Wallace DC - Search Results

1

Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming.

Picard M, Zhang J, Hancock S, Derbeneva O, Golhar R, Golik P, O'Hearn S, Levy S, Potluri P, Lvova M, Davila A, Lin CS, Perin JC, Rappaport EF, Hakonarson H, Trounce IA, Procaccio V, Wallace DC. Picard M, et al. Among authors: wallace dc. Proc Natl Acad Sci U S A. 2014 Sep 23;111(38):E4033-42. doi: 10.1073/pnas.1414028111. Epub 2014 Sep 5. Proc Natl Acad Sci U S A. 2014. PMID: 25192935 Free PMC article.

2

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.

Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC. Ballinger SW, et al. Among authors: wallace dc. Nat Genet. 1992 Apr;1(1):11-5. doi: 10.1038/ng0492-11. Nat Genet. 1992. PMID: 1301992

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

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. 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.

5

Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.

Trounce I, Neill S, Wallace DC. Trounce I, et al. Among authors: wallace dc. Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8334-8. doi: 10.1073/pnas.91.18.8334. Proc Natl Acad Sci U S A. 1994. PMID: 8078883 Free PMC article.

6

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.

Jun AS, Trounce IA, Brown MD, Shoffner JM, Wallace DC. Jun AS, et al. Among authors: wallace dc. Mol Cell Biol. 1996 Mar;16(3):771-7. doi: 10.1128/MCB.16.3.771. Mol Cell Biol. 1996. PMID: 8622678 Free PMC article.

7

Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells.

Trounce I, Wallace DC. Trounce I, et al. Among authors: wallace dc. Somat Cell Mol Genet. 1996 Jan;22(1):81-5. doi: 10.1007/BF02374379. Somat Cell Mol Genet. 1996. PMID: 8643997

8

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines.

Trounce IA, Kim YL, Jun AS, Wallace DC. Trounce IA, et al. Among authors: wallace dc. Methods Enzymol. 1996;264:484-509. doi: 10.1016/s0076-6879(96)64044-0. Methods Enzymol. 1996. PMID: 8965721 No abstract available.

9

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.

Graham BH, Waymire KG, Cottrell B, Trounce IA, MacGregor GR, Wallace DC. Graham BH, et al. Among authors: wallace dc. Nat Genet. 1997 Jul;16(3):226-34. doi: 10.1038/ng0797-226. Nat Genet. 1997. PMID: 9207786

10

Transfer of chloramphenicol-resistant mitochondrial DNA into the chimeric mouse.

Levy SE, Waymire KG, Kim YL, MacGregor GR, Wallace DC. Levy SE, et al. Among authors: wallace dc. Transgenic Res. 1999 Apr;8(2):137-45. doi: 10.1023/a:1008967412955. Transgenic Res. 1999. PMID: 10481313 Free PMC article.

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