In Situ Visualization of DNA Double-Strand Break Repair in Human Fibroblasts

The double-strand-break repair model for recombination

Szostak, J. W., Orr-Weaver, T. L., Rothstein, R. J., & Stahl, F. W. (1983) · Cell · doi:10.1016/0092-8674(83)90331-8 · Cited by 2,437

Dynamic changes of BRCA1 subnuclear location and phosphorylation state are initiated by DNA damage

Scully, R., Chen, J., Ochs, R. L., Keegan, K., Hoekstra, M., Feunteun, J., & Livingston, D. M. (1997) · Cell · doi:10.1016/s0092-8674(00)80503-6 · Cited by 900

DNA Strand Breaks: the DNA Template Alterations That Trigger p53-Dependent DNA Damage Response Pathways

Nelson, W. G., & Kastan, M. B. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.3.1815 · Cited by 855

Human Rad51 Protein Promotes ATP-Dependent Homologous Pairing and Strand Transfer Reactions In Vitro

Baumann, P., Benson, F. E., & West, S. C. (1996) · Cell · doi:10.1016/s0092-8674(00)81394-x · Cited by 689

Nuclear foci of mammalian Rad51 recombination protein in somatic cells after DNA damage and its localization in synaptonemal complexes.

Haaf, T., Golub, E. I., Reddy, G., Radding, C. M., & Ward, D. C. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.6.2298 · Cited by 552

DNA strand exchange mediated by a RAD51-ssDNA nucleoprotein filament with polarity opposite to that of RecA

Sung, P., & Robberson, D. L. (1995) · Cell · doi:10.1016/0092-8674(95)90434-4 · Cited by 501

hMre11 and hRad50 Nuclear Foci Are Induced During the Normal Cellular Response to DNA Double-Strand Breaks †

Maser, R. S., Monsen, K. J., Nelms, B. E., & Petrini, J. H. J. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.10.6087 · Cited by 499

ATAXIA-TELANGIECTASIA AND THE NIJMEGEN BREAKAGE SYNDROME: Related Disorders But Genes Apart

Shiloh, Y. (1997) · Annual Review of Genetics · doi:10.1146/annurev.genet.31.1.635 · Cited by 482

Visualization of replication factories attached to a nucleoskeleton

Hozák, P., Hassan, A. B., Jackson, D. A., & Cook, P. R. (1993) · Cell · doi:10.1016/0092-8674(93)90235-i · Cited by 466

Sensitivity and selectivity of the DNA damage sensor responsible for activating p53-dependent G1 arrest.

Huang, L. C., Clarkin, K. C., & Wahl, G. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.10.4827 · Cited by 384

A versatile system to introduce clusters of genomic double‐strand breaks in large cell populations

Kolb, T., Khalid, U., Simovic-Lorenz, M., Ratnaparkhe, M., Wong, J., Jauch, A. S., Schmezer, P., Rode, A., Sebban, S., Haag, D., et al. (2020) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22890 · Cited by 5

Microscopic visualization of a biological response to charged particle traversal

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The MRE11-RAD50 Complex

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DNA double-strand breaks induce formation of RP-A/Ku foci on in vitro reconstitutedXenopussperm nuclei

Grandi, P., Eltsov, M., Nielsen, I. S., & Raška, I. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.18.3345 · Cited by 5

The human Werner Syndrome as a model system for aging

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Repair of DNA Double-Strand Breaks

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Repair of DNA Double-Strand Breaks and Mismatches in Drosophila

Flores, C. C. (2001) · Humana Press eBooks · doi:10.1007/978-1-59259-095-7_8 · Cited by 5

Neocarzinostatin-induced Rad51 nuclear focus formation is cell cycle regulated and aberrant in AT cells

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Role of ATM in Radiation Signal Transduction

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Biochemical and Cellular Aspects of Homologous Recombination

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Meiotic localization of Mre11 and Rad50 in wild type, spo11-1, and MRN complex mutants of Coprinus cinereus

