A citation-based method for searching scientific literature

Nicole L Batenburg, Sofiane Y Mersaoui, John R Walker, Yan Coulombe, Ian Hammond-Martel, Hugo Wurtele, Jean-Yves Masson, Xu-Dong Zhu. Nucleic Acids Res 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity



A ubiquitylation site in Cockayne syndrome B required for repair of oxidative DNA damage, but not for transcription-coupled nucleotide excision repair.
Michael Ranes, Stefan Boeing, Yuming Wang, Franziska Wienholz, Hervé Menoni, Jane Walker, Vesela Encheva, Probir Chakravarty, Pierre-Olivier Mari, Aengus Stewart,[...]. Nucleic Acids Res 2016
27
66

Principles and concepts of DNA replication in bacteria, archaea, and eukarya.
Michael O'Donnell, Lance Langston, Bruce Stillman. Cold Spring Harb Perspect Biol 2013
216
66

Time for remodeling: SNF2-family DNA translocases in replication fork metabolism and human disease.
Sarah A Joseph, Angelo Taglialatela, Giuseppe Leuzzi, Jen-Wei Huang, Raquel Cuella-Martin, Alberto Ciccia. DNA Repair (Amst) 2020
12
66

Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition.
G T van der Horst, H van Steeg, R J Berg, A J van Gool, J de Wit, G Weeda, H Morreau, R B Beems, C F van Kreijl, F R de Gruijl,[...]. Cell 1997
267
66

Hallmarks of cancer: the next generation.
Douglas Hanahan, Robert A Weinberg. Cell 2011
66

The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging.
Tinna Stevnsner, Meltem Muftuoglu, Maria Diget Aamann, Vilhelm A Bohr. Mech Ageing Dev 2008
106
66

The Winged Helix Domain of CSB Regulates RNAPII Occupancy at Promoter Proximal Pause Sites.
Nicole L Batenburg, Shixin Cui, John R Walker, Herb E Schellhorn, Xu-Dong Zhu. Int J Mol Sci 2021
4
66

RECQ5 Helicase Cooperates with MUS81 Endonuclease in Processing Stalled Replication Forks at Common Fragile Sites during Mitosis.
Stefano Di Marco, Zdenka Hasanova, Radhakrishnan Kanagaraj, Nagaraja Chappidi, Veronika Altmannova, Shruti Menon, Hana Sedlackova, Jana Langhoff, Kalpana Surendranath, Daniela Hühn,[...]. Mol Cell 2017
55
66

ROS-induced R loops trigger a transcription-coupled but BRCA1/2-independent homologous recombination pathway through CSB.
Yaqun Teng, Tribhuwan Yadav, Meihan Duan, Jun Tan, Yufei Xiang, Boya Gao, Jianquan Xu, Zhuobin Liang, Yang Liu, Satoshi Nakajima,[...]. Nat Commun 2018
78
66

Cockayne syndrome group B protein regulates DNA double-strand break repair and checkpoint activation.
Nicole L Batenburg, Elizabeth L Thompson, Eric A Hendrickson, Xu-Dong Zhu. EMBO J 2015
40
66


CSB interacts with BRCA1 in late S/G2 to promote MRN- and CtIP-mediated DNA end resection.
Nicole L Batenburg, John R Walker, Yan Coulombe, Alana Sherker, Jean-Yves Masson, Xu-Dong Zhu. Nucleic Acids Res 2019
15
66

Cockayne syndrome group B protein has novel strand annealing and exchange activities.
Meltem Muftuoglu, Sudha Sharma, Tina Thorslund, Tinna Stevnsner, Martin M Soerensen, Robert M Brosh, Vilhelm A Bohr. Nucleic Acids Res 2006
38
66

Cyclin-dependent kinase suppression by WEE1 kinase protects the genome through control of replication initiation and nucleotide consumption.
Halfdan Beck, Viola Nähse-Kumpf, Marie Sofie Yoo Larsen, Karen A O'Hanlon, Sebastian Patzke, Christian Holmberg, Jakob Mejlvang, Anja Groth, Olaf Nielsen, Randi G Syljuåsen,[...]. Mol Cell Biol 2012
189
66

The CSB repair factor is overexpressed in cancer cells, increases apoptotic resistance, and promotes tumor growth.
Manuela Caputo, Mattia Frontini, Renier Velez-Cruz, Serena Nicolai, Giorgio Prantera, Luca Proietti-De-Santis. DNA Repair (Amst) 2013
22
66

Identification of multiple distinct Snf2 subfamilies with conserved structural motifs.
Andrew Flaus, David M A Martin, Geoffrey J Barton, Tom Owen-Hughes. Nucleic Acids Res 2006
474
66

ATM and CDK2 control chromatin remodeler CSB to inhibit RIF1 in DSB repair pathway choice.
Nicole L Batenburg, John R Walker, Sylvie M Noordermeer, Nathalie Moatti, Daniel Durocher, Xu-Dong Zhu. Nat Commun 2017
42
66

