Cree L - Search Results

1

Transmission of mitochondrial DNA disorders: possibilities for the future.

Brown DT, Herbert M, Lamb VK, Chinnery PF, Taylor RW, Lightowlers RN, Craven L, Cree L, Gardner JL, Turnbull DM. Brown DT, et al. Among authors: cree l. Lancet. 2006 Jul 1;368(9529):87-9. doi: 10.1016/S0140-6736(06)68972-1. Lancet. 2006. PMID: 16815383 No abstract available.

2

The inheritance of pathogenic mitochondrial DNA mutations.

Cree LM, Samuels DC, Chinnery PF. Cree LM, et al. Biochim Biophys Acta. 2009 Dec;1792(12):1097-102. doi: 10.1016/j.bbadis.2009.03.002. Epub 2009 Mar 19. Biochim Biophys Acta. 2009. PMID: 19303927 Free PMC article. Review.

3

Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease.

Craven L, Tuppen HA, Greggains GD, Harbottle SJ, Murphy JL, Cree LM, Murdoch AP, Chinnery PF, Taylor RW, Lightowlers RN, Herbert M, Turnbull DM. Craven L, et al. Among authors: cree lm. Nature. 2010 May 6;465(7294):82-5. doi: 10.1038/nature08958. Epub 2010 Apr 14. Nature. 2010. PMID: 20393463 Free PMC article.

4

Single-cell analysis of mitochondrial DNA.

Payne BA, Cree L, Chinnery PF. Payne BA, et al. Among authors: cree l. Methods Mol Biol. 2015;1264:67-76. doi: 10.1007/978-1-4939-2257-4_7. Methods Mol Biol. 2015. PMID: 25631004

5

Age-related decline in mitochondrial DNA copy number in isolated human pancreatic islets.

Cree LM, Patel SK, Pyle A, Lynn S, Turnbull DM, Chinnery PF, Walker M. Cree LM, et al. Diabetologia. 2008 Aug;51(8):1440-3. doi: 10.1007/s00125-008-1054-4. Epub 2008 Jun 5. Diabetologia. 2008. PMID: 18528676

6

Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->G.

Durham SE, Samuels DC, Cree LM, Chinnery PF. Durham SE, et al. Am J Hum Genet. 2007 Jul;81(1):189-95. doi: 10.1086/518901. Epub 2007 May 23. Am J Hum Genet. 2007. PMID: 17564976 Free PMC article.

7

The implications of mitochondrial DNA copy number regulation during embryogenesis.

Carling PJ, Cree LM, Chinnery PF. Carling PJ, et al. Mitochondrion. 2011 Sep;11(5):686-92. doi: 10.1016/j.mito.2011.05.004. Epub 2011 May 27. Mitochondrion. 2011. PMID: 21635974 Review.

8

A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes.

Cree LM, Samuels DC, de Sousa Lopes SC, Rajasimha HK, Wonnapinij P, Mann JR, Dahl HH, Chinnery PF. Cree LM, et al. Nat Genet. 2008 Feb;40(2):249-54. doi: 10.1038/ng.2007.63. Epub 2008 Jan 27. Nat Genet. 2008. PMID: 18223651

9

Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy.

Yu-Wai-Man P, Davies VJ, Piechota MJ, Cree LM, Votruba M, Chinnery PF. Yu-Wai-Man P, et al. Invest Ophthalmol Vis Sci. 2009 Oct;50(10):4561-6. doi: 10.1167/iovs.09-3634. Epub 2009 May 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19443720 Free PMC article.

10

Age-related mitochondrial DNA depletion and the impact on pancreatic Beta cell function.

Nile DL, Brown AE, Kumaheri MA, Blair HR, Heggie A, Miwa S, Cree LM, Payne B, Chinnery PF, Brown L, Gunn DA, Walker M. Nile DL, et al. Among authors: cree lm. PLoS One. 2014 Dec 22;9(12):e115433. doi: 10.1371/journal.pone.0115433. eCollection 2014. PLoS One. 2014. PMID: 25532126 Free PMC article.

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