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Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Browsing publications by Dr Denise Kirby

Newcastle AuthorsTitleYearFull text
Professor Robert Taylor
Dr Helen Swalwell
Dr Denise Kirby
Emeritus Professor Doug Turnbull
Professor Bobby McFarland
Respiratory chain complex I deficiency caused by mitochondrial DNA mutations2011
Dr Helen Swalwell
Dr Denise Kirby
Dr Anna Mitchell
Emeritus Professor Doug Turnbull
Professor Bobby McFarland
et al.
Respiratory chain complex I deficiency caused by mitochondrial DNA mutations2011
Dr Tora Smulders-Srinivasan
Dr Denise Kirby
Emeritus Professor Robert Lightowlers
Emeritus Professor Doug Turnbull
Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations2010
Professor Andrew Trevelyan
Dr Denise Kirby
Dr Tora Smulders-Srinivasan
Marco Nooteboom
Professor Miles Whittington
et al.
Mitochondrial DNA mutations affect calcium handling in differentiated neurons2010
Dr Denise Kirby
Dr Kate Rennie
Dr Tora Smulders-Srinivasan
Professor Miles Whittington
Professor Andrew Trevelyan
et al.
Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiation2009
Dr Denise Kirby
Emeritus Professor Doug Turnbull
Professor Robert Taylor
Biochemical Assays of Respiratory Chain Complex Activity2007
Professor Robert Taylor
Dr Helen Swalwell
Dr Denise Kirby
Professor Bobby McFarland
Dr Anna Mitchell
[abstract] The molecular genetic basis of respiratory chain complex I deficiency: Clinical presentations and mtDNA mutations2006
Professor Bobby McFarland
Dr Denise Kirby
Emeritus Professor Doug Turnbull
Professor Robert Taylor
De Novo Mutations in the Mitochondrial ND3 Gene as a Cause of Infantile Mitochondrial Encephalopathy and Complex I Deficiency2004
Dr Denise Kirby
Professor Bobby McFarland
Emeritus Professor Doug Turnbull
Professor Robert Taylor
Mutations of the mitochondrial ND1 gene as a cause of MELAS2004
Dr Denise Kirby
Professor Robert Taylor
NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency2004
Professor Bobby McFarland
Dr Denise Kirby
Emeritus Professor Doug Turnbull
Professor Robert Taylor
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency2003