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

A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1

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Lessons from hereditary colorectal cancer

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A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

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

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Enhanced Phosphorylation of p53 by ATM in Response to DNA Damage

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Association of BRCA1 with Rad51 in Mitotic and Meiotic Cells

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The Bloom's syndrome gene product is homologous to RecQ helicases

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BRCA1 mutations in primary breast and ovarian carcinomas.

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Linkage of ATM to Cell Cycle Regulation by the Chk2 Protein Kinase

Matsuoka, S. (1998) · Science · doi:10.1126/science.282.5395.1893 · Cited by 1,322

The RXFP3 receptor is functionally associated with cellular responses to oxidative stress and DNA damage

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Polyploidization and Cancer

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MSH2 role in BRCA1-driven tumorigenesis: A preliminary study in yeast and in human tumors from BRCA1-VUS carriers

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Boosted Network Classifiers for Local Feature Selection

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Tailoring heated intraperitoneal mitomycin C for peritoneal metastases originating from colorectal carcinoma: a translational approach to improve survival

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DNA Transcription and Repair: A Confluence

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What is wrong with Fanconi anemia cells?

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Mismatch repair dependence of replication stress-associated DSB recognition and repair

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AURKA overexpression accompanies dysregulation of DNA-damage response genes in invasive urothelial cell carcinoma

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Interactions between BRCA Proteins and DNA Structure

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The tumor suppressor activity induced by adenovirus-mediated BRCA1 overexpression is not restricted to breast cancers

Marot, D., Opolon, P., Brailly‐Tabard, S., Elie, N., Randrianarison-Huetz, V., Connault, E., Foray, N., Feunteun, J., & Perricaudet, M. (2005) · Gene Therapy · doi:10.1038/sj.gt.3302637 · Cited by 16

Differing Responses of Nijmegen Breakage Syndrome and Ataxia Telangiectasia Cells to Ionizing Radiation

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Salivary Biomarkers in Breast Cancer: From Salivaomics to Salivaoncoomics

Bel’skaya, L. V., & Dyachenko, E. I. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2907253 · Cited by 16

Nuclear matrix contains novel WD‐repeat and disordered‐region‐rich proteins

Ishii, K., Hirano, Y., Araki, N., Oda, T., Kumeta, M., Takeyasu, K., Furukawa, K., & Horigome, T. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.09.019 · Cited by 15

BRCA1 requirement for the fidelity of plasmid DNA double‐strand break repair in cultured breast epithelial cells

Thompson, E. G., Fares, H., & Dixon, K. (2011) · Environmental and Molecular Mutagenesis · doi:10.1002/em.21674 · Cited by 15

Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells

Björkman, A., Qvist, P., Du, L., Bartish, M., Zaravinos, A., Georgiou, K. E., Børglum, A. D., Gatti, R. A., Törngren, T., & Pan‐Hammarström, Q. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418947112 · Cited by 15

Genomic destabilization and its associated mutagenesis increase with senescence‐associated phenotype expression

Yoshioka, K., & Matsuno, Y. (2020) · Cancer Science · doi:10.1111/cas.14746 · Cited by 15

BRCA1 5083del19 Mutant Allele Selectively Up-Regulates Periostin Expression In vitro and In vivo

Quaresima, B., Romeo, F., Faniello, M. C., Sanzo, M. D., Liu, C., Lavecchia, A. M., Taccioli, C., Gaudio, E., Baudi, F., Trapasso, F., et al. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-5208 · Cited by 15

DNA damage checkpoints in nasopharyngeal carcinoma

Poon, R. Y. C. (2014) · Oral Oncology · doi:10.1016/j.oraloncology.2014.01.009 · Cited by 15

Does breast carcinoma belong to the Lynch syndrome tumor spectrum? – Somatic mutational profiles vs. ovarian and colorectal carcinomas

Porkka, N., Olkinuora, A. P., Kuopio, T., Ahtiainen, M., Eldfors, S., Almusa, H., Mecklin, J., & Peltomäki, P. (2020) · Oncotarget · doi:10.18632/oncotarget.27538 · Cited by 15

Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

Bogdanova, N. V., Togo, A. V., Ratajska, M., Kluźniak, W., Takhirova, Z., Tarp, T., Prokofyeva, D. S., Bermisheva, M., Yanus, G. A., Gorodnova, T. V., et al. (2014) · Familial Cancer · doi:10.1007/s10689-014-9748-x · Cited by 15

Genetically determined subdivision of human populations with respect to the risk of breast cancer in women

Va, T., Aslanyan, M. M., Tsyrendorzhiyeva, E. S., Litvinov, S., Гарькавцева, Р. Ф., & Altukhov, Y. P. (2006) · Doklady Biological Sciences · doi:10.1134/s0012496606010182 · Cited by 15

Analysis of the DNA Binding Activity of BRCA1 and Its Modulation by the Tumour Suppressor p53

Naseem, R., & Webb, M. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002336 · Cited by 15

Highlight: BRCA1 and BRCA2 proteins in breast cancer

Daniel, D. C. (2002) · Microscopy Research and Technique · doi:10.1002/jemt.10178 · Cited by 15

RecQ helicases and topoisomerase III in cancer and aging

Laursen, L. V., Bjergbæk, L., Murray, J. M., & Andersen, A. H. (2003) · Biogerontology · doi:10.1023/a:1026218513772 · Cited by 15

The FHA Domain, a Phosphoamino Acid Binding Domain Involved in the DNA Damage Response PathwayPreprint

Huang, M., & Elledge, S. J. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.413 · Cited by 15

Pooling-analysis on hMLH1 polymorphisms and cancer risk: evidence based on 31,484 cancer cases and 45,494 cancer-free controls

Li, S., Zheng, Y., Tian, T., Wang, M., Liu, X., Liu, K., Zhai, Y., Dai, C., Deng, Y., Li, S., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.21810 · Cited by 14

Monopolar Spindle 1 (MPS1) Protein-dependent Phosphorylation of RecQ-mediated Genome Instability Protein 2 (RMI2) at Serine 112 Is Essential for BLM-Topo III α-RMI1-RMI2 (BTR) Protein Complex Function upon Spindle Assembly Checkpoint (SAC) Activation during Mitosis

Pradhan, A., Singh, T. R., Ali, A. M., Wahengbam, K., & Meetei, A. R. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.470823 · Cited by 14

Impact of α-Targeted Radiation Therapy on Gene Expression in a Pre-Clinical Model for Disseminated Peritoneal Disease when Combined with Paclitaxel

Yong, K. J., Milenic, D. E., Baidoo, K. E., & Brechbiel, M. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108511 · Cited by 14

ATM Paradoxically Promotes Oncogenic Transformation via Transcriptional Reprogramming

Liu, X., Hu, M., Liu, P., Jiao, M., Zhou, M., Lee, A. K., Li, F., & Li, C. (2020) · Cancer Research · doi:10.1158/0008-5472.can-19-2255 · Cited by 14

Alteration of the fragile histidine triad gene in intrahepatic cholangiocarcinoma

Koch, E., Fiedler, W., Tannapfel, A., & Ballhausen, W. G. (2003) · European Journal of Gastroenterology & Hepatology · doi:10.1097/00042737-200308000-00012 · Cited by 14

The MRE11/RAD50/NBS1 complex destabilization in Lynch-syndrome patients

Alemayehu, A., & Fridrichová, I. (2007) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201858 · Cited by 14

Cell Killing Mechanisms and Impact on Gene Expression by Gemcitabine and 212Pb-Trastuzumab Treatment in a Disseminated i.p. Tumor Model

Yong, K. J., Milenic, D. E., Baidoo, K. E., & Brechbiel, M. W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159904 · Cited by 14

HERC2 inactivation abrogates nucleolar localization of RecQ helicases BLM and WRN

