Ageing and Parkinson's disease: Why is advancing age the biggest risk factor?()

Por Reeve, Amy, Simcox, Eve, Turnbull, Doug
Publicado em 2014

Mitochondrial Mutations: Newly Discovered Players in Neuronal Degeneration

Por Lax, Nichola Z., Turnbull, Doug M., Reeve, Amy K.
Publicado em 2011

The ageing mitochondrial genome

Por Krishnan, Kim J., Greaves, Laura C., Reeve, Amy K., Turnbull, Doug
Publicado em 2007

Mitochondrial dysfunction in neurodegenerative disorders

Por Reeve, Amy Katherine., Krishnan, Kim Jennifer., Duchen, Michael R., Turnbull, Doug M.
Publicado em 2012

No excess of mitochondrial DNA deletions within muscle in progressive multiple sclerosis

Por Campbell, Graham R, Reeve, Amy K, Ziabreva, Iryna, Reynolds, Richard, Turnbull, Doug M, Mahad, Don J
Publicado no Mult Scler (2013)

Nature of Mitochondrial DNA Deletions in Substantia Nigra Neurons

Por Reeve, Amy K., Krishnan, Kim J., Elson, Joanna L., Morris, Christopher M., Bender, Andreas, Lightowlers, Robert N., Turnbull, Douglass M.
Publicado em 2008

The low abundance of clonally expanded mitochondrial DNA point mutations in aged substantia nigra neurons

Por Reeve, Amy K, Krishnan, Kim J, Taylor, Geoffrey, Elson, Joanna L, Bender, Andreas, Taylor, Robert W, Morris, Christopher M, Turnbull, Doug M
Publicado em 2009

Cerebellar Ataxia in Patients with Mitochondrial DNA Disease: A Molecular Clinicopathological Study

Por Lax, Nichola Zoe, Hepplewhite, Philippa Denis, Reeve, Amy Katherine, Nesbitt, Victoria, McFarland, Robert, Jaros, Evelyn, Taylor, Robert William, Turnbull, Douglass Matthew
Publicado em 2012

Microangiopathy in the cerebellum of patients with mitochondrial DNA disease

Por Lax, Nichola Z., Pienaar, Ilse S., Reeve, Amy K., Hepplewhite, Philippa D., Jaros, Evelyn, Taylor, Robert W., Kalaria, Raj N., Turnbull, Doug M.
Publicado em 2012

OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules

Por Yu-Wai-Man, Patrick, Sitarz, Kamil S., Samuels, David C., Griffiths, Philip G., Reeve, Amy K., Bindoff, Laurence A., Horvath, Rita, Chinnery, Patrick F.
Publicado em 2010

Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis

Por Campbell, Graham R, Ziabreva, Iryna, Reeve, Amy K, Krishnan, Kim J, Reynolds, Richard, Howell, Owen, Lassmann, Hans, Turnbull, Doug M, Mahad, Don J
Publicado em 2011

Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue

Por Grünewald, Anne, Lax, Nichola Z., Rocha, Mariana C., Reeve, Amy K., Hepplewhite, Philippa D., A. Rygiel, Karolina, Taylor, Robert W., Turnbull, Doug M.
Publicado em 2014

Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis

Por Rygiel, Karolina A., Tuppen, Helen A., Grady, John P., Vincent, Amy, Blakely, Emma L., Reeve, Amy K., Taylor, Robert W., Picard, Martin, Miller, James, Turnbull, Doug M.
Publicado no Nucleic Acids Res (2016)

Clonal Expansion of Mitochondrial DNA Deletions in Multiple Sclerosis

Por Campbell, Graham R, Kraytsberg, Yevgenya, Krishnan, Kim J, Ohno, Nobuhiko, Ziabreva, Iryna, Reeve, Amy, Newcombe, Jia, Reynolds, Richard, Lassmann, Hans, Khrapko, Konstantin, Turnbull, Doug M, Mahad, Don J
Publicado em 2012

Sensory neuronopathy in patients harbouring recessive polymerase γ mutations

Por Lax, Nichola Z., Whittaker, Roger G., Hepplewhite, Philippa D., Reeve, Amy K., Blakely, Emma L., Jaros, Evelyn, Ince, Paul G., Taylor, Robert W., Fawcett, Peter R. W., Turnbull, Doug M.
Publicado em 2012

Loss of Myelin-Associated Glycoprotein in Kearns-Sayre Syndrome

Por Lax, Nichola Z., Campbell, Graham R., Reeve, Amy K., Ohno, Nobuhiko, Zambonin, Jessica, Blakely, Emma L., Taylor, Robert W., Bonilla, Eduardo, Tanji, Kurenai, DiMauro, Salvatore, Jaros, Evelyn, Lassmann, Hans, Turnbull, Doug M., Mahad, Don J.
Publicado em 2012