Poulton J - Search Results

1

Detailed analysis of variation at and around mitochondrial position 16189 in a large Finnish cohort reveals no significant associations with early growth or metabolic phenotypes at age 31 years.

Das S, Bennett AJ, Sovio U, Ruokonen A, Martikainen H, Pouta A, Hartikainen AL, Franks S, Elliott P, Poulton J, Järvelin MR, McCarthy MI. Das S, et al. Among authors: poulton j. J Clin Endocrinol Metab. 2007 Aug;92(8):3219-23. doi: 10.1210/jc.2007-0702. Epub 2007 May 29. J Clin Endocrinol Metab. 2007. PMID: 17535991

2

Correction: no evidence of an association between the T16189C mtDNA variant and late onset dementia (Gibson et al).

Poulton J, Das S. Poulton J, et al. J Med Genet. 2004 Dec;41(12):957; author reply 957-8. doi: 10.1136/jmg.2004.019208. J Med Genet. 2004. PMID: 15591285 Free PMC article. No abstract available.

3

Fetal and neonatal exposure to AZT and low-protein diet affects glucose homeostasis: a model with implications for AIDS prevention.

Morten K, Field P, Ashley N, Williams KA, Harris D, Hartley M, Clark A, Poulton J. Morten K, et al. Among authors: poulton j. Am J Physiol Endocrinol Metab. 2005 Dec;289(6):E1115-8. doi: 10.1152/ajpendo.00226.2005. Epub 2005 Jul 12. Am J Physiol Endocrinol Metab. 2005. PMID: 16014351 Free article.

4

Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1).

Poulton J, Hirano M, Spinazzola A, Arenas Hernandez M, Jardel C, Lombès A, Czermin B, Horvath R, Taanman JW, Rotig A, Zeviani M, Fratter C. Poulton J, et al. Biochim Biophys Acta. 2009 Dec;1792(12):1109-12. doi: 10.1016/j.bbadis.2009.08.016. Epub 2009 Sep 11. Biochim Biophys Acta. 2009. PMID: 19748572 Free article. Review.

5

Information for genetic management of mtDNA disease: sampling pathogenic mtDNA mutants in the human germline and in placenta.

Marchington D, Malik S, Banerjee A, Turner K, Samuels D, Macaulay V, Oakeshott P, Fratter C, Kennedy S, Poulton J. Marchington D, et al. Among authors: poulton j. J Med Genet. 2010 Apr;47(4):257-61. doi: 10.1136/jmg.2009.072900. Epub 2009 Nov 12. J Med Genet. 2010. PMID: 19914907

6

Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck.

Marchington DR, Hartshorne GM, Barlow D, Poulton J. Marchington DR, et al. Among authors: poulton j. Am J Hum Genet. 1997 Feb;60(2):408-16. Am J Hum Genet. 1997. PMID: 9012414 Free PMC article.

7

Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion.

Morten KJ, Ashley N, Wijburg F, Hadzic N, Parr J, Jayawant S, Adams S, Bindoff L, Bakker HD, Mieli-Vergani G, Zeviani M, Poulton J. Morten KJ, et al. Among authors: poulton j. Mitochondrion. 2007 Dec;7(6):386-95. doi: 10.1016/j.mito.2007.09.001. Epub 2007 Sep 21. Mitochondrion. 2007. PMID: 17981517

8

Forecasting stroke-like episodes and outcomes in mitochondrial disease.

Ng YS, Lax NZ, Blain AP, Erskine D, Baker MR, Polvikoski T, Thomas RH, Morris CM, Lai M, Whittaker RG, Gebbels A, Winder A, Hall J, Feeney C, Farrugia ME, Hirst C, Roberts M, Lawthom C, Chrysostomou A, Murphy K, Baird T, Maddison P, Duncan C, Poulton J, Nesbitt V, Hanna MG, Pitceathly RDS, Taylor RW, Blakely EL, Schaefer AM, Turnbull DM, McFarland R, Gorman GS. Ng YS, et al. Among authors: poulton j. Brain. 2022 Apr 18;145(2):542-554. doi: 10.1093/brain/awab353. Brain. 2022. PMID: 34927673 Free PMC article.

9

Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study.

Poulton J, Luan J, Macaulay V, Hennings S, Mitchell J, Wareham NJ. Poulton J, et al. Hum Mol Genet. 2002 Jun 15;11(13):1581-3. doi: 10.1093/hmg/11.13.1581. Hum Mol Genet. 2002. PMID: 12045211

10

Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations.

Ashley N, O'Rourke A, Smith C, Adams S, Gowda V, Zeviani M, Brown GK, Fratter C, Poulton J. Ashley N, et al. Among authors: poulton j. Hum Mol Genet. 2008 Aug 15;17(16):2496-506. doi: 10.1093/hmg/ddn150. Epub 2008 May 16. Hum Mol Genet. 2008. PMID: 18487244 Free PMC article.

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