Zhu, M., Wu, W., Togashi, Y., Liang, W., Miyoshi, Y., & Ohta, T. (2021) · Scientific Reports · doi:10.1038/s41598-020-79715-y · Cited by 14

Haplotypic variation inMRE11,RAD50 and NBS1and risk of non-Hodgkin's lymphoma

Rollinson, S. J., Kesby, H., & Morgan, G. J. (2006) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428190600909743 · Cited by 14

Radiation clastogenesis and cell cycle checkpoint function as functional markers of breast cancer risk

Kaufmann, W. K., Filatov, L. V., Oglesbee, S. E., Simpson, D. A., Lotano, M. A., McKeen, H. D., Sawyer, L., Moore, D. T., Millikan, R. C., Cordeiro‐Stone, M., et al. (2006) · Carcinogenesis · doi:10.1093/carcin/bgl103 · Cited by 14

No MSH6 germline mutations in breast cancer families with colorectal and/or endometrial cancer

Vahteristo, P., Ojala, S., Tamminen, A., Tommiska, J., Sammalkorpi, H., Kiuru-Kuhlefelt, S., Eerola, H., Aaltonen, L. A., Aittomäki, K., & Nevanlinna, H. A. (2005) · Journal of Medical Genetics · doi:10.1136/jmg.2004.022327 · Cited by 15

DNA Damage Response Pathways and Cancer

Ford, J. M., & Kastan, M. B. (2014) · Elsevier eBooks · doi:10.1016/b978-1-4557-2865-7.00010-2 · Cited by 14

Connecting Fanconi anemia to BRCA1

Joenje, H., & Arwert, F. (2001) · Nature Medicine · doi:10.1038/86458 · Cited by 14

Dynamics of DNA repair suggested by the subcellular localization of Brca1 and Brca2 proteins

Huber, L. J., & Chodosh, L. A. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20517 · Cited by 14

Associations between NBS1 Polymorphisms and Colorectal Cancer in Chinese Population

Li, J.-T., Zhong, B., Xu, H., Qiao, S.-Y., Wang, G., Huang, J., Fan, H., & Zhao, H.-C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132332 · Cited by 13

A New Rapid Methodological Strategy to Assess BRCA Mutational Status

Vuttariello, E., Borra, M., Calise, C., Mauriello, E., Greggi, S., Vecchione, A., Biffali, E., & Chiappetta, G. (2013) · Molecular Biotechnology · doi:10.1007/s12033-012-9646-0 · Cited by 13

What's Your Poison? Impact of Individual Repair Capacity on the Outcomes of Genotoxic Therapies in Cancer. Part I—Role of Individual Repair Capacity in the Constitution of Risk for Late-Onset Multifactorial Disease

Petkova, R., Chelenkova, P., Georgieva, E., & Chakarov, S. (2013) · Biotechnology & Biotechnological Equipment · doi:10.5504/bbeq.2013.0097 · Cited by 13

DNA Topoisomerase III Alpha Regulates p53-Mediated Tumor Suppression

Hsieh, M., Fan, J.-R., Chang, H., Chen, H.-C., Shen, T., Teng, S., Yeh, Y.-H., & Li, T. (2014) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-13-1997 · Cited by 13

A Rad53 Independent Function of Rad9 Becomes Crucial for Genome Maintenance in the Absence of the RecQ Helicase Sgs1

Nielsen, I., Bentsen, I. B., Andersen, A. H., Gasser, S. M., & Bjergbæk, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081015 · Cited by 13

The fellowship of the RING: BRCA1, its partner BARD1 and their liaison in DNA repair and cancer

Russi, M., Marson, D., Fermeglia, A., Aulić, S., Fermeglia, M., Laurini, E., & Pricl, S. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.108009 · Cited by 14

A Conditional Mouse Model for Measuring the Frequency of Homologous Recombination Events In Vivo in the Absence of Essential Genes

Brown, A., Claybon, A. B., & Bishop, A. J. R. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.00848-10 · Cited by 13

