A superfamily of conserved domains in DNA damage‐ responsive cell cycle checkpoint proteins

The nuclear protein PH5P of the inter‐α‐inhibitor superfamily: a missing link between poly(ADP‐ribose)polymerase and the inter‐α‐inhibitor family and a novel actor of DNA repair?

Jean, L., Risler, J., Nagase, T., Coulouarn, C., Nomura, N., & Salier, J. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)00173-8 · Cited by 18

The Knowns Unknowns: Exploring the Homologous Recombination Repair Pathway in Toxoplasma gondii

Fenoy, I. M., Bogado, S. S., Contreras, M., Gottifredi, V., & Angel, S. O. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00627 · Cited by 15

Computational Prediction of Protein Complexes from Protein Interaction Networks

Srihari, S., Yong, C. H., & Wong, L. (2017) · doi:10.1145/3064650 · Cited by 17

Expression pattern of p53-binding protein 1 as a new molecular indicator of genomic instability in bladder urothelial carcinoma

Matsuda, K., Kawasaki, T., Akazawa, Y., Hasegawa, Y., Kondo, H., Suzuki, K., Iseki, M., & Nakashima, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-33761-9 · Cited by 17

Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin

Ghani, M., Robinson, P. N., Morlot, S., Mitter, D., Trimborn, M., Albrecht, B. E., Varon, R., Sperling, K., & Neitzel, H. (2012) · Molecular Syndromology · doi:10.1159/000338975 · Cited by 17

BRIT1 regulates p53 stability and functions as a tumor suppressor in breast cancer

Zhang, B., Wang, E., Dai, H., Hu, R., Liang, Y., Li, K., Wang, G., Peng, G., & Lin, S. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt190 · Cited by 17

Identification of TopBP1 as a c-Abl-interacting Protein and a Repressor for c-Abl Expression

Zeng, L., Hu, Y., & Li, B. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503016200 · Cited by 17

Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer

Zuhlke, K. A., Johnson, A., Okoth, L. A., Stoffel, E. M., Robbins, C. M., Tembe, W. A., Salinas, C. A., Zheng, S.-S., Xu, J., Carpten, J. D., et al. (2012) · Familial Cancer · doi:10.1007/s10689-012-9555-1 · Cited by 16

Role of Rap1 in DNA damage response: implications in stem cell homeostasis and cancer

Khattar, E., & Tergaonkar, V. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.08.009 · Cited by 16

Dictyostelium nucleomorphin is a member of the BRCT-domain family of cell cycle checkpoint proteins

Myre, M. A., & O’Day, D. H. (2004) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2004.08.002 · Cited by 16

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

Solution Structure of the Carboxyl-Terminal Domain of RAP74 and NMR Characterization of the FCP1-Binding Sites of RAP74 and Human TFIIB,

Nguyen, B. D., Chen, H., Kobor, M. S., Greenblatt, J. F., Legault, P., & Omichinski, J. G. (2003) · Biochemistry · doi:10.1021/bi0265473 · Cited by 16

Genome sequences: Genome sequence of a model prokaryote

Koonin, E. V. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00328-9 · Cited by 16

Interactions of the HIV-1 Tat and RAP74 Proteins with the RNA Polymerase II CTD Phosphatase FCP1

Abbott, K. L., Archambault, J., Xiao, H., Nguyen, B. D., Roeder, R. G., Greenblatt, J., Omichinski, J. G., & Legault, P. (2005) · Biochemistry · doi:10.1021/bi047957p · Cited by 16

Functional deficiency of NBN, the Nijmegen breakage syndrome protein, in a p.R215W mutant breast cancer cell line

Schröder‐Heurich, B., Bogdanova, N. V., Wieland, B., Xie, X., Noskowicz, M., Park‐Simon, T., Hillemanns, P., Christiansen, H., & Dörk, T. (2014) · BMC Cancer · doi:10.1186/1471-2407-14-434 · Cited by 15

