A citation-based method for searching scientific literature

Yu Wang, Yiwei Wang, S Marcus, L S Busenlehner. Biochim Biophys Acta 2014
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Overexpression of human and fly frataxins in Drosophila provokes deleterious effects at biochemical, physiological and developmental levels.
Juan A Navarro, José V Llorens, Sirena Soriano, José A Botella, Stephan Schneuwly, María J Martínez-Sebastián, María D Moltó. PLoS One 2011
28
54

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
54

Prevention and reversal of severe mitochondrial cardiomyopathy by gene therapy in a mouse model of Friedreich's ataxia.
Morgane Perdomini, Brahim Belbellaa, Laurent Monassier, Laurence Reutenauer, Nadia Messaddeq, Nathalie Cartier, Ronald G Crystal, Patrick Aubourg, Hélène Puccio. Nat Med 2014
136
36

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
H Puccio, D Simon, M Cossée, P Criqui-Filipe, F Tiziano, J Melki, C Hindelang, R Matyas, P Rustin, M Koenig. Nat Genet 2001
536
36

Frataxin activates mitochondrial energy conversion and oxidative phosphorylation.
M Ristow, M F Pfister, A J Yee, M Schubert, L Michael, C Y Zhang, K Ueki, M D Michael, B B Lowell, C R Kahn. Proc Natl Acad Sci U S A 2000
184
36

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.
V Campuzano, L Montermini, Y Lutz, L Cova, C Hindelang, S Jiralerspong, Y Trottier, S J Kish, B Faucheux, P Trouillas,[...]. Hum Mol Genet 1997
559
27

A TAT-frataxin fusion protein increases lifespan and cardiac function in a conditional Friedreich's ataxia mouse model.
Piyush M Vyas, Wendy J Tomamichel, P Melanie Pride, Clifford M Babbey, Qiujuan Wang, Jennifer Mercier, Elizabeth M Martin, R Mark Payne. Hum Mol Genet 2012
64
27

An AAV9 coding for frataxin clearly improved the symptoms and prolonged the life of Friedreich ataxia mouse models.
Catherine Gérard, Xiao Xiao, Mohammed Filali, Zoé Coulombe, Marie Arsenault, Jacques Couet, Juan Li, Marie-Claude Drolet, Pierre Chapdelaine, Amina Chikh,[...]. Mol Ther Methods Clin Dev 2014
32
27

Frataxin promotes antioxidant defense in a thiol-dependent manner resulting in diminished malignant transformation in vitro.
Sarah A Shoichet, Anselm T Bäumer, Djordje Stamenkovic, Heinrich Sauer, Andreas F H Pfeiffer, C Ronald Kahn, Dirk Müller-Wieland, Christoph Richter, Michael Ristow. Hum Mol Genet 2002
69
27

Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation.
M Cossée, H Puccio, A Gansmuller, H Koutnikova, A Dierich, M LeMeur, K Fischbeck, P Dollé, M Koenig. Hum Mol Genet 2000
265
27

Friedreich ataxia: the clinical picture.
Massimo Pandolfo. J Neurol 2009
262
27

Frataxin overexpressing mice.
Carlos J Miranda, Manuela M Santos, Keiichi Ohshima, Marco Tessaro, Jorge Sequeiros, Massimo Pandolfo. FEBS Lett 2004
22
27

GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology.
Sahar Al-Mahdawi, Ricardo Mouro Pinto, Dhaval Varshney, Lorraine Lawrence, Margaret B Lowrie, Sian Hughes, Zoe Webster, Julian Blake, J Mark Cooper, Rosalind King,[...]. Genomics 2006
163
27

Adding a temporal dimension to the study of Friedreich's ataxia: the effect of frataxin overexpression in a human cell model.
Tommaso Vannocci, Roberto Notario Manzano, Ombretta Beccalli, Barbara Bettegazzi, Fabio Grohovaz, Gianfelice Cinque, Antonio de Riso, Luca Quaroni, Franca Codazzi, Annalisa Pastore. Dis Model Mech 2018
18
27

Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis.
M A Pook, S Al-Mahdawi, C J Carroll, M Cossée, H Puccio, L Lawrence, P Clark, M B Lowrie, J L Bradley, J M Cooper,[...]. Neurogenetics 2001
52
18

Novel frataxin isoforms may contribute to the pathological mechanism of Friedreich ataxia.
Haiyan Xia, Yun Cao, Xiaoman Dai, Zvonimir Marelja, Di Zhou, Ran Mo, Sahar Al-Mahdawi, Mark A Pook, Silke Leimkühler, Tracey A Rouault,[...]. PLoS One 2012
39
18

Long range regulation of human FXN gene expression.
Novita Puspasari, Simone M Rowley, Lavinia Gordon, Paul J Lockhart, Panos A Ioannou, Martin B Delatycki, Joseph P Sarsero. PLoS One 2011
9
22

Functional recovery in a Friedreich's ataxia mouse model by frataxin gene transfer using an HSV-1 amplicon vector.
Filip Lim, Gloria M Palomo, Christina Mauritz, Alfredo Giménez-Cassina, Belen Illana, Francisco Wandosell, Javier Díaz-Nido. Mol Ther 2007
39
18

Friedreich ataxia: neuropathology revised.
Arnulf H Koeppen, Joseph E Mazurkiewicz. J Neuropathol Exp Neurol 2013
160
18

Clinical features of Friedreich's ataxia: classical and atypical phenotypes.
Michael H Parkinson, Sylvia Boesch, Wolfgang Nachbauer, Caterina Mariotti, Paola Giunti. J Neurochem 2013
135
18

A pool of extramitochondrial frataxin that promotes cell survival.
Ivano Condò, Natascia Ventura, Florence Malisan, Barbara Tomassini, Roberto Testi. J Biol Chem 2006
74
18

Partial correction of sensitivity to oxidant stress in Friedreich ataxia patient fibroblasts by frataxin-encoding adeno-associated virus and lentivirus vectors.
Jane Fleming, Afroditi Spinoulas, Maolin Zheng, Sharon C Cunningham, Samantha L Ginn, Robert C McQuilty, Peter B Rowe, Ian E Alexander. Hum Gene Ther 2005
25
18

Gene regulation and epigenetics in Friedreich's ataxia.
Cihangir Yandim, Theona Natisvili, Richard Festenstein. J Neurochem 2013
36
18


Rescue of the Friedreich ataxia knockout mutation in transgenic mice containing an FXN-EGFP genomic reporter.
Joseph P Sarsero, Timothy P Holloway, Lingli Li, David I Finkelstein, Panos A Ioannou. PLoS One 2014
6
33

Normal and Friedreich ataxia cells express different isoforms of frataxin with complementary roles in iron-sulfur cluster assembly.
Oleksandr Gakh, Tibor Bedekovics, Samantha F Duncan, Douglas Y Smith, Donald S Berkholz, Grazia Isaya. J Biol Chem 2010
61
18

Identification of a novel transcript of X25, the human gene involved in Friedreich ataxia.
Luigi Pianese, Angela Tammaro, Mimmo Turano, Irene De Biase, Antonella Monticelli, Sergio Cocozza. Neurosci Lett 2002
17
18

Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice.
Joseph P Sarsero, Lingli Li, Timothy P Holloway, Lucille Voullaire, Sophie Gazeas, Kerry J Fowler, Denise M Kirby, David R Thorburn, Adam Galle, Surindar Cheema,[...]. Mamm Genome 2004
38
18

Infectious Delivery and Expression of a 135 kb Human FRDA Genomic DNA Locus Complements Friedreich's Ataxia Deficiency in Human Cells.
Silvia Gomez-Sebastian, Alfredo Gimenez-Cassina, Javier Diaz-Nido, Filip Lim, Richard Wade-Martins. Mol Ther 2007
30
18

