The DOI matches its Crossref record; 108 of the 110 references it cites were found in a registry or an index.
PCNA, the Maestro of the Replication Fork
Open accessAbstract
Inheritance requires genome duplication, reproduction of chromatin and its epigenetic information, mechanisms to ensure genome integrity, and faithful transmission of the information to progeny. Proliferating cell nuclear antigen (PCNA)-a cofactor of DNA polymerases that encircles DNA-orchestrates several of these functions by recruiting crucial players to the replication fork. Remarkably, many factors that are involved in replication-linked processes interact with a particular face of PCNA and through the same interaction domain, indicating that these interactions do not occur simultaneously during replication. Switching of PCNA partners may be triggered by affinity-driven competition, phosphorylation, proteolysis, and modification of PCNA by ubiquitin and SUMO.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“And, although PCNA is a crucial component of the replication fork during the cell cycle, it also functions in DNA repair.167”
From Census and evaluation of p53 target genes (2017) · cites this paper as [167]
Citations
Cites
1 retracted
Sarraf, S. A., & Stancheva, I. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.06.043 · Cited by 501
RetractedDNA methylation patterns and epigenetic memory
Bird, A. (2002) · Genes & Development · doi:10.1101/gad.947102 · Cited by 7,124
Molecular Mechanisms of Mammalian DNA Repair and the DNA Damage Checkpoints
Sancar, A., Lindsey-Boltz, L. A., Ünsal-Kaçmaz, K., & Linn, S. (2004) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.073723 · Cited by 3,317
RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO
Hoege, C., Pfander, B., Moldovan, G., Pyrowolakis, G., & Jentsch, S. (2002) · Nature · doi:10.1038/nature00991 · Cited by 2,202
Self-citationDNA Replication in Eukaryotic Cells
Bell, S. P., & Dutta, A. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.110601.135425 · Cited by 2,065
The p21 inhibitor of cyclin-dependent kinases controls DNA replication by interaction with PCNA
Waga, S., Hannon, G. J., Beach, D., & Stillman, B. (1994) · Nature · doi:10.1038/369574a0 · Cited by 1,655
The multifaceted mismatch-repair system
Jiricny, J. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1907 · Cited by 1,375
Human DNA-(Cytosine-5) Methyltransferase-PCNA Complex as a Target for p21 WAF1
Chuang, L. S.-H., Ian, H.-I., Koh, T., Ng, H., Xu, G., & Li, B. F. L. (1997) · Science · doi:10.1126/science.277.5334.1996 · Cited by 902
Control of spontaneous and damage-induced mutagenesis by SUMO and ubiquitin conjugation
Stelter, P., & Ulrich, H. D. (2003) · Nature · doi:10.1038/nature01965 · Cited by 850
Interaction of Human DNA Polymerase η with Monoubiquitinated PCNA
Kannouche, P. L., Wing, J., & Lehmann, A. R. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00259-x · Cited by 845
Flagged first, then by citations
2 of the 110 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
The DNA Damage Response: Making It Safe to Play with Knives
Ciccia, A., & Elledge, S. J. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.019 · Cited by 4,368
Komander, D., & Rape, M. (2012) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060310-170328 · Cited by 3,679
p21 in cancer: Intricate networks and multiple activities
Abbas, T., & Dutta, A. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2657 · Cited by 2,712
The DNA Damage Response: Ten Years After
Harper, J. W., & Elledge, S. J. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.11.015 · Cited by 1,705
The SUMO pathway: emerging mechanisms that shape specificity, conjugation and recognition
Gareau, J. R., & Lima, C. D. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3011 · Cited by 1,145
Census and evaluation of p53 target genes
Fischer, M. (2017) · Oncogene · doi:10.1038/onc.2016.502 · Cited by 971
Epigenetic inheritance during the cell cycle