Many, A. M., Melki, C., Savytskyy, O. P., Maillet, D. S., Acharya, S. N., & Zolan, M. E. (2009) · Chromosoma · doi:10.1007/s00412-009-0209-5 · Cited by 3

Studies of the DNA Damage Response by Using the Lac Operator/Repressor (LacO/LacR) Tethering System

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Targeted nuclear irradiation with a proton microbeam induces oxidative DNA base damage and triggers the recruitment of DNA glycosylases OGG1 and NTH1

Robeska, E., Lalanne, K., Vianna, F., Sutcu, H. H., Khobta, A., Busso, D., Radicella, J. P., Campalans, A., & Baldeyron, C. (2023) · DNA repair · doi:10.1016/j.dnarep.2023.103610 · Cited by 4

Identification of different classes of genome instability suppressor genes through analysis of DNA damage response markers

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Using Transcriptomics to Evaluate Thresholds in Genotoxicity Dose–Response

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Nijmegen Breakage syndrome

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Characterization of theNbs1Gene and Analysis of the Expression of Homologous and Homoeologous MRN Complex Genes in Meiocytes and Somatic Cells of Different Wheat Species

Pérez, R., Cuadrado, Á., Jouve, N., & de Bustos, A. (2011) · International Journal of Plant Sciences · doi:10.1086/661296 · Cited by 3

Nijmegen Breakage Syndrome

Digweed, M., & Fritz, E. (2003) · CRC Press eBooks · doi:10.1201/9780203911709.ch14 · Cited by 3

Synaptic and Recombination Nodules in Mammals: Structural Continuity with Shifting Protein Composition

Ashley, T. (2007) · Springer eBooks · doi:10.1007/7050_2007_035 · Cited by 3

The Causes of Structural Aberrations

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Chromosomeninstabilitätssyndrome

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DNA Repair, Cancer and Cancer Therapy - The Current State of Art

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MRE11A Gene Mutations Responsible for the Rare Ataxia Telangiectasia-Like Disorder

Alsbeih, G. (2011) · InTech eBooks · doi:10.5772/24560 · Cited by 2

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SYNDROMIC IMMUNODEFICIENCES WITH HUMORAL DEFECTS

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The role of DNA polymerases, in particular DNA polymerase ε in DNA repair and replication

Pospiech, H. (2002) · Cited by 2

A nucleoskeleton network preserves genomic integrity by promoting NHEJ and restraining chromosome translocations

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Spatio-temporal analysis of DNA damage repair using the X-ray microbeam

Schettino, G., Ghita, M., & Prise, K. M. (2010) · The European Physical Journal D · doi:10.1140/epjd/e2010-00076-9 · Cited by 1

Microbeam Radiation Biology

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DNA Repair Defects

Porras, Ó. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405546-9.00007-8 · Cited by 1

DNA stability defects

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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

A large scale genomic screen reveals mechanisms of yeast postreplication repair in Saccharomyces cerevisiae

Ball, L. G. (2011) · University Library - University of Saskatchewan (University of Saskatchewan) · Cited by 1

Ataxia-Telangiectasia

Meyn, M. S. (2003) · CRC Press eBooks · doi:10.1201/9780203911709.ch13 · Cited by 1

Genomic Instability in Fanconi Anaemia and Nijmegen Breakage Syndrome

Digweed, M. (2006) · Springer eBooks · doi:10.1007/7050_013 · Cited by 1

The Cell Biology of Rad54: Implications for homologous recombination

Agarwal, S. (2008) · RePub (Erasmus University Rotterdam)

ATM Deficiency -- A Multifaceted Defect in Lymphocyte Development

Helmink, B. A. (2012) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7k07291

Characterization of human MRE11 and MLH1 interacting domains, and the effects of pathogenic mutations on protein interaction

Vo, A. T. (2003) · Research Exchange (Washington State University)

The cell biology of homologous recombination

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DNA Repair, Cancer and Cancer Therapy

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

DNA Double-Strand Break Repair Through Non-Homologous End-Joining: Recruitment and Assembly of the Players

