Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins

ATM and ATR Substrate Analysis Reveals Extensive Protein Networks Responsive to DNA Damage

Matsuoka, S., Ballif, B. A., Smogorzewska, A., McDonald, E. R., Hurov, K. E., Luo, J., Bakalarski, C. E., Zhao, Z., Solimini, N., Lerenthal, Y., et al. (2007) · Science · doi:10.1126/science.1140321 · Cited by 3,075

Hallmarks of 'BRCAness' in sporadic cancers

Turner, N. C., Tutt, A. N. J., & Ashworth, A. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1457 · Cited by 1,690

Interaction of the Fanconi Anemia Proteins and BRCA1 in a Common Pathway

Garcia-Higuera, I., Taniguchi, T., Ganesan, S., Meyn, M. S., Timmers, C., Hejna, J., Grompe, M., & D'Andrea, A. D. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00173-3 · Cited by 1,198

Biallelic Inactivation of BRCA2 in Fanconi Anemia

Howlett, N. G., Taniguchi, T., Olson, S., Cox, B., Waisfisz, Q., de Die-Smulders, C., Persky, N., Grompe, M., Joenje, H., Pals, G., et al. (2002) · Science · doi:10.1126/science.1073834 · Cited by 1,149

Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2

Sharan, S. K., Morimatsu, M., Albrecht, U., Lim, D., Regel, E., Dinh, C. Q., Sands, A., Gregor Eichele, C., Hasty, P., & Bradley, A. (1997) · Nature · doi:10.1038/386804a0 · Cited by 1,087

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

Rahman, N., Seal, S., Thompson, D. J., Kelly, P. F., Renwick, A., Elliott, A., Reid, S., Spanova, K., Barfoot, R., Chagtai, T., et al. (2006) · Nature Genetics · doi:10.1038/ng1959 · Cited by 1,026

BRCA2 Is Required for Homology-Directed Repair of Chromosomal Breaks

Moynahan, M. E., Pierce, A. J., & Jasin, M. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00174-5 · Cited by 1,007

Control of BRCA2 Cellular and Clinical Functions by a Nuclear Partner, PALB2

Xia, B., Sheng, Q., Nakanishi, K., Ohashi, A., Wu, J., Christ, N., Liu, X., Jasin, M., Couch, F. J., & Livingston, D. M. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.05.022 · Cited by 861

Interaction of Human DNA Polymerase η with Monoubiquitinated PCNA

Kannouche, P. L., Wing, J., & Lehmann, A. R. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00259-x · Cited by 845

BRCA2 Function in DNA Binding and Recombination from a BRCA2-DSS1-ssDNA Structure

Yang, H., Jeffrey, P. D., Miller, J. J., Kinnucan, E., Sun, Y., Thomä, N. H., Zheng, N., Chen, P., Lee, W., & Pavletich, N. P. (2002) · Science · doi:10.1126/science.297.5588.1837 · Cited by 719

Promotion of BRCA1-associated triple-negative breast cancer by ovarian hormones

Lee, E. Y.-H. P. (2008) · Current Opinion in Obstetrics & Gynecology · doi:10.1097/gco.0b013e3282f42237 · Cited by 20

The Molecular Basis of Cancer and the Development of Targeted Therapy

Riley, L. B., & Desai, D. C. (2009) · Surgical Clinics of North America · doi:10.1016/j.suc.2008.09.016 · Cited by 21

Sleeping Beauty‐mediated correction of Fanconi anemia type C

Hyland, K. A., Olson, E. R., Clark, K. J., Aronovich, E. L., Hackett, P. B., Blazar, B. R., Tolar, J., & McIvor, R. S. (2011) · The Journal of Gene Medicine · doi:10.1002/jgm.1589 · Cited by 19

Chronic treatment with cisplatin induces replication-dependent sister chromatid recombination to confer cisplatin-resistant phenotype in nasopharyngeal carcinoma

Su, W., Hsu, S.-H., Wu, C.-K., Chang, S., Lin, Y.-J., Yang, W., Hung, J., Chiu, W., Tzeng, S., Tseng, Y., et al. (2014) · Oncotarget · doi:10.18632/oncotarget.2210 · Cited by 20

Chronic treatment with cisplatin induces chemoresistance through the TIP60-mediated Fanconi anemia and homologous recombination repair pathways

