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Neil Howell

Showing results (21-30 of 44) with videos related to

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Human Genetics|December 16, 2004
Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigreeNeil Howell, Iwona Kubacka, Sharon M Keers, et al.
Neuromuscular Disorders : NMD|January 22, 2004
A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysisRobert McFarland, Robert W Taylor, Patrick F Chinnery, et al.
Trends in Genetics : TIG|November 4, 2004
Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enoughRobert McFarland, Joanna L Elson, Robert W Taylor, et al.
International Journal of Cardiology|October 30, 2015
National administrative data produces an accurate and stable risk prediction model for short-term and 1-year mortality following cardiac surgeryDincer Aktuerk, David McNulty, Daniel Ray, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patientsElena Pegoraro, Andrea Vettori, Maria L Valentino, et al.
Clinical Science (London, England : 1979)|January 22, 2009
Titin isoform expression in aortic stenosisLynne Williams, Neil Howell, Domenico Pagano, et al.
American Journal of Human Genetics|February 7, 2003
The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree ratesNeil Howell, Christy Bogolin Smejkal, D A Mackey, et al.
Asian Cardiovascular & Thoracic Annals|February 21, 2015
Coronary ostial compromise in aortic valve replacement: an avoidable complicationShakil Farid, Aravinda Page, Neil Howell, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|December 5, 2002
Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutationsNeil Howell, Neil R Miller, David A Mackey, et al.
Mutation Research|April 6, 2002
A high frequency of mtDNA polymorphisms in HeLa cell sublinesCorinna Herrnstadt, Gwen Preston, Richard Andrews, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Human Genetics|December 16, 2004
Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigreeNeil Howell, Iwona Kubacka, Sharon M Keers, et al.
Neuromuscular Disorders : NMD|January 22, 2004
A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysisRobert McFarland, Robert W Taylor, Patrick F Chinnery, et al.
Trends in Genetics : TIG|November 4, 2004
Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enoughRobert McFarland, Joanna L Elson, Robert W Taylor, et al.
International Journal of Cardiology|October 30, 2015
National administrative data produces an accurate and stable risk prediction model for short-term and 1-year mortality following cardiac surgeryDincer Aktuerk, David McNulty, Daniel Ray, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patientsElena Pegoraro, Andrea Vettori, Maria L Valentino, et al.
Clinical Science (London, England : 1979)|January 22, 2009
Titin isoform expression in aortic stenosisLynne Williams, Neil Howell, Domenico Pagano, et al.
American Journal of Human Genetics|February 7, 2003
The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree ratesNeil Howell, Christy Bogolin Smejkal, D A Mackey, et al.
Asian Cardiovascular & Thoracic Annals|February 21, 2015
Coronary ostial compromise in aortic valve replacement: an avoidable complicationShakil Farid, Aravinda Page, Neil Howell, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|December 5, 2002
Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutationsNeil Howell, Neil R Miller, David A Mackey, et al.
Mutation Research|April 6, 2002
A high frequency of mtDNA polymorphisms in HeLa cell sublinesCorinna Herrnstadt, Gwen Preston, Richard Andrews, et al.
Pageof 5