Probst, A. V., Dunleavy, E. M., & Almouzni, G. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2640 · Cited by 857
Structure of replicating SARS-CoV-2 polymerase
Hillen, H. S., Kokić, G., Farnung, L., Dienemann, C., Tegunov, D., & Cramer, P. (2020) · Nature · doi:10.1038/s41586-020-2368-8 · Cited by 813
Proliferating cell nuclear antigen (PCNA): a key factor in DNA replication and cell cycle regulation
Strzałka, W., & Ziemienowicz, A. (2010) · Annals of Botany · doi:10.1093/aob/mcq243 · Cited by 804
Chromatin structure and the inheritance of epigenetic information
Margueron, R., & Reinberg, D. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2752 · Cited by 761
The emerging complexity of protein ubiquitination
Komander, D. (2009) · Biochemical Society Transactions · doi:10.1042/bst0370937 · Cited by 821
A model for transmission of the H3K27me3 epigenetic mark
Hansen, K. H., Bracken, A. P., Pasini, D., Dietrich, N., Gehani, S. S., Monrad, A., Rappsilber, J., Lerdrup, M., & Helin, K. (2008) · Nature Cell Biology · doi:10.1038/ncb1787 · Cited by 748
Y-family DNA polymerases and their role in tolerance of cellular DNA damage
Sale, J. E., Lehmann, A. R., & Woodgate, R. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3289 · Cited by 665
Murine features of neurogenesis in the human hippocampus across the lifespan from 0 to 100 years
Knoth, R., Singec, I., Ditter, M., Pantazis, G., Capetian, P., Meyer, R. P., Horvat, V., Volk, B., & Kempermann, G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008809 · Cited by 650
Most Random Gene Expression Signatures Are Significantly Associated with Breast Cancer Outcome
Venet, D., Dumont, J. E., & Detours, V. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002240 · Cited by 614
How the Fanconi Anemia Pathway Guards the Genome
Moldovan, G., & D’Andrea, A. D. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102108-134222 · Cited by 601
Self-citationRad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis
Hashimoto, Y., Chaudhuri, A. R., Lopes, M., & Costanzo, V. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1927 · Cited by 537
Principles of ubiquitin and SUMO modifications in DNA repair
Bergink, S., & Jentsch, S. (2009) · Nature · doi:10.1038/nature07963 · Cited by 554
Self-citationRegulation of DNA cross-link repair by the Fanconi anemia/BRCA pathwayPreprint
Kim, H., & D’Andrea, A. D. (2012) · Genes & Development · doi:10.1101/gad.195248.112 · Cited by 534
The Biochemistry of Somatic Hypermutation
Peled, J. U., Kuang, F. L., Iglesias-Ussel, M. D., Roa, S., Kalis, S. L., Goodman, M. F., & Scharff, M. D. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090236 · Cited by 460
Multiple roles of the cell cycle inhibitor p21CDKN1A in the DNA damage response
Cazzalini, O., Scovassi, A. I., Savio, M., Stivala, L. A., & Prosperi, E. (2010) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2010.01.009 · Cited by 445
The Ubiquitin–Proteasome System of Saccharomyces cerevisiae
Finley, D. J., Ulrich, H. D., Sommer, T., & Kaiser, P. (2012) · Genetics · doi:10.1534/genetics.112.140467 · Cited by 449
Examination of the expanding pathways for the regulation of p21 expression and activity
Jung, Y.-S., Qian, Y., & Chen, X. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.01.013 · Cited by 428
CRL4s: the CUL4-RING E3 ubiquitin ligases
Jackson, S., & Xiong, Y. (2009) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2009.07.002 · Cited by 420
Barr, A. R., Cooper, S., Heldt, F. S., Butera, F., Stoy, H., Mansfeld, J., Novák, B., & Bakal, C. (2017) · Nature Communications · doi:10.1038/ncomms14728 · Cited by 403
Ogi, T., Limsirichaikul, S., Overmeer, R. M., Volker, M., Takenaka, K., Cloney, R., Nakazawa, Y., Niimi, A., Miki, Y., Jaspers, N. G., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.02.009 · Cited by 392
Dungrawala, H., Rose, K. L., Bhat, K. P., Mohni, K. N., Glick, G. G., Couch, F. B., & Cortez, D. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.07.030 · Cited by 395
