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J M Shoffner

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Neurology|October 1, 1995
Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patientsT M Horton, B H Graham, M Corral-Debrinski, et al.
Genomics|September 15, 1994
Marked changes in mitochondrial DNA deletion levels in Alzheimer brainsM Corral-Debrinski, T Horton, M T Lott, et al.
American Journal of Medical Genetics|January 22, 1996
Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patientsM D Brown, J M Shoffner, Y L Kim, et al.
Cell|November 18, 1988
Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA diseaseD C Wallace, X X Zheng, M T Lott, et al.
Annals of Neurology|August 1, 1995
Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutationJ M Shoffner, M D Brown, C Stugard, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA mutations in human degenerative diseases and agingD C Wallace, J M Shoffner, I Trounce, et al.
Genomics|May 1, 1993
Genetic mapping of human heart-skeletal muscle adenine nucleotide translocator and its relationship to the facioscapulohumeral muscular dystrophy locusY Haraguchi, A B Chung, A Torroni, et al.
Genomics|July 1, 1993
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patientsJ M Shoffner, M D Brown, A Torroni, et al.
Neurology|November 1, 1992
Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutationJ M Shoffner, P M Fernhoff, N S Krawiecki, et al.
Journal of Neuropathology and Experimental Neurology|April 28, 1999
Tau pathology in a family with dementia and a P301L mutation in tauS S Mirra, J R Murrell, M Gearing, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Neurology|October 1, 1995
Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patientsT M Horton, B H Graham, M Corral-Debrinski, et al.
Genomics|September 15, 1994
Marked changes in mitochondrial DNA deletion levels in Alzheimer brainsM Corral-Debrinski, T Horton, M T Lott, et al.
American Journal of Medical Genetics|January 22, 1996
Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patientsM D Brown, J M Shoffner, Y L Kim, et al.
Cell|November 18, 1988
Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA diseaseD C Wallace, X X Zheng, M T Lott, et al.
Annals of Neurology|August 1, 1995
Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutationJ M Shoffner, M D Brown, C Stugard, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA mutations in human degenerative diseases and agingD C Wallace, J M Shoffner, I Trounce, et al.
Genomics|May 1, 1993
Genetic mapping of human heart-skeletal muscle adenine nucleotide translocator and its relationship to the facioscapulohumeral muscular dystrophy locusY Haraguchi, A B Chung, A Torroni, et al.
Genomics|July 1, 1993
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patientsJ M Shoffner, M D Brown, A Torroni, et al.
Neurology|November 1, 1992
Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutationJ M Shoffner, P M Fernhoff, N S Krawiecki, et al.
Journal of Neuropathology and Experimental Neurology|April 28, 1999
Tau pathology in a family with dementia and a P301L mutation in tauS S Mirra, J R Murrell, M Gearing, et al.
Pageof 5