Kamdar, R. P., & Matsumoto, Y. (2011) · InTech eBooks · doi:10.5772/21262

E2F1 AND TUMOR SUPPRESSION: THE ROLE OF p21, miRNAS, AND THE DNA DAMAGE RESPONSE

Weaks, R. L. (2010) · Digital Commons-TMC (Texas Medical Center)

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

Jalili, E. (2013)

ATM Mediated Signaling Defends the Integrity of the Genome

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Targeting Radiation at the Subcellular, Cellular and Tissue Levels: Future Strategies

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

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Telomere Dysfunction and the DNA Damage Response

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Using Imaging Methods to Interrogate Radiation-Induced Cell Signaling

Shankaran, H., Weber, T. J., von Neubeck, C., & Sowa, M. B. (2012) · Radiation Research · doi:10.1667/rr2669.1

An oncogene-induced DNA replication stress model for human cancer development

Halazonetis, T. D., Zgheib, O., Gorgoulis, V. G., & Bártek, J. (2008) · European Journal of Cancer Supplements · doi:10.1016/s1359-6349(08)71417-4

Functions of the MRE11-RAD50-NBS1 complex in DNA double strand break repair

Konkow, S. (2012) · DuEPublico (University of Duisburg-Essen)

Analysis of DNA Recombination Proteins in DNA Damage Response

Tan, T. (2005) · EUR Research Repository (Erasmus University Rotterdam)

A Microscopic Study of the DNA Damage Response

Dinant, C. (2008) · RePub (Erasmus University Rotterdam)

Structural and functional characterization of the budding yeast Mus81-Mms4 complex

Fu, Y. V. (2003) · University Library - University of Saskatchewan (University of Saskatchewan)

Characterization of the mechanisms of ATM activation by the MRN complex and DNA

Lee, J. H. (2005) · Texas ScholarWorks (Texas Digital Library)

GENOTOXIN-INDUCED ACETYLATION OF THE WERNER SYNDROME PROTEIN (WRN) AND EFFECT ON ITS DNA METABOLIC FUNCTION

Lozada, E., & Santiago, L. (2011) · UKnowledge (University of Kentucky)

REVIEW Cancer Risk and the ATM Gene: a Continuing Debate

Khanna, K. K. (2015)

Commentary BRCA2 and homologous recombination

Orelli, B. J., & Bishop, D. K. (2001)

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)

Nuclear Architecture: Topology and Function of Chromatin- and Non-Chromatin Nuclear Domains

Tashiro, S., Cremer, M., Solovei, I. V., & Cremer, T. (2007) · Springer eBooks · doi:10.1007/978-4-431-30130-1_9

DNA polymerase ε : structure of the human and mouse genes for the catalytic A-subunit, transcriptional regulation of the human gene for the B-subunit, and identification of DNA topoisomerase IIβ binding protein as a partner of DNA polymerase ε

Huang, D. (2000)

Distribution and dynamics of charged particle-induced DNA double-strand breaks

Splinter, J. (2010) · GSI Repository (German Federal Government) · doi:10.26083/tuprints-00002228

Live-cell visualisation of chromatin for the study of radiation-induced chromosome aberrations

Malis, G. (2011) · Brunel University Research Archive (BURA) (Brunel University London)

Genetic Control of the Trigger for the G2/M Checkpoint

Hall, E. J., Smilenov, L. B., & Young, E. F. (2013) · OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) · doi:10.2172/1095188

TECHNICAL ADVANCE Live Cell Imaging of Heavy-Ion-Induced Radiation Responses by Beamline Microscopy

Jakob, B., Rudolph, J. H., Gueven, N., Lavin, M., & Taucher-Scholz, G. (2005)

Interaction of the Mre11/Rad50/Nbs1 (MRN) complex and replication protein A (RPA) in response to DNA damage.

