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Geoffrey A Taylor

Showing results (1-10 of 12) with videos related to

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Aging Cell|July 24, 2009
Quantification of mitochondrial DNA mutation loadLaura C Greaves, Nina E Beadle, Geoffrey A Taylor, et al.
Radiation Research|January 27, 2006
Mitochondrial DNA mutations in individuals occupationally exposed to ionizing radiationCraig S Wilding, Kevin Cadwell, E Janet Tawn, et al.
Journal of Neurology|April 3, 2007
Investigation of the mitochondrial genome in patients with atypical motor neuron diseaseCatherine Phoenix, Geoffrey A Taylor, Judith Hartley, et al.
Annals of Neurology|December 17, 2005
Motor neuron disease in a patient with a mitochondrial tRNAIle mutationGillian M Borthwick, Robert W Taylor, Timothy J Walls, et al.
Annals of Neurology|October 2, 2003
Genotypes from patients indicate no paternal mitochondrial DNA contributionRobert W Taylor, Martina T McDonnell, Emma L Blakely, et al.
Diabetes|June 28, 2002
Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genomeAlan T W Choo-Kang, Stephen Lynn, Geoffrey A Taylor, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
Plos Genetics|November 21, 2012
Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutationsLaura C Greaves, Joanna L Elson, Marco Nooteboom, et al.
Nucleic Acids Research|August 4, 2006
Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variantsDeborah Pye, Dimitra S Kyriakouli, Geoffrey A Taylor, et al.
Nature Genetics|April 11, 2006
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson diseaseAndreas Bender, Kim J Krishnan, Christopher M Morris, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Aging Cell|July 24, 2009
Quantification of mitochondrial DNA mutation loadLaura C Greaves, Nina E Beadle, Geoffrey A Taylor, et al.
Radiation Research|January 27, 2006
Mitochondrial DNA mutations in individuals occupationally exposed to ionizing radiationCraig S Wilding, Kevin Cadwell, E Janet Tawn, et al.
Journal of Neurology|April 3, 2007
Investigation of the mitochondrial genome in patients with atypical motor neuron diseaseCatherine Phoenix, Geoffrey A Taylor, Judith Hartley, et al.
Annals of Neurology|December 17, 2005
Motor neuron disease in a patient with a mitochondrial tRNAIle mutationGillian M Borthwick, Robert W Taylor, Timothy J Walls, et al.
Annals of Neurology|October 2, 2003
Genotypes from patients indicate no paternal mitochondrial DNA contributionRobert W Taylor, Martina T McDonnell, Emma L Blakely, et al.
Diabetes|June 28, 2002
Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genomeAlan T W Choo-Kang, Stephen Lynn, Geoffrey A Taylor, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
Plos Genetics|November 21, 2012
Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutationsLaura C Greaves, Joanna L Elson, Marco Nooteboom, et al.
Nucleic Acids Research|August 4, 2006
Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variantsDeborah Pye, Dimitra S Kyriakouli, Geoffrey A Taylor, et al.
Nature Genetics|April 11, 2006
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson diseaseAndreas Bender, Kim J Krishnan, Christopher M Morris, et al.
Pageof 2