G0500695/MRC_/Medical Research Council/United Kingdom[Grants and Funding] - Search Results

Year	Number of Results
2006	1
2007	4
2008	2
2009	11
2010	8
2011	3
2012	1
2013	1
2015	1
2017	3
2019	1
2024	0

1

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.

2

Therapeutic treatments of mtDNA diseases at the earliest stages of human development.

Chiaratti MR, Meirelles FV, Wells D, Poulton J. Chiaratti MR, et al. Mitochondrion. 2011 Sep;11(5):820-8. doi: 10.1016/j.mito.2010.11.004. Epub 2010 Dec 14. Mitochondrion. 2011. PMID: 21147275 Review.

3

Preventing transmission of maternally inherited mitochondrial DNA diseases.

Poulton J, Kennedy S, Oakeshott P, Wells D. Poulton J, et al. BMJ. 2009 Jan 30;338:b94. doi: 10.1136/bmj.b94. BMJ. 2009. PMID: 19181733 Review. No abstract available.

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

Diagnosis of mitochondrial DNA depletion syndromes.

Rahman S, Poulton J. Rahman S, et al. Arch Dis Child. 2009 Jan;94(1):3-5. doi: 10.1136/adc.2008.147983. Arch Dis Child. 2009. PMID: 19103785 No abstract available.

6

Anticancer DNA intercalators cause p53-dependent mitochondrial DNA nucleoid re-modelling.

Ashley N, Poulton J. Ashley N, et al. Oncogene. 2009 Nov 5;28(44):3880-91. doi: 10.1038/onc.2009.242. Epub 2009 Aug 17. Oncogene. 2009. PMID: 19684617 Free PMC article.

7

Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease.

Uusimaa J, Jungbluth H, Fratter C, Crisponi G, Feng L, Zeviani M, Hughes I, Treacy EP, Birks J, Brown GK, Sewry CA, McDermott M, Muntoni F, Poulton J. Uusimaa J, et al. J Med Genet. 2011 Oct;48(10):660-668. doi: 10.1136/jmg.2011.089995. J Med Genet. 2011. PMID: 21931168 Free PMC article.

8

Genetic causes of mitochondrial DNA depletion in humans.

Rötig A, Poulton J. Rötig A, et al. Biochim Biophys Acta. 2009 Dec;1792(12):1103-8. doi: 10.1016/j.bbadis.2009.06.009. Epub 2009 Jul 9. Biochim Biophys Acta. 2009. PMID: 19596444 Free article. Review.

9

The mitochondrial DNA T16189C polymorphism and HIV-associated cardiomyopathy: a genotype-phenotype association study.

Shaboodien G, Engel ME, Syed FF, Poulton J, Badri M, Mayosi BM. Shaboodien G, et al. BMC Med Genet. 2009 Apr 27;10:37. doi: 10.1186/1471-2350-10-37. BMC Med Genet. 2009. PMID: 19397801 Free PMC article.

10

Insights into pancreatic β cell energy metabolism using rodent β cell models.

Morten KJ, Potter M, Badder L, Sivathondan P, Dragovic R, Neumann A, Gavin J, Shrestha R, Reilly S, Phadwal K, Lodge TA, Borzychowski A, Cookson S, Mitchell C, Morovat A, Simon AK, Uusimaa J, Hynes J, Poulton J. Morten KJ, et al. Wellcome Open Res. 2019 Sep 25;2:14. doi: 10.12688/wellcomeopenres.10535.3. eCollection 2017. Wellcome Open Res. 2019. PMID: 31754635 Free PMC article.

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