Mitochondrial content is central to nuclear gene expression: Profound implications for human health

por Muir, Rebecca, Diot, Alan, Poulton, Joanna
Publicado 2016

Mitophagy plays a central role in mitochondrial ageing

por Diot, Alan, Morten, Karl, Poulton, Joanna
Publicado 2016

Staphylococcal Adhesion and Host Cell Invasion: Fibronectin-Binding and Other Mechanisms

por Josse, Jérôme, Laurent, Frédéric, Diot, Alan
Publicado 2017

Interaction Between Staphylococcal Biofilm and Bone: How Does the Presence of Biofilm Promote Prosthesis Loosening?

por Josse, Jérôme, Valour, Florent, Maali, Yousef, Diot, Alan, Batailler, Cécile, Ferry, Tristan, Laurent, Frédéric
Publicado 2019

Differential Early in vivo Dynamics and Functionality of Recruited Polymorphonuclear Neutrophils After Infection by Planktonic or Biofilm Staphylococcus aureus

por Abdul Hamid, Aizat Iman, Cara, Andréa, Diot, Alan, Laurent, Frédéric, Josse, Jérôme, Gueirard, Pascale
Publicado 2021

Acute nutritional stress during pregnancy affects placental efficiency, fetal growth and adult glucose homeostasis

por Malik, Sajida, Diot, Alan, Morten, Karl, Dombi, Eszter, Vatish, Manu, Boyd, C.A. Richard, Poulton, Joanna
Publicado 2017

Investigation of a Staphylococcus argenteus Strain Involved in a Chronic Prosthetic-Joint Infection

por Diot, Alan, Dyon-Tafani, Virginie, Bergot, Marine, Tasse, Jason, Martins-Simões, Patricia, Josse, Jérôme, Valour, Florent, Laurent, Frédéric
Publicado 2020

Is Placental Mitochondrial Function a Regulator that Matches Fetal and Placental Growth to Maternal Nutrient Intake in the Mouse?

por Chiaratti, Marcos R., Malik, Sajida, Diot, Alan, Rapa, Elizabeth, Macleod, Lorna, Morten, Karl, Vatish, Manu, Boyd, Richard, Poulton, Joanna
Publicado 2015

Correction: Is Placental Mitochondrial Function a Regulator that Matches Fetal and Placental Growth to Maternal Nutrient Intake in the Mouse?

por Chiaratti, Marcos R., Malik, Sajida, Diot, Alan, Rapa, Elizabeth, Macleod, Lorna, Morten, Karl, Vatish, Manu, Boyd, Richard, Poulton, Joanna
Publicado 2017

Understanding the Virulence of Staphylococcus pseudintermedius: A Major Role of Pore-Forming Toxins

por Maali, Yousef, Badiou, Cédric, Martins-Simões, Patrícia, Hodille, Elisabeth, Bes, Michele, Vandenesch, François, Lina, Gérard, Diot, Alan, Laurent, Frederic, Trouillet-Assant, Sophie
Publicado 2018

Bone and Joint Infection Involving Corynebacterium spp.: From Clinical Features to Pathophysiological Pathways

por Chauvelot, Pierre, Ferry, Tristan, Tafani, Virginie, Diot, Alan, Tasse, Jason, Conrad, Anne, Chidiac, Christian, Braun, Evelyne, Lustig, Sébastien, Laurent, Frédéric, Valour, Florent
Publicado 2021

Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children

por Diot, Alan, Dombi, Eszter, Lodge, Tiffany, Liao, Chunyan, Morten, Karl, Carver, Janet, Wells, Dagan, Child, Tim, Johnston, Iain G., Williams, Suzannah, Poulton, Joanna
Publicado 2016

Staphylococcus aureus Small Colony Variants (SCVs): News From a Chronic Prosthetic Joint Infection

por Loss, Guilherme, Simões, Patricia Martins, Valour, Florent, Cortês, Marina Farrel, Gonzaga, Luiz, Bergot, Marine, Trouillet-Assant, Sophie, Josse, Jêrome, Diot, Alan, Ricci, Emiliano, Vasconcelos, Ana Tereza, Laurent, Frédéric
Publicado 2019

