Lott MT - Search Results

1

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants.

Bianco SD, Parca L, Petrizzelli F, Biagini T, Giovannetti A, Liorni N, Napoli A, Carella M, Procaccio V, Lott MT, Zhang S, Vescovi AL, Wallace DC, Caputo V, Mazza T. Bianco SD, et al. Among authors: lott mt. Nat Commun. 2023 Aug 19;14(1):5058. doi: 10.1038/s41467-023-40797-7. Nat Commun. 2023. PMID: 37598215 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

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.

5

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.

6

Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

Brown MD, Voljavec AS, Lott MT, Torroni A, Yang CC, Wallace DC. Brown MD, et al. Among authors: lott mt. Genetics. 1992 Jan;130(1):163-73. doi: 10.1093/genetics/130.1.163. Genetics. 1992. PMID: 1732158 Free PMC article.

7

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.

8

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

9

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.

Singh G, Lott MT, Wallace DC. Singh G, et al. Among authors: lott mt. N Engl J Med. 1989 May 18;320(20):1300-5. doi: 10.1056/NEJM198905183202002. N Engl J Med. 1989. PMID: 2566116

10

Mitochondrial DNA mutations in human degenerative diseases and aging.

Wallace DC, Shoffner JM, Trounce I, Brown MD, Ballinger SW, Corral-Debrinski M, Horton T, Jun AS, Lott MT. Wallace DC, et al. Among authors: lott mt. Biochim Biophys Acta. 1995 May 24;1271(1):141-51. doi: 10.1016/0925-4439(95)00021-u. Biochim Biophys Acta. 1995. PMID: 7599200 Free article. Review.

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