ATR and ATRIP: Partners in Checkpoint Signaling

Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells

Elbashir, S. M., Harborth, J., Lendeckel, W., Yalcin, A., Weber, K., & Tuschl, T. (2001) · Nature · doi:10.1038/35078107 · Cited by 9,456

Activation of the ATM Kinase by Ionizing Radiation and Phosphorylation of p53

Canman, C. E., Lim, D.-S., Cimprich, K. A., Taya, Y., Tamai, K., Sakaguchi, K., Appella, E., Kastan, M. B., & Siliciano, J. D. (1998) · Science · doi:10.1126/science.281.5383.1677 · Cited by 2,042

BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures.

Wang, Y., Cortez, D., Yazdi, P., Neff, N., Elledge, S. J., & Qin, J. (2000) · Genes & Development · doi:10.1101/gad.14.8.927 · Cited by 1,221

A role for ATR in the DNA damage-induced phosphorylation of p53

Tibbetts, R. S., Brumbaugh, K. M., Williams, J. M., Sarkaria, J. N., Cliby, W. A., Shieh, S.-Y., Taya, Y., Prives, C., & Abraham, R. T. (1999) · Genes & Development · doi:10.1101/gad.13.2.152 · Cited by 1,046

ATR disruption leads to chromosomal fragmentation and early embryonic lethality

Brown, E. J., & Baltimore, D. (2000) · Genes & Development · doi:10.1101/gad.14.4.397 · Cited by 951

A Suppressor of Two Essential Checkpoint Genes Identifies a Novel Protein that Negatively Affects dNTP Pools

Zhao, X., Muller, E. G. D., & Rothstein, R. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80277-4 · Cited by 728

ATM and ATR: networking cellular responses to DNA damage

Shiloh, Y. (2001) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(00)00159-3 · Cited by 601

Involvement of Brca1 in S-Phase and G 2 -Phase Checkpoints after Ionizing Irradiation

Xu, B., Kim, S., & Kastan, M. B. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.10.3445-3450.2001 · Cited by 550

Overexpression of a kinase‐inactive ATR protein causes sensitivity to DNA‐damaging agents and defects in cell cycle checkpoints

Cliby, W. A., Roberts, C. J., Cimprich, K. A., Stringer, C. M., Lamb, J. R., Schreiber, S. L., & Friend, S. H. (1998) · The EMBO Journal · doi:10.1093/emboj/17.1.159 · Cited by 542

DNA-PK, ATM and ATR as sensors of DNA damage: variations on a theme?

Durocher, D., & Jackson, S. P. (2001) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(00)00201-5 · Cited by 523

Distinct Pathways Involved in S-Phase Checkpoint Control

Hurley, P. J., & Bunz, F. (2009) · Humana Press eBooks · doi:10.1007/978-1-60761-178-3_2 · Cited by 2

Characterization and function of the nek11 kinase in cancer cells

Sabir, S. R. (2015) · Figshare · Cited by 2

Interaction of DDB1 with NBS1 in a DNA Damage Checkpoint Pathway

Lim, H. J., Lim, H. J., & Yoo, H. Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252313097 · Cited by 1

Tumorigenesis Caused by Aberrant Expression of GANP, a Central Component in the Mammalian TREX-2 Complex—Lessons from Transcription-Coupled DNA Damages

Rezano, A., Gondo, N., Sakai, Y., Nakamura, Y., Phimsen, S., Tani, T., Ito, A., Okada, S., & Kuwahara, K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413612 · Cited by 1

Mono-ubiquitination of TopBP1 by PHRF1 enhances ATR activation and genomic stability

Zhao, F., Cai, C., Gao, H., Moon, J., Christyani, G., Qin, S., Hao, Y., Liu, T., Lou, Z., & Kim, W. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf073 · Cited by 1

Distinct ATRX functions cooperate with 9-1-1 and CST complexes to safeguard replication and telomere integrity

