Howell N - Search Results

1

Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodies.

Chinnery PF, Taylor GA, Howell N, Andrews RM, Morris CM, Taylor RW, McKeith IG, Perry RH, Edwardson JA, Turnbull DM. Chinnery PF, et al. Among authors: howell n. Neurology. 2000 Jul 25;55(2):302-4. doi: 10.1212/wnl.55.2.302. Neurology. 2000. PMID: 10908912

2

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: howell n. Ann Neurol. 2003 Oct;54(4):521-4. doi: 10.1002/ana.10673. Ann Neurol. 2003. PMID: 14520666

3

Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection.

Elson JL, Turnbull DM, Howell N. Elson JL, et al. Among authors: howell n. Am J Hum Genet. 2004 Feb;74(2):229-38. doi: 10.1086/381505. Epub 2004 Jan 7. Am J Hum Genet. 2004. PMID: 14712420 Free PMC article.

4

Does the mitochondrial genome play a role in the etiology of Alzheimer's disease?

Elson JL, Herrnstadt C, Preston G, Thal L, Morris CM, Edwardson JA, Beal MF, Turnbull DM, Howell N. Elson JL, et al. Among authors: howell n. Hum Genet. 2006 Apr;119(3):241-54. doi: 10.1007/s00439-005-0123-8. Epub 2006 Jan 12. Hum Genet. 2006. PMID: 16408223

5

Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

Chinnery PF, Andrews RM, Turnbull DM, Howell NN. Chinnery PF, et al. Among authors: howell nn. Am J Med Genet. 2001 Jan 22;98(3):235-43. doi: 10.1002/1096-8628(20010122)98:3<235::aid-ajmg1086>3.0.co;2-o. Am J Med Genet. 2001. PMID: 11169561

6

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

Chinnery PF, Howell N, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Among authors: howell n. Brain. 1997 Oct;120 ( Pt 10):1713-21. doi: 10.1093/brain/120.10.1713. Brain. 1997. PMID: 9365365

7

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.

Lightowlers RN, Chinnery PF, Turnbull DM, Howell N. Lightowlers RN, et al. Among authors: howell n. Trends Genet. 1997 Nov;13(11):450-5. doi: 10.1016/s0168-9525(97)01266-3. Trends Genet. 1997. PMID: 9385842 Review.

8

MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring.

Chinnery PF, Howell N, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Among authors: howell n. Brain. 1998 Oct;121 ( Pt 10):1889-94. doi: 10.1093/brain/121.10.1889. Brain. 1998. PMID: 9798744

9

Mitochondrial DNA analysis: polymorphisms and pathogenicity.

Chinnery PF, Howell N, Andrews RM, Turnbull DM. Chinnery PF, et al. Among authors: howell n. J Med Genet. 1999 Jul;36(7):505-10. J Med Genet. 1999. PMID: 10424809 Free PMC article. Review.

10

Clinical mitochondrial genetics.

Chinnery PF, Howell N, Andrews RM, Turnbull DM. Chinnery PF, et al. Among authors: howell n. J Med Genet. 1999 Jun;36(6):425-36. J Med Genet. 1999. PMID: 10874629 Free PMC article. Review.

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