The role of BRCA1 in non-small cell lung cancer

Gachechiladze, M. A., & Škarda, J. (2012) · Biomedical Papers · doi:10.5507/bp.2012.049 · Cited by 13

BRCA1 involvement in toxicological responses and human cancer etiology

Georgakilas, A. G., Aziz, K., Ziech, D., Georgakila, S., & Panayiotidis, M. I. (2009) · Toxicology Letters · doi:10.1016/j.toxlet.2009.04.006 · Cited by 13

Molecular Oncology of Breast Cancer

Ioan, A.-M., Klobocista, M. M., Shirazi, S., & Press, M. F. (2009) · Elsevier eBooks · doi:10.1016/b978-1-4160-5221-0.00028-0 · Cited by 13

Response to environmental carcinogens in DNA-repair-deficient disorders

Digweed, M. (2003) · Toxicology · doi:10.1016/s0300-483x(03)00292-0 · Cited by 14

A Novel BRCA2-Binding Protein and Breast and Ovarian Tumorigenesis

King, M. (2004) · New England Journal of Medicine · doi:10.1056/nejmcibr033528 · Cited by 13

BRCA proteins AND DNA damage checkpoints

Chen, J. (2003) · Frontiers in bioscience · doi:10.2741/1127 · Cited by 13

Breast Cancer Susceptibility Genes

Apostolou, P., Vratimos, A., & Fostira, F. (2015) · Wiley eBooks · doi:10.1002/9780470015902.a0025847 · Cited by 13

Biological Responses to DNA Damage: A Perspective in the New MillenniumPreprint

Friedberg, E. C. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.593 · Cited by 13

Protein-DNA Interactions

Pandey, P., Hasnain, S., & Ahmad, S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809633-8.20217-3 · Cited by 13

Crunch: integrated processing and modeling of ChIP-seq data in terms of regulatory motifsPreprint

Berger, S., Omidi, S., Pachkov, M., Arnold, P., Kelley, N. W., Salatino, S., & van Nimwegen, E. (2019) · Genome Research · doi:10.1101/gr.239319.118 · Cited by 13

BLM’s balancing act and the involvement of FANCJ in DNA repair

Dhar, S., & Brosh, R. M. (2018) · Cell Cycle · doi:10.1080/15384101.2018.1520567 · Cited by 13

Human Immunodeficiency Virus Type 1 Vpr Mediates Degradation of APC1, a Scaffolding Component of the Anaphase-Promoting Complex/Cyclosome

Barbosa, J. A. F., Sparapani, S., Boulais, J., Lodge, R., & Cohen, É. A. (2021) · Journal of Virology · doi:10.1128/jvi.00971-20 · Cited by 13

Integrative analysis and prediction of human R-loop binding proteins

Fournier, L.-A., Kumar, A., Smith, T., Su, E., Moksa, M., Hirst, M., & Stirling, P. C. (2022) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkac142 · Cited by 12

TRIP13 Participates in Immediate-Early Sensing of DNA Strand Breaks and ATM Signaling Amplification through MRE11

Jeong, H., Wie, M., Baek, I., Sohn, G., Um, S.-H., Lee, S., Seo, Y., Ra, J., Lee, E. A., Kim, S., et al. (2022) · Cells · doi:10.3390/cells11244095 · Cited by 12

Genetic variations in the homologous recombination repair pathway genes modify risk of glioma

Zhang, H., Liu, Y., Zhou, K., Zhou, C., Zhou, R., Cheng, C., Wei, Q., Li, J., & Zhou, L. (2015) · Journal of Neuro-Oncology · doi:10.1007/s11060-015-1892-0 · Cited by 12

Msh2 Deficiency Attenuates But Does Not Abolish Thiopurine Hematopoietic Toxicity in Msh2-- Mice

Krynetskaia, N. F., Brenner, T. L., Krynetski, E. Y., Du, W., Panetta, J. C., Pui, C., & Evans, W. E. (2003) · Molecular Pharmacology · doi:10.1124/mol.64.2.456 · Cited by 12

