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Annals of Neurology|February 1, 1997
Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndromeP L Adams, R N Lightowlers, D M TurnbullGene Therapy|July 1, 1995
Gene therapy for mitochondrial DNA defects: is it possible?Z M Chrzanowska-Lightowlers, R N Lightowlers, D M TurnbullAnalytical Biochemistry|October 1, 1993
A microtiter plate assay for cytochrome c oxidase in permeabilized whole cellsZ M Chrzanowska-Lightowlers, D M Turnbull, R N LightowlersTrends in Genetics : TIG|January 10, 1998
Mammalian mitochondrial genetics: heredity, heteroplasmy and diseaseR N Lightowlers, P F Chinnery, D M Turnbull, et al.Brain : a Journal of Neurology|November 20, 1997
Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypesP F Chinnery, N Howell, R N Lightowlers, et al.Brain : a Journal of Neurology|November 3, 1998
MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspringP F Chinnery, N Howell, R N Lightowlers, et al.Human Reproduction (Oxford, England)|October 21, 2000
In-vitro genetic modification of mitochondrial functionR W Taylor, P F Chinnery, D M Turnbull, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Molecular basis for treatment of mitochondrial myopathiesR W Taylor, T M Wardell, R N Lightowlers, et al.British Medical Bulletin|November 22, 2015
Potential compounds for the treatment of mitochondrial diseaseP K Rai, O M Russell, R N Lightowlers, et al.Nature Genetics|February 1, 1997
Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acidsR W Taylor, P F Chinnery, D M Turnbull, et al.Pageof 23