What a difference a decade makes: Insights into translesion DNA synthesis
Yang, W., & Woodgate, R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704219104 · Cited by 380
Regulation of PCNA–protein interactions for genome stability
Mailand, N., Gibbs‐Seymour, I., & Bekker‐Jensen, S. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3562 · Cited by 395
Alabert, C., Bukowski-Wills, J.-C., Lee, S.-B., Kustatscher, G., Nakamura, K., Alves, F. D. L., Ménard, P., Mejlvang, J., Rappsilber, J., & Groth, A. (2014) · Nature Cell Biology · doi:10.1038/ncb2918 · Cited by 334
Forging Ahead through Darkness: PCNA, Still the Principal Conductor at the Replication Fork
Choe, K. N., & Moldovan, G.-L. (2017) · Molecular Cell · doi:10.1016/j.molcel.2016.12.020 · Cited by 325
Self-citationDamage to dopaminergic neurons by oxidative stress in Parkinson's disease (Review)
Guo, J., Zhao, X., Li, Y., Li, G., & Liu, X. (2018) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2018.3406 · Cited by 353
DNA polymerases and human disease
Loeb, L. A., & Monnat, R. J. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2345 · Cited by 330
Mechanisms that regulate localization of a DNA double-strand break to the nuclear peripheryPreprint
Oza, P., Jaspersen, S. L., Miele, A., Dekker, J., & Peterson, C. L. (2009) · Genes & Development · doi:10.1101/gad.1782209 · Cited by 334
Zharkov, D. O. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-7543-2 · Cited by 314
Motegi, A., Liaw, H.-J., Lee, K.-Y., Roest, H. P., Maas, A., Wu, X., Moinova, H., Markowitz, S. D., Ding, H., Hoeijmakers, J. H. J., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805685105 · Cited by 304
The Many Roles of PCNA in Eukaryotic DNA Replication
Boehm, E. M., Gildenberg, M. S., & Washington, M. T. (2016) · The Enzymes · doi:10.1016/bs.enz.2016.03.003 · Cited by 306
Ciccia, A., Nimonkar, A. V., Hu, Y., Hajdú, I., Achar, Y. J., Izhar, L., Petit, S. A., Adamson, B., Yoon, J. C., Kowalczykowski, S. C., et al. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.05.024 · Cited by 308
Karras, G. I., & Jentsch, S. (2010) · Cell · doi:10.1016/j.cell.2010.02.028 · Cited by 282
Self-citationPCNA: a silent housekeeper or a potential therapeutic target?
Wang, S.-C. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.02.004 · Cited by 285
Human PCNA Structure, Function and Interactions
Magaña, A. G., & Blanco, F. J. (2020) · Biomolecules · doi:10.3390/biom10040570 · Cited by 288
Povlsen, L. K., Beli, P., Wagner, S., Poulsen, S. L., Sylvestersen, K. B., Poulsen, J. W., Nielsen, M. L., Bekker‐Jensen, S., Mailand, N., & Choudhary, C. (2012) · Nature Cell Biology · doi:10.1038/ncb2579 · Cited by 288
ELM—the eukaryotic linear motif resource in 2020
Kumar, M., Gouw, M., Michael, S., Sámano‐Sánchez, H., Pancsa, R., Glavina, J., Diakogianni, A., Alvarado-Valverde, J., Bukirova, D., Čalyševa, J., et al. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz1030 · Cited by 278
Abbas, T., Shibata, E., Park, J.-H., Jha, S., Karnani, N., & Dutta, A. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.014 · Cited by 280
The Elg1 replication factor C-like complex functions in PCNA unloading during DNA replication
Kubota, T., Nishimura, K., Kanemaki, M. T., & Donaldson, A. D. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.02.012 · Cited by 279
Circadian molecular clocks and cancer
Kelleher, F. C., Rao, A. D., & Maguire, A. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.09.040 · Cited by 283
Molecular Mechanisms of Somatic Hypermutation and Class Switch Recombination
Methot, S. P., & Noia, J. M. D. (2016) · Advances in immunology · doi:10.1016/bs.ai.2016.11.002 · Cited by 273
Chi, X., Li, Y., & Qiu, X. (2020) · Immunology · doi:10.1111/imm.13176 · Cited by 299
Rescuing Stalled or Damaged Replication ForksPreprint
Yeeles, J. T. P., Poli, J., Marians, K. J., & Pasero, P. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012815 · Cited by 269
Translesion DNA polymerases in eukaryotes: what makes them tick?