The Cockayne syndrome group A and B proteins are part of a ubiquitin-proteasome degradation complex regulating cell division.
Elena Paccosi, Federico Costanzo, Michele Costantino, Alessio Balzerano, Laura Monteonofrio, Silvia Soddu, Giorgio Prantera, Stefano Brancorsini, Jean-Marc Egly, Luca Proietti-De-Santis. Proc Natl Acad Sci U S A 2020
10
66

Mechanisms of action and regulation of ATP-dependent chromatin-remodelling complexes.
Cedric R Clapier, Janet Iwasa, Bradley R Cairns, Craig L Peterson. Nat Rev Mol Cell Biol 2017
458
66

DNA replication stress as a hallmark of cancer.
Morgane Macheret, Thanos D Halazonetis. Annu Rev Pathol 2015
408
66


Replication stress activates DNA repair synthesis in mitosis.
Sheroy Minocherhomji, Songmin Ying, Victoria A Bjerregaard, Sara Bursomanno, Aiste Aleliunaite, Wei Wu, Hocine W Mankouri, Huahao Shen, Ying Liu, Ian D Hickson. Nature 2015
326
66


Replication stress induces sister-chromatid bridging at fragile site loci in mitosis.
Kok Lung Chan, Timea Palmai-Pallag, Songmin Ying, Ian D Hickson. Nat Cell Biol 2009
434
66

Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
V Laugel, C Dalloz, M Durand, F Sauvanaud, U Kristensen, M C Vincent, L Pasquier, S Odent, V Cormier-Daire, B Gener,[...]. Hum Mutat 2010
156
66

Structural basis of human transcription-DNA repair coupling.
Goran Kokic, Felix R Wagner, Aleksandar Chernev, Henning Urlaub, Patrick Cramer. Nature 2021
19
66

Measurement of replication structures at the nanometer scale using super-resolution light microscopy.
D Baddeley, V O Chagin, L Schermelleh, S Martin, A Pombo, P M Carlton, A Gahl, P Domaing, U Birk, H Leonhardt,[...]. Nucleic Acids Res 2010
75
66

Current and emerging roles of Cockayne syndrome group B (CSB) protein.
Vinod Tiwari, Beverly A Baptiste, Mustafa N Okur, Vilhelm A Bohr. Nucleic Acids Res 2021
19
66


UV-induced association of the CSB remodeling protein with chromatin requires ATP-dependent relief of N-terminal autorepression.
Robert J Lake, Anastasia Geyko, Girish Hemashettar, Yu Zhao, Hua-Ying Fan. Mol Cell 2010
79
66

Replication stress and cancer.
Hélène Gaillard, Tatiana García-Muse, Andrés Aguilera. Nat Rev Cancer 2015
514
66

Cockayne Syndrome group B protein interacts with TRF2 and regulates telomere length and stability.
Nicole L Batenburg, Taylor R H Mitchell, Derrik M Leach, Andrew J Rainbow, Xu-Dong Zhu. Nucleic Acids Res 2012
39
66

RAD52 Facilitates Mitotic DNA Synthesis Following Replication Stress.
Rahul Bhowmick, Sheroy Minocherhomji, Ian D Hickson. Mol Cell 2016
214
66

53BP1 nuclear bodies form around DNA lesions generated by mitotic transmission of chromosomes under replication stress.
Claudia Lukas, Velibor Savic, Simon Bekker-Jensen, Carsten Doil, Beate Neumann, Ronni Sølvhøj Pedersen, Merete Grøfte, Kok Lung Chan, Ian David Hickson, Jiri Bartek,[...]. Nat Cell Biol 2011
478
66

CSB cooperates with SMARCAL1 to maintain telomere stability in ALT cells.
Emily Feng, Nicole L Batenburg, John R Walker, Angus Ho, Taylor R H Mitchell, Jian Qin, Xu-Dong Zhu. J Cell Sci 2020
12
66



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
799
66

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
62
66

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
398
66

Replication fork reversal in eukaryotes: from dead end to dynamic response.
Kai J Neelsen, Massimo Lopes. Nat Rev Mol Cell Biol 2015
296
66

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
278
66

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
69
66

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
194
66

Role of double-stranded DNA translocase activity of human HLTF in replication of damaged DNA.
András Blastyák, Ildikó Hajdú, Ildikó Unk, Lajos Haracska. Mol Cell Biol 2010
135
66

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
197
66

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
130
66

HLTF Promotes Fork Reversal, Limiting Replication Stress Resistance and Preventing Multiple Mechanisms of Unrestrained DNA Synthesis.
Gongshi Bai, Chames Kermi, Henriette Stoy, Carl J Schiltz, Julien Bacal, Angela M Zaino, M Kyle Hadden, Brandt F Eichman, Massimo Lopes, Karlene A Cimprich. Mol Cell 2020
57
66

To skip or not to skip: choosing repriming to tolerate DNA damage.
Annabel Quinet, Stephanie Tirman, Emily Cybulla, Alice Meroni, Alessandro Vindigni. Mol Cell 2021
19
66


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.