BRCA1 alterations are associated with endometriosis, but BRCA2 alterations show no detectable endometriosis risk: a study in Indian population

Govatati, S., Challa, K., Reddy, S. B., Pramod, K., Deenadayal, M., Chakravarty, B., Shivaji, S., & Bhanoori, M. (2014) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-014-0379-9 · Cited by 12

Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation

Uribe-Bojanini, E., Hernandez-Quiceno, S., & Cock-Rada, A. M. (2017) · Case Reports in Medicine · doi:10.1155/2017/7162737 · Cited by 12

Induced in vivo knockdown of the Brca1 gene in skeletal muscle results in skeletal muscle weakness

Tarpey, M. D., Valencia, A. P., Jackson, K. C., Amorese, A. J., Balestrieri, N. P., Renegar, R. H., Pratt, S. J. P., RYAN, T. E., McClung, J. M., Lovering, R. M., et al. (2018) · The Journal of Physiology · doi:10.1113/jp276863 · Cited by 12

Missense mutations of BRCA1 gene affect the binding with p53 both in vitro and in vivo

Quaresima, B., Faniello, M. C., Baudi, F., Crugliano, T., Sanzo, M. D., Cuda, G., Costanzo, F. S., & Venuta, S. (2006) · Oncology Reports · doi:10.3892/or.16.4.811 · Cited by 12

Downregulation of BRCA1 in A375 Melanoma Cell Line Increases Radio-Sensitivity and Modifies Metastatic and Angiogenic Gene Expression

Hesling, C., D'Incan, M., Souteyrand, P., Monboisse, J., Brassart‐Pasco, S., D'Incan, C., Madelmont, J., & Bignon, Y. J. (2004) · Journal of Investigative Dermatology · doi:10.1046/j.0022-202x.2004.22212.x · Cited by 12

Crosstalk between the DNA damage response, histone modifications and neovascularisation

Vassilopoulos, A., Deng, C., & Chavakis, T. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.11.020 · Cited by 12

Proteomic Characterization of Cerebrospinal Fluid from Ataxia-Telangiectasia (A-T) Patients Using a LC/MS-Based Label-Free Protein Quantification Technology

Dzieciątkowska, M., Qi, G. D., You, J., Bemis, K. G., Sahm, H., Lederman, H. M., Crawford, T. O., Gelbert, L. M., Rothblum‐Oviatt, C., & Wang, M. (2011) · International Journal of Proteomics · doi:10.1155/2011/578903 · Cited by 12

Deficiency of the DNA repair protein nibrin increases the basal but not the radiation induced mutation frequency in vivo

Wessendorf, P., Vijg, J., Nussenzweig, A., & Digweed, M. (2014) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2014.07.001 · Cited by 12

hSSB1 associates with and promotes stability of the BLM helicase

Croft, L. V., Ashton, N. W., Paquet, N., Bolderson, E., O'Byrne, K. J., & Richard, D. J. (2017) · BMC Molecular Biology · doi:10.1186/s12867-017-0090-3 · Cited by 12

DNA repair helicases: from mechanistic understanding to therapeutic implications

Menon, V., & Gueble, S. E. (2025) · NAR Cancer · doi:10.1093/narcan/zcaf034 · Cited by 12

Identification of proteins associated with Aha1 in HeLa cells by quantitative proteomics

Sun, L., Hartson, S. D., & Matts, R. L. (2015) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2015.01.002 · Cited by 11

BRCA1-BRCTMutations Alter the Subcellular Localization of BRCA1In Vitro

Drikos, I. G., Boutou, E., Kastritis, P. L., & Vorgias, C. E. (2021) · Anticancer Research · doi:10.21873/anticanres.15077 · Cited by 15

Computational structural assessment of BReast CAncer type 1 susceptibility protein (BRCA1) and BRCA1-Associated Ring Domain protein 1 (BARD1) mutations on the protein-protein interface