Vaisman, A., & Woodgate, R. (2017) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2017.1291576 · Cited by 261
Replication-Coupled DNA Repair
Cortez, D. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.04.027 · Cited by 250
Terminal deoxynucleotidyl transferase: The story of a misguided DNA polymerase
Motea, E. A., & Berdis, A. J. (2009) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2009.06.030 · Cited by 259
Sirbu, B. M., McDonald, W. H., Dungrawala, H., Badu-Nkansah, A., Kavanaugh, G. M., Chen, Y., Tabb, D. L., & Cortez, D. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.511337 · Cited by 251
Oda, H., Hübner, M. R., Beck, D. B., Vermeulen, M., Hurwitz, J., Spector, D. L., & Reinberg, D. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.10.011 · Cited by 253
TrxG and PcG Proteins but Not Methylated Histones Remain Associated with DNA through Replication
Petruk, S., Sedkov, Y., Johnston, D. M., Hodgson, J. W., Black, K. L., Kovermann, S. K., Beck, S., Canaani, E., Brock, H. W., & Mazo, A. (2012) · Cell · doi:10.1016/j.cell.2012.06.046 · Cited by 251
Phytochrome regulation of branching in Arabidopsis
Finlayson, S. A., Krishnareddy, S. R., Kebrom, T. H., & Casal, J. J. (2010) · Plant Physiology · doi:10.1104/pp.109.148833 · Cited by 240
The CRL4Cdt2 ubiquitin ligase targets the degradation of p21Cip1 to control replication licensing
Kim, Y., Starostina, N. G., & Kipreos, E. T. (2008) · Genes & Development · doi:10.1101/gad.1703708 · Cited by 240
Herpes Simplex Viruses: Mechanisms of DNA ReplicationPreprint
Weller, S. K., & Coen, D. M. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a013011 · Cited by 239
SUMO-targeted ubiquitin ligases
Sriramachandran, A. M., & Dohmen, R. J. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.08.022 · Cited by 241
Dutto, I., Tillhon, M., Cazzalini, O., Stivala, L. A., & Prosperi, E. (2014) · Archives of Toxicology · doi:10.1007/s00204-014-1430-4 · Cited by 242
Inhibition of Homologous Recombination by the PCNA-Interacting Protein PARI
Moldovan, G., Dejsuphong, D., Petalcorin, M. I. R., Hofmann, K., Takeda, S., Boulton, S. J., & D’Andrea, A. D. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.11.010 · Cited by 242
Self-citationDNA Repair Mechanisms and the Bypass of DNA Damage in Saccharomyces cerevisiae
Boiteux, S., & Jinks-Robertson, S. (2013) · Genetics · doi:10.1534/genetics.112.145219 · Cited by 250
Proliferating cell nuclear antigen: a proteomics view
Naryzhny, S. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8305-x · Cited by 256
The ubiquitous role of ubiquitin in the DNA damage response
Al-Hakim, A., Escribano‐Diaz, C., Landry, M.-C., O’Donnell, L., Panier, S., Szilard, R. K., & Durocher, D. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.09.011 · Cited by 240
Bitar, S. A., & Gali‐Muhtasib, H. U. (2019) · Cancers · doi:10.3390/cancers11101475 · Cited by 231
Mechanism of CRL4Cdt2, a PCNA-dependent E3 ubiquitin ligasePreprint
Havens, C. G., & Walter, J. C. (2011) · Genes & Development · doi:10.1101/gad.2068611 · Cited by 228
Cotta‐Ramusino, C., McDonald, E. R., Hurov, K. E., Sowa, M. E., Harper, J. W., & Elledge, S. J. (2011) · Science · doi:10.1126/science.1203430 · Cited by 229
Histone Lysine Methyltransferase SETD8 Promotes Carcinogenesis by Deregulating PCNA Expression
Takawa, M., Cho, H., Hayami, S., Toyokawa, G., Kogure, M., Yamane, Y., Iwai, Y., Maejima, K., Ueda, K., Masuda, A., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-11-3701 · Cited by 217
Ling, X., Chen, X., Riddell, I. A., Tao, W., Wang, J., Hollett, G., Lippard, S. J., Farokhzad, O. C., Shi, J., & Wu, J. (2018) · Nano Letters · doi:10.1021/acs.nanolett.8b01924 · Cited by 209
Reshaping the Endogenous Electric Field to Boost Wound Repair via Electrogenerative Dressing
Luo, R., Liang, Y., Yang, J., Feng, H., Chen, Y., Jiang, X., Zhang, Z., Liu, J., Bai, Y., Xue, J., et al. (2023) · Advanced Materials · doi:10.1002/adma.202208395 · Cited by 210
DNA damage tolerance: when it's OK to make mistakes
Chang, D. J., & Cimprich, K. A. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.139 · Cited by 213
Eukaryotic DNA damage tolerance and translesion synthesis through covalent modifications of PCNA
Andersen, P. L., Xu, F., & Xiao, W. (2007) · Cell Research · doi:10.1038/cr.2007.114 · Cited by 204
DNA damage tolerance: a double-edged sword guarding the genome.
