Wallace DC - Search Results

1

Core mitochondrial genes are down-regulated during SARS-CoV-2 infection of rodent and human hosts.

Guarnieri JW, Dybas JM, Fazelinia H, Kim MS, Frere J, Zhang Y, Soto Albrecht Y, Murdock DG, Angelin A, Singh LN, Weiss SL, Best SM, Lott MT, Zhang S, Cope H, Zaksas V, Saravia-Butler A, Meydan C, Foox J, Mozsary C, Bram Y, Kidane Y, Priebe W, Emmett MR, Meller R, Demharter S, Stentoft-Hansen V, Salvatore M, Galeano D, Enguita FJ, Grabham P, Trovao NS, Singh U, Haltom J, Heise MT, Moorman NJ, Baxter VK, Madden EA, Taft-Benz SA, Anderson EJ, Sanders WA, Dickmander RJ, 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: wallace dc. Sci Transl Med. 2023 Aug 9;15(708):eabq1533. doi: 10.1126/scitranslmed.abq1533. Epub 2023 Aug 9. Sci Transl Med. 2023. PMID: 37556555 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: wallace dc. 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: wallace dc. 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: wallace dc. 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. 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: wallace dc. 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: wallace dc. FASEB J. 1992 Jul;6(10):2791-9. doi: 10.1096/fasebj.6.10.1634041. FASEB J. 1992. PMID: 1634041 Review.

8

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: wallace dc. Genetics. 1992 Jan;130(1):163-73. doi: 10.1093/genetics/130.1.163. Genetics. 1992. PMID: 1732158 Free PMC article.

9

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: wallace dc. JAMA. 1991 Oct 2;266(13):1812-6. JAMA. 1991. PMID: 1890710

10

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

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

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