A citation-based method for searching scientific literature

R W Taylor, P F Chinnery, K M Clark, R N Lightowlers, D M Turnbull. J Bioenerg Biomembr 1997
Times Cited: 52







List of co-cited articles
671 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids.
R W Taylor, P F Chinnery, D M Turnbull, R N Lightowlers. Nat Genet 1997
177
44

Sequence and organization of the human mitochondrial genome.
S Anderson, A T Bankier, B G Barrell, M H de Bruijn, A R Coulson, J Drouin, I C Eperon, D P Nierlich, B A Roe, F Sanger,[...]. Nature 1981
26

Reversal of a mitochondrial DNA defect in human skeletal muscle.
K M Clark, L A Bindoff, R N Lightowlers, R M Andrews, P G Griffiths, M A Johnson, E J Brierley, D M Turnbull. Nat Genet 1997
116
26

Molecular genetic aspects of human mitochondrial disorders.
N G Larsson, D A Clayton. Annu Rev Genet 1995
365
21


Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
R N Lightowlers, P F Chinnery, D M Turnbull, N Howell. Trends Genet 1997
294
21

Peptide nucleic acid delivery to human mitochondria.
P F Chinnery, R W Taylor, K Diekert, R Lill, D M Turnbull, R N Lightowlers. Gene Ther 1999
125
21

Gene therapy for mitochondrial DNA defects: is it possible?
Z M Chrzanowska-Lightowlers, R N Lightowlers, D M Turnbull. Gene Ther 1995
44
22

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.
S Eleff, N G Kennaway, N R Buist, V M Darley-Usmar, R A Capaldi, W J Bank, B Chance. Proc Natl Acad Sci U S A 1984
234
19

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
J M Shoffner, M T Lott, A M Lezza, P Seibel, S W Ballinger, D C Wallace. Cell 1990
19

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
D C Wallace, G Singh, M T Lott, J A Hodge, T G Schurr, A M Lezza, L J Elsas, E K Nikoskelainen. Science 1988
19


Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseases.
P Seibel, J Trappe, G Villani, T Klopstock, S Papa, H Reichmann. Nucleic Acids Res 1995
114
17



Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial.
N Bresolin, C Doriguzzi, C Ponzetto, C Angelini, I Moroni, E Castelli, E Cossutta, A Binda, A Gallanti, S Gabellini. J Neurol Sci 1990
104
17


Gene shifting: a novel therapy for mitochondrial myopathy.
T Taivassalo, K Fu, T Johns, D Arnold, G Karpati, E A Shoubridge. Hum Mol Genet 1999
114
15

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
C T Moraes, S DiMauro, M Zeviani, A Lombes, S Shanske, A F Miranda, H Nakase, E Bonilla, L C Werneck, S Servidei. N Engl J Med 1989
857
15




A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.
K Weber, J N Wilson, L Taylor, E Brierley, M A Johnson, D M Turnbull, L A Bindoff. Am J Hum Genet 1997
163
15

PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules.
M Egholm, O Buchardt, L Christensen, C Behrens, S M Freier, D A Driver, R H Berg, S K Kim, B Norden, P E Nielsen. Nature 1993
15

The epidemiology of pathogenic mitochondrial DNA mutations.
P F Chinnery, M A Johnson, T M Wardell, R Singh-Kler, C Hayes, D T Brown, R W Taylor, L A Bindoff, D M Turnbull. Ann Neurol 2000
279
15


Mitochondria and apoptosis.
D R Green, J C Reed. Science 1998
13



Mitochondrial myopathy caused by long-term zidovudine therapy.
M C Dalakas, I Illa, G H Pezeshkpour, J P Laukaitis, B Cohen, J L Griffin. N Engl J Med 1990
698
13

Mitochondrial toxicity of antiviral drugs.
W Lewis, M C Dalakas. Nat Med 1995
601
13

Coenzyme Q10 with multiple vitamins is generally ineffective in treatment of mitochondrial disease.
P M Matthews, B Ford, R J Dandurand, D H Eidelman, D O'Connor, A Sherwin, G Karpati, F Andermann, D L Arnold. Neurology 1993
103
13

Mitochondrial DNA mutations and pathogenesis.
E A Schon, E Bonilla, S DiMauro. J Bioenerg Biomembr 1997
354
11

Clinical mitochondrial genetics.
P F Chinnery, N Howell, R M Andrews, D M Turnbull. J Med Genet 1999
71
11

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.
X Estivill, N Govea, E Barceló, C Badenas, E Romero, L Moral, R Scozzri, L D'Urbano, M Zeviani, A Torroni. Am J Hum Genet 1998
377
11

Stability of peptide nucleic acids in human serum and cellular extracts.
V V Demidov, V N Potaman, M D Frank-Kamenetskii, M Egholm, O Buchard, S H Sönnichsen, P E Nielsen. Biochem Pharmacol 1994
486
11

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase.
S Melov, J A Schneider, B J Day, D Hinerfeld, P Coskun, S S Mirra, J D Crapo, D C Wallace. Nat Genet 1998
374
11

Protein import into mitochondria.
W Neupert. Annu Rev Biochem 1997
927
11

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.
T Bourgeron, P Rustin, D Chretien, M Birch-Machin, M Bourgeois, E Viegas-Péquignot, A Munnich, A Rötig. Nat Genet 1995
529
11

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
I J Holt, A E Harding, R K Petty, J A Morgan-Hughes. Am J Hum Genet 1990
796
11

Adverse effects of reverse transcriptase inhibitors: mitochondrial toxicity as common pathway.
K Brinkman, H J ter Hofstede, D M Burger, J A Smeitink, P P Koopmans. AIDS 1998
676
11

Treatment of complex I deficiency with riboflavin.
P L Bernsen, F J Gabreëls, W Ruitenbeek, H L Hamburger. J Neurol Sci 1993
73
11

Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disorders.
N De Stefano, P M Matthews, B Ford, A Genge, G Karpati, D L Arnold. Neurology 1995
127
11

Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication.
Y Michikawa, F Mazzucchelli, N Bresolin, G Scarlato, G Attardi. Science 1999
530
11

Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes.
R B Blok, D A Gook, D R Thorburn, H H Dahl. Am J Hum Genet 1997
127
11


Mitochondrial DNA and disease.
P F Chinnery, D M Turnbull. Lancet 1999
86
11


Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene.
G Manfredi, N Gupta, M E Vazquez-Memije, J E Sadlock, A Spinazzola, D C De Vivo, E A Schon. J Biol Chem 1999
77
9



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.