Su, W., Ho, Y.-C., Wu, C.-K., Hsu, S.-H., Shiu, J.-L., Huang, J.-C., Chang, S., Chiu, W., Hung, J., Liu, T.-L., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-04223-5 · Cited by 19

Involvement of p29 in DNA damage responses and Fanconi anemia pathway

Chu, P., Wang, T., Lu, Y., Chou, C.-K., Yang, Y., & Chang, M.-S. (2009) · Carcinogenesis · doi:10.1093/carcin/bgp204 · Cited by 19

Synchronous multifocal HPV-related neoplasm involving both the genital tract and the head-and-neck area: A case report of Fanconi anemia

Han, T.-J., Lee, C. H., Yoo, C.-W., Shin, H., Park, H., Cho, K. H., Park, J. Y., Choi, S.-W., & Kim, J. (2009) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2009.03.009 · Cited by 19

The Fanconi anemia pathway: Insights from somatic cell genetics using DT40 cell line

Takata, M., Ishiai, M., & Kitao, H. (2009) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2008.12.012 · Cited by 18

Identification of Tat-SF1 cellular targets by exon array analysis reveals dual roles in transcription and splicing

Miller, H. B., Robinson, T. J., Gordân, R., Hartemink, A. J., & García-Blanco, M. A. (2011) · RNA · doi:10.1261/rna.2462011 · Cited by 18

SCAI promotes error‐free repair of DNA interstrand crosslinks via the Fanconi anemia pathway

Schubert, L. A., Hendriks, I. A., Hertz, E. P. T., Wu, W., Sellés‐Baiget, S., Hoffmann, S., Viswalingam, K. S., Gallina, I., Pentakota, S., Benedict, B., et al. (2022) · EMBO Reports · doi:10.15252/embr.202153639 · Cited by 18

Topo IIIα and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Hemphill, A., Akkari, Y. M. N., Newell, A. H., Schultz, R. A., Grompe, M., North, P. S., Hickson, I. D., Jakobs, P. M., Rennie, S., Pauw, D., et al. (2009) · Cytogenetic and Genome Research · doi:10.1159/000230001 · Cited by 19

Protein Degradation Pathways Regulate the Functions of Helicases in the DNA Damage Response and Maintenance of Genomic Stability

Sommers, J. A., Suhasini, A. N., & Brosh, R. M. (2015) · Biomolecules · doi:10.3390/biom5020590 · Cited by 19

Discovering gene functional relationships using FAUN (Feature Annotation Using Nonnegative matrix factorization)

Tjioe, E., Berry, M. W., & Homayouni, R. (2010) · BMC Bioinformatics · doi:10.1186/1471-2105-11-s6-s14 · Cited by 18

Uncoupling of transcription and translation of Fanconi anemia (FANC) complex proteins during spermatogenesis

Jamsai, D., O’Connor, A. E., O’Donnell, L., Lo, J. C. Y., & O’Bryan, M. K. (2014) · Spermatogenesis · doi:10.4161/21565562.2014.979061 · Cited by 18

BRCA2 Variants and cardiovascular disease in a multi-ethnic study

Zbuk, K. M., Xie, C., Young, R., Heydarpour, M., Paré, G., Davis, A. D., Miller, R., Lanktree, M. B., Saleheen, D., Danesh, J., et al. (2012) · BMC Medical Genetics · doi:10.1186/1471-2350-13-56 · Cited by 18

Lack of large genomic deletions in BRIP1, PALB2, and FANCD2 genes in BRCA1/2 negative familial breast cancer

Ameziane, N., van den Ouweland, A. M. W., Adank, M. A., Vijzelaar, R., Errami, A., Dorsman, J. C., Joenje, H., Meijers-Heijboer, H. E. J., & Waisfisz, Q. (2009) · Breast Cancer Research and Treatment · doi:10.1007/s10549-009-0428-8 · Cited by 19

The ubiquitin family meets the Fanconi anemia proteins

Renaudin, X., Lerner, L. K., Menck, C. F. M., & Rosselli, F. (2016) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2016.06.004 · Cited by 18

Chromatin Ubiquitination Guides DNA Double Strand Break Signaling and Repair

Kolobynina, K. G., Rapp, A. W., & Cardoso, M. C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.928113 · Cited by 17