Kaposi’s sarcoma-associated herpesvirus processivity factor (PF-8) recruits cellular E3 ubiquitin ligase CHFR to promote PARP1 degradation and lytic replication

Chung, W.-C., Lee, S., Kim, Y., Seo, J. B., & Song, M. J. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009261 · Cited by 16

PES1 regulates sensitivity of colorectal cancer cells to anticancer drugs

Xie, W., Qu, L., Meng, L., Liu, C., Wu, J. L., & Shou, C. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.12.145 · Cited by 16

Boundaries and physical characterization of a new domain shared between mammalian 53BP1 and yeast Rad9 checkpoint proteins

Alpha‐Bazin, B., Lorphelin, A., Nozerand, N., Charier, G., Marchetti, C., Bérenguer, F., Couprie, J., Gilquin, B., Zinn‐Justin, S., & Quéméneur, É. (2005) · Protein Science · doi:10.1110/ps.041305205 · Cited by 15

Germline alterations in the 53BP1 gene in breast and ovarian cancer families

Rapakko, K., Heikkinen, K., Karppinen, S., Erkko, H., & Winqvist, R. (2006) · Cancer Letters · doi:10.1016/j.canlet.2006.01.021 · Cited by 15

Multi-BRCT scaffolds use distinct strategies to support genome maintenance

Wan, B., Hang, L. E., & Zhao, X. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1218102 · Cited by 14

The Schizosaccharomyces pombe cfr1+ gene participates in mating through a new pathway that is independent of fus1+

Cartagena‐Lirola, H., Durán, Á., & Valdivieso, M. ‐. (2006) · Yeast · doi:10.1002/yea.1361 · Cited by 15

Hymenoic acid, a novel specific inhibitor of human DNA polymerase λ from a fungus of Hymenochaetaceae sp.

Nishida, M., Ida, N., Horio, M., Takeuchi, T., Kamisuki, S., Murata, H., Kuramochi, K., Sugawara, F., Yoshida, H., & Mizushina, Y. (2008) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2008.03.021 · Cited by 15

Sequential, Structural, and Phylogenetic Study of BRCT Module in Plants

Singh, S. K., Choudhury, S. R., Roy, S., & Sengupta, D. N. (2008) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2008.10507239 · 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

Discovery and Validation of Lmj_04_BRCT Domain, a Novel Therapeutic Target: Identification of Candidate Drugs for Leishmaniasis

Guerrero, J. P., Fernández-Rubio, C., Burguete-Mikeo, A., El-Dirany, R., García‐Sosa, A. T., & Nguewa, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910493 · Cited by 14

Analysis of BRCT5 domain-containing proteins reveals a new component of DNA damage repair in Arabidopsis

Vladejić, J., Yang, F., Tomaštíková, E. D., Doležel, J., Palecek, J. J., & Pečinka, A. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1023358 · Cited by 13

Linking up and interacting with BRCT domains

Watts, F. Z., & Brissett, N. C. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.10.010 · Cited by 14

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

Role of multifunctional transcription factor TFII-I and putative tumour suppressor DBC1 in cell cycle and DNA double strand damage repair

Tanikawa, M., Wada‐Hiraike, O., Yoshizawa-Sugata, N., Shirane, A., Hirano, M., Hiraike, H., Miyamoto, Y., Sone, K., Ikeda, Y., Kashiyama, T., et al. (2013) · British Journal of Cancer · doi:10.1038/bjc.2013.532 · Cited by 14

Rtt107 BRCT domains act as a targeting module in the DNA damage response

Leung, G. P., Brown, J. A. R., Glover, J. N. M., & Kobor, M. S. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.10.007 · Cited by 14

Mutational Analyses of Aquifex pyrophilus DNA Ligase Define Essential Domains for Self-Adenylation and DNA Binding Activity

Lim, J. H., Choi, J., Kim, W., Ahn, B.-Y., & Han, Y. S. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2291 · Cited by 14

With the ends in sight: images from the BRCA1 tumor suppressor.

