Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy

Por Yu-Wai-Man, Patrick, Soiferman, Devorah, Moore, David G., Burté, Florence, Saada, Ann
Publicado no Mitochondrion (2017)

A neurodegenerative perspective on mitochondrial optic neuropathies

Por Yu-Wai-Man, Patrick, Votruba, Marcela, Burté, Florence, La Morgia, Chiara, Barboni, Piero, Carelli, Valerio
Publicado no Acta Neuropathol (2016)

metabolic profiling of Parkinson's disease and mild cognitive impairment

Por Burté, Florence, Houghton, David, Lowes, Hannah, Pyle, Angela, Nesbitt, Sarah, Yarnall, Alison, Yu‐Wai‐Man, Patrick, Burn, David J., Santibanez‐Koref, Mauro, Hudson, Gavin
Publicado no Mov Disord (2017)

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions

Por Rouzier, Cécile, Moore, David, Delorme, Cécile, Lacas-Gervais, Sandra, Ait-El-Mkadem, Samira, Fragaki, Konstantina, Burté, Florence, Serre, Valérie, Bannwarth, Sylvie, Chaussenot, Annabelle, Catala, Martin, Yu-Wai-Man, Patrick, Paquis-Flucklinger, Véronique
Publicado no Hum Mol Genet (2017)

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions

Por Rouzier, Cécile, Moore, David, Delorme, Cécile, Lacas-Gervais, Sandra, Ait-El-Mkadem, Samira, Fragaki, Konstantina, Burté, Florence, Serre, Valérie, Bannwarth, Sylvie, Chaussenot, Annabelle, Catala, Martin, Yu-Wai-Man, Patrick, Paquis-Flucklinger, Véronique
Publicado no Hum Mol Genet (2017)

Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation

Por Spiegel, Ronen, Saada, Ann, Flannery, Padraig J, Burté, Florence, Soiferman, Devorah, Khayat, Morad, Eisner, Verónica, Vladovski, Eugene, Taylor, Robert W, Bindoff, Laurence A, Shaag, Avraham, Mandel, Hanna, Schuler-Furman, Ora, Shalev, Stavit A, Elpeleg, Orly, Yu-Wai-Man, Patrick
Publicado no J Med Genet (2016)

Severe Childhood Malaria Syndromes Defined by Plasma Proteome Profiles

Por Burté, Florence, Brown, Biobele J., Orimadegun, Adebola E., Ajetunmobi, Wasiu A., Battaglia, Francesca, Ely, Barry K., Afolabi, Nathaniel K., Athanasakis, Dimitrios, Akinkunmi, Francis, Kowobari, Olayinka, Omokhodion, Samuel, Osinusi, Kikelomo, Akinbami, Felix O., Shokunbi, Wuraola A., Sodeinde, Olugbemiro, Fernandez-Reyes, Delmiro
Publicado em 2012

A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria

Por Marquet, Sandrine, Conte, Ianina, Poudiougou, Belco, Argiro, Laurent, Dessein, Hélia, Couturier, Charlène, Burté, Florence, Oumar, Aboubacar A., Brown, Biobele J., Traore, Abdoualye, Afolabi, Nathaniel K., Barry, Abdoulaye, Omokhodion, Samuel, Shokunbi, Wuraola A., Sodeinde, Olugbemiro, Doumbo, Ogobara, Fernandez-Reyes, Delmiro, Dessein, Alain J.
Publicado no Sci Rep (2017)

Malaria Induces Anemia through CD8(+) T Cell-Dependent Parasite Clearance and Erythrocyte Removal in the Spleen

Por Safeukui, Innocent, Gomez, Noé D., Adelani, Aanuoluwa A., Burte, Florence, Afolabi, Nathaniel K., Akondy, Rama, Velazquez, Peter, Holder, Anthony, Tewari, Rita, Buffet, Pierre, Brown, Biobele J., Shokunbi, Wuraola A., Olaleye, David, Sodeinde, Olugbemiro, Kazura, James, Ahmed, Rafi, Mohandas, Narla, Fernandez-Reyes, Delmiro, Haldar, Kasturi
Publicado no mBio (2015)

The IL17F and IL17RA Genetic Variants Increase Risk of Cerebral Malaria in Two African Populations

Por Marquet, Sandrine, Conte, Ianina, Poudiougou, Belco, Argiro, Laurent, Cabantous, Sandrine, Dessein, Hélia, Burté, Florence, Oumar, Aboubacar A., Brown, Biobele J., Traore, Abdoualye, Afolabi, Nathaniel K., Barry, Abdoulaye, Omokhodion, Samuel, Ndoumbe, Ursule Ewanda, Shokunbi, Wuraola A., Sodeinde, Olugbemiro, Doumbo, Ogobara, Fernandez-Reyes, Delmiro, Dessein, Alain J.
Publicado no Infect Immun (2016)

Affinity Proteomics Reveals Elevated Muscle Proteins in Plasma of Children with Cerebral Malaria

Por Bachmann, Julie, Burté, Florence, Pramana, Setia, Conte, Ianina, Brown, Biobele J., Orimadegun, Adebola E., Ajetunmobi, Wasiu A., Afolabi, Nathaniel K., Akinkunmi, Francis, Omokhodion, Samuel, Akinbami, Felix O., Shokunbi, Wuraola A., Kampf, Caroline, Pawitan, Yudi, Uhlén, Mathias, Sodeinde, Olugbemiro, Schwenk, Jochen M., Wahlgren, Mats, Fernandez-Reyes, Delmiro, Nilsson, Peter
Publicado em 2014

CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis

Por Genin, Emmanuelle C, Plutino, Morgane, Bannwarth, Sylvie, Villa, Elodie, Cisneros‐Barroso, Eugenia, Roy, Madhuparna, Ortega‐Vila, Bernardo, Fragaki, Konstantina, Lespinasse, Françoise, Pinero‐Martos, Estefania, Augé, Gaëlle, Moore, David, Burté, Florence, Lacas‐Gervais, Sandra, Kageyama, Yusuke, Itoh, Kie, Yu‐Wai‐Man, Patrick, Sesaki, Hiromi, Ricci, Jean‐Ehrland, Vives‐Bauza, Cristofol, Paquis‐Flucklinger, Véronique
Publicado no EMBO Mol Med (2015)