FANCJ protein is important for the stability of FANCD2/FANCI proteins and protects them from proteasome and caspase-3 dependent degradation

Clark, D. W., Tripathi, K. K., Dorsman, J. C., & Palle, K. (2015) · Oncotarget · doi:10.18632/oncotarget.5006 · Cited by 17

Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes

Gayarre, J., Martín, P., Osório, A., Paumard‐Hernández, B., Barroso, A., Fernández, V., de la Hoya, M., Rojo‐Sebastián, A., Caldés, T., Palacios, J., et al. (2017) · British Journal of Cancer · doi:10.1038/bjc.2017.286 · Cited by 17

Spectrin and its interacting partners in nuclear structure and function

Lambert, M. W. (2018) · Experimental Biology and Medicine · doi:10.1177/1535370218763563 · Cited by 17

The nuclease FAN1 is involved in DNA crosslink repair in Arabidopsis thaliana independently of the nuclease MUS81

Herrmann, N. J., Knoll, A., & Puchta, H. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv208 · Cited by 16

Physical and functional crosstalk between Fanconi anemia core components and the GINS replication complex

Tumini, E., Plevani, P., Muzi-Falconi, M., & Marini, F. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.10.006 · Cited by 16

Advances in the understanding of the Fanconi anemia tumor suppressor pathway

Pickering, A., Zhang, J., Panneerselvam, J., & Fei, P. (2013) · Cancer Biology & Therapy · doi:10.4161/cbt.26380 · Cited by 18

Human Fanconi Anemia Complementation Group A Protein Stimulates the 5’ Flap Endonuclease Activity of FEN1

Qian, L., Yuan, F., Rodriguez-Tello, P., Padgaonkar, S., & Zhang, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082666 · Cited by 16

Role of Germline Predisposition to Therapy-Related Myeloid Neoplasms

Baranwal, A., Hahn, C. N., Shah, M. V., & Hiwase, D. (2022) · Current Hematologic Malignancy Reports · doi:10.1007/s11899-022-00676-2 · Cited by 16

DNA Repair and Resistance to Cancer Therapy

Antnio, S., Costa, B. A., Martins, C., Gromicho, M., Nuno, G., Patrcia, S., & Rueff, J. (2013) · InTech eBooks · doi:10.5772/53952 · Cited by 18

FANCD2 but not FANCA promotes cellular resistance to type II topoisomerase poisons

Kachnic, L. A., Li, L., Fournier, L., Ferraiolo, N., Dahm‐Daphi, J., Borgmann, K., & Willers, H. (2011) · Cancer Letters · doi:10.1016/j.canlet.2011.02.030 · Cited by 16

Alpha-fetoprotein and Fanconi Anemia: Relevance to DNA Repair and Breast Cancer Susceptibility

Lakhi, N. A., & Mizejewski, G. J. (2016) · Fetal and Pediatric Pathology · doi:10.1080/15513815.2016.1225873 · Cited by 16

Genetic variants of the DNA repair genes from Exome Aggregation Consortium (EXAC) database: significance in cancer

Das, R., & Ghosh, S. K. (2017) · DNA repair · doi:10.1016/j.dnarep.2017.02.013 · Cited by 16

Breast cancer genetic susceptibility: With focus in Saudi Arabia

Alshammari, F. D. (2019) · Journal of Oncological Sciences · doi:10.1016/j.jons.2019.02.001 · Cited by 16

The Clinical Utility of Biomarkers in the Management of Pancreatic Adenocarcinoma

Jazieh, K., Foote, M. B., & Diaz, L. A. (2014) · Seminars in Radiation Oncology · doi:10.1016/j.semradonc.2013.11.007 · Cited by 16

Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families

Fernández‐Rodríguez, J., Quiles, F., Blanco, I., Teulé, À., Feliubadaló, L., Valle, J. D., Salinas, M., Izquierdo, Á., Darder, E., Schindler, D., et al. (2012) · BMC Cancer · doi:10.1186/1471-2407-12-84 · Cited by 16

Ubiquitin control of S phase: a new role for the ubiquitin conjugating enzyme, UbcH7

