Brown DT - Search Results

1

Spinocerebellar ataxia and the A3243G and A8344G mtDNA mutations.

Chinnery PF, Brown DT, Archibald K, Curtis A, Turnbull DM. Chinnery PF, et al. Among authors: brown dt. J Med Genet. 2002 May;39(5):E22. doi: 10.1136/jmg.39.5.e22. J Med Genet. 2002. PMID: 12011163 Free PMC article. No abstract available.

2

Random genetic drift determines the level of mutant mtDNA in human primary oocytes.

Brown DT, Samuels DC, Michael EM, Turnbull DM, Chinnery PF. Brown DT, et al. Am J Hum Genet. 2001 Feb;68(2):533-6. doi: 10.1086/318190. Epub 2000 Dec 29. Am J Hum Genet. 2001. PMID: 11133360 Free PMC article.

3

Point mutations of the mtDNA control region in normal and neurodegenerative human brains.

Chinnery PF, Taylor GA, Howell N, Brown DT, Parsons TJ, Turnbull DM. Chinnery PF, et al. Among authors: brown dt. Am J Hum Genet. 2001 Feb;68(2):529-32. doi: 10.1086/318204. Epub 2000 Dec 21. Am J Hum Genet. 2001. PMID: 11133363 Free PMC article.

4

Progressive depletion of mtDNA in mitochondrial myopathy.

Durham SE, Brown DT, Turnbull DM, Chinnery PF. Durham SE, et al. Among authors: brown dt. Neurology. 2006 Aug 8;67(3):502-4. doi: 10.1212/01.wnl.0000227961.55640.2f. Neurology. 2006. PMID: 16894115

5

The epidemiology of pathogenic mitochondrial DNA mutations.

Chinnery PF, Johnson MA, Wardell TM, Singh-Kler R, Hayes C, Brown DT, Taylor RW, Bindoff LA, Turnbull DM. Chinnery PF, et al. Among authors: brown dt. Ann Neurol. 2000 Aug;48(2):188-93. Ann Neurol. 2000. PMID: 10939569

6

The epidemiology of Leber hereditary optic neuropathy in the North East of England.

Yu-Wai-Man P, Griffiths PG, Brown DT, Howell N, Turnbull DM, Chinnery PF. Yu-Wai-Man P, et al. Among authors: brown dt. Am J Hum Genet. 2003 Feb;72(2):333-9. doi: 10.1086/346066. Epub 2002 Jan 7. Am J Hum Genet. 2003. PMID: 12518276 Free PMC article.

7

Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo.

Chinnery PF, Taylor DJ, Brown DT, Manners D, Styles P, Lodi R. Chinnery PF, et al. Among authors: brown dt. Ann Neurol. 2000 Mar;47(3):381-4. Ann Neurol. 2000. PMID: 10716261

8

The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.

Chinnery PF, Brown DT, Andrews RM, Singh-Kler R, Riordan-Eva P, Lindley J, Applegarth DA, Turnbull DM, Howell N. Chinnery PF, et al. Among authors: brown dt. Brain. 2001 Jan;124(Pt 1):209-18. doi: 10.1093/brain/124.1.209. Brain. 2001. PMID: 11133798

9

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. Lancet. 2006 Jul 1;368(9529):87-9. doi: 10.1016/S0140-6736(06)68972-1. Lancet. 2006. PMID: 16815383 No abstract available.

10

NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathy.

Yu-Wai-Man P, Brown DT, Wehnert MS, Zeviani M, Carrara F, Turnbull DM, Chinnery PF. Yu-Wai-Man P, et al. Among authors: brown dt. Neurology. 2002 Jun 25;58(12):1861-2. doi: 10.1212/wnl.58.12.1861. Neurology. 2002. PMID: 12084895 No abstract available.

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