A citation-based method for searching scientific literature

S Dhe-Paganon, R Shigeta, Y I Chi, M Ristow, S E Shoelson. J Biol Chem 2000
Times Cited: 170







List of co-cited articles
1048 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
64

Towards a structural understanding of Friedreich's ataxia: the solution structure of frataxin.
G Musco, G Stier, B Kolmerer, S Adinolfi, S Martin, T Frenkiel, T Gibson, A Pastore. Structure 2000
138
56


Yeast frataxin solution structure, iron binding, and ferrochelatase interaction.
Yanan He, Steven L Alam, Simona V Proteasa, Yan Zhang, Emmanuel Lesuisse, Andrew Dancis, Timothy L Stemmler. Biochemistry 2004
125
42


Bacterial frataxin CyaY is the gatekeeper of iron-sulfur cluster formation catalyzed by IscS.
Salvatore Adinolfi, Clara Iannuzzi, Filippo Prischi, Chiara Pastore, Stefania Iametti, Stephen R Martin, Franco Bonomi, Annalisa Pastore. Nat Struct Mol Biol 2009
189
37

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
36

Frataxin acts as an iron chaperone protein to modulate mitochondrial aconitase activity.
Anne-Laure Bulteau, Heather A O'Neill, Mary Claire Kennedy, Masao Ikeda-Saito, Grazia Isaya, Luke I Szweda. Science 2004
292
35

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
34

In vivo maturation of human frataxin.
Ivano Condò, Natascia Ventura, Florence Malisan, Alessandra Rufini, Barbara Tomassini, Roberto Testi. Hum Mol Genet 2007
90
37

Solution structure of the bacterial frataxin ortholog, CyaY: mapping the iron binding sites.
Margie Nair, Salvatore Adinolfi, Chiara Pastore, Geoff Kelly, Pierandrea Temussi, Annalisa Pastore. Structure 2004
105
34

Mammalian frataxin: an essential function for cellular viability through an interaction with a preformed ISCU/NFS1/ISD11 iron-sulfur assembly complex.
Stéphane Schmucker, Alain Martelli, Florent Colin, Adeline Page, Marie Wattenhofer-Donzé, Laurence Reutenauer, Hélène Puccio. PLoS One 2011
176
34




The in vivo mitochondrial two-step maturation of human frataxin.
Stéphane Schmucker, Manuela Argentini, Nadège Carelle-Calmels, Alain Martelli, Hélène Puccio. Hum Mol Genet 2008
97
31

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
30

A structural approach to understanding the iron-binding properties of phylogenetically different frataxins.
S Adinolfi, M Trifuoggi, A S Politou, S Martin, A Pastore. Hum Mol Genet 2002
110
30


Acidic residues of yeast frataxin have an essential role in Fe-S cluster assembly.
Françoise Foury, Annalisa Pastore, Mathieu Trincal. EMBO Rep 2007
67
43

Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia.
Patrizia Cavadini, Heather A O'Neill, Oldrich Benada, Grazia Isaya. Hum Mol Genet 2002
163
29

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
29


Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia.
J Adamec, F Rusnak, W G Owen, S Naylor, L M Benson, A M Gacy, G Isaya. Am J Hum Genet 2000
211
28

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
28

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
M Cossée, A Dürr, M Schmitt, N Dahl, P Trouillas, P Allinson, M Kostrzewa, A Nivelon-Chevallier, K H Gustavson, A Kohlschütter,[...]. Ann Neurol 1999
262
27

Monomeric yeast frataxin is an iron-binding protein.
Jeremy D Cook, Krisztina Z Bencze, Ana D Jankovic, Anna K Crater, Courtney N Busch, Patrick B Bradley, Ann J Stemmler, Mark R Spaller, Timothy L Stemmler. Biochemistry 2006
101
27

The structure and function of frataxin.
Krisztina Z Bencze, Kalyan C Kondapalli, Jeremy D Cook, Stephen McMahon, César Millán-Pacheco, Nina Pastor, Timothy L Stemmler. Crit Rev Biochem Mol Biol 2006
107
25


Iron use for haeme synthesis is under control of the yeast frataxin homologue (Yfh1).
Emmanuel Lesuisse, Renata Santos, Berthold F Matzanke, Simon A B Knight, Jean-Michel Camadro, Andrew Dancis. Hum Mol Genet 2003
195
25

Dynamics, stability and iron-binding activity of frataxin clinical mutants.
Ana R Correia, Chiara Pastore, Salvatore Adinolfi, Annalisa Pastore, Cláudio M Gomes. FEBS J 2008
47
51


The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins.
Ulrich Mühlenhoff, Nadine Richhardt, Michael Ristow, Gyula Kispal, Roland Lill. Hum Mol Genet 2002
265
23

Iron-induced oligomerization of yeast frataxin homologue Yfh1 is dispensable in vivo.
Kerman Aloria, Brenda Schilke, Amy Andrew, Elizabeth A Craig. EMBO Rep 2004
86
26

The structures of frataxin oligomers reveal the mechanism for the delivery and detoxification of iron.
Tobias Karlberg, Ulrika Schagerlöf, Oleksandr Gakh, Sungjo Park, Ulf Ryde, Martin Lindahl, Kirstin Leath, Elspeth Garman, Grazia Isaya, Salam Al-Karadaghi. Structure 2006
68
33

Iron binding and oxidation kinetics in frataxin CyaY of Escherichia coli.
Fadi Bou-Abdallah, Salvatore Adinolfi, Annalisa Pastore, Thomas M Laue, N Dennis Chasteen. J Mol Biol 2004
98
23


Mitochondrial iron detoxification is a primary function of frataxin that limits oxidative damage and preserves cell longevity.
Oleksandr Gakh, Sungjo Park, Gang Liu, Lee Macomber, James A Imlay, Gloria C Ferreira, Grazia Isaya. Hum Mol Genet 2006
161
22

Clinical and genetic abnormalities in patients with Friedreich's ataxia.
A Dürr, M Cossee, Y Agid, V Campuzano, C Mignard, C Penet, J L Mandel, A Brice, M Koenig. N Engl J Med 1996
739
21

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
21

Conformational stability of human frataxin and effect of Friedreich's ataxia-related mutations on protein folding.
Ana R Correia, Salvatore Adinolfi, Annalisa Pastore, Cláudio M Gomes. Biochem J 2006
37
56

Frataxin interacts with Isu1 through a conserved tryptophan in its beta-sheet.
Sébastien Leidgens, Sébastien De Smet, Françoise Foury. Hum Mol Genet 2010
38
55

Yeast frataxin sequentially chaperones and stores iron by coupling protein assembly with iron oxidation.
Sungjo Park, Oleksandr Gakh, Heather A O'Neill, Arianna Mangravita, Helen Nichol, Gloria C Ferreira, Grazia Isaya. J Biol Chem 2003
137
20

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin.
H Koutnikova, V Campuzano, F Foury, P Dollé, O Cazzalini, M Koenig. Nat Genet 1997
378
20




Friedreich ataxia: the clinical picture.
Massimo Pandolfo. J Neurol 2009
262
20


Oligomeric yeast frataxin drives assembly of core machinery for mitochondrial iron-sulfur cluster synthesis.
Hongqiao Li, Oleksandr Gakh, Douglas Y Smith, Grazia Isaya. J Biol Chem 2009
50
38


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.