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

Por Muir, Rebecca, Diot, Alan, Poulton, Joanna
Publicado no Bioessays (2016)

Mitophagy plays a central role in mitochondrial ageing

Por Diot, Alan, Morten, Karl, Poulton, Joanna
Publicado no Mamm Genome (2016)

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

Por Josse, Jérôme, Laurent, Frédéric, Diot, Alan
Publicado no Front Microbiol (2017)

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 no Oncotarget (2017)

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 no PLoS One (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 no PLoS One (2017)

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 no Biochem Soc Trans (2016)

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 no Neurology (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 em 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 no Neurology (2017)