Schon EA - Search Results

1

Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cells.

Santra S, Gilkerson RW, Davidson M, Schon EA. Santra S, et al. Among authors: schon ea. Ann Neurol. 2004 Nov;56(5):662-9. doi: 10.1002/ana.20240. Ann Neurol. 2004. PMID: 15389892

2

Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation.

Gilkerson RW, Schon EA, Hernandez E, Davidson MM. Gilkerson RW, et al. Among authors: schon ea. J Cell Biol. 2008 Jun 30;181(7):1117-28. doi: 10.1083/jcb.200712101. Epub 2008 Jun 23. J Cell Biol. 2008. PMID: 18573913 Free PMC article.

3

Functional complementation of mitochondrial DNAs: mobilizing mitochondrial genetics against dysfunction.

Schon EA, Gilkerson RW. Schon EA, et al. Biochim Biophys Acta. 2010 Mar;1800(3):245-9. doi: 10.1016/j.bbagen.2009.07.007. Epub 2009 Jul 17. Biochim Biophys Acta. 2010. PMID: 19616602 Review.

4

Therapeutic prospects for mitochondrial disease.

Schon EA, DiMauro S, Hirano M, Gilkerson RW. Schon EA, et al. Trends Mol Med. 2010 Jun;16(6):268-76. doi: 10.1016/j.molmed.2010.04.007. Trends Mol Med. 2010. PMID: 20556877 Free PMC article. Review.

5

An algal nucleus-encoded subunit of mitochondrial ATP synthase rescues a defect in the analogous human mitochondrial-encoded subunit.

Ojaimi J, Pan J, Santra S, Snell WJ, Schon EA. Ojaimi J, et al. Among authors: schon ea. Mol Biol Cell. 2002 Nov;13(11):3836-44. doi: 10.1091/mbc.e02-05-0306. Mol Biol Cell. 2002. PMID: 12429828 Free PMC article.

6

Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiency.

Tay SK, Nesti C, Mancuso M, Schon EA, Shanske S, Bonilla E, Davidson MM, Dimauro S. Tay SK, et al. Among authors: schon ea. Arch Neurol. 2004 Dec;61(12):1935-7. doi: 10.1001/archneur.61.12.1935. Arch Neurol. 2004. PMID: 15596615

7

Nucleoid autonomy: An underlying mechanism of mitochondrial genetics with therapeutic potential.

Gilkerson RW, Schon EA. Gilkerson RW, et al. Among authors: schon ea. Commun Integr Biol. 2008;1(1):34-6. doi: 10.4161/cib.1.1.6622. Commun Integr Biol. 2008. PMID: 19704786 Free PMC article.

8

Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition.

Gilkerson RW, De Vries RL, Lebot P, Wikstrom JD, Torgyekes E, Shirihai OS, Przedborski S, Schon EA. Gilkerson RW, et al. Among authors: schon ea. Hum Mol Genet. 2012 Mar 1;21(5):978-90. doi: 10.1093/hmg/ddr529. Epub 2011 Nov 11. Hum Mol Genet. 2012. PMID: 22080835 Free PMC article.

9

Mitophagy in cells with mtDNA mutations: being sick is not enough.

de Vries RL, Gilkerson RW, Przedborski S, Schon EA. de Vries RL, et al. Among authors: schon ea. Autophagy. 2012 Apr;8(4):699-700. doi: 10.4161/auto.19470. Epub 2012 Apr 1. Autophagy. 2012. PMID: 22361618

10

Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.

Koga Y, Davidson M, Schon EA, King MP. Koga Y, et al. Among authors: schon ea. Nucleic Acids Res. 1993 Feb 11;21(3):657-62. doi: 10.1093/nar/21.3.657. Nucleic Acids Res. 1993. PMID: 7680123 Free PMC article.

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