Baer, R. J. (2001) · Nature Structural Biology · doi:10.1038/nsb1001-822 · Cited by 14

Fins, limbs, and tails: outgrowths and axial patterning in vertebrate evolution

Coates, M. I., & Cohn, M. J. (1998) · BioEssays · doi:10.1002/(sici)1521-1878(199805)20:5 · Cited by 107

ECT2 promotes malignant phenotypes through the activation of the AKT/mTOR pathway and cisplatin resistance in cervical cancer

Liu, X., Zhang, J., Ju, S., Liu, L., Sun, Y., Guo, L., Zhen, Q., Han, S., Lü, W., & Zhang, Y. (2022) · Cancer Gene Therapy · doi:10.1038/s41417-022-00525-7 · Cited by 13

Mechanistic insight into the role of Poly(ADP-ribosyl)ation in DNA topology modulation and response to DNA damage

Matkarimov, B. T., Zharkov, D. O., & Saparbaev, M. K. (2019) · Mutagenesis · doi:10.1093/mutage/gez045 · Cited by 14

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

Poly(ADP-ribose) polymerase-1: A Regulator of Protein–Nucleic Acid Interactions in Processes Responding to Genotoxic Impact

Sukhanova, M. V., Lavrik, O. I., & Khodyreva, S. N. (2004) · Molecular Biology · doi:10.1023/b:mbil.0000043940.06762.39 · Cited by 13

NFBD1/MDC1 Regulates Cav1 and Cav2 Independently of DNA Damage and p53

Wilson, K. A., Colavito, S. A., Schulz, V., Wakefield, P. H., Sessa, W. C., Tuck, D. P., & Stern, D. F. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-10-0317 · Cited by 11

Association between p53-binding protein 1 expression and genomic instability in oncocytic follicular adenoma of the thyroid

Mussazhanova, Z., Akazawa, Y., Matsuda, K., Shichijo, K., Miura, S., Otsubo, R., Oikawa, M., Yoshiura, K.-I., Mitsutake, N., Rogounovitch, T., et al. (2016) · Endocrine Journal · doi:10.1507/endocrj.ej15-0629 · Cited by 12

In silico analysis for determining the deleterious nonsynonymous single nucleotide polymorphisms of BRCA genes.

Yadegari, F., & Majidzadeh‐A, K. (2019) · PubMed Central · doi:10.22099/mbrc.2019.34198.1420 · Cited by 12

Cryo-EM structure of the Rev1–Polζ holocomplex reveals the mechanism of their cooperativity in translesion DNA synthesis

Malik, R., Johnson, R. E., Ubarretxena‐Belandia, I., Prakash, L., Prakash, S., & Aggarwal, A. K. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01302-w · Cited by 12

5-(Hydroxymethyl)-2-furfural: A selective inhibitor of DNA polymerase λ and terminal deoxynucleotidyltransferase

Mizushina, Y., Yagita, E., Kuramochi, K., Kuriyama, I., Shimazaki, N., Koiwai, O., Uchiyama, Y., Yomezawa, Y., Sugawara, F., Kobayashi, S. S., et al. (2005) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2005.11.015 · Cited by 12

Molecular Characterization of NAD+-Dependent DNA Ligase from Wolbachia Endosymbiont of Lymphatic Filarial Parasite Brugia malayi

Shrivastava, N., Nag, J. K., & Misra‐Bhattacharya, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041113 · Cited by 12

Simulations of DNA Pol λ R517 Mutants Indicate 517's Crucial Role in Ternary Complex Stability and Suggest DNA Slippage Origin

Foley, M. C., & Tamar Schlick, A. (2008) · Journal of the American Chemical Society · doi:10.1021/ja077982t · Cited by 12

BRCTx Is a Novel, Highly Conserved RAD18-Interacting Protein

Adams, D. J., van der Weyden, L., Gergely, F. V., Arends, M. J., Ng, B. L., Tannahill, D., Kanaar, R., Markus, M. A., Morris, B. J., & Bradley, A. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.2.779-788.2005 · Cited by 12

