Chinnery PF - Search Results

1

Pathogenic mitochondrial DNA mutations are common in the general population.

Elliott HR, Samuels DC, Eden JA, Relton CL, Chinnery PF. Elliott HR, et al. Among authors: chinnery pf. Am J Hum Genet. 2008 Aug;83(2):254-60. doi: 10.1016/j.ajhg.2008.07.004. Am J Hum Genet. 2008. PMID: 18674747 Free PMC article.

2

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

3

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.

4

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. Brain. 1997 Oct;120 ( Pt 10):1713-21. doi: 10.1093/brain/120.10.1713. Brain. 1997. PMID: 9365365

5

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.

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

6

Mitochondrial medicine.

Chinnery PF, Turnbull DM. Chinnery PF, et al. QJM. 1997 Nov;90(11):657-67. doi: 10.1093/qjmed/90.11.657. QJM. 1997. PMID: 9474346 Review. No abstract available.

7

Mitochondrial genotype and clinical phenotype.

Chinnery PF, Turnbull DM. Chinnery PF, et al. J Inherit Metab Dis. 1998 Jun;21(4):321-5. doi: 10.1023/a:1005357221101. J Inherit Metab Dis. 1998. PMID: 9700589 Review. No abstract available.

8

Relaxed replication of mtDNA: A model with implications for the expression of disease.

Chinnery PF, Samuels DC. Chinnery PF, et al. Am J Hum Genet. 1999 Apr;64(4):1158-65. doi: 10.1086/302311. Am J Hum Genet. 1999. PMID: 10090901 Free PMC article.

9

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.

10

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

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