A conserved mitochondrial ATP-binding cassette transporter exports glutathione polysulfide for cytosolic metal cofactor assembly.
Theresia A Schaedler, Jeremy D Thornton, Inga Kruse, Markus Schwarzländer, Andreas J Meyer, Hendrik W van Veen, Janneke Balk. J Biol Chem 2014
104
18

The role of mitochondria in cellular iron-sulfur protein biogenesis and iron metabolism.
Roland Lill, Bastian Hoffmann, Sabine Molik, Antonio J Pierik, Nicole Rietzschel, Oliver Stehling, Marta A Uzarska, Holger Webert, Claudia Wilbrecht, Ulrich Mühlenhoff. Biochim Biophys Acta 2012
336
18

Human frataxin activates Fe-S cluster biosynthesis by facilitating sulfur transfer chemistry.
Jennifer Bridwell-Rabb, Nicholas G Fox, Chi-Lin Tsai, Andrew M Winn, David P Barondeau. Biochemistry 2014
107
18


Global analysis of protein localization in budding yeast.
Won-Ki Huh, James V Falvo, Luke C Gerke, Adam S Carroll, Russell W Howson, Jonathan S Weissman, Erin K O'Shea. Nature 2003
18



Activation of the iron regulon by the yeast Aft1/Aft2 transcription factors depends on mitochondrial but not cytosolic iron-sulfur protein biogenesis.
Julian C Rutherford, Luis Ojeda, Janneke Balk, Ulrich Mühlenhoff, Roland Lill, Dennis R Winge. J Biol Chem 2005
190
18

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin.
M Babcock, D de Silva, R Oaks, S Davis-Kaplan, S Jiralerspong, L Montermini, M Pandolfo, J Kaplan. Science 1997
726
18

Causative role of oxidative stress in a Drosophila model of Friedreich ataxia.
José V Llorens, Juan A Navarro, Maria J Martínez-Sebastián, Mary K Baylies, S Schneuwly, José A Botella, Maria D Moltó. FASEB J 2007
93
18

Structural bases for the interaction of frataxin with the central components of iron-sulphur cluster assembly.
Filippo Prischi, Petr V Konarev, Clara Iannuzzi, Chiara Pastore, Salvatore Adinolfi, Stephen R Martin, Dmitri I Svergun, Annalisa Pastore. Nat Commun 2010
136
18

Overexpression of the yeast frataxin homolog (Yfh1): contrasting effects on iron-sulfur cluster assembly, heme synthesis and resistance to oxidative stress.
Alexandra Seguin, Aurélien Bayot, Andrew Dancis, Adelina Rogowska-Wrzesinska, Françoise Auchère, Jean-Michel Camadro, Anne-Laure Bulteau, Emmanuel Lesuisse. Mitochondrion 2009
42
18

Frataxin: a protein in search for a function.
Annalisa Pastore, Helene Puccio. J Neurochem 2013
132
18

Time-resolved functional analysis of acute impairment of frataxin expression in an inducible cell model of Friedreich ataxia.
Dörte Poburski, Josefine Barbara Boerner, Michel Koenig, Michael Ristow, René Thierbach. Biol Open 2016
15
18

Loss of Frataxin activates the iron/sphingolipid/PDK1/Mef2 pathway in mammals.
Kuchuan Chen, Tammy Szu-Yu Ho, Guang Lin, Kai Li Tan, Matthew N Rasband, Hugo J Bellen. Elife 2016
39
18


Chronochemistry in neurodegeneration.
Annalisa Pastore, Salvatore Adinolfi. Front Mol Neurosci 2014
7
28


A new cellular model to follow Friedreich's ataxia development in a time-resolved way.
Tommaso Vannocci, Nathalie Faggianelli, Silvia Zaccagnino, Ilaria della Rosa, Salvatore Adinolfi, Annalisa Pastore. Dis Model Mech 2015
14
18


Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
A Rötig, P de Lonlay, D Chretien, F Foury, M Koenig, D Sidi, A Munnich, P Rustin. Nat Genet 1997
774
18


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.