A citation-based method for searching scientific literature

András Blastyák, Ildikó Hajdú, Ildikó Unk, Lajos Haracska. Mol Cell Biol 2010
Times Cited: 130







List of co-cited articles
1503 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


HLTF's Ancient HIRAN Domain Binds 3' DNA Ends to Drive Replication Fork Reversal.
Andrew C Kile, Diana A Chavez, Julien Bacal, Sherif Eldirany, Dmitry M Korzhnev, Irina Bezsonova, Brandt F Eichman, Karlene A Cimprich. Mol Cell 2015
119
56

Polyubiquitinated PCNA recruits the ZRANB3 translocase to maintain genomic integrity after replication stress.
Alberto Ciccia, Amitabh V Nimonkar, Yiduo Hu, Ildiko Hajdu, Yathish Jagadheesh Achar, Lior Izhar, Sarah A Petit, Britt Adamson, John C Yoon, Stephen C Kowalczykowski,[...]. Mol Cell 2012
189
51

SMARCAL1 catalyzes fork regression and Holliday junction migration to maintain genome stability during DNA replication.
Rémy Bétous, Aaron C Mason, Robert P Rambo, Carol E Bansbach, Akosua Badu-Nkansah, Bianca M Sirbu, Brandt F Eichman, David Cortez. Genes Dev 2012
189
45

Polyubiquitination of proliferating cell nuclear antigen by HLTF and SHPRH prevents genomic instability from stalled replication forks.
Akira Motegi, Hung-Jiun Liaw, Kyoo-Young Lee, Henk P Roest, Alex Maas, Xiaoli Wu, Helen Moinova, Sanford D Markowitz, Hao Ding, Jan H J Hoeijmakers,[...]. Proc Natl Acad Sci U S A 2008
194
44

Human HLTF functions as a ubiquitin ligase for proliferating cell nuclear antigen polyubiquitination.
Ildiko Unk, Ildikó Hajdú, Károly Fátyol, Jerard Hurwitz, Jung-Hoon Yoon, Louise Prakash, Satya Prakash, Lajos Haracska. Proc Natl Acad Sci U S A 2008
164
42

Yeast Rad5 protein required for postreplication repair has a DNA helicase activity specific for replication fork regression.
András Blastyák, Lajos Pintér, Ildiko Unk, Louise Prakash, Satya Prakash, Lajos Haracska. Mol Cell 2007
218
40

Rad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells.
Ralph Zellweger, Damian Dalcher, Karun Mutreja, Matteo Berti, Jonas A Schmid, Raquel Herrador, Alessandro Vindigni, Massimo Lopes. J Cell Biol 2015
375
37

RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO.
Carsten Hoege, Boris Pfander, George-Lucian Moldovan, George Pyrowolakis, Stefan Jentsch. Nature 2002
36

Replication fork reversal in eukaryotes: from dead end to dynamic response.
Kai J Neelsen, Massimo Lopes. Nat Rev Mol Cell Biol 2015
281
36

Substrate-selective repair and restart of replication forks by DNA translocases.
Rémy Bétous, Frank B Couch, Aaron C Mason, Brandt F Eichman, Maria Manosas, David Cortez. Cell Rep 2013
108
35

Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11.
Katharina Schlacher, Nicole Christ, Nicolas Siaud, Akinori Egashira, Hong Wu, Maria Jasin. Cell 2011
765
33

Coordinated protein and DNA remodeling by human HLTF on stalled replication fork.
Yathish Jagadheesh Achar, David Balogh, Lajos Haracska. Proc Natl Acad Sci U S A 2011
56
58


Structure of a Novel DNA-binding Domain of Helicase-like Transcription Factor (HLTF) and Its Functional Implication in DNA Damage Tolerance.
Asami Hishiki, Kodai Hara, Yuzu Ikegaya, Hideshi Yokoyama, Toshiyuki Shimizu, Mamoru Sato, Hiroshi Hashimoto. J Biol Chem 2015
50
64

SHPRH and HLTF act in a damage-specific manner to coordinate different forms of postreplication repair and prevent mutagenesis.
Jia-Ren Lin, Michelle K Zeman, Jia-Yun Chen, Muh-Ching Yee, Karlene A Cimprich. Mol Cell 2011
124
31

Role of yeast Rad5 and its human orthologs, HLTF and SHPRH in DNA damage tolerance.
Ildiko Unk, Ildikó Hajdú, András Blastyák, Lajos Haracska. DNA Repair (Amst) 2010
131
30