BRCT domain of DNA polymerase μ has DNA ‐binding activity and promotes the DNA polymerization activity

Matsumoto, T., Go, K., Hyodo, M., Koiwai, K., Maezawa, S., Hayano, T., Suzuki, M., & Koiwai, O. (2012) · Genes to Cells · doi:10.1111/j.1365-2443.2012.01628.x · Cited by 11

Functional Domains of the BRCA1 and BRCA2 Proteins

Baer, R. J., & Lee, W. (1998) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1023/a:1018736115722 · Cited by 11

Insect-Resistant Transgenic Brassicas

Earle, E. D., Cao, J. W., & Shelton, A. M. (2004) · Biotechnology in agriculture and forestry · doi:10.1007/978-3-662-06164-0_12 · Cited by 11

Purification, crystallization and preliminary X-ray analysis of the BRCT domains of human 53BP1 bound to the p53 tumour suppressor

Derbyshire, D. J., Basu, B. P., Date, T., Iwabuchi, K., & Doherty, A. J. (2002) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444902010910 · Cited by 11

Functional Characterization of BRCA1 and BRCA2: Clues from Their Interacting Proteins

Sharan, S. K., & Bradley, A. (1998) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1023/a:1018788132560 · Cited by 11

DNA Damage Response Checkpoint Activation Drives KP1019 Dependent Pre-Anaphase Cell Cycle Delay in S. cerevisiae

Bierle, L. A., Reich, K. L., Taylor, B. E., Blatt, E. B., Middleton, S. M., Burke, S. D., Stultz, L. K., Hanson, P. K., Partridge, J. F., & Miller, M. E. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138085 · Cited by 10

Significant association between 53 BP1 expression and grade of intraepithelial neoplasia of esophagus: Alteration during esophageal carcinogenesis

Ueki, N., Akazawa, Y., Miura, S., Matsuda, K., Kurohama, H., Imaizumi, T., Kondo, H., & Nakashima, M. (2019) · Pathology - Research and Practice · doi:10.1016/j.prp.2019.152601 · Cited by 10

The Staining Patterns of 53BP1 Nuclear Foci and 53BP1 mRNA Level are Associated With Cervical Cancer Progression and Metastasis

Zhu, H., Yan, H., Jin, W., Dai, C., Chen, Z., Zheng, F., & Chen, X. (2014) · International Journal of Gynecological Pathology · doi:10.1097/pgp.0000000000000079 · Cited by 10

Human pescadillo induces large-scale chromatin unfolding

Zhang, H., Yan, F., Huang, C., Yang, X. Y., & Ye, Q. (2005) · Science in China Series C Life Sciences · doi:10.1007/bf03183621 · Cited by 10

Localization of BRCA1 Protein at the Cellular Level

Potter, C. R. D., Coene, E. D., & Schelfhout, V. (1998) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1023/a:1018740216630 · Cited by 10

Rad9 Comes of Age

Walworth, N. C. (1998) · Science · doi:10.1126/science.281.5374.185 · Cited by 10

Retinoblastoma susceptibility protein, Rb, possesses multiple BRCT-Ws, BRCA1 carboxyl-terminus-related W regions with DNA break-binding activity

Yamane, K., Katayama, E., Sugasawa, K., & Tsuruo, T. (2000) · Oncogene · doi:10.1038/sj.onc.1203528 · Cited by 10

Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome

Vissinga, C. S., Yeo, T. C., Woessner, J., Massa, H. F., Wilson, R. K., Trask, B. J., & CONCANNON, P. J. (1999) · Cytogenetic and Genome Research · doi:10.1159/000015396 · 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

Mutations in XRCC1 Gene Alters the Genetic Risks of Head and Neck Cancer Patients

Sabitha, K., Reddy, M. V., & Jamil, M. K. (2009) · International Journal of Cancer Research · doi:10.3923/ijcr.2009.58.68 · Cited by 9