Whitcomb, E. A., & Taylor, A. (2009) · Cell Division · doi:10.1186/1747-1028-4-17 · Cited by 15

Hawaii natural compounds are promising to reduce ovarian cancer deaths

Fei‐Zhang, D. J., Li, C., & Cao, S. (2016) · Cancer Biology & Therapy · doi:10.1080/15384047.2016.1178428 · Cited by 15

A Hidden Role of the Inactivated FANCD2: Upregulating ΔNp63

Panneerselvam, J., Pickering, A., Zhang, J., Wang, H., Tian, H., Zheng, J., & Fei, P. (2013) · Oncotarget · doi:10.18632/oncotarget.1217 · Cited by 15

Inherited bone marrow failure syndromes

Dokal, I. S. (2011) · Journal of Hematopathology · doi:10.1007/s12308-011-0089-5 · Cited by 15

Damage-dependent regulation of MUS81-EME1 by Fanconi anemia complementation group A protein

Benitez, A., Yuan, F., Nakajima, S., Wei, L., Qian, L., Myers, R. S., Hu, J. J., Lan, L., & Zhang, Y. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt975 · Cited by 15

The FANC pathway is activated by adenovirus infection and promotes viral replication-dependent recombination

Cherubini, G., Naim, V., Caruso, P., Burla, R., Bogliolo, M., Cundari, E., Benihoud, K., Saggio, I., & Rosselli, F. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr084 · Cited by 15

Emerging roles for centromere-associated proteins in DNA repair and genetic recombination

Osman, F., & Whitby, M. C. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130200 · Cited by 15

Identification of polymorphisms in ultraconserved elements associated with clinical outcomes in locally advanced colorectal adenocarcinoma

Lin, M., Eng, C., Hawk, E. T., Huang, M., Lin, J. M., Gu, J. H., Ellis, L. M., & Wu, X. (2012) · Cancer · doi:10.1002/cncr.27653 · Cited by 16

The phenotype of FancB-mutant mouse embryonic stem cells

Kim, T. M., Ko, J. H., Choi, Y. J., Hu, L., & Hasty, P. (2011) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2011.03.010 · Cited by 15

Structural aspects of multi-domain RING/Ubox E3 ligases in DNA repair

Hibbert, R. G., Mattiroli, F., & Sixma, T. K. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.01.014 · Cited by 15

Advances in the Understanding of Fanconi Anemia Complementation Group D2 Protein (FANCD2) in Human Cancer

Shen, Y., Zhang, J., Yu, H., & Fei, P. (2015) · Cancer Cell & Microenvironment · doi:10.14800/ccm.986 · Cited by 14

The translesion polymerase ζ has roles dependent and independent of the nuclease MUS81 and the helicase RECQ4A in DNA damage repair in Arabidopsis

Kobbe, S., Trapp, O., Knoll, A., Mannuß, A., & Puchta, H. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00806 · Cited by 14

Nucleotide Excision Repair and Response and Survival to Chemotherapy in Colorectal Cancer Patients

Kap, E. J., Popanda, O., & Chang-Claude, J. C. (2016) · Pharmacogenomics · doi:10.2217/pgs-2015-0017 · Cited by 14

Phase I Study of Veliparib on an Intermittent and Continuous Schedule in Combination with Carboplatin in Metastatic Breast Cancer: A Safety and [18F]-Fluorothymidine Positron Emission Tomography Biomarker Study

Wesolowski, R., Stover, D. G., Lustberg, M. B., Shoben, A. B., Zhao, M., Mrózek, E., Layman, R. M., Macrae, E. R., Duan, W., Zhang, J., et al. (2020) · The Oncologist · doi:10.1634/theoncologist.2020-0039 · Cited by 14

Deacetylase Plus Bromodomain Inhibition Downregulates ERCC2 and Suppresses the Growth of Metastatic Colon Cancer Cells

Kapoor, S., Gustafson, T. A., Zhang, M., Chen, Y., Li, J., Nhung, N. T., Perez, J. E. T., Dashwood, W. M., Rajendran, P., & Dashwood, R. H. (2021) · Cancers · doi:10.3390/cancers13061438 · Cited by 15

Defects in DNA Lesion Bypass Lead to Spontaneous Chromosomal Rearrangements and Increased Cell Death

