plutino, S Bannwarth, E Villa, E Cisneros‐Barroso, M Roy, ...
EMBO molecular medicine 8 (1), 58-72, 2016
1822016
A neurodegenerative perspective on mitochondrial optic neuropathies
P Yu-Wai-Man, M Votruba, F Burté, C La Morgia, P Barboni, V Carelli
Acta neuropathologica 132, 789-806, 2016
1562016
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation
R Spiegel, A Saada, PJ Flannery, F Burté, D Soiferman, M Khayat, ...
Journal of medical genetics 53 (2), 127-131, 2016
1072016
Metabolic profiling of Parkinson's disease and mild cognitive impairment
F Burté, D Houghton, H Lowes, A Pyle, S Nesbitt, A Yarnall, ...
Movement Disorders 32 (6), 927-932, 2017
722017
A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions
C Rouzier, D Moore, C Delorme, S Lacas-Gervais, S Ait-El-Mkadem, ...
Human molecular genetics 26 (9), 1599-1611, 2017
712017
Alterations in the mitochondrial proteome of neuroblastoma cells in response to complex 1 inhibition
F Burté, LA De Girolamo, AJ Hargreaves, EE Billett
Journal of proteome research 10 (4), 1974-1986, 2011
692011
Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy
P Yu-Wai-Man, D Soiferman, DG Moore, F Burté, A Saada
Mitochondrion 36, 36-42, 2017
582017
Malaria Induces Anemia through CD8+ T Cell-Dependent Parasite Clearance and Erythrocyte Removal in the Spleen
I Safeukui, ND Gomez, AA Adelani, F Burte, NK Afolabi, R Akondy, ...
MBio 6 (1), 10.1128/mbio. 02493-14, 2015
552015
Circulatory hepcidin is associated with the anti-inflammatory response but not with iron or anemic status in childhood malaria
F Burté, BJ Brown, AE Orimadegun, WA Ajetunmobi, NK Afolabi, ...
Blood, The Journal of the American Society of Hematology 121 (15), 3016-3022, 2013
522013
Affinity proteomics reveals elevated muscle proteins in plasma of children with cerebral malaria
J Bachmann, F Burté, S Pramana, I Conte, BJ Brown, AE Orimadegun, ...
PLoS pathogens 10 (4), e1004038, 2014
512014
Altered ceramide metabolism is a feature in the extracellular vesicle-mediated spread of alpha-synuclein in Lewy body disorders
M Kurzawa-Akanbi, S Tammireddy, I Fabrik, L Gliaudelytė, MK Doherty, ...
Acta neuropathologica 142, 961-984, 2021
362021
Monoamine oxidase-A promotes protective autophagy in human SH-SY5Y neuroblastoma cells through Bcl-2 phosphorylation
A Ugun-Klusek, TS Theodosi, JC Fitzgerald, F Burté, C Ufer, DJ Boocock, ...
Redox Biology 20, 167-181, 2019
342019
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells
S Trifunov, A Pyle, ML Valentino, R Liguori, P Yu-Wai-Man, F Burté, J Duff, ...
Scientific reports 8 (1), 11682, 2018
292018
The IL17F and IL17RA Genetic Variants Increase Risk of Cerebral Malaria in Two African Populations
S Marquet, I Conte, B Poudiougou, L Argiro, S Cabantous, H Dessein, ...
Infection and immunity 84 (2), 590-597, 2016
252016
Severe childhood malaria syndromes defined by plasma proteome profiles
F Burté, BJ Brown, AE Orimadegun, WA Ajetunmobi, F Battaglia, BK Ely, ...
PLoS One 7 (12), e49778, 2012
202012
A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria
S Marquet, I Conte, B Poudiougou, L Argiro, H Dessein, C Couturier, ...
Scientific reports 7 (1), 41636, 2017
172017
Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis
SE Abah, F Burté, S Marquet, BJ Brown, F Akinkunmi, G Oyinloye, ...
Scientific Reports 8 (1), 17527, 2018
112018
A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delay
G Cairns, F Burté, R Price, E O’Connor, M Toms, R Mishra, M Moosajee, ...
Scientific Reports 11 (1), 20491, 2021
102021
WFS1-associated optic neuropathy: genotype-phenotype correlations and disease progression
A Majander, N Jurkute, F Burté, K Brock, C João, H Huang, MM Neveu, ...
American Journal of Ophthalmology 241, 9-27, 2022
92022
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