A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs.
Sandra R Bacman, Siôn L Williams, Milena Pinto, Susana Peralta, Carlos T Moraes. Nat Med 2013
215
70


Mitochondrially targeted ZFNs for selective degradation of pathogenic mitochondrial genomes bearing large-scale deletions or point mutations.
Payam A Gammage, Joanna Rorbach, Anna I Vincent, Edward J Rebar, Michal Minczuk. EMBO Mol Med 2014
137
51

Development of a single-chain, quasi-dimeric zinc-finger nuclease for the selective degradation of mutated human mitochondrial DNA.
Michal Minczuk, Monika A Papworth, Jeffrey C Miller, Michael P Murphy, Aaron Klug. Nucleic Acids Res 2008
109
50

Rapid directional shift of mitochondrial DNA heteroplasmy in animal tissues by a mitochondrially targeted restriction endonuclease.
Maria Pilar Bayona-Bafaluy, Bas Blits, Brendan J Battersby, Eric A Shoubridge, Carlos T Moraes. Proc Natl Acad Sci U S A 2005
99
50


Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.
Masashi Tanaka, Harm-Jan Borgeld, Jin Zhang, Shin-ichi Muramatsu, Jian-Sheng Gong, Makoto Yoneda, Wakako Maruyama, Makoto Naoi, Tohru Ibi, Ko Sahashi,[...]. J Biomed Sci 2002
131
45


Selective elimination of mutant mitochondrial genomes as therapeutic strategy for the treatment of NARP and MILS syndromes.
M F Alexeyev, N Venediktova, V Pastukh, I Shokolenko, G Bonilla, G L Wilson. Gene Ther 2008
56
44

Sequence-specific modification of mitochondrial DNA using a chimeric zinc finger methylase.
Michal Minczuk, Monika A Papworth, Paulina Kolasinska, Michael P Murphy, Aaron Klug. Proc Natl Acad Sci U S A 2006
97
40

Selective elimination of mitochondrial mutations in the germline by genome editing.
Pradeep Reddy, Alejandro Ocampo, Keiichiro Suzuki, Jinping Luo, Sandra R Bacman, Sion L Williams, Atsushi Sugawara, Daiji Okamura, Yuji Tsunekawa, Jun Wu,[...]. Cell 2015
151
36

MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases.
Masami Hashimoto, Sandra R Bacman, Susana Peralta, Marni J Falk, Anne Chomyn, David C Chan, Sion L Williams, Carlos T Moraes. Mol Ther 2015
85
35

Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction.
Sami Ellouze, Sébastien Augustin, Aicha Bouaita, Crystel Bonnet, Manuel Simonutti, Valérie Forster, Serge Picaud, Jose-Alain Sahel, Marisol Corral-Debrinski. Am J Hum Genet 2008
140
26

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

Correcting human mitochondrial mutations with targeted RNA import.
Geng Wang, Eriko Shimada, Jin Zhang, Jason S Hong, Geoffrey M Smith, Michael A Teitell, Carla M Koehler. Proc Natl Acad Sci U S A 2012
82
26

Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus.
Giovanni Manfredi, Jin Fu, Joseline Ojaimi, James E Sadlock, Jennifer Q Kwong, John Guy, Eric A Schon. Nat Genet 2002
184
25

Allotopic expression of mitochondrial-encoded genes in mammals: achieved goal, undemonstrated mechanism or impossible task?
Ester Perales-Clemente, Patricio Fernández-Silva, Rebeca Acín-Pérez, Acisclo Pérez-Martos, Jose Antonio Enríquez. Nucleic Acids Res 2011
152
25

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, Nicholas Gomez, Emma L Blakely, Charlotte L Alston, Catherine Feeney, Rita Horvath, Patrick Yu-Wai-Man, Patrick F Chinnery,[...]. Ann Neurol 2015
395
25

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
176
23

Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.
Olga A Kolesnikova, Nina S Entelis, Clarisse Jacquin-Becker, Francine Goltzene, Zofia M Chrzanowska-Lightowlers, Robert N Lightowlers, Robert P Martin, Ivan Tarassov. Hum Mol Genet 2004
105
23


