Poulton J - Search Results

1

Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants.

Vergani L, Malena A, Sabatelli P, Loro E, Cavallini L, Magalhaes P, Valente L, Bragantini F, Carrara F, Leger B, Poulton J, Russell AP, Holt IJ. Vergani L, et al. Among authors: poulton j. Brain. 2007 Oct;130(Pt 10):2715-24. doi: 10.1093/brain/awm151. Epub 2007 Jul 11. Brain. 2007. PMID: 17626036

2

163rd ENMC International Workshop: nucleoid and nucleotide biology in syndromes of mitochondrial DNA depletion myopathy 12-14 December 2008, Naarden, The Netherlands.

Poulton J, Holt IJ. Poulton J, et al. Neuromuscul Disord. 2009 Jun;19(6):439-43. doi: 10.1016/j.nmd.2009.04.009. Epub 2009 May 21. Neuromuscul Disord. 2009. PMID: 19464176 No abstract available.

3

Mitochondrial DNA: does more lead to less?

Poulton J, Holt IJ. Poulton J, et al. Nat Genet. 1994 Dec;8(4):313-5. doi: 10.1038/ng1294-313. Nat Genet. 1994. PMID: 7894476 No abstract available.

4

Transmission of mitochondrial DNA diseases and ways to prevent them.

Poulton J, Chiaratti MR, Meirelles FV, Kennedy S, Wells D, Holt IJ. Poulton J, et al. PLoS Genet. 2010 Aug 12;6(8):e1001066. doi: 10.1371/journal.pgen.1001066. PLoS Genet. 2010. PMID: 20711358 Free PMC article. Review.

5

Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number.

Tyynismaa H, Sembongi H, Bokori-Brown M, Granycome C, Ashley N, Poulton J, Jalanko A, Spelbrink JN, Holt IJ, Suomalainen A. Tyynismaa H, et al. Among authors: poulton j. Hum Mol Genet. 2004 Dec 15;13(24):3219-27. doi: 10.1093/hmg/ddh342. Epub 2004 Oct 27. Hum Mol Genet. 2004. PMID: 15509589

6

Mice expressing an error-prone DNA polymerase in mitochondria display elevated replication pausing and chromosomal breakage at fragile sites of mitochondrial DNA.

Bailey LJ, Cluett TJ, Reyes A, Prolla TA, Poulton J, Leeuwenburgh C, Holt IJ. Bailey LJ, et al. Among authors: poulton j. Nucleic Acids Res. 2009 Apr;37(7):2327-35. doi: 10.1093/nar/gkp091. Epub 2009 Feb 25. Nucleic Acids Res. 2009. PMID: 19244310 Free PMC article.

7

Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.

Bugiardini E, Poole OV, Manole A, Pittman AM, Horga A, Hargreaves I, Woodward CE, Sweeney MG, Holton JL, Taanman JW, Plant GT, Poulton J, Zeviani M, Ghezzi D, Taylor J, Smith C, Fratter C, Kanikannan MA, Paramasivam A, Thangaraj K, Spinazzola A, Holt IJ, Houlden H, Hanna MG, Pitceathly RDS. Bugiardini E, et al. Among authors: poulton j. Neurol Genet. 2017 May 2;3(3):e149. doi: 10.1212/NXG.0000000000000149. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28508084 Free PMC article.

8

Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?

Marchington DR, Poulton J, Sellar A, Holt IJ. Marchington DR, et al. Among authors: poulton j. Hum Mol Genet. 1996 Apr;5(4):473-9. doi: 10.1093/hmg/5.4.473. Hum Mol Genet. 1996. PMID: 8845839

9

MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria.

Dalla Rosa I, Cámara Y, Durigon R, Moss CF, Vidoni S, Akman G, Hunt L, Johnson MA, Grocott S, Wang L, Thorburn DR, Hirano M, Poulton J, Taylor RW, Elgar G, Martí R, Voshol P, Holt IJ, Spinazzola A. Dalla Rosa I, et al. Among authors: poulton j. PLoS Genet. 2016 Jan 13;12(1):e1005779. doi: 10.1371/journal.pgen.1005779. eCollection 2016 Jan. PLoS Genet. 2016. PMID: 26760297 Free PMC article.

10

Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states.

Kajander OA, Rovio AT, Majamaa K, Poulton J, Spelbrink JN, Holt IJ, Karhunen PJ, Jacobs HT. Kajander OA, et al. Among authors: poulton j. Hum Mol Genet. 2000 Nov 22;9(19):2821-35. doi: 10.1093/hmg/9.19.2821. Hum Mol Genet. 2000. PMID: 11092758

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