Causes and consequences of replication stress.
Michelle K Zeman, Karlene A Cimprich. Nat Cell Biol 2014
30

Strand invasion by HLTF as a mechanism for template switch in fork rescue.
Peter Burkovics, Marek Sebesta, David Balogh, Lajos Haracska, Lumir Krejci. Nucleic Acids Res 2014
45
64

Human HLTF mediates postreplication repair by its HIRAN domain-dependent replication fork remodelling.
Yathish Jagadheesh Achar, David Balogh, Dante Neculai, Szilvia Juhasz, Monika Morocz, Himabindu Gali, Sirano Dhe-Paganon, Česlovas Venclovas, Lajos Haracska. Nucleic Acids Res 2015
45
64

Smarcal1-Mediated Fork Reversal Triggers Mre11-Dependent Degradation of Nascent DNA in the Absence of Brca2 and Stable Rad51 Nucleofilaments.
Arun Mouli Kolinjivadi, Vincenzo Sannino, Anna De Antoni, Karina Zadorozhny, Mairi Kilkenny, Hervé Técher, Giorgio Baldi, Rong Shen, Alberto Ciccia, Luca Pellegrini,[...]. Mol Cell 2017
179
29


Replication Fork Slowing and Reversal upon DNA Damage Require PCNA Polyubiquitination and ZRANB3 DNA Translocase Activity.
Marko Vujanovic, Jana Krietsch, Maria Chiara Raso, Nastassja Terraneo, Ralph Zellweger, Jonas A Schmid, Angelo Taglialatela, Jen-Wei Huang, Cory L Holland, Katharina Zwicky,[...]. Mol Cell 2017
121
28


DNA2 drives processing and restart of reversed replication forks in human cells.
Saravanabhavan Thangavel, Matteo Berti, Maryna Levikova, Cosimo Pinto, Shivasankari Gomathinayagam, Marko Vujanovic, Ralph Zellweger, Hayley Moore, Eu Han Lee, Eric A Hendrickson,[...]. J Cell Biol 2015
209
25

Human SHPRH is a ubiquitin ligase for Mms2-Ubc13-dependent polyubiquitylation of proliferating cell nuclear antigen.
Ildiko Unk, Ildikó Hajdú, Károly Fátyol, Barnabás Szakál, András Blastyák, Vladimir Bermudez, Jerard Hurwitz, Louise Prakash, Satya Prakash, Lajos Haracska. Proc Natl Acad Sci U S A 2006
170
24

ATR phosphorylates SMARCAL1 to prevent replication fork collapse.
Frank B Couch, Carol E Bansbach, Robert Driscoll, Jessica W Luzwick, Gloria G Glick, Rémy Bétous, Clinton M Carroll, Sung Yun Jung, Jun Qin, Karlene A Cimprich,[...]. Genes Dev 2013
248
24

Replication fork reversal triggers fork degradation in BRCA2-defective cells.
Sofija Mijic, Ralph Zellweger, Nagaraja Chappidi, Matteo Berti, Kurt Jacobs, Karun Mutreja, Sebastian Ursich, Arnab Ray Chaudhuri, Andre Nussenzweig, Pavel Janscak,[...]. Nat Commun 2017
174
24

Restoration of Replication Fork Stability in BRCA1- and BRCA2-Deficient Cells by Inactivation of SNF2-Family Fork Remodelers.
Angelo Taglialatela, Silvia Alvarez, Giuseppe Leuzzi, Vincenzo Sannino, Lepakshi Ranjha, Jen-Wei Huang, Chioma Madubata, Roopesh Anand, Brynn Levy, Raul Rabadan,[...]. Mol Cell 2017
175
24

MRE11 and EXO1 nucleases degrade reversed forks and elicit MUS81-dependent fork rescue in BRCA2-deficient cells.
Delphine Lemaçon, Jessica Jackson, Annabel Quinet, Joshua R Brickner, Shan Li, Stephanie Yazinski, Zhongsheng You, Grzegorz Ira, Lee Zou, Nima Mosammaparast,[...]. Nat Commun 2017
187
24

Rad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis.
Yoshitami Hashimoto, Arnab Ray Chaudhuri, Massimo Lopes, Vincenzo Costanzo. Nat Struct Mol Biol 2010
339
23