Near-complete elimination of mutant mtDNA by iterative or dynamic dose-controlled treatment with mtZFNs.
Payam A Gammage, Edoardo Gaude, Lindsey Van Haute, Pedro Rebelo-Guiomar, Christopher B Jackson, Joanna Rorbach, Marcin L Pekalski, Alan J Robinson, Marine Charpentier, Jean-Paul Concordet,[...]. Nucleic Acids Res 2016
51
27

Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo.
Payam A Gammage, Carlo Viscomi, Marie-Lune Simard, Ana S H Costa, Edoardo Gaude, Christopher A Powell, Lindsey Van Haute, Beverly J McCann, Pedro Rebelo-Guiomar, Raffaele Cerutti,[...]. Nat Med 2018
106
23


The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes.
Crystel Bonnet, Sébastien Augustin, Sami Ellouze, Paule Bénit, Aicha Bouaita, Pierre Rustin, José-Alain Sahel, Marisol Corral-Debrinski. Biochim Biophys Acta 2008
63
21

Efficient Mitochondrial Genome Editing by CRISPR/Cas9.
Areum Jo, Sangwoo Ham, Gum Hwa Lee, Yun-Il Lee, SangSeong Kim, Yun-Song Lee, Joo-Ho Shin, Yunjong Lee. Biomed Res Int 2015
98
21

MitoTALEN reduces mutant mtDNA load and restores tRNAAla levels in a mouse model of heteroplasmic mtDNA mutation.
Sandra R Bacman, Johanna H K Kauppila, Claudia V Pereira, Nadee Nissanka, Maria Miranda, Milena Pinto, Sion L Williams, Nils-Göran Larsson, James B Stewart, Carlos T Moraes. Nat Med 2018
91
21

Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy.
John Guy, Xiaoping Qi, Francesco Pallotti, Eric A Schon, Giovanni Manfredi, Valerio Carelli, Andrea Martinuzzi, William W Hauswirth, Alfred S Lewin. Ann Neurol 2002
176
20

Towards germline gene therapy of inherited mitochondrial diseases.
Masahito Tachibana, Paula Amato, Michelle Sparman, Joy Woodward, Dario Melguizo Sanchis, Hong Ma, Nuria Marti Gutierrez, Rebecca Tippner-Hedges, Eunju Kang, Hyo-Sang Lee,[...]. Nature 2013
228
20

Mitochondrial DNA mutations and human disease.
Helen A L Tuppen, Emma L Blakely, Douglass M Turnbull, Robert W Taylor. Biochim Biophys Acta 2010
360
18

Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease.
Lyndsey Craven, Helen A Tuppen, Gareth D Greggains, Stephen J Harbottle, Julie L Murphy, Lynsey M Cree, Alison P Murdoch, Patrick F Chinnery, Robert W Taylor, Robert N Lightowlers,[...]. Nature 2010
284
18

Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized.
Payam A Gammage, Carlos T Moraes, Michal Minczuk. Trends Genet 2018
103
18

Targeting peptide nucleic acid (PNA) oligomers to mitochondria within cells by conjugation to lipophilic cations: implications for mitochondrial DNA replication, expression and disease.
A Muratovska, R N Lightowlers, R W Taylor, D M Turnbull, R A Smith, J A Wilce, S W Martin, M P Murphy. Nucleic Acids Res 2001
117
16

Construction and testing of engineered zinc-finger proteins for sequence-specific modification of mtDNA.
Michal Minczuk, Paulina Kolasinska-Zwierz, Michael P Murphy, Monika A Papworth. Nat Protoc 2010
35
28

Mitochondrial threshold effects.
Rodrigue Rossignol, Benjamin Faustin, Christophe Rocher, Monique Malgat, Jean-Pierre Mazat, Thierry Letellier. Biochem J 2003
455
16