Segura‐Bayona, S., Maric, M., Takaki, T., Manova, Z., Stanage, T. H., Idilli, A. I., Idilli, A. I., Hewitt, G., Machour, F. E., Millar, R., et al. (2026) · Nature Structural & Molecular Biology · doi:10.1038/s41594-026-01827-2 · Cited by 2

Targeting ATR in Cancer therapy: A drug discovery perspective

Lai, Y., Zhao, W., Wang, Y., & Zhang, L. (2026) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2026.109707 · Cited by 1

β-tubulin phosphorylation by Chk1 is required for normal spindle formation during cell division

Boutakoglou, N., Petsalaki, E., Balafouti, S., Efthymiou, D., Lilla, S., Giatagana, E.-M., Zanivan, S. R., & Zachos, G. (2026) · Communications Biology · doi:10.1038/s42003-026-09862-x · Cited by 1

Structural mechanism of TOPBP1 activating the ATR–ATRIP replication checkpoint kinase

Li, B., Yaseen, A., & Pavletich, N. P. (2026) · Nature Structural & Molecular Biology · doi:10.1038/s41594-026-01844-1 · Cited by 1

Targeting DNA Damage Response Pathways for Cancer Therapy

Polu, P. R., & Vyas, M. (2026) · Springer eBooks · doi:10.1007/978-981-92-0477-9_3 · Cited by 1

Mechanistic insights into phosphorylation-driven activation and therapeutic inhibition of human ATR–ATRIP

Wang, L., Wang, M., Zhao, L., Rao, Q., Wu, H., Ma, B., Wang, J., Zheng, J., Li, Y., Xu, Y., et al. (2026) · Nature Structural & Molecular Biology · doi:10.1038/s41594-026-01887-4 · Cited by 1

Evelyn Witkin and Stephen Elledge share the 2015 Lasker Basic Medical Award

Jackson, S. (2015) · Journal of Clinical Investigation · doi:10.1172/jci84318 · Cited by 1

The ATM-mediated DNA-damage response

Shiloh, Y. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139046947.035 · Cited by 1

Checkpoint Control Following Radiation Exposure

Löbrich, M., Goodarzi, A. A., Stiff, T., & Jeggo, P. A. (2011) · Springer eBooks · doi:10.1007/978-1-4419-8044-1_3 · Cited by 1

Preparation of endogenous TopBP1/Dpb11 and effect on central checkpoint kinase Mec1- Ddc2 (human ATR-ATRIP homolog)

Wu, T., Zhang, Z., & Wang, X. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.07.055 · Cited by 1

Damage and Replication Stress Responses

Wang, H., Shen, P., & Zhu, W. (2011) · InTech eBooks · doi:10.5772/21986 · Cited by 1

Xeroderma Pigmentosum and the DNA Damage Response to Ultraviolet Light

Cleaver, J. E. (2016) · Springer eBooks · doi:10.1007/978-1-59745-458-2_24 · Cited by 1

Mechanisms of Cardiovascular Damage Induced by Traditional Chemotherapy

Mercurio, V., Agnetti, G., Pagliaro, P., & Tocchetti, C. G. (2018) · Current clinical pathology · doi:10.1007/978-3-319-93402-0_2 · Cited by 1

Proteins Involved in Colorectal Cancer: Identification Strategies and Possible Roles

Kumar, S., Goel, D., Neeraj, & Maurya, V. K. (2021) · Springer eBooks · doi:10.1007/978-3-030-63369-1_9 · Cited by 1

DNA mismatch repair in mammals

Cherkasova, V. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85679-9.00018-0 · Cited by 1

Recognition of DNA Damage as the Initial Step of Eukaryotic Checkpoint Arrest

Siede, W. (2005) · CRC Press eBooks · doi:10.1201/9780849352683.ch36 · Cited by 1

DNA Damage: Sensing

Yang, X. H., & Zou, L. (2008) · Wiley eBooks · doi:10.1002/9780470048672.wecb132 · Cited by 1