Horizontal transfer generates genetic variation in an asexual pathogen

Huang, X. (2014) · PeerJ · doi:10.7717/peerj.650 · Cited by 9

Development, evaluation and application of tripeptidyl-peptidase II sequence signatures

Eriksson, S., Gutierrez‐Arenas, O., Bjerling, P., & Tomkinson, B. (2009) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2009.01.007 · Cited by 9

Heterozygous p.I171V mutation of the NBN gene as a risk factor for lung cancer development

Kałużna, E. M., Rembowska, J., Ziółkowska‐Suchanek, I., Świątek-Kościelna, B., Gabryel, P., Dyszkiewicz, W., & Nowak, J. (2015) · Oncology Letters · doi:10.3892/ol.2015.3715 · Cited by 9

Kinetics of BRCA1 regulation in response to UVC radiation

Clarkin, C. E. K., Zhang, H., & Weber, B. L. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000749 · Cited by 9

TopBP1 deficiency impairs V(D)J recombination during lymphocyte development

Kim, J., Lee, S. K., Jeon, Y., Kim, Y.-H., Lee, C., Jeon, S. H., Shim, J., Kim, I.-H., Hong, S., Kim, N., et al. (2014) · The EMBO Journal · doi:10.1002/embj.201284316 · Cited by 11

Crystallization of the catalytic domain of murine terminal deoxynucleotidyl transferase

Sukumar, N., Boulé, J.-B., Expert-Bezançon, N., Jourdan, N., Lescar, J., Rougeon, F., Papanicolaou, C., & Delarue, M. H. (2000) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s090744490001297x · Cited by 9

StrucBreak: A Computational Framework for Structural Break Detection in DNA Sequences

Kamal, M. S., & Nimmy, S. F. (2016) · Interdisciplinary Sciences Computational Life Sciences · doi:10.1007/s12539-016-0158-7 · Cited by 8

The BRCT Domain from the Homologue of the Oncogene PES1 in Leishmania major (LmjPES) Promotes Malignancy and Drug Resistance in Mammalian Cells

Larrea, E., Fernández-Rubio, C., Guerrero, J. P., Guruceaga, E., & Nguewa, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113203 · Cited by 8

The antibody preparation and expression of human Pescadillo

Zhang, H., Li, J., Wang, X., Sun, Y., Yuan, B., Yang, Z., Jiang, Y., Zeng, M., Ding, L., Ning, K., et al. (2007) · Science in China Series C Life Sciences · doi:10.1007/s11427-007-0045-x · Cited by 8

Multimodal approach to explore the pathogenicity of BARD1, ARG 658 CYS, and ILE 738 VAL mutants

Choudhary, R. K., Vikrant, Siddiqui, M. Q., Thapa, P. S., Raikundalia, S., Gadewal, N., Kumar, N. S., Hosur, M. V., & Varma, A. K. (2015) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2015.1082149 · Cited by 8

The BRCT domain and the specific loop 1 of human Polμ are targets of Cdk2/cyclin A phosphorylation

Esteban, V., Martín, M. J., & Blanco, L. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.07.007 · Cited by 8

Increased expression of the 58-kD microspherule protein (MSP58) is correlated with poor prognosis in glioma patients

Lin, W., Li, X.-M., Zhang, J., Huang, Y., Wang, J., Zhang, J., Jiang, X., & Fei, Z. (2013) · Medical Oncology · doi:10.1007/s12032-013-0677-6 · Cited by 8

The DNA-binding subunit p140 of replication factor C is upregulated in cycling cells and associates with G 1 phase cell cycle regulatory proteins

van der Kuip, H., Carius, B., Haque, S. J., Williams, B. R. G., Huber, C., & Fischer, T. H. (1999) · Journal of Molecular Medicine · doi:10.1007/s001090050365 · Cited by 8

Purification, Characterization, and Crystallization of the Distal BRCT Domain of the Human XRCC1 DNA Repair Protein

