Publications by David Moore - ePrints

Browsing publications by David Moore.

Newcastle Authors	Title	Year
Rebecca Hanna David Moore Professor Mark Birch-Machin	Optimised detection of mitochondrial DNA strand breaks	2019
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 interactions	2017
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/ddx060	2017
Dr Patrick Yu Wai Man David Moore Dr Florence Burte	Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy	2017
David Moore Dr Patrick Yu Wai Man	Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China	2016
David Moore Professor Patrick Chinnery Dr Patrick Yu Wai Man	Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies	2015
David Moore	Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis	2015
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 involvement	2014
Dr Gerald Pfeffer Professor 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 maintenance	2014
David Moore Dr Patrick Yu Wai Man	Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?	2014
David Moore Dr Patrick Yu Wai Man	Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis	2014
David Moore Dr Patrick Yu Wai Man	Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease	2014