Anti-cancer DNA Intercalators cause p53 Dependent Mitochondrial DNA Nucleoid Re-modelling

por Ashley, Neil, Poulton, Joanna
Publicado 2009

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

The role of mitophagy during oocyte aging in human, mouse, and Drosophila: implications for oocyte quality and mitochondrial disease

por Cox, Rachel T, Poulton, Joanna, Williams, Suzannah A
Publicado 2021

Mitochondrial DNA disease and developmental implications for reproductive strategies

por Burgstaller, Joerg Patrick, Johnston, Iain G., Poulton, Joanna
Publicado 2015

The mitochondrial DNA T16189C polymorphism and HIV-associated cardiomyopathy: a genotype-phenotype association study

por Shaboodien, Gasnat, Engel, Mark E, Syed, Faisal F, Poulton, Joanna, Badri, Motasim, Mayosi, Bongani M
Publicado 2009

Transmission of Mitochondrial DNA Diseases and Ways to Prevent Them

por Poulton, Joanna, Chiaratti, Marcos R., Meirelles, Flávio V., Kennedy, Stephen, Wells, Dagan, Holt, Ian J.
Publicado 2010

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

No evidence for age-related differences in mitochondrial RNA quality in the female germline

por Hartley, Fiona, Alageel, Arwa, Appeltant, Ruth, Gray, Nicki, Repapi, Emmanouela, Wells, Dagan, Williams, Suzannah A, Poulton, Joanna
Publicado 2022

Mice expressing an error-prone DNA polymerase in mitochondria display elevated replication pausing and chromosomal breakage at fragile sites of mitochondrial DNA

por Bailey, Laura J., Cluett, Tricia J., Reyes, Aurelio, Prolla, Tom A., Poulton, Joanna, Leeuwenburgh, Christiaan, Holt, Ian J.
Publicado 2009

The association of the mitochondrial DNA OriB variant (16184–16193 polycytosine tract) with type 2 diabetes in Europid populations

por Ye, Zheng, Gillson, Christopher, Sims, Matt, Khaw, Kay-Tee, Plotka, Magdalena, Poulton, Joanna, Langenberg, Claudia, Wareham, Nicholas J.
Publicado 2013

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

Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations

por Ashley, Neil, O'Rourke, Anthony, Smith, Conrad, Adams, Susan, Gowda, Vasantha, Zeviani, Massimo, Brown, Garry K., Fratter, Carl, Poulton, Joanna
Publicado 2008

Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice

por Morovat, Alireza, Weerasinghe, Gayani, Nesbitt, Victoria, Hofer, Monika, Agnew, Thomas, Quaghebeur, Geralrine, Sergeant, Kate, Fratter, Carl, Guha, Nishan, Mirzazadeh, Mehdi, Poulton, Joanna
Publicado 2017

The Mitochondrion-lysosome Axis in Adaptive and Innate Immunity: Effect of Lupus Regulator Peptide P140 on Mitochondria Autophagy and NETosis

por Bendorius, Mykolas, Neeli, Indira, Wang, Fengjuan, Bonam, Srinivasa Reddy, Dombi, Eszter, Buron, Nelly, Borgne-Sanchez, Annie, Poulton, Joanna, Radic, Marko, Muller, Sylviane
Publicado 2018

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

Pigmentary retinopathy, rod–cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNA(Lys) (m.8340G>A) gene variant

por Gill, Jaidip S, Hardy, Steven A, Blakely, Emma L, Hopton, Sila, Nemeth, Andrea H, Fratter, Carl, Poulton, Joanna, Taylor, Robert W, Downes, Susan M
Publicado 2017

Large-scale genetic analysis reveals mammalian mtDNA heteroplasmy dynamics and variance increase through lifetimes and generations

por Burgstaller, Joerg P., Kolbe, Thomas, Havlicek, Vitezslav, Hembach, Stephanie, Poulton, Joanna, Piálek, Jaroslav, Steinborn, Ralf, Rülicke, Thomas, Brem, Gottfried, Jones, Nick S., Johnston, Iain G.
Publicado 2018

De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity

por Ladds, Emma, Whitney, Andrea, Dombi, Eszter, Hofer, Monika, Anand, Geetha, Harrison, Victoria, Fratter, Carl, Carver, Janet, Barbosa, Ines A., Simpson, Michael, Jayawant, Sandeep, Poulton, Joanna
Publicado 2018