Joanna Poulton
Joanna Poulton is a British medical researcher, and Professor of Mitochondrial Genetics at the University of Oxford. She is an honorary consultant in Oxford, where she works on diseases caused by mutations in mitochondrial DNA. Such mutations are associated with many diseases, including diabetes, organ failure, deafness, and blindness, and are also important in neurodegeneration and aging. Poulton has spoken up on behalf of women in academia, as well as on the effects of neurodiversity on women's careers. Provided by Wikipedia
Showing 1 - 6 results of 6 for search 'Joanna Poulton', query time: 0.03s
Refine Results
-
1
Transmission of mitochondrial DNA diseases and ways to prevent them. by Joanna Poulton, Marcos R Chiaratti, Flávio V Meirelles, Stephen Kennedy, Dagan Wells, Ian J Holt
Published 2010-08-01Get full text
Article -
2
Correction: Is Placental Mitochondrial Function a Regulator that Matches Fetal and Placental Growth to Maternal Nutrient Intake in the Mouse? by Marcos R Chiaratti, Sajida Malik, Alan Diot, Elizabeth Rapa, Lorna Macleod, Karl Morten, Manu Vatish, Richard Boyd, Joanna Poulton
Published 2017-01-01Get full text
Article -
3
Is Placental Mitochondrial Function a Regulator that Matches Fetal and Placental Growth to Maternal Nutrient Intake in the Mouse? by Marcos R Chiaratti, Sajida Malik, Alan Diot, Elizabeth Rapa, Lorna Macleod, Karl Morten, Manu Vatish, Richard Boyd, Joanna Poulton
Published 2015-01-01Get full text
Article -
4
MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria. by Ilaria Dalla Rosa, Yolanda Cámara, Romina Durigon, Chloe F Moss, Sara Vidoni, Gokhan Akman, Lilian Hunt, Mark A Johnson, Sarah Grocott, Liya Wang, David R Thorburn, Michio Hirano, Joanna Poulton, Robert W Taylor, Greg Elgar, Ramon Martí, Peter Voshol, Ian J Holt, Antonella Spinazzola
Published 2016-01-01Get full text
Article -
5
Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability by Direnis Erdinc, Alejandro Rodríguez‐Luis, Mahmoud R Fassad, Sarah Mackenzie, Christopher M Watson, Sebastian Valenzuela, Xie Xie, Katja E Menger, Kate Sergeant, Kate Craig, Sila Hopton, Gavin Falkous, Genomics England Research Consortium, Joanna Poulton, Hector Garcia‐Moreno, Paola Giunti, Carlos A de Moura Aschoff, Jonas A Morales Saute, Amelia J Kirby, Camilo Toro, Lynne Wolfe, Danica Novacic, Lior Greenbaum, Aviva Eliyahu, Ortal Barel, Yair Anikster, Robert McFarland, Gráinne S Gorman, Andrew M Schaefer, Claes M Gustafsson, Robert W Taylor, Maria Falkenberg, Thomas J Nicholls
Published 2023-04-01Get full text
Article -
6
Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder by Bobby G. Ng, Erik A. Eklund, Jill A. Rosenfeld, Abdallah F. Elias, Aya Abu-El-Haija, Celine Bris, Magalie Barth, Jong-Hee Chae, Murim Choi, Holly A. Dubbs, Carl Fratter, Nicola Foulds, Candace Gamble, Ralitza H. Gavrilova, Jaclyn Haven, Trevor L. Hoffman, Jill V. Hunter, Austin Larson, Timothy Edward Lotze, Pilar Magoulas, Emily C. Magness, Debra M. Bootin, Eric D. Marsh, Victoria Nesbitt, Matthew T. Pastore, Joanna Poulton, Shamima Rahman, Fernando Scaglia, Chaya Murali, Jennifer Posey, Joshua Rotenberg, Betsy Schmalz, Deepali N. Shinde, Zöe Powis, Rivka Sukenik-Halevy, Kristen V. Truxal, Tami Uster, Matheus Vernet Machado Bressan Wilke, Erik Klee, Hyewon Woo, Donald Younkin, Jianhua Zhao, Jorge Granadillo, Seema Lalani, David Chitayat, Wendy K. Chung, Hudson H. Freeze, Volkan Okur
Published 2025-01-01Get full text
Article