Lott MT - Search Results

1

TARGETED DOWN REGULATION OF CORE MITOCHONDRIAL GENES DURING SARS-COV-2 INFECTION.

Guarnieri JW, Dybas JM, Fazelinia H, Kim MS, Frere J, Zhang Y, Albrecht YS, Murdock DG, Angelin A, Singh LN, Weiss SL, Best SM, Lott MT, Cope H, Zaksas V, Saravia-Butler A, Meydan C, Foox J, Mozsary C, Kidane YH, Priebe W, Emmett MR, Meller R, Singh U, Bram Y, tenOever BR, Heise MT, Moorman NJ, Madden EA, Taft-Benz SA, Anderson EJ, Sanders WA, Dickmander RJ, Baxter VK, Baylin SB, Wurtele ES, Moraes-Vieira PM, Taylor D, Mason CE, Schisler JC, Schwartz RE, Beheshti A, Wallace DC. Guarnieri JW, et al. Among authors: lott mt. bioRxiv [Preprint]. 2022 Feb 22:2022.02.19.481089. doi: 10.1101/2022.02.19.481089. bioRxiv. 2022. PMID: 35233572 Free PMC article. Preprint.

2

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.

3

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.

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

Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease.

Corral-Debrinski M, Stepien G, Shoffner JM, Lott MT, Kanter K, Wallace DC. Corral-Debrinski M, et al. Among authors: lott mt. JAMA. 1991 Oct 2;266(13):1812-6. JAMA. 1991. PMID: 1890710

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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