Coskun PE - Search Results

1

Adeno-associated virus-mediated gene transfer of the heart/muscle adenine nucleotide translocator (ANT) in mouse.

Flierl A, Chen Y, Coskun PE, Samulski RJ, Wallace DC. Flierl A, et al. Among authors: coskun pe. Gene Ther. 2005 Apr;12(7):570-8. doi: 10.1038/sj.gt.3302443. Gene Ther. 2005. PMID: 15647764 Free PMC article.

2

The mitochondrial adenine nucleotide transporters in myogenesis.

Flierl A, Schriner SE, Hancock S, Coskun PE, Wallace DC. Flierl A, et al. Among authors: coskun pe. Free Radic Biol Med. 2022 Aug 1;188:312-327. doi: 10.1016/j.freeradbiomed.2022.05.022. Epub 2022 Jun 15. Free Radic Biol Med. 2022. PMID: 35714845 Free article. Review.

3

Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum.

Coskun PE, Ruiz-Pesini E, Wallace DC. Coskun PE, et al. Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2174-6. doi: 10.1073/pnas.0630589100. Epub 2003 Feb 26. Proc Natl Acad Sci U S A. 2003. PMID: 12606714 Free PMC article. No abstract available.

4

MITOCHIP assessment of differential gene expression in the skeletal muscle of Ant1 knockout mice: coordinate regulation of OXPHOS, antioxidant, and apoptotic genes.

Subramaniam V, Golik P, Murdock DG, Levy S, Kerstann KW, Coskun PE, Melkonian GA, Wallace DC. Subramaniam V, et al. Among authors: coskun pe. Biochim Biophys Acta. 2008 Jul-Aug;1777(7-8):666-75. doi: 10.1016/j.bbabio.2008.03.015. Epub 2008 Mar 28. Biochim Biophys Acta. 2008. PMID: 18439414 Free PMC article.

5

Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication.

Coskun PE, Beal MF, Wallace DC. Coskun PE, et al. Proc Natl Acad Sci U S A. 2004 Jul 20;101(29):10726-31. doi: 10.1073/pnas.0403649101. Epub 2004 Jul 9. Proc Natl Acad Sci U S A. 2004. PMID: 15247418 Free PMC article.

6

A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.

Fan W, Waymire KG, Narula N, Li P, Rocher C, Coskun PE, Vannan MA, Narula J, Macgregor GR, Wallace DC. Fan W, et al. Among authors: coskun pe. Science. 2008 Feb 15;319(5865):958-62. doi: 10.1126/science.1147786. Science. 2008. PMID: 18276892 Free PMC article.

7

Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome.

Yazdi PG, Su H, Ghimbovschi S, Fan W, Coskun PE, Nalbandian A, Knoblach S, Resnick JL, Hoffman E, Wallace DC, Kimonis VE. Yazdi PG, et al. Among authors: coskun pe. Clin Transl Sci. 2013 Oct;6(5):347-55. doi: 10.1111/cts.12083. Epub 2013 Jul 29. Clin Transl Sci. 2013. PMID: 24127921 Free PMC article.

8

Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome.

Su H, Fan W, Coskun PE, Vesa J, Gold JA, Jiang YH, Potluri P, Procaccio V, Acab A, Weiss JH, Wallace DC, Kimonis VE. Su H, et al. Among authors: coskun pe. Neurosci Lett. 2011 Jan 7;487(2):129-33. doi: 10.1016/j.neulet.2009.06.079. Epub 2009 Jun 27. Neurosci Lett. 2011. PMID: 19563863 Free PMC article.

9

Accumulation of mitochondrial DNA damage in keratoconus corneas.

Atilano SR, Coskun P, Chwa M, Jordan N, Reddy V, Le K, Wallace DC, Kenney MC. Atilano SR, et al. Invest Ophthalmol Vis Sci. 2005 Apr;46(4):1256-63. doi: 10.1167/iovs.04-1395. Invest Ophthalmol Vis Sci. 2005. PMID: 15790887

10

Mitochondrial DNA haplogroups associated with age-related macular degeneration.

Udar N, Atilano SR, Memarzadeh M, Boyer DS, Chwa M, Lu S, Maguen B, Langberg J, Coskun P, Wallace DC, Nesburn AB, Khatibi N, Hertzog D, Le K, Hwang D, Kenney MC. Udar N, et al. Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2966-74. doi: 10.1167/iovs.08-2646. Epub 2009 Jan 17. Invest Ophthalmol Vis Sci. 2009. PMID: 19151382

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