DNA damage signalling in eukaryotes: learning from budding yeast

Menacho-Márquez, M., & Ibañez, J. R. M. (2003) · Revista de Oncología · doi:10.1007/bf02712848 · Cited by 1

Analysis of Rad9 Functions; Roles in the Checkpoint Response, DNA Damage Processing, and Prevention of Genomic Instability

Nyberg, K. A., & Weinert, T. A. (2003) · Defense Technical Information Center (DTIC) · doi:10.21236/ada418042 · Cited by 1

Targeting ATM/ATR in the DNA Damage Checkpoint

Ackermann, J. M., & El‐Deiry, W. S. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-274-8_4 · Cited by 1

Chromatin: The Entry to and Exit from DNA Repair

Gospodinov, A. G., & Herceg, Z. (2010) · Springer eBooks · doi:10.1007/978-1-4419-6382-6_16 · Cited by 1

Differential Effect of Selected Methylxanthine Derivatives on Radiosensitization and Cell Cycle in Normal and Lung Cancer Cell Lines

Malki, A. M. (2006) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1

A UVB-hypersensitive mutant in Arabidopsis thaliana is defective in the DNA damage response

Nam, V. (2009) · Cited by 1

The kinase MK2 in DNA replication upon genotoxic stress and chemotherapy

Köpper, F. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1445 · Cited by 1

The role of telomere damage in cardiomyocyte ageing

Anderson, R. K. (2016) · Cited by 1

CDKs-mediated phosphorylation of PNKP is required for end-processing of single-strand DNA gaps on Okazaki Fragments and genome stabilityPreprint

Tsukada, K., Miyake, T., Imamura, R., Saikawa, K., Saito, M., Kase, N., Ishiai, M., Matsumoto, Y., & Shimada, M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.29.452278 · Cited by 1

Widespread roles of Trypanosoma brucei ATR in nuclear genome function and transmission are linked to R-loopsPreprint

Black, J. A., Crouch, K., Briggs, E. M., Lemgruber, L., Lapsely, C., Tosi, L. R. O., Mottram, J. C., & McCulloch, R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.09.459654 · Cited by 1

Chapter 3

Valentin, J. (2005) · Annals of the ICRP · doi:10.1016/j.icrp.2005.11.003 · Cited by 1

Thymidine rescues ATR kinase inhibition induced deoxyuridine contamination in genomic DNA, cell death, and Type 1 interferon expressionPreprint

Sugitani, N., Vendetti, F. P., Cipriano, A. J., Pandya, P., Deppas, J. J., Moiseeva, T. N., Schamus-Haynes, S., Wang, Y., Palmer, D., Osmanbeyoglu, H. U., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.24.481821 · Cited by 1

ATR Kinase Inhibition Induces Thymineless Death in Proliferating CD8 + T CellsPreprint

Sugitani, N., Vendetti, F. P., Cipriano, A. J., Deppas, J. J., Moiseeva, T. N., Schamus-Haynes, S., Wang, Y., Palmer, D., Osmanbeyoglu, H. U., Bostwick, A., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4093292 · Cited by 1

A phosphorylation code coordinating transcription condensate dynamics with DNA replicationPreprint

Marmolejo, C. A. O., Sanchez, C., Lee, J., Werner, M., Roberts, P. A., Hamperl, S., & Saldivar, J. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.10.593572 · Cited by 1

Saccharomyces cerevisiae DNA helicases Mph1, Srs2 and Sgs1 collaborate for the reinitiation of stalled or collapsed replication forks

Panico, E. R. (2006) · doi:10.53846/goediss-148

The DNA damage response pathway in oral squamous cell carcinoma

Parikh, R. A. (2006) · D-Scholarship@Pitt (University of Pittsburgh)

GENETIC AND EVOLUTIONARY ANALYSIS OF PLANT REPLICATION PROTEIN A 1 (RPA1)

Aklilu, B. B. (2015) · University of New Hampshire Scholars Repository (University of New Hampshire at Manchester)

