Mitochondrial DNA density homeostasis accounts for a threshold effect in a cybrid model of a human mitochondrial disease

di Aryaman, Juvid, Johnston, Iain G., Jones, Nick S.
Pubblicato in Biochem J (2017)

Mitochondrial Heterogeneity

di Aryaman, Juvid, Johnston, Iain G., Jones, Nick S.
Pubblicato in Front Genet (2019)

Mitochondrial Network State Scales mtDNA Genetic Dynamics

di Aryaman, Juvid, Bowles, Charlotte, Jones, Nick S., Johnston, Iain G.
Pubblicato in Genetics (2019)

Oxygen tension modulates the mitochondrial genetic bottleneck and influences the segregation of a heteroplasmic mtDNA variant in vitro

di Pezet, Mikael G., Gomez-Duran, Aurora, Klimm, Florian, Aryaman, Juvid, Burr, Stephen, Wei, Wei, Saitou, Mitinori, Prudent, Julien, Chinnery, Patrick F.
Pubblicato in Commun Biol (2021)

High prevalence of focal and multi-focal somatic genetic variants in the human brain

di Keogh, Michael J., Wei, Wei, Aryaman, Juvid, Walker, Lauren, van den Ameele, Jelle, Coxhead, Jon, Wilson, Ian, Bashton, Matthew, Beck, Jon, West, John, Chen, Richard, Haudenschild, Christian, Bartha, Gabor, Luo, Shujun, Morris, Chris M., Jones, Nick S., Attems, Johannes, Chinnery, Patrick F.
Pubblicato in Nat Commun (2018)

Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains

di Keogh, Michael J, Wei, Wei, Aryaman, Juvid, Wilson, Ian, Talbot, Kevin, Turner, Martin R, McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Al Sarraj, Safa, Morris, Chris M, Ansorge, Olaf, Pickering-Brown, Stuart, Jones, Nick, Ironside, James W, Chinnery, Patrick F
Pubblicato in J Neurol Neurosurg Psychiatry (2018)

Frequency and signature of somatic variants in 1461 human brain exomes

di Wei, Wei, Keogh, Michael J., Aryaman, Juvid, Golder, Zoe, Kullar, Peter J., Wilson, Ian, Talbot, Kevin, Turner, Martin R., McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Sarraj, Safa Al, Morris, Chris M., Ansorge, Olaf, Jones, Nick S., Ironside, James W., Chinnery, Patrick F.
Pubblicato in Genet Med (2018)