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
16

A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease.
Johanna H K Kauppila, Holly L Baines, Ana Bratic, Marie-Lune Simard, Christoph Freyer, Arnaud Mourier, Craig Stamp, Roberta Filograna, Nils-Göran Larsson, Laura C Greaves,[...]. Cell Rep 2016
56
17

mitoTev-TALE: a monomeric DNA editing enzyme to reduce mutant mitochondrial DNA levels.
Claudia V Pereira, Sandra R Bacman, Tania Arguello, Ugne Zekonyte, Sion L Williams, David R Edgell, Carlos T Moraes. EMBO Mol Med 2018
32
31

Limitations of allotopic expression of mitochondrial genes in mammalian cells.
Jose Oca-Cossio, Lesley Kenyon, Huiling Hao, Carlos T Moraes. Genetics 2003
68
15

Mitochondrial gene replacement in primate offspring and embryonic stem cells.
Masahito Tachibana, Michelle Sparman, Hathaitip Sritanaudomchai, Hong Ma, Lisa Clepper, Joy Woodward, Ying Li, Cathy Ramsey, Olena Kolotushkina, Shoukhrat Mitalipov. Nature 2009
334
15

Functional delivery of a cytosolic tRNA into mutant mitochondria of human cells.
Bidesh Mahata, Saikat Mukherjee, Sumita Mishra, Arun Bandyopadhyay, Samit Adhya. Science 2006
70
15

Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Aleksandra Trifunovic, Anna Wredenberg, Maria Falkenberg, Johannes N Spelbrink, Anja T Rovio, Carl E Bruder, Mohammad Bohlooly-Y, Sebastian Gidlöf, Anders Oldfors, Rolf Wibom,[...]. Nature 2004
15


PNPASE regulates RNA import into mitochondria.
Geng Wang, Hsiao-Wen Chen, Yavuz Oktay, Jin Zhang, Eric L Allen, Geoffrey M Smith, Kelly C Fan, Jason S Hong, Samuel W French, J Michael McCaffery,[...]. Cell 2010
218
15

Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber's hereditary optic neuropathy in a mouse model.
Hong Yu, Rajeshwari D Koilkonda, Tsung-Han Chou, Vittorio Porciatti, Sacide S Ozdemir, Vince Chiodo, Sanford L Boye, Shannon E Boye, William W Hauswirth, Alfred S Lewin,[...]. Proc Natl Acad Sci U S A 2012
100
15

Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome.
Caroline Comte, Yann Tonin, Anne-Marie Heckel-Mager, Abdeldjalil Boucheham, Alexandre Smirnov, Karine Auré, Anne Lombès, Robert P Martin, Nina Entelis, Ivan Tarassov. Nucleic Acids Res 2013
39
23

New treatments for mitochondrial disease-no time to drop our standards.
Gerald Pfeffer, Rita Horvath, Thomas Klopstock, Vamsi K Mootha, Anu Suomalainen, Saskia Koene, Michio Hirano, Massimo Zeviani, Laurence A Bindoff, Patrick Yu-Wai-Man,[...]. Nat Rev Neurol 2013
108
15

Enhancing zinc-finger-nuclease activity with improved obligate heterodimeric architectures.
Yannick Doyon, Thuy D Vo, Matthew C Mendel, Shon G Greenberg, Jianbin Wang, Danny F Xia, Jeffrey C Miller, Fyodor D Urnov, Philip D Gregory, Michael C Holmes. Nat Methods 2011
280
15

Linear mitochondrial DNA is rapidly degraded by components of the replication machinery.
Viktoriya Peeva, Daniel Blei, Genevieve Trombly, Sarah Corsi, Maciej J Szukszto, Pedro Rebelo-Guiomar, Payam A Gammage, Alexei P Kudin, Christian Becker, Janine Altmüller,[...]. Nat Commun 2018
60
15

Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits.
Crystel Bonnet, Valérie Kaltimbacher, Sami Ellouze, Sébastien Augustin, Paule Bénit, Valérie Forster, Pierre Rustin, José-Alain Sahel, Marisol Corral-Debrinski. Rejuvenation Res 2007
49
16


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.