The Role of the ATR-CHEK1 Pathway in Therapeutic Resistance Resulting from Distal 11q Loss in Carcinoma Cells

Sankunny, M. (2013) · D-Scholarship@Pitt (University of Pittsburgh)

Prospects for Research in Radiation Biology

Limoli, C. L. (2004) · Springer eBooks · doi:10.1007/978-3-642-18687-5_3

In vitro models for investigating keratinocyte responses to ultraviolet B radiation

Fernandez, T. L. (2013)

Cyclin A/CDK2 regulates multiple G2 phase pathways

Oakes, V. (2012)

Cellular Responses to Replication Problems

Budzowska, M. (2008) · EUR Research Repository (Erasmus University Rotterdam)

DNA Damage Checkpoint Signaling Pathways in Human Cancer

Abraham, R. T., & Halazonetis, T. D. (2011) · Springer eBooks · doi:10.1007/978-1-4614-1216-8_3

DNA Damage Response

Khanna, K. K., & Tibbetts, R. S. (2006) · Wiley eBooks · doi:10.1038/npg.els.0006107

Xenopus laevis as a model system for evaluating the function of fanconi anemia proteins

Stone, S. (2008) · Pure Amsterdam UMC

Role Of Hippocampal Neurogenesis In The Etiology And Treatment Of Mood & Anxiety Disorders

Onksen, J. L. (2011) · ScholarlyCommons (University of Pennsylvania)

Replication fork stability in mammalian cells

Elvers, I. (2011) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Checkpoint Kinase-Dependent Regulation of DNA Repair and Genome Instability in Breast Cancer

Lovejoy, C. A. (2007) · Defense Technical Information Center (DTIC) · doi:10.21236/ada473781

DNA Repair, Cancer and Cancer Therapy

Wang, M. (2011) · InTech eBooks · doi:10.5772/20855

Mechanisms of DNA Double-Strand Break Repair in Hematopoietic Homeostasis and Oncogenesis

Maas, S. A., Caddle, L. B., & Mills, K. D. (2008) · Springer eBooks · doi:10.1007/978-0-387-69132-9_4

DNA Strand Break Repair and Human Genetic Disease

García‐Muse, T., & Aguilera, A. (2018) · Wiley eBooks · doi:10.1002/9780470015902.a0021478.pub2

Regulation of cellular signalling pathways by Adenovirus

Forrester, N. A. (2012) · University of Birmingham Institutional Research Archive (University of Birmingham)

The Rad9-Rad1-Hus1 complex and Bif-1 regulate multiple mechanisms that affect sensitivity to DNA damage

Meyerkord, C. L. (2009) · Digital Commons - University of South Florida (University of South Florida)

Consequences of Interstrand Crosslinks in Hematopoiesis: Tipping the balance between senescence and proliferation

Verhagen-Oldenampsen, J. (2013) · EUR Research Repository (Erasmus University Rotterdam)

Spy1 Regulation of the DNA Damage Response; Checkpoint Activation and Cellular Senescence

Jalili, E. (2013)

Signaling at Stalled Replication Forks

Mordes, D. A., & Cortez, D. (2009) · Springer eBooks · doi:10.1007/978-90-481-2561-6_2

Avaliação da expressão de genes processadores de danos oxidativos em pacientes com Alzheimer

de Oliveira, D. V. N. P. (2007) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2007.tde-17042009-152311

DNA Repair of Eukaryotes Associated with Non-coding Small RNAs

Kang, H., Yoon, S.-H., Lee, C., & Roh, K. H. (2013) · Journal of Applied Biological Chemistry · doi:10.3839/jabc.2013.007

Dissecting Layers of Mitotic Regulation Essential for Maintaining Genomic Stability

Searle, J. S., & Sánchez, Y. (2007) · Springer eBooks · doi:10.1007/978-1-4020-5963-6_2

ATR (ataxia telangiectasia and Rad3 related)