Ghosal, G., & Chen, J. (2013) · PubMed · doi:10.3978/j.issn.2218-676x.2013.04.01 · Cited by 215
Regulation of heterochromatic DNA replication by histone H3 lysine 27 methyltransferases
Jacob, Y., Stroud, H., LeBlanc, C., Feng, S., Zhuo, L., Caro, E., Hassel, C. A., Gutiérrez, C., Michaels, S. D., & Jacobsen, S. E. (2010) · Nature · doi:10.1038/nature09290 · Cited by 198
DNA Damage and P53-Mediated Growth Arrest in Human Cells Treated with Platinum Nanoparticles
Asharani, P. V., Xinyi, N., Hande, M. P., & Valiyaveettil, S. (2009) · Nanomedicine · doi:10.2217/nnm.09.85 · Cited by 198
Yu, C., Gan, H., Han, J., Zhou, Z.-X., Jia, S., Chabes, A., Farrugia, G., Ördög, T., & Zhang, Z. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.09.017 · Cited by 190
DNA mismatch repair and its many roles in eukaryotic cells
Liu, D., Keijzers, G., & Rasmussen, L. J. (2017) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2017.07.001 · Cited by 209
Ghazal, S., McKinnon, B. D., Zhou, J., Mueller, M., Men, Y., Yang, L., Mueller, M. D., Flannery, C. A., Huang, Y., & Taylor, H. S. (2015) · EMBO Molecular Medicine · doi:10.15252/emmm.201505245 · Cited by 198
DNA Mismatch Repair in Eukaryotes and Bacteria
Fukui, K. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/260512 · Cited by 192
Cellular responses to DNA double-strand breaks after low-dose γ-irradiation
Asaithamby, A., & Chen, D. J. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp237 · Cited by 194
Rowbotham, S. P., Barki‐Celli, L., Neves‐Costa, A., Santos, F., Dean, W., Hawkes, N. A., Choudhary, P., Will, W. R., Webster, J. A., Oxley, D., et al. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.02.036 · Cited by 186
Ma, H., Luo, J., Sun, Z., Xia, L., Shi, M., Liu, M., Chang, J., & Wu, C. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.10.005 · Cited by 190
Behera, S. S., Das, U., Kumar, A., Bissoyi, A., & Singh, A. K. (2017) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2017.02.017 · Cited by 189
Molecular Markers for Breast Cancer: Prediction on Tumor Behavior
Hirata, B. K. B., Oda, J. M. M., Guembarovski, R. L., Ariza, C. B., de Oliveira, C. E. C., & Watanabe, M. A. E. (2014) · Disease Markers · doi:10.1155/2014/513158 · Cited by 192
Landmann, F., Orsi, G. A., Loppin, B., & Sullivan, W. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000343 · Cited by 184
Cardano, M., Tribioli, C., & Prosperi, E. (2020) · Current Cancer Drug Targets · doi:10.2174/1568009620666200115162814 · Cited by 189
Lydeard, J. R., Lipkin-Moore, Z., Sheu, Y.-J., Stillman, B., Burgers, P., & Haber, J. E. (2010) · Genes & Development · doi:10.1101/gad.1922610 · Cited by 194
Smeets, D., Markaki, Y., Schmid, V. J., Kraus, F., Tattermusch, A., Cerase, A., Sterr, M., Fiedler, S., Demmerle, J., Popken, J., et al. (2014) · Epigenetics & Chromatin · doi:10.1186/1756-8935-7-8 · Cited by 186
Havens, C. G., & Walter, J. C. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.05.012 · Cited by 178
Oligonucleotide/oligosaccharide-binding fold proteins: a growing family of genome guardians
Flynn, R. L., & Zou, L. (2010) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2010.488216 · Cited by 186
Tissue Biomarkers for Prognosis in Cutaneous Melanoma: A Systematic Review and Meta-analysis
Rothberg, B. E. G., Bracken, M. B., & Rimm, D. L. (2009) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djp038 · Cited by 183
