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P F Chinnery

Showing results (81-90 of 152) with videos related to

Pageof 16
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Journal of Medical Genetics|April 5, 2003
The role of APOE in the phenotypic expression of Leber hereditary optic neuropathyP Yu-Wai-Man, C M Morris, M Zeviani, et al.
The British Journal of Ophthalmology|March 21, 2006
The role of mitochondrial haplogroups in primary open angle glaucomaR Andrews, T Ressiniotis, D M Turnbull, et al.
American Journal of Human Genetics|January 3, 2001
Point mutations of the mtDNA control region in normal and neurodegenerative human brainsP F Chinnery, G A Taylor, N Howell, et al.
American Journal of Human Genetics|January 9, 2003
The epidemiology of Leber hereditary optic neuropathy in the North East of EnglandP Yu-Wai-Man, P G Griffiths, D T Brown, et al.
Journal of Medical Genetics|January 20, 2004
No evidence of an association between the T16189C mtDNA variant and late onset dementiaA M Gibson, J A Edwardson, D M Turnbull, et al.
Brain : a Journal of Neurology|December 28, 1999
The spectrum of hearing loss due to mitochondrial DNA defectsP F Chinnery, C Elliott, G R Green, et al.
Journal of Medical Genetics|June 27, 2009
A common UCP2 polymorphism predisposes to stress hyperglycaemia in severe sepsisA Pyle, I M Ibbett, C Gordon, et al.
Diabetes|October 29, 1998
Mitochondrial diabetes: investigation and identification of a novel mutationS Lynn, T Wardell, M A Johnson, et al.
Journal of Medical Genetics|March 19, 2002
Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndromeJ A Goodship, J O'Sullivan, P F Chinnery, et al.
Diabetologia|June 6, 2008
Age-related decline in mitochondrial DNA copy number in isolated human pancreatic isletsL M Cree, S K Patel, A Pyle, et al.
Pageof 16

Showing results (81-90 of 152) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|April 5, 2003
The role of APOE in the phenotypic expression of Leber hereditary optic neuropathyP Yu-Wai-Man, C M Morris, M Zeviani, et al.
The British Journal of Ophthalmology|March 21, 2006
The role of mitochondrial haplogroups in primary open angle glaucomaR Andrews, T Ressiniotis, D M Turnbull, et al.
American Journal of Human Genetics|January 3, 2001
Point mutations of the mtDNA control region in normal and neurodegenerative human brainsP F Chinnery, G A Taylor, N Howell, et al.
American Journal of Human Genetics|January 9, 2003
The epidemiology of Leber hereditary optic neuropathy in the North East of EnglandP Yu-Wai-Man, P G Griffiths, D T Brown, et al.
Journal of Medical Genetics|January 20, 2004
No evidence of an association between the T16189C mtDNA variant and late onset dementiaA M Gibson, J A Edwardson, D M Turnbull, et al.
Brain : a Journal of Neurology|December 28, 1999
The spectrum of hearing loss due to mitochondrial DNA defectsP F Chinnery, C Elliott, G R Green, et al.
Journal of Medical Genetics|June 27, 2009
A common UCP2 polymorphism predisposes to stress hyperglycaemia in severe sepsisA Pyle, I M Ibbett, C Gordon, et al.
Diabetes|October 29, 1998
Mitochondrial diabetes: investigation and identification of a novel mutationS Lynn, T Wardell, M A Johnson, et al.
Journal of Medical Genetics|March 19, 2002
Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndromeJ A Goodship, J O'Sullivan, P F Chinnery, et al.
Diabetologia|June 6, 2008
Age-related decline in mitochondrial DNA copy number in isolated human pancreatic isletsL M Cree, S K Patel, A Pyle, et al.
Pageof 16