Chinnery PF - Search Results

1

A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegia.

Deschauer M, Hudson G, Müller T, Taylor RW, Chinnery PF, Zierz S. Deschauer M, et al. Among authors: chinnery pf. Neuromuscul Disord. 2005 Apr;15(4):311-5. doi: 10.1016/j.nmd.2004.12.004. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15792871

2

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

Taylor RW, Chinnery PF, Haldane F, Morris AA, Bindoff LA, Wilson J, Turnbull DM. Taylor RW, et al. Among authors: chinnery pf. Ann Neurol. 1996 Sep;40(3):459-62. doi: 10.1002/ana.410400318. Ann Neurol. 1996. PMID: 8797538

3

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids.

Taylor RW, Chinnery PF, Turnbull DM, Lightowlers RN. Taylor RW, et al. Among authors: chinnery pf. Nat Genet. 1997 Feb;15(2):212-5. doi: 10.1038/ng0297-212. Nat Genet. 1997. PMID: 9020853

4

A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis.

Chinnery PF, Johnson MA, Taylor RW, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Ann Neurol. 1997 Mar;41(3):408-10. doi: 10.1002/ana.410410319. Ann Neurol. 1997. PMID: 9066365

5

Treatment of mitochondrial disease.

Taylor RW, Chinnery PF, Clark KM, Lightowlers RN, Turnbull DM. Taylor RW, et al. Among authors: chinnery pf. J Bioenerg Biomembr. 1997 Apr;29(2):195-205. doi: 10.1023/a:1022646215643. J Bioenerg Biomembr. 1997. PMID: 9239544 Review.

6

A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegia.

Chinnery PF, Johnson MA, Taylor RW, Durward WF, Turnbull DM. Chinnery PF, et al. Neurology. 1997 Oct;49(4):1166-8. doi: 10.1212/wnl.49.4.1166. Neurology. 1997. PMID: 9339712

7

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: chinnery pf. Biochem Biophys Res Commun. 1998 Feb 4;243(1):47-51. doi: 10.1006/bbrc.1997.8055. Biochem Biophys Res Commun. 1998. PMID: 9473477

8

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: chinnery pf. Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361. Am J Hum Genet. 1999. PMID: 10205264 Free PMC article.

9

Nonrandom tissue distribution of mutant mtDNA.

Chinnery PF, Zwijnenburg PJ, Walker M, Howell N, Taylor RW, Lightowlers RN, Bindoff L, Turnbull DM. Chinnery PF, et al. Am J Med Genet. 1999 Aug 27;85(5):498-501. Am J Med Genet. 1999. PMID: 10405450

10

Peptide nucleic acid delivery to human mitochondria.

Chinnery PF, Taylor RW, Diekert K, Lill R, Turnbull DM, Lightowlers RN. Chinnery PF, et al. Gene Ther. 1999 Dec;6(12):1919-28. doi: 10.1038/sj.gt.3301061. Gene Ther. 1999. PMID: 10637443

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