Andrews RM - Search Results

1

Reversal of a mitochondrial DNA defect in human skeletal muscle.

Clark KM, Bindoff LA, Lightowlers RN, Andrews RM, Griffiths PG, Johnson MA, Brierley EJ, Turnbull DM. Clark KM, et al. Among authors: andrews rm. Nat Genet. 1997 Jul;16(3):222-4. doi: 10.1038/ng0797-222. Nat Genet. 1997. PMID: 9207784 No abstract available.

2

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.

Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N. Andrews RM, et al. Nat Genet. 1999 Oct;23(2):147. doi: 10.1038/13779. Nat Genet. 1999. PMID: 10508508 No abstract available.

3

Mitochondrial DNA mutations and pathogenicity.

Chinnery PF, Turnbull DM, Howell N, Andrews RM. Chinnery PF, et al. Among authors: andrews rm. J Med Genet. 1998 Aug;35(8):701-2. doi: 10.1136/jmg.35.8.701-a. J Med Genet. 1998. PMID: 9719386 Free PMC article. No abstract available.

4

Clinical mitochondrial genetics.

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

5

Mitochondrial DNA analysis: polymorphisms and pathogenicity.

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

6

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.

Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM. Clark KM, et al. Among authors: andrews rm. Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361. Am J Hum Genet. 1999. PMID: 10205264 Free PMC article.

7

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: andrews rm. 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

8

A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis.

Taylor RW, Chinnery PF, Bates MJ, Jackson MJ, Johnson MA, Andrews RM, Turnbull DM. Taylor RW, et al. Among authors: andrews rm. Biochem Biophys Res Commun. 1998 Feb 4;243(1):47-51. doi: 10.1006/bbrc.1997.8055. Biochem Biophys Res Commun. 1998. PMID: 9473477

9

Histochemical localisation of mitochondrial enzyme activity in human optic nerve and retina.

Andrews RM, Griffiths PG, Johnson MA, Turnbull DM. Andrews RM, et al. Br J Ophthalmol. 1999 Feb;83(2):231-5. doi: 10.1136/bjo.83.2.231. Br J Ophthalmol. 1999. PMID: 10396204 Free PMC article.

10

The distribution of mitochondrial activity in relation to optic nerve structure.

Bristow EA, Griffiths PG, Andrews RM, Johnson MA, Turnbull DM. Bristow EA, et al. Among authors: andrews rm. Arch Ophthalmol. 2002 Jun;120(6):791-6. doi: 10.1001/archopht.120.6.791. Arch Ophthalmol. 2002. PMID: 12049585

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