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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. Among authors: lightowlers rn. Nat Genet. 1999 Oct;23(2):147. doi: 10.1038/13779. Nat Genet. 1999. PMID: 10508508 No abstract available.
Mitochondrial DNA recombination.
Morris AA, Lightowlers RN. Morris AA, et al. Among authors: lightowlers rn. Lancet. 2000 Sep 9;356(9233):941. doi: 10.1016/s0140-6736(05)73923-4. Lancet. 2000. PMID: 11036918 No abstract available.
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.
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.
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: lightowlers rn. Nat Genet. 1997 Jul;16(3):222-4. doi: 10.1038/ng0797-222. Nat Genet. 1997. PMID: 9207784 No abstract available.
Human mitochondria: distinct organelles or dynamic network?
Preiss T, Lowerson SA, Weber K, Lightowlers RN. Preiss T, et al. Among authors: lightowlers rn. Trends Genet. 1995 Jun;11(6):211-2. doi: 10.1016/s0168-9525(00)89048-4. Trends Genet. 1995. PMID: 7638898 No abstract available.
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
Lightowlers RN, Chinnery PF, Turnbull DM, Howell N. Lightowlers RN, et al. Trends Genet. 1997 Nov;13(11):450-5. doi: 10.1016/s0168-9525(97)01266-3. Trends Genet. 1997. PMID: 9385842 Review.
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.
Mitochondrial DNA deletion in "identical" twin brothers.
Blakely EL, He L, Taylor RW, Chinnery PF, Lightowlers RN, Schaefer AM, Turnbull DM. Blakely EL, et al. Among authors: lightowlers rn. J Med Genet. 2004 Feb;41(2):e19. doi: 10.1136/jmg.2003.011296. J Med Genet. 2004. PMID: 14757869 Free PMC article. No abstract available.
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
Chinnery PF, Thorburn DR, Samuels DC, White SL, Dahl HM, Turnbull DM, Lightowlers RN, Howell N. Chinnery PF, et al. Among authors: lightowlers rn. Trends Genet. 2000 Nov;16(11):500-5. doi: 10.1016/s0168-9525(00)02120-x. Trends Genet. 2000. PMID: 11074292
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