Gagou, M., & Meuth, M. (2011) · Atlas of Genetics and Cytogenetics in Oncology and Haematology · doi:10.4267/2042/44954

Chemosensitivity of testicular germ cell tumors is based on high constitutive Noxa protein levels and a functional p53 response

Gutekunst, M. (2013) · OPUS Publication Server of the University of Stuttgart (University of Stuttgart) · doi:10.18419/opus-8157

Defects in the ATR-dependent DNA damage response pathway and human syndromes

O’Driscoll, M. (2009) · Institutional Repositories DataBase (IRDB) · doi:10.11343/amn.53.s23

Interplay between ATM and ATR for the regulation of cellular responses to DNA damage

Fan, X. (2010) · DuEPublico (University of Duisburg-Essen)

Molecular Characterization of the Dbf4/Drf1-Dependent Kinase (DDK) and the DNA Replication Checkpoint Mediator Claspin in Xenopus Egg Extracts

Gold, D. A. (2009) · CaltechTHESIS (California Institute of Technology) · doi:10.7907/xg90-5475

p53 and DNA damage checkpoint responses in the human prostate

af Hällström, T. (2007)

Nuclear Subdomains and Cancer

Cann, K. L., Huang, S., & Dellaire, G. (2010) · Springer eBooks · doi:10.1007/978-90-481-9899-3_1

DNA damage-induced cell death : The role of caspase-2

Vakifahmetoglu, H. (2009) · Figshare

Protein Dynamics in Mammalian Genome Maintenance

Zotter, A. (2008) · RePub (Erasmus University Rotterdam)

Inhibiting Cell Cycle Kinases in Cancer Therapy

de Cárcer, G., de Castro, I. P., & Malumbres, M. (2012) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9781608054640113060009

Studies on early cellular responses during Epstein-Barr virus infection

Chen, X. (2015) · Figshare

Bedeutung der c-Abl-Aktivität für die Reaktion auf DNA-Schädigung und für die genetische Stabilität Bcr-Abl-negativer Zellen Dissertation zur Erlangung des Doktorgrades der Naturwissenschaften (Dr. rer. nat.)

Naturwissenschaften, F., & Fischer-Bosch-Institut, M. (2011)

Stephen Elledge and the DNA damage response

Cortez, D., Zhou, Z. Y., & Sánchez, Y. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.11.001

Aberrations of DNA Damage in Checkpoints in Cancer

Laiho, M. (2007) · Humana Press eBooks · doi:10.1007/978-1-59745-200-7_5

DNA damage signaling in response to etoposide

Siponen, M. I. (2005) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/17380

Development and Validation of an Assay for the Characterization of the DNA Damage Response to Damage Caused by Superfund Chemicals

Ridpath, J. R. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/1dj8-fy53

Meccanismi di controllo della proliferazione delle cellule germinali primordiali

Sorrentino, E. (2007) · Cineca Institutional Research Information System (Tor Vergata University) · doi:10.58015/sorrentino-eleonora_phd2007-05

Genetics of DNA replication and homologous recombination in arabidopsis

Schürmann, D. (2005) · edoc (University of Basel) · doi:10.5451/unibas-003646982

The DNA damage and the DNA synthesis checkpoints converge at the MBF transcription factor

Ivanova, T. G. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Combining gemcitabine with checkpoint kinase inhibitors to sensitize pancreatic tumors

Saini, P. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5028

immunoglobulin class switch recombination and somatic hypermutation

Pan‐Hammarström, Q., Lähdesmäki, A., Zhao, Y., Du, L., Zhao, Z., Wen, S., Ruiz‐Pérez, V. L., Dunn‐Walters, D. K., Goodship, J. A., & Hammarström, L. L. G. (2006)

ATM-Independent Manner Mutated (ATM)-Dependent and an Apoptosis in both an Ataxia Telangiectasia Chk2 Is a Tumor Suppressor That Regulates

Jeggo, P. A., Elledge, S. J., Mak, T. W., Bristow, R. G., Suda, T., Lowe, S. W., Sarkissian, T., Wong, J. A., Sakai, T., Elia, A., et al. (2014)

The role of hnRNP A1 and hnRNP C1/C2 in the regulation of the stress responsive genes Cyp2a5/2A6 and p53.