Izhar, L., Adamson, B., Ciccia, A., Lewis, J., Vaites, L. P., Leng, Y., Liang, A. C. T., Westbrook, T. F., Harper, J. W., & Elledge, S. J. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.04.053 · Cited by 178
Silibinin Inhibits Colorectal Cancer Growth by Inhibiting Tumor Cell Proliferation and Angiogenesis
Singh, R. P., Gu, M., & Agarwal, R. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-6247 · Cited by 176
Witko‐Sarsat, V., Mocek, J., Bouayad, D., Tamassia, N., Ribeil, J., Candalh, C., Davezac, N., Reuter, N., Mouthon, L., Hermine, O., et al. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20092241 · Cited by 173
Mosbech, A., Gibbs‐Seymour, I., Kagias, K., Thorslund, T., Beli, P., Povlsen, L. K., Nielsen, S. V., Smedegaard, S. B., Sedgwick, G. G., Lukas, C., et al. (2012) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2395 · Cited by 181
Lim, S., Khoo, R., Peh, K. M., Teo, J., Chang, S. C., Ng, S., Beilhartz, G. L., Melnyk, R. A., Johannes, C. W., Brown, C. J., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1920251117 · Cited by 170
H2AX Is Required for Cell Cycle Arrest via the p53/p21 Pathway
Fragkos, M., Jurvansuu, J., & Beard, P. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01830-08 · Cited by 176
Regulating post-translational modifications of the eukaryotic replication clamp PCNA
Ulrich, H. D. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.01.006 · Cited by 172
Identification of a novel, widespread, and functionally important PCNA-binding motif
Gilljam, K. M., Feyzi, E., Aas, P. A., de Sousa, M. M. L., Müller, R., Vågbø, C. B., Catterall, T., Liabakk, N., Slupphaug, G., Drabløs, F., et al. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200903138 · Cited by 179
LncRNA PCNAP1 modulates hepatitis B virus replication and enhances tumor growth of liver cancer
Feng, J., Yang, G., Liu, Y., Gao, Y., Zhao, M., Bu, Y., Yuan, H., Yuan, Y., Yun, H., Sun, M., et al. (2019) · Theranostics · doi:10.7150/thno.34273 · Cited by 168
Metadata
- Authors
- Moldovan, G.-L., Pfander, B., & Jentsch, S.
- Affiliations
- Harvard University (US)
- Cancer Research UK (GB)
- Max Planck Institute of Biochemistry (DE)
- Corresponding author
- Jentsch, Stefan
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2007-05
- Volume
- 129
- Issue
- 4
- Pages
- 665-679
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2072747624
- Cited by
- 1,796
- References
- 110
- Citations by year
- 2026: 53 · 2025: 70 · 2024: 77 · 2023: 84 · 2022: 80 · 2021: 86 · 2020: 87 · 2019: 97 · 2018: 87 · 2017: 111 · 2016: 113 · 2015: 92 · 2014: 113 · 2013: 106 · 2012: 125
- FWCI
- 8.35
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2269 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- proliferating cell nuclear antigen, PCNA, DNA replication, replication fork, genome stability, epigenetic inheritance, whole-genome duplication, protein-protein interaction, phosphorylation, ubiquitination, SUMOylation, proteolysis, chromatin inheritance
- MeSH terms
- Animals, DNA-Directed DNA Polymerase, DNA Repair, DNA Replication, DNA-Binding Proteins, Humans, S Phase, Cell Cycle Proteins, Proliferating Cell Nuclear Antigen, Genomic Instability, Epigenesis, Genetic
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review