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M T Lott

Showing results (11-20 of 33) with videos related to

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Nucleic Acids Research|January 1, 1996
MITOMAP: a human mitochondrial genome databaseA M Kogelnik, M T Lott, M D Brown, et al.
Nucleic Acids Research|February 21, 1998
MITOMAP: a human mitochondrial genome database--1998 updateA M Kogelnik, M T Lott, M D Brown, et al.
Nucleic Acids Research|January 1, 1997
MITOMAP: an update on the status of the human mitochondrial genome databaseA M Kogelnik, M T Lott, M D Brown, et al.
American Journal of Human Genetics|August 1, 1992
A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit IM D Brown, C C Yang, I Trounce, et al.
JAMA|October 2, 1991
Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac diseaseM Corral-Debrinski, G Stepien, J M Shoffner, et al.
American Journal of Human Genetics|October 1, 1994
mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop regionA Torroni, M T Lott, M F Cabell, et al.
Archives of Neurology|May 1, 1993
Atypical Leber's hereditary optic neuropathy with molecular confirmationN C Weiner, N J Newman, S Lessell, et al.
Pediatric Research|November 1, 1990
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reactionD C Wallace, M T Lott, A M Lezza, et al.
Nature Genetics|December 1, 1992
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced ageM Corral-Debrinski, T Horton, M T Lott, et al.
Cell|June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutationJ M Shoffner, M T Lott, A M Lezza, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Nucleic Acids Research|January 1, 1996
MITOMAP: a human mitochondrial genome databaseA M Kogelnik, M T Lott, M D Brown, et al.
Nucleic Acids Research|February 21, 1998
MITOMAP: a human mitochondrial genome database--1998 updateA M Kogelnik, M T Lott, M D Brown, et al.
Nucleic Acids Research|January 1, 1997
MITOMAP: an update on the status of the human mitochondrial genome databaseA M Kogelnik, M T Lott, M D Brown, et al.
American Journal of Human Genetics|August 1, 1992
A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit IM D Brown, C C Yang, I Trounce, et al.
JAMA|October 2, 1991
Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac diseaseM Corral-Debrinski, G Stepien, J M Shoffner, et al.
American Journal of Human Genetics|October 1, 1994
mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop regionA Torroni, M T Lott, M F Cabell, et al.
Archives of Neurology|May 1, 1993
Atypical Leber's hereditary optic neuropathy with molecular confirmationN C Weiner, N J Newman, S Lessell, et al.
Pediatric Research|November 1, 1990
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reactionD C Wallace, M T Lott, A M Lezza, et al.
Nature Genetics|December 1, 1992
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced ageM Corral-Debrinski, T Horton, M T Lott, et al.
Cell|June 15, 1990
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutationJ M Shoffner, M T Lott, A M Lezza, et al.
Pageof 4