Thornton, K. H., Forstner, M., Shen, M. R., West, M. G., Rupp, B., & Thelen, M. P. (1999) · Protein Expression and Purification · doi:10.1006/prep.1999.1070 · Cited by 8

A novel domain of BRCA1 interacts with p53 in breast cancer cells

Buck, M. (2008) · Cancer Letters · doi:10.1016/j.canlet.2008.03.061 · Cited by 8

Establishment of and Recovery from Damage Checkpoint Requires Sequential Interactions of Crb2 with Protein Kinases Rad3, Chk1, and Cdc2Preprint

Esashi, F., Mochida, S., Matsusaka, T., OBARA, T., OGAWA, A., Tamai, K., & Yanagida, M. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.443 · Cited by 8

The Rtt107 BRCT scaffold and its partner modification enzymes collaborate to promote replication

Hang, L. E., & Zhao, X. (2016) · Nucleus · doi:10.1080/19491034.2016.1201624 · Cited by 7

A sulfoglycolipid beta-sulfoquinovosyldiacylglycerol ( SQDG) binds to Met1-Arg95 region of murine DNA polymerase lambda (Mmpol ) and inhibits its nuclear transit

Takakusagi, K., Takakusagi, Y., Ohta, K., Aoki, S., Sugawara, F., & Sakaguchi, K. (2009) · Protein Engineering Design and Selection · doi:10.1093/protein/gzp064 · Cited by 7

Genetic instability in the RAD51 and BRCA1 regions in breast cancer

Nowacka‐Zawisza, M., Bryś, M., Romanowicz‐Makowska, H., Kulig, A., & Krajewska, W. M. (2006) · Cellular & Molecular Biology Letters · doi:10.2478/s11658-006-0063-x · Cited by 7

Staurosporine‐sensitive protein phosphorylation is required for postreplication DNA repair in human cells

Svetlova, M., Solovjeva, L., Nikiforov, A. A., Chagin, V. A., Lehmann, A. R., & Tomilin, N. V. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00477-3 · Cited by 7

p53 contains a DNA break-binding motif similar to the functional part of BRCT-related region of Rb

Yamane, K., Katayama, E., & Tsuruo, T. (2001) · Oncogene · doi:10.1038/sj.onc.1204408 · Cited by 7

The mutation landscape of multiple cancer predisposition genes in Chinese familial/hereditary breast cancer families

Dong, L., & #x2019 (2021) · Cancer Biology and Medicine · doi:10.20892/j.issn.2095-3941.2021.0011 · Cited by 6

Evolution of the triplet BRCT domain

Mota, M. B. S., Woods, N. T., Carvalho, M. A., Monteiro, Á. N. A., & Mesquita, R. D. (2023) · DNA repair · doi:10.1016/j.dnarep.2023.103532 · Cited by 6

Cholesterol hemisuccinate: A selective inhibitor of family X DNA polymerases

Ishimaru, C., Kuriyama, I., Shimazaki, N., Koiwai, O., Sakaguchi, K., Kato, I., Yoshida, H., & Mizushina, Y. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.01.034 · Cited by 6

Expression of 58-kD Microspherule Protein (MSP58) is Highly Correlated with PET Imaging of Tumor Malignancy and Cell Proliferation in Glioma Patients

Lin, W. J., Dai, S., Chen, T., Kawai, N., Miyake, K., Okada, M., Haba, R., Yamamoto, Y., Tamiya, T., & Fei, Z. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000438656 · Cited by 6

Mechanistic Insights into Phosphopeptide–BRCT Domain Association: Preorganization, Flexibility, and Phosphate Recognition

Huang, Y. M., Kang, M., & Chang, C. A. (2012) · The Journal of Physical Chemistry B · doi:10.1021/jp305028d · Cited by 7

An array of basic residues is essential for the nucleolytic activity of the PHP domain of bacterial/archaeal PolX DNA polymerases

Rodríguez, G., Martín, M. T., & de Vega, M. (2019) · Scientific Reports · doi:10.1038/s41598-019-46349-8 · Cited by 8