Robison, J. G. (2005) · OhioLink ETD Center (Ohio Library and Information Network)

ELUCIDATION OF FACTORS IMPACTING HOMOLOGOUS RECOMBINATION IN MAMMALIAN MEIOSIS

Cherry, S. M. (2007) · OhioLink ETD Center (Ohio Library and Information Network)

Spatial and Temporal Aspects of Radiation Response in Cell and Tissue Models

Prise, K. M., & Schettino, G. (2011) · Biological and medical physics series · doi:10.1007/978-94-007-2564-5_23

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

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

Comparison of several protocols for the increase in homologous recombination in normal porcine fetal fibroblasts and the application to an actual locus

Zaunbrecher, G. M. (2004) · OakTrust (Texas A&M University Libraries)

The Recognition and Mobility of DNA-Double Strand Breaks

Strecker, J. (2016) · TSpace (University of Toronto)

The Mre11-Rad50-Xrs2 Complex in the DNA Damage Response

Oh, J. (2018) · doi:10.7916/d8sj33hs

Morphological and molecular changes induced in the callus culture of peanut (Arachis hypogaea L.) after γ-irradiation of 137Cs

Hlinková, E., & Bobák, M. (2004) · Journal of Applied Biomedicine · doi:10.32725/jab.2004.012

The Molecular Physiology of Ageing: New Targets for Regenerative Medicine

Macip, S., & Althubiti, M. (2019) · Springer eBooks · doi:10.1007/978-3-030-15458-5_3

Non-targeted effects of ionising radiation. Proceedings of the RISC-RAD specialised training course

Belyakov, O. V. (2008)

The Study of Fork Processing and DSB Repair in Bacteriophage T4: Roles of the MR Complex and Endonuclease VII

Almond, J. R. (2013) · DukeSpace (Duke University)

XRCC1, un élément clef de la réparation des dommages de l'ADN couplée à la réplication

Lévy, N. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique)

Faculty Opinions recommendation of Dynamic formation of RecA filaments at DNA double strand break repair centers in live cells.

Norris, V. (2005) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1027895.335852

An Oncogene-Induced DNA Replication Stress Model for Cancer Development

Halazonetis, T. D. (2009) · Springer eBooks · doi:10.1007/978-90-481-2561-6_3

Managing DNA Strand Breaks in Eukaryotic Cells

Friedberg, E. C., Walker, G. C., Siede, W., Wood, R. D., Schultz, R. A., & Ellenberger, T. E. (2014) · ASM Press eBooks · doi:10.1128/9781555816704.ch19

Diseases Associated with Defective Responses to DNA Strand Breaks

Friedberg, E. C., Walker, G. C., Siede, W., Wood, R. D., Schultz, R. A., & Ellenberger, T. E. (2014) · ASM Press eBooks · doi:10.1128/9781555816704.ch26

Production and Acceleration of Ions

(2007) · Springer eBooks · doi:10.1007/0-387-25586-9_2

Faculty Opinions recommendation of Cancer predisposition and hematopoietic failure in Rad50(S/S) mice.

Jackson, S. P. (2002) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1009247.121957

Supplementary Figure Legends from Evidence for the Direct Binding of Phosphorylated p53 to Sites of DNA Breaks In vivo

Rashid, S. T. A., Dellaire, G., Cuddihy, A. R., Jalali, F., Vaid, M., Coackley, C. L., Folkard, M., Xu, Y., Chen, B. P. C., Chen, D. J., et al. (2023) · doi:10.1158/0008-5472.22364979

Data from Distinct RAD51 Associations with RAD52 and BCCIP in Response to DNA Damage and Replication Stress

Wray, J. W., Liu, J., Nickoloff, J. A., & Shen, Z. (2023) · doi:10.1158/0008-5472.c.6497168.v1

Data from Distinct RAD51 Associations with RAD52 and BCCIP in Response to DNA Damage and Replication Stress

Wray, J. W., Liu, J., Nickoloff, J. A., & Shen, Z. (2023) · doi:10.1158/0008-5472.c.6497168

Réparation des cassures double brin de l'adn chez les mammifères : rôle des protéines MRE11 et BLM dans l’initiation de la ligature d’extrémités non homologues (NHEJ )

