Lott MT - Search Results

1

Toward a mtDNA locus-specific mutation database using the LOVD platform.

Elson JL, Sweeney MG, Procaccio V, Yarham JW, Salas A, Kong QP, van der Westhuizen FH, Pitceathly RD, Thorburn DR, Lott MT, Wallace DC, Taylor RW, McFarland R. Elson JL, et al. Among authors: lott mt. Hum Mutat. 2012 Sep;33(9):1352-8. doi: 10.1002/humu.22118. Epub 2012 Jul 2. Hum Mutat. 2012. PMID: 22581690 Free PMC article.

2

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age.

Corral-Debrinski M, Horton T, Lott MT, Shoffner JM, Beal MF, Wallace DC. Corral-Debrinski M, et al. Among authors: lott mt. Nat Genet. 1992 Dec;2(4):324-9. doi: 10.1038/ng1292-324. Nat Genet. 1992. PMID: 1303288

3

A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.

Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC. Brown MD, et al. Among authors: lott mt. Am J Hum Genet. 1992 Aug;51(2):378-85. Am J Hum Genet. 1992. PMID: 1322638 Free PMC article.

4

Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease.

Corral-Debrinski M, Shoffner JM, Lott MT, Wallace DC. Corral-Debrinski M, et al. Among authors: lott mt. Mutat Res. 1992 Sep;275(3-6):169-80. doi: 10.1016/0921-8734(92)90021-g. Mutat Res. 1992. PMID: 1383759 Review.

5

Diseases resulting from mitochondrial DNA point mutations.

Wallace DC, Lott MT, Shoffner JM, Brown MD. Wallace DC, et al. Among authors: lott mt. J Inherit Metab Dis. 1992;15(4):472-9. doi: 10.1007/BF01799605. J Inherit Metab Dis. 1992. PMID: 1528007 Review.

6

Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.

Stone EM, Newman NJ, Miller NR, Johns DR, Lott MT, Wallace DC. Stone EM, et al. Among authors: lott mt. J Clin Neuroophthalmol. 1992 Mar;12(1):10-4. J Clin Neuroophthalmol. 1992. PMID: 1532593

7

Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.

Brown MD, Voljavec AS, Lott MT, MacDonald I, Wallace DC. Brown MD, et al. Among authors: lott mt. FASEB J. 1992 Jul;6(10):2791-9. doi: 10.1096/fasebj.6.10.1634041. FASEB J. 1992. PMID: 1634041 Review.

8

MERRF: a model disease for understanding the principles of mitochondrial genetics.

Shoffner JM, Lott MT, Wallace DC. Shoffner JM, et al. Among authors: lott mt. Rev Neurol (Paris). 1991;147(6-7):431-5. Rev Neurol (Paris). 1991. PMID: 1962048 Review.

9

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

Newman NJ, Lott MT, Wallace DC. Newman NJ, et al. Among authors: lott mt. Am J Ophthalmol. 1991 Jun 15;111(6):750-62. doi: 10.1016/s0002-9394(14)76784-4. Am J Ophthalmol. 1991. PMID: 2039048

10

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Shoffner JM, Lott MT, Lezza AM, Seibel P, Ballinger SW, Wallace DC. Shoffner JM, et al. Among authors: lott mt. Cell. 1990 Jun 15;61(6):931-7. doi: 10.1016/0092-8674(90)90059-n. Cell. 1990. PMID: 2112427

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