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Browsing publications by David Moore

Newcastle AuthorsTitleYearFull text
Rebecca Hanna
David Moore
Professor Mark Birch-Machin
Optimised detection of mitochondrial DNA strand breaks2019
David Moore
Dr Florence Burte
Dr Patrick Yu Wai Man
A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions2017
David Moore
Dr Florence Burte
Dr Patrick Yu Wai Man
Corrigendum: A novel CISD2 mutation associated with a classical wolfram syndrome phenotype alters Ca21 homeostasis and ER-mitochondria interactions. [Human Molecular Genetics (2017)], doi: 10.1093/hmg/ddx0602017
Dr Patrick Yu Wai Man
David Moore
Dr Florence Burte
Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy2017
David Moore
Dr Patrick Yu Wai Man
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China2016
David Moore
Professor Patrick Chinnery
Dr Patrick Yu Wai Man
Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies2015
David Moore
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis2015
David Moore
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?2015
David Moore
Dr Patrick Yu Wai Man
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement2014
Dr Gerald Pfeffer
Dr Grainne Gorman
Dr Helen Griffin
Dr Marzena Kurzawa-Akanbi
Dr Ian Wilson
et al.
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance2014
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