Unbiased yeast screens identify cellular pathways affected in Niemann–Pick disease type C

por Colaco, Alexandria, Fernández-Suárez, María E, Shepherd, Dawn, Gal, Lihi, Bibi, Chen, Chuartzman, Silvia, Diot, Alan, Morten, Karl, Eden, Emily, Porter, Forbes D, Poulton, Joanna, Platt, Nick, Schuldiner, Maya, Platt, Frances M
Publicado 2020

Transcriptome Architecture of Osteoblastic Cells Infected With Staphylococcus aureus Reveals Strong Inflammatory Responses and Signatures of Metabolic and Epigenetic Dysregulation

por Nicolas, Aurélie, Deplanche, Martine, Commere, Pierre-Henri, Diot, Alan, Genthon, Clemence, Marques da Silva, Wanderson, Azevedo, Vasco, Germon, Pierre, Jamme, Hélène, Guédon, Eric, Le Loir, Yves, Laurent, Fréderic, Bierne, Hélène, Berkova, Nadia
Publicado 2022

Staphylococcus aureus induces DNA damage in host cell

por Deplanche, Martine, Mouhali, Nassim, Nguyen, Minh-Thu, Cauty, Chantal, Ezan, Frédéric, Diot, Alan, Raulin, Lesly, Dutertre, Stephanie, Langouet, Sophie, Legembre, Patrick, Taieb, Frederic, Otto, Michael, Laurent, Frédéric, Götz, Friedrich, Le Loir, Yves, Berkova, Nadia
Publicado 2019

Validating the RedMIT/GFP-LC3 Mouse Model by Studying Mitophagy in Autosomal Dominant Optic Atrophy Due to the OPA1Q285STOP Mutation

por Diot, Alan, Agnew, Thomas, Sanderson, Jeremy, Liao, Chunyan, Carver, Janet, Neves, Ricardo Pires das, Gupta, Rajeev, Guo, Yanping, Waters, Caroline, Seto, Sharon, Daniels, Matthew J., Dombi, Eszter, Lodge, Tiffany, Morten, Karl, Williams, Suzannah A., Enver, Tariq, Iborra, Francisco J., Votruba, Marcela, Poulton, Joanna
Publicado 2018

The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy

por Dombi, Eszter, Diot, Alan, Morten, Karl, Carver, Janet, Lodge, Tiffany, Fratter, Carl, Ng, Yi Shiau, Liao, Chunyan, Muir, Rebecca, Blakely, Emma L., Hargreaves, Iain, Al-Dosary, Mazhor, Sarkar, Gopa, Hickman, Simon J., Downes, Susan M., Jayawant, Sandeep, Yu-Wai-Man, Patrick, Taylor, Robert W., Poulton, Joanna
Publicado 2016

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

por Uusimaa, Johanna, Evans, Julie, Smith, Conrad, Butterworth, Anna, Craig, Kate, Ashley, Neil, Liao, Chunyan, Carver, Janet, Diot, Alan, Macleod, Lorna, Hargreaves, Iain, Al-Hussaini, Abdulrahman, Faqeih, Eissa, Asery, Ali, Al Balwi, Mohammed, Eyaid, Wafaa, Al-Sunaid, Areej, Kelly, Deirdre, van Mourik, Indra, Ball, Sarah, Jarvis, Joanna, Mulay, Arundhati, Hadzic, Nedim, Samyn, Marianne, Baker, Alastair, Rahman, Shamima, Stewart, Helen, Morris, Andrew AM, Seller, Anneke, Fratter, Carl, Taylor, Robert W, Poulton, Joanna
Publicado 2014

Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations

por Liao, Chunyan, Ashley, Neil, Diot, Alan, Morten, Karl, Phadwal, Kanchan, Williams, Andrew, Fearnley, Ian, Rosser, Lyndon, Lowndes, Jo, Fratter, Carl, Ferguson, David J.P., Vay, Laura, Quaghebeur, Gerardine, Moroni, Isabella, Bianchi, Stefania, Lamperti, Costanza, Downes, Susan M., Sitarz, Kamil S., Flannery, Padraig J., Carver, Janet, Dombi, Eszter, East, Daniel, Laura, Matilde, Reilly, Mary M., Mortiboys, Heather, Prevo, Remko, Campanella, Michelangelo, Daniels, Matthew J., Zeviani, Massimo, Yu-Wai-Man, Patrick, Simon, Anna Katharina, Votruba, Marcela, Poulton, Joanna
Publicado 2017