Christian, K. J. (2008) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Gene Targeting in Cultured Human Cells

Waldman, T. A. (2004) · Humana Press eBooks · doi:10.1385/1-59259-646-0:163

Strategies to Isolate Evolutionarily Conserved Cell Cycle Regulatory Genes

Davey, S. K. (2004) · Humana Press eBooks · doi:10.1385/1-59259-646-0:115

Signaling of DNA Replication Stress Through the ATR Checkpoint

Shiotani, B., & Zou, L. (2016) · Springer eBooks · doi:10.1007/978-4-431-55873-6_16 · Cited by 1

Activation of the DNA damage checkpointandgenomicinstabilityin human precancerous lesions

Gorgoulis, V. G., Vassiliou, L. V., Karakaidos, P., Zacharatos, P., Kotsinas, A., Liloglou, T., Venere, M., DiTullio, R. A., Herlyn, M., Kittas, C. N., et al. (2005)

Recognition of DNA Damage as the Initial Step of Eukaryotic Checkpoint Arrest

Siede, W. (2005) · doi:10.1201/9780849352683-46

Checkpoint kinase (Chk1) and reactive oxygen species induced oncotic cell death during the cell cycle in LLC-PK1 cells.

Ehsan, H. (2012)

Integration of ATM, ATR, and DNA-PKcs Signaling Maintains Genome Integrity During Neurogenesis

Enriquez-Rios, V. D. (2015) · doi:10.21007/etd.cghs.2015.0085

Characterization of p53 in rainbow trout cell lines

Liu, M. (2010) · UWSpace (University of Waterloo)

The interaction between Rad9 and Tousled-like kinase 1 in the cell cycle and the DNA damage response

Kelly, R. M. (2013) · QSpace (Queen's University Library)

A. Apoptosis and the Genesis of Tumors

Stewart, B. W. (2003)

The effect of UVA irradiation on the DNA damage response in a human keratinocyte cell line

Eastham, M. (2016) · Lancaster EPrints (Lancaster University)

Identification and characterization of tac5, a telomerase activation mutant, characterization of DNA damage responses and assessment of interactions between telomere-related proteins in Arabidopsis thaliana

Jasti, M. (2009) · OakTrust (Texas A&M University Libraries)

Experimental study of the combined effect of irradiation, lovastatin, and monoclonal antibodies on tumour and normal tissue cell lines. Its genesis and mechanisms of action

Miglierini, P. (2014) · doi:10.53846/goediss-4708

A Genome-scale RNA Interference Screen Identifies Novel Regulators of DNA Double-strand Break Repair

Young, J. T. F. (2016) · TSpace (University of Toronto)

Control of DNA Replication by ATR

Lecona, E., & Fernández-Capetillo, Ó. (2018) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-75836-7_3

A deficiência das proteínas de checkpoint HUS1 e RAD9 promove a variação do número de cópias no genoma de Leishmania major

Gomez, R. O. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2018.tde-25042018-163036

Coordinated Effort Against DNA Damage

(2001) · Science Signaling · doi:10.1126/scisignal.1102001tw436

Mechanisms of ATR-mediated checkpoint signalling

Smits, V. A. J. (2010) · Frontiers in bioscience · doi:10.2741/3649 · Cited by 46

Interplay between ATM and ATR for the regulation of cellular responses to DNA damage

Fan, X. (2010) · DuEPublico (University of Duisburg-Essen)

Identifying Inhibitors of ATM and ATR Kinase Activities

Sarkaria, J. N. (2003) · Humana Press eBooks · doi:10.1385/1-59259-380-1:49 · Cited by 15

ATR Is Not Required for p53 Activation but Synergizes with p53 in the Replication Checkpoint*

(2001)