Cloning and characterization of a new BRCA1 variant: A role for BRCT domains in apoptosis

Gu, M., Li, H., Shen, C., Wu, L., Liu, W., Miao, L., & Zheng, C. (2010) · Cancer Letters · doi:10.1016/j.canlet.2010.03.002 · Cited by 7

Problèmes posés par la prise en charge gynécologique des femmes porteuses d’une mutation germinale des gènes BRCA 1 & 2

Cabaret, A.-S., Lévêque, J., Dugast, C., Blanchot, J., & Grall, J. Y. (2003) · Gynécologie Obstétrique & Fertilité · doi:10.1016/s1297-9589(03)00058-4 · Cited by 6

Diverse functions of BRCA1 in the DNA damage response

Lee, J., & Chung, J. H. (2001) · Expert Reviews in Molecular Medicine · doi:10.1017/s1462399401003131 · Cited by 6

Characterization of a 3′–5′ Exonuclease Associated with VDJP

Zhu, L., & Halligan, B. D. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.0774 · Cited by 6

Celebrating Similarities—Embracing DifferencesPreprint

Goodman, L. (1999) · Genome Research · doi:10.1101/gr.9.9.797 · Cited by 6

Structural insights into Rad18 targeting by the SLF1 BRCT domains

Huang, W., Qiu, F., Zheng, L., Shi, M., Shen, M., Zhao, X., & Xiang, S. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105288 · Cited by 5

Association of XRCC1 genetic polymorphism (Arg399Gln) with laryngeal cancer: a meta-analysis based on 4,031 subjects

Chen, W., Wang, Z., Xu, F., Wu, K., Zhang, Y., Xu, L., & Wang, Q. P. (2013) · Tumor Biology · doi:10.1007/s13277-013-1225-x · Cited by 5

Isolation and characterization of ZePES and AtPES, the pescadillo orthologs from Zinnia and Arabidopsis

Zografidis, A., Καπόλας, Γ., Kitsios, G. D., McCann, M. C., Roberts, K., Milioni, D., & Haralampidis, K. (2007) · Plant Science · doi:10.1016/j.plantsci.2007.06.009 · Cited by 5

The Three-Dimensional Structure of p53

Stavridi, E. S., Huyen, Y., Sheston, E. A., & Halazonetis, T. D. (2007) · Springer eBooks · doi:10.1007/0-387-30127-5_2 · Cited by 5

Significance of abnormal 53BP1 expression as a novel molecular pathologic parameter of follicular-shaped B-cell lymphoid lesions in human digestive tract

Luong, T. M. H., Matsuda, K., Niino, D., Kurohama, H., Ito, M., & Nakashima, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-82867-0 · Cited by 5

Identification of proteins that interact with BRCA1 by Far‐Western library screening

Yarden, R. I., & Brody, L. C. (2001) · Journal of Cellular Biochemistry · doi:10.1002/jcb.1257 · Cited by 5

BRCT domains as chromatin readers: Structure, function, and clinical implications

Kruswick, A., Lam, F. C., Kong, Y. W., Smerdon, S. J., & Yaffe, M. B. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823376-4.00012-4 · Cited by 4

Mapping BRCT Interactions

(2004) · Science s STKE · doi:10.1126/stke.2142004tw6 · Cited by 1

The BRCT domain of the S. cerevisiae checkpoint protein Rad9 mediates a Rad9–Rad9 interaction after DNA damage

Soulier, J., & Lowndes, N. F. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80242-5 · Cited by 101

The BRCA1 C-terminal domain: structure and function

Huyton, T., Bates, P. A., Zhang, X., Sternberg, M. J. E., & Freemont, P. S. (2000) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(00)00034-3 · Cited by 147

From BRCA1 to RAP1: a widespread BRCT module closely associated with DNA repair

Callebaut, I., & Mornon, J. (1997) · FEBS Letters · doi:10.1016/s0014-5793(96)01312-9 · Cited by 524