Kumar, D. T., Kumar, S. U., Jain, N., Sowmya, B., Balsekar, K., Siva, R., Kamaraj, B., Sidenna, M., Doss, C. G. P., & Zayed, H. (2022) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2022.02.003 · Cited by 11

Causal Link between Microsatellite Instability and hMRE11 Dysfunction in Human Cancers

Wu, X., Yang, X., Chai, W., & Her, C. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-11-0322 · Cited by 11

The Hsp90 inhibitor SNX-7081 is synergistic with fludarabine nucleoside via DNA damage and repair mechanisms in human, p53-negative chronic lymphocytic leukemia

Alexander, K. L., Jenkins, Y., Alomari, M., Mirzaei, M., Best, G., Pascovici, D., Mactier, S., Mulligan, S. P., Haynes, P. A., & Christopherson, R. I. (2015) · Oncotarget · doi:10.18632/oncotarget.5715 · Cited by 11

The Aspergillus nidulans musN Gene Encodes a RecQ Helicase That Interacts With the PI-3K-Related Kinase UVSB

Hofmann, A. F., & Harris, S. D. (2001) · Genetics · doi:10.1093/genetics/159.4.1595 · Cited by 11

An Antisense Construct of Full-Length HumanRAD50cDNA Confers Sensitivity to Ionizing Radiation and Alkylating Agents on Human Cell Lines

Kim, Y. C., Koh, J. T., Shin, B. A., Ahn, K. Y., Choi, B. K., Kim, C. G., & Kim, K. K. (2002) · Radiation Research · doi:10.1667/0033-7587(2002)157[0019:aacofl]2.0.co;2 · Cited by 11

Genomic Instability and DNA Repair

Kohn, K. W., & Bohr, V. A. (2005) · Wiley eBooks · doi:10.1002/0470025077.chap07 · Cited by 11

Analysis of the Fission Yeast Checkpoint Rad ProteinsPreprint

Caspari, T., Davies, C., & Carr, A. M. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.451 · Cited by 11

Multiple functions of the ALT favorite helicase, BLM

Chang, S., Jiang, T., Bao, R., Zhang, Y., Tong, J., Jia, T., Liu, J., Dan, J., & Jia, S. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01372-3 · Cited by 10

Functional assessment of intrinsic disorder central domains of BRCA1

Yadav, L. R., Rai, S., Hosur, M. V., & Varma, A. K. (2015) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2014.1000973 · Cited by 10

Identification of novel potential homologous repair deficiency-associated genes in pancreatic adenocarcinoma via WGCNA coexpression network analysis and machine learning

Liu, C., Fang, J., Kang, W., Yang, Y., Yu, C., Chen, H., Zhang, Y., & Ouyang, H. (2023) · Cell Cycle · doi:10.1080/15384101.2023.2293594 · Cited by 10

Assessment of Anti-recombination and Double-strand Break-induced Gene Conversion in Human Cells by a Chromosomal Reporter

Xu, K., Wu, X., Tompkins, J. D., & Her, C. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.352302 · Cited by 11

Critical Interaction Domains between Bloom Syndrome Protein and RAD51

Bergeron, K. L., Murphy, E. L., Brown, L. W., & Almeida, K. H. (2010) · The Protein Journal · doi:10.1007/s10930-010-9295-8 · Cited by 10

Determination of Molecular Markers for BRCA1 and BRCA2 Heterozygosity Using Gene Expression Profiling

Salmon, A. Y., Salmon‐Divon, M., Zahavi, T., Barash, Y., Levy‐Drummer, R. S., Jacob‐Hirsch, J., & Peretz, T. (2013) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-12-0105 · Cited by 10

Intrachromosomal recombination between highly diverged DNA sequences is enabled in human cells deficient in Bloom helicase

Wang, Y., Shen, L., Smith, K., Waldman, B. C., & Waldman, A. S. (2016) · DNA repair · doi:10.1016/j.dnarep.2016.03.005 · Cited by 10

