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Genetic counseling and prenatal diagnosis for mtDNA disease.
Chinnery PF, Howell N, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Among authors: lightowlers rn. Am J Hum Genet. 1998 Dec;63(6):1908-11. doi: 10.1086/302157. Am J Hum Genet. 1998. PMID: 9837843 Free PMC article. No abstract available.
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. Among authors: lightowlers rn. Am J Med Genet. 1999 Aug 27;85(5):498-501. Am J Med Genet. 1999. PMID: 10405450
Treatment of mitochondrial disease.
Taylor RW, Chinnery PF, Clark KM, Lightowlers RN, Turnbull DM. Taylor RW, et al. Among authors: lightowlers rn. J Bioenerg Biomembr. 1997 Apr;29(2):195-205. doi: 10.1023/a:1022646215643. J Bioenerg Biomembr. 1997. PMID: 9239544 Review.
An essential guide to mtDNA maintenance.
Turnbull DM, Lightowlers RN. Turnbull DM, et al. Among authors: lightowlers rn. Nat Genet. 1998 Mar;18(3):199-200. doi: 10.1038/ng0398-199. Nat Genet. 1998. PMID: 9500531 No abstract available.
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: lightowlers rn. Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361. Am J Hum Genet. 1999. PMID: 10205264 Free PMC article.
In-vitro genetic modification of mitochondrial function.
Taylor RW, Chinnery PF, Turnbull DM, Lightowlers RN. Taylor RW, et al. Among authors: lightowlers rn. Hum Reprod. 2000 Jul;15 Suppl 2:79-85. doi: 10.1093/humrep/15.suppl_2.79. Hum Reprod. 2000. PMID: 11041515 Review.
194 results