Blakely EL - Search Results

1

Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

Rocha MC, Rosa HS, Grady JP, Blakely EL, He L, Romain N, Haller RG, Newman J, McFarland R, Ng YS, Gorman GS, Schaefer AM, Tuppen HA, Taylor RW, Turnbull DM. Rocha MC, et al. Among authors: blakely el. Ann Neurol. 2018 Jan;83(1):115-130. doi: 10.1002/ana.25127. Ann Neurol. 2018. PMID: 29283441 Free PMC article.

2

Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorder.

Cottrell DA, Ince PG, Blakely EL, Johnson MA, Chinnery PF, Hanna M, Turnbull DM. Cottrell DA, et al. Among authors: blakely el. J Neuropathol Exp Neurol. 2000 Jul;59(7):621-7. doi: 10.1093/jnen/59.7.621. J Neuropathol Exp Neurol. 2000. PMID: 10901234

3

Role of mitochondrial DNA mutations in disease and aging.

Cottrell DA, Blakely EL, Borthwick GM, Johnson MA, Taylor GA, Brierley EJ, Ince PG, Turnbull DM. Cottrell DA, et al. Among authors: blakely el. Ann N Y Acad Sci. 2000 Jun;908:199-207. doi: 10.1111/j.1749-6632.2000.tb06647.x. Ann N Y Acad Sci. 2000. PMID: 10911959 Review.

4

Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age.

Cottrell DA, Blakely EL, Johnson MA, Ince PG, Borthwick GM, Turnbull DM. Cottrell DA, et al. Among authors: blakely el. Neurobiol Aging. 2001 Mar-Apr;22(2):265-72. doi: 10.1016/s0197-4580(00)00234-7. Neurobiol Aging. 2001. PMID: 11182476

5

Mitochondrial DNA mutations in disease and ageing.

Cottrell DA, Blakely EL, Johnson MA, Borthwick GM, Ince PI, Turnbull DM. Cottrell DA, et al. Among authors: blakely el. Novartis Found Symp. 2001;235:234-43; discussion 243-6. doi: 10.1002/0470868694.ch19. Novartis Found Symp. 2001. PMID: 11280028 Review.

6

Mitochondrial enzyme-deficient hippocampal neurons and choroidal cells in AD.

Cottrell DA, Blakely EL, Johnson MA, Ince PG, Turnbull DM. Cottrell DA, et al. Among authors: blakely el. Neurology. 2001 Jul 24;57(2):260-4. doi: 10.1212/wnl.57.2.260. Neurology. 2001. PMID: 11468310

7

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

He L, Chinnery PF, Durham SE, Blakely EL, Wardell TM, Borthwick GM, Taylor RW, Turnbull DM. He L, et al. Among authors: blakely el. Nucleic Acids Res. 2002 Jul 15;30(14):e68. doi: 10.1093/nar/gnf067. Nucleic Acids Res. 2002. PMID: 12136116 Free PMC article.

8

A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia.

Deschauer M, Kiefer R, Blakely EL, He L, Zierz S, Turnbull DM, Taylor RW. Deschauer M, et al. Among authors: blakely el. Neuromuscul Disord. 2003 Sep;13(7-8):568-72. doi: 10.1016/s0960-8966(03)00071-3. Neuromuscul Disord. 2003. PMID: 12921794

9

Genotypes from patients indicate no paternal mitochondrial DNA contribution.

Taylor RW, McDonnell MT, Blakely EL, Chinnery PF, Taylor GA, Howell N, Zeviani M, Briem E, Carrara F, Turnbull DM. Taylor RW, et al. Among authors: blakely el. Ann Neurol. 2003 Oct;54(4):521-4. doi: 10.1002/ana.10673. Ann Neurol. 2003. PMID: 14520666

10

Somatic mitochondrial DNA mutations in adult-onset leukaemia.

He L, Luo L, Proctor SJ, Middleton PG, Blakely EL, Taylor RW, Turnbull DM. He L, et al. Among authors: blakely el. Leukemia. 2003 Dec;17(12):2487-91. doi: 10.1038/sj.leu.2403146. Leukemia. 2003. PMID: 14523470

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