Radiosensitivity is predicted by DNA end-binding complex density, but not by nuclear levels of band components

Ismail, S. M., Buchholz, T. A., Story, M. D., Brock, W. A., & Stevens, C. W. (2004) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2004.07.003 · Cited by 10

MLH1 Polymorphisms and Cancer risk: a Meta-analysis Based on 33 Case-control Studies

Xu, J., Yin, Z., Huang, M., Wang, X., Gao, W., Liu, L., Wang, R., Huang, P.-W., Yin, Y., Liu, P., et al. (2012) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2012.13.3.901 · Cited by 10

Proteomic Analysis of Human Angiogenin Interactions Reveals Cytoplasmic PCNA as a Putative Binding Partner

Chatzileontiadou, D. S. M., Samiotaki, M. K., Alexopoulou, A. N., Cotsiki, M., Panayotou, G., Stamatiadi, M., Balatsos, N. A. A., Leonidas, D. D., & Kontou, M. (2017) · Journal of Proteome Research · doi:10.1021/acs.jproteome.7b00335 · Cited by 10

Role of BRCA1 and BRCA2 gene mutations in epithelial ovarian cancer in Indian population: a pilot study.

Sharma, S., Rajaram, S., Sharma, T., Goel, N., Agarwal, S., & Banerjee, B. D. (2014) · Europe PMC (PubMed Central) · Cited by 10

Mechanisms of topoisomerase I inhibition by anticancer drugs

Pommier, Y. G., Barceló, J. M., Furuta, T., Takemura, H., & Sordet, O. (2003) · Springer eBooks · doi:10.1007/978-1-4615-0141-1_2 · Cited by 10

Function of RECQ family helicase in genome stability

Seki, M., Tada, S., & Enomoto, T. (2006) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-1-4020-4896-8_5 · Cited by 10

BRCA1-associated complexes: new targets to overcome breast cancer radiation resistance

Chen, X., Arciero, C. A., & Godwin, A. K. (2006) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.6.2.187 · Cited by 10

Mechanisms of Repair of Interstrand Crosslinks in DNA

Legerski, R. J., & Richie, C. T. (2002) · Cancer treatment and research · doi:10.1007/978-1-4615-1173-1_6 · Cited by 10

TOWARD MAINTAINING THE GENOME

Nyberg, K. A., Michelson, R. J., Putnam, C. W., & Weinert, T. A. (2002) · Cited by 10

BRCA1 and BRCA2 in DNA Repair and Genome Stability

Brenneman, M. A. (2001) · Humana Press eBooks · doi:10.1007/978-1-59259-095-7_10 · Cited by 10

FBP1 Is an Interacting Partner of Menin

Zaman, S., Sukhodolets, K. E., Wang, P., Qin, J., Levens, D., Agarwal, S. K., & Marx, S. J. (2014) · International Journal of Endocrinology · doi:10.1155/2014/535401 · Cited by 9

BASC (BRCA1‐associated genome surveillance complex)

(2008) · Springer eBooks · doi:10.1007/978-1-4020-6754-9_1584

Coordination of BRCA1/BARD1- and MRE11/RAD50/NBS1-dependent DNA Transactions in Breast Tumor Suppression

Gautier, J., & Greene, E. C. (2009) · doi:10.21236/ada519536

Factors forming the BRCA1-A complex orchestrate BRCA1 recruitment to the sites of DNA damage

Her, J., Lee, N. S., Kim, Y., & Kim, H. (2016) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmw047 · Cited by 43

Вовлеченность генов белков BRСA1-ассоциированного комплекса наблюдения за геномом (BASC) в развитие многофакторной патологии

Бабушкина, Н. П., Postrigan, A. E., & Николаевна, К. А. (2021) · Molecular Biology · doi:10.31857/s0026898421020038 · Cited by 7

Evaluation of BRCA1 related DNA repair genes in breast and ovarian carcinogenesis

MARESCA, L. (2017) · Electronic Theses and Dissertations Repository (University of Pisa)