Schmidt, K. H., Viebranz, E., Harris, L., Mirzaei, H., Syed, S., & Medicus, R. (2009) · Eukaryotic Cell · doi:10.1128/ec.00260-09 · Cited by 14

The role of the Fanconi anemia network in the response to DNA replication stress

Gari, K., & Constantinou, A. (2009) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230903154150 · Cited by 14

Oxidative Stress-Associated Protein Tyrosine Kinases and Phosphatases in Fanconi Anemia

Li, J., & Pang, Q. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5715 · Cited by 14

Replication Protein A (RPA) deficiency activates the Fanconi anemia DNA repair pathway

Jang, S.-W., Jung, J. K., & Kim, J. M. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1201621 · Cited by 14

Analysis of polymorphisms in genes associated with the FA/BRCA pathway in three patients with multiple primary malignant neoplasms

Wang, L., Wang, H., Wang, T., Liu, J., Chen, W., Wang, Y., Chen, C., Zhu, H., & Dai, P. (2019) · Artificial Cells Nanomedicine and Biotechnology · doi:10.1080/21691401.2019.1575846 · Cited by 14

Upregulated ATM Gene Expression and Activated DNA Crosslink-Induced Damage Response Checkpoint in Fanconi Anemia: Implications for Carcinogenesis

Yamamoto, K., Nihrane, A., Aglipay, J. A., Sironi, J., Arkin, S., Lipton, J. M. M., Ouchi, T., & Liu, J. M. (2008) · Molecular Medicine · doi:10.2119/2007-00122.yamamoto · Cited by 14

The role of poly adenosine diphosphate ribose polymerase inhibitors in breast and ovarian cancer: Current status and future directions

Chionh, F. J. M., Mitchell, G., Lindeman, G. J., Friedlander, M. L., & Scott, C. L. (2011) · Asia-Pacific Journal of Clinical Oncology · doi:10.1111/j.1743-7563.2011.01430.x · Cited by 16

The RecQ helicase RECQL5 participates in psoralen-induced interstrand cross-link repair

Ramamoorthy, M., May, A., Tadokoro, T., Popuri, V., Seidman, M. M., Croteau, D. L., & Bohr, V. A. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt183 · Cited by 13

New insights into redox response modulation in Fanconi’s anemia cells by hydrogen peroxide and glutathione depletors

Cuccarolo, P., Viaggi, S., & Degan, P. (2012) · FEBS Journal · doi:10.1111/j.1742-4658.2012.08629.x · Cited by 13

Effects of Breast Cancer Genes 1 and 2 on Cardiovascular Diseases

Zhou, S., Jin, J., Wang, J., Zhang, Z., Huang, S., Zheng, Y., & Cai, L. (2019) · Current Problems in Cardiology · doi:10.1016/j.cpcardiol.2019.04.001 · Cited by 13

Low incidence of methylation of the promoter region of the FANCF gene in Japanese primary breast cancer

Tokunaga, E., Okada, S., Kitao, H., Shiotani, S., Saeki, H., Endo, K., Morita, M., Kakeji, Y., & Maehara, Y. (2009) · Breast Cancer · doi:10.1007/s12282-009-0175-z · Cited by 13

Phenotyping Genetic Diseases Using an Extension of µ-Scores for Multivariate Data

Morales, J. F., Song, T., Auerbach, A. D., & Wittkowski, K. M. (2008) · Statistical Applications in Genetics and Molecular Biology · doi:10.2202/1544-6115.1372 · Cited by 13

Papel das proteínas XPD e DNA polimerase eta nas respostas de células humanas a danos no genoma

Lerner, L. K. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2014.tde-20102014-103732 · Cited by 13

Fanconi anemia is a highly penetrant cancer susceptibility syndrome.

