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M T Lott

Showing results (1-10 of 33) with videos related to

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The New England Journal of Medicine|May 18, 1989
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathyG Singh, M T Lott, D C Wallace
Gene|November 26, 1999
Mitochondrial DNA variation in human evolution and diseaseD C Wallace, M D Brown, M T Lott
American Journal of Ophthalmology|June 15, 1990
Variable genotype of Leber's hereditary optic neuropathy patientsM T Lott, A S Voljavec, D C Wallace
American Journal of Ophthalmology|June 15, 1991
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutationN J Newman, M T Lott, D C Wallace
Revue Neurologique|January 1, 1991
MERRF: a model disease for understanding the principles of mitochondrial geneticsJ M Shoffner, M T Lott, D C Wallace
Epilepsia|January 1, 1994
Mitochondrial DNA mutations in epilepsy and neurological diseaseD C Wallace, M T Lott, J M Shoffner, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Diseases resulting from mitochondrial DNA point mutationsD C Wallace, M T Lott, J M Shoffner, et al.
Mutation Research|September 1, 1992
Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart diseaseM Corral-Debrinski, J M Shoffner, M T Lott, et al.
Human Mutation|January 1, 1995
African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Cuba Neuropathy Field Investigation TeamA Torroni, M D Brown, M T Lott, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseasesM D Brown, A S Voljavec, M T Lott, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
The New England Journal of Medicine|May 18, 1989
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathyG Singh, M T Lott, D C Wallace
Gene|November 26, 1999
Mitochondrial DNA variation in human evolution and diseaseD C Wallace, M D Brown, M T Lott
American Journal of Ophthalmology|June 15, 1990
Variable genotype of Leber's hereditary optic neuropathy patientsM T Lott, A S Voljavec, D C Wallace
American Journal of Ophthalmology|June 15, 1991
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutationN J Newman, M T Lott, D C Wallace
Revue Neurologique|January 1, 1991
MERRF: a model disease for understanding the principles of mitochondrial geneticsJ M Shoffner, M T Lott, D C Wallace
Epilepsia|January 1, 1994
Mitochondrial DNA mutations in epilepsy and neurological diseaseD C Wallace, M T Lott, J M Shoffner, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Diseases resulting from mitochondrial DNA point mutationsD C Wallace, M T Lott, J M Shoffner, et al.
Mutation Research|September 1, 1992
Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart diseaseM Corral-Debrinski, J M Shoffner, M T Lott, et al.
Human Mutation|January 1, 1995
African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Cuba Neuropathy Field Investigation TeamA Torroni, M D Brown, M T Lott, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseasesM D Brown, A S Voljavec, M T Lott, et al.
Pageof 4