Grabarz, A. (2011) · theses.fr (ABES) · doi:10.70675/02d2d5f8z36aaz4d04z9d37z5384351bf9cf

Recombinaison homologue protège contre les défauts de la mitose et la ségrégation des chromosomes déséquilibre causé par le stress de réplication spontanée

Wilhelm, T. (2011) · theses.fr (ABES) · doi:10.70675/8f8f5907z32edz4a84zb3c8zc042507f5b0d

Rôle du complexe de cohésion sur la ligature d'extrémités d'ADN non homologues et la stabilité du génome

Gelot, C. (2014) · theses.fr (ABES) · doi:10.70675/e3a4a46bzed37z4f21zb647z0313e5cd5811

Etude de la réparation des cassures double-brin de l'ADN dans les cellules souches du muscle squelettique et leurs progéniteurs

Ferdousi, L. V. (2014) · theses.fr (ABES) · doi:10.70675/9d73199ez7949z4602zadcfz6763e4bdd1b0

Role of Poly-(ADP-ribose)-ylation signaling pathway in the chromatin remodeling after DNA damage

Sellou, H. (2016) · theses.fr (ABES) · doi:10.70675/c2e900e6zb02ez4a12zb3fazc621be99e611

Multiscale analysis of poly-ADP-ribosylation dependent chromatin remodeling mechanisms at DNA breaks

Lebeaupin, T. (2017) · theses.fr (ABES) · doi:10.70675/e61e4cf3z6af7z4766z8412zde6fc6de0dbe

Gene editing approaches of microsatellite disorders : shortening expanded repeats

Poggi, L. (2020) · theses.fr (ABES) · doi:10.70675/741f0470z28a0z4c3bz9e75ze578bdc49074 · Cited by 1

Factors That Affect Chromosomal Translocations in Cells

Canoy, R. J. (2021) · theses.fr (ABES) · doi:10.70675/9f331f7az9151z4c95zbf47zbc6ed65a5896

Mécanismes de réparations d’une cassure double-brin et résection au sein d’un microsatellite humain

Vaysse-Zinkhöfer, W. (2021) · theses.fr (ABES) · doi:10.70675/315e7956zf006z4518z99adz6282679fa7af

Factors that contribute to B cell oncogenesis in people living with HIV

Shmakova, A. (2023) · theses.fr (ABES) · doi:10.70675/1d51b9d6z9a12z41f9z8f98z0c7f955aeb54

Epigenomic and 3D-genomic changes in Mantle Cell Lymphoma

Karpukhina, A. A. (2024) · theses.fr (ABES) · doi:10.70675/07b193edz7113z43b1z8a89zf8e13bc9f359

The interaction of CtIP with DNA damage response proteins

Abramowiçz, I. (2010) · University of Birmingham Institutional Research Archive (University of Birmingham)

Conserved genetic programs in insect and mammalian brain development

(1999) · doi:10.1002/(sici)1521-1878(199908)21:8

hMre11 and hRad50 Nuclear Foci Are Induced During the Normal Cellular Response to DNA Double-Strand Breaks †

Maser, R. S., Monsen, K. J., Nelms, B. E., & Petrini, J. H. J. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.10.6087 · Cited by 499

Dynamics of DNA-repair factors and chromosomes studied by laser-UVA-microirradiation and laser-photobleaching

Walter, J. K. (2003) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.1458

In situ visualization of ultraviolet-light-induced DNA damage repair in locally irradiated human fibroblasts

Katsumi, S., Kobayashi, N., Imoto, K., Nakagawa, A., Yamashina, Y., Muramatsu, T., Shirai, T., Miyagawa, S., Sugiura, S., Hanaoka, F., et al. (2001) · Journal of Investigative Dermatology · doi:10.1046/j.0022-202x.2001.01540.x · Cited by 119

Rad51 Accumulation at Sites of DNA Damage and in

Chromatin, P., Tashiro, S., Walter, J., Shinohara, A., Kamada, N., & Cremer, T. (2000)

Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage

Raderschall, E., Golub, E. I., & Haaf, T. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.1921 · Cited by 350