Human RECQ1 promotes restart of replication forks reversed by DNA topoisomerase I inhibition.
Matteo Berti, Arnab Ray Chaudhuri, Saravanabhavan Thangavel, Shivasankari Gomathinayagam, Sasa Kenig, Marko Vujanovic, Federico Odreman, Timo Glatter, Simona Graziano, Ramiro Mendoza-Maldonado,[...]. Nat Struct Mol Biol 2013
265
22

Topoisomerase I poisoning results in PARP-mediated replication fork reversal.
Arnab Ray Chaudhuri, Yoshitami Hashimoto, Raquel Herrador, Kai J Neelsen, Daniele Fachinetti, Rodrigo Bermejo, Andrea Cocito, Vincenzo Costanzo, Massimo Lopes. Nat Struct Mol Biol 2012
315
22

Human SHPRH suppresses genomic instability through proliferating cell nuclear antigen polyubiquitination.
Akira Motegi, Raman Sood, Helen Moinova, Sanford D Markowitz, Pu Paul Liu, Kyungjae Myung. J Cell Biol 2006
145
21


FBH1 Catalyzes Regression of Stalled Replication Forks.
Kasper Fugger, Martin Mistrik, Kai J Neelsen, Qi Yao, Ralph Zellweger, Arne Nedergaard Kousholt, Peter Haahr, Wai Kit Chu, Jiri Bartek, Massimo Lopes,[...]. Cell Rep 2015
65
30

Y-family DNA polymerases and their role in tolerance of cellular DNA damage.
Julian E Sale, Alan R Lehmann, Roger Woodgate. Nat Rev Mol Cell Biol 2012
442
20



The SIOD disorder protein SMARCAL1 is an RPA-interacting protein involved in replication fork restart.
Alberto Ciccia, Andrea L Bredemeyer, Mathew E Sowa, Marie-Emilie Terret, Prasad V Jallepalli, J Wade Harper, Stephen J Elledge. Genes Dev 2009
146
19

The annealing helicase SMARCAL1 maintains genome integrity at stalled replication forks.
Carol E Bansbach, Rémy Bétous, Courtney A Lovejoy, Gloria G Glick, David Cortez. Genes Dev 2009
171
19

Eukaryotic translesion synthesis DNA polymerases: specificity of structure and function.
Satya Prakash, Robert E Johnson, Louise Prakash. Annu Rev Biochem 2005
771
18

Remodeling of DNA replication structures by the branch point translocase FANCM.
Kerstin Gari, Chantal Décaillet, Mathieu Delannoy, Leonard Wu, Angelos Constantinou. Proc Natl Acad Sci U S A 2008
172
18

Hydroxyurea-stalled replication forks become progressively inactivated and require two different RAD51-mediated pathways for restart and repair.
Eva Petermann, Manuel Luís Orta, Natalia Issaeva, Niklas Schultz, Thomas Helleday. Mol Cell 2010
562
18

RADX Promotes Genome Stability and Modulates Chemosensitivity by Regulating RAD51 at Replication Forks.
Huzefa Dungrawala, Kamakoti P Bhat, Rémy Le Meur, Walter J Chazin, Xia Ding, Shyam K Sharan, Sarah R Wessel, Aditya A Sathe, Runxiang Zhao, David Cortez. Mol Cell 2017
95
18

Functions of SMARCAL1, ZRANB3, and HLTF in maintaining genome stability.
Lisa A Poole, David Cortez. Crit Rev Biochem Mol Biol 2017
69
26

HLTF gene silencing in human colon cancer.
Helen R Moinova, Wei-Dong Chen, Lanlan Shen, Dominic Smiraglia, Joseph Olechnowicz, Lakshmeswari Ravi, Lakshmi Kasturi, Lois Myeroff, Christoph Plass, Ramon Parsons,[...]. Proc Natl Acad Sci U S A 2002
126
17


The HIRAN domain and recruitment of chromatin remodeling and repair activities to damaged DNA.
Lakshminarayan M Iyer, M Madan Babu, L Aravind. Cell Cycle 2006
72
23

Functional uncoupling of MCM helicase and DNA polymerase activities activates the ATR-dependent checkpoint.
Tony S Byun, Marcin Pacek, Muh-ching Yee, Johannes C Walter, Karlene A Cimprich. Genes Dev 2005
545
17

Cooperation of RAD51 and RAD54 in regression of a model replication fork.
Dmitry V Bugreev, Matthew J Rossi, Alexander V Mazin. Nucleic Acids Res 2011
60
28


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.