Dokal, I. S. (2008) · PubMed · Cited by 13

Connecting the Dots: Interplay between Ubiquitylation and SUMOylation at DNA Double-Strand Breaks

Tang, J.-B., & Greenberg, R. A. (2010) · Genes & Cancer · doi:10.1177/1947601910382774 · Cited by 12

Nonsense Suppression Therapy: New Hypothesis for the Treatment of Inherited Bone Marrow Failure Syndromes

Bezzerri, V., Api, M., Allegri, M., Fabrizzi, B., Corey, S. J., & Cipolli, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134672 · Cited by 13

Impaired function of Fanconi anemia type C-deficient macrophages

Liu, Y., Ballman, K. K., Li, D., Khan, S., Derr-Yellin, E. C., Shou, W., & Haneline, L. S. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.0811418 · Cited by 12

Evolutionary genomics of human intellectual disability

Crespi, B. J., Summers, K., & Dorus, S. (2009) · Evolutionary Applications · doi:10.1111/j.1752-4571.2009.00098.x · Cited by 12

Interactome Networks

Carvunis, A., Roth, F. P., Calderwood, M. A., Cusick, M. E., Superti‐Furga, G., & Vidal, M. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-385944-0.00003-4 · Cited by 12

The Impact of Whole Genome Data on Therapeutic Decision-Making in Metastatic Prostate Cancer: A Retrospective Analysis

Crumbaker, M., Chan, E. K. F., Gong, T., Corcoran, N. M., Jaratlerdsiri, W., Lyons, R. J., Haynes, A., Kulidjian, A., Kalsbeek, A. M. F., Petersen, D. C., et al. (2020) · Cancers · doi:10.3390/cancers12051178 · Cited by 12

Research progress of the Fanconi anemia pathway and premature ovarian insufficiency

Zhao, J., Zhang, Y., Li, W., Yao, M., Liu, C., Zhang, Z., Wang, C., Wang, X., & Meng, K. (2023) · Biology of Reproduction · doi:10.1093/biolre/ioad110 · Cited by 11

Insights into common fragile site instability: DNA replication challenges at DNA repeat sequences

Sinai, M. I., & Kerem, B. (2023) · Emerging Topics in Life Sciences · doi:10.1042/etls20230023 · Cited by 11

Clinical implications of using molecular diagnostics for ovarian cancers

Kohn, E. C., Romano, S., & Lee, J.-M. (2013) · Annals of Oncology · doi:10.1093/annonc/mdt464 · Cited by 11

Four-Dimensional Orthogonal Electrophoresis System for Screening Protein Complexes and Protein−Protein Interactions Combined with Mass Spectrometry

Wang, X., Chen, G., Liu, H., Zhao, Z., & Li, Z. (2010) · Journal of Proteome Research · doi:10.1021/pr100581x · Cited by 11

Structure analysis of FAAP24 reveals single-stranded DNA-binding activity and domain functions in DNA damage response

Wang, Y., Han, X. Y., Wu, F., Leung, J. W. C., Lowery, M. G., Do, H., Chen, J., Shi, C., Tian, C., Li, L., et al. (2013) · Cell Research · doi:10.1038/cr.2013.124 · Cited by 11

TREX2 Exonuclease Causes Spontaneous Mutations and Stress-Induced Replication Fork Defects in Cells Expressing RAD51K133A

Ko, J. H., Son, M. Y., Zhou, Q., Molnárová, L., Song, L., Mlčoušková, J., Je̅kabsons, A., Montagna, C., Krejčí, L., & Hasty, P. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108543 · Cited by 11

The role of USP 1 autocleavage in DNA interstrand crosslink repair

Kim, M., & Kim, J. M. (2016) · FEBS Letters · doi:10.1002/1873-3468.12060 · Cited by 11

Contemplating chemosensitivity of basal-like breast cancer based on BRCA1 dysfunction

Ohta, T., Wu, W., Koike, A., Asakawa, H., Koizumi, H., & Fukuda, M. (2009) · Breast Cancer · doi:10.1007/s12282-009-0115-y · Cited by 11

The role of BACH1 , BARD1 and TOPBP1 genes in familial breast cancer

Karppinen, S. (2009) · Cited by 11

PALB2 mutations 1592delT and 229delT are not present in Korean breast cancer patients negative for BRCA1 and BRCA2 mutations

Kim, J. H., Choi, D. H., Cho, D. Y., Ahn, S. H., Son, B. H., & Haffty, B. G. (2010) · Breast Cancer Research and Treatment · doi:10.1007/s10549-010-0806-2 · Cited by 10

Nuclear α Spectrin Differentially Affects Monoubiquitinated Versus Non-Ubiquitinated FANCD2 Function After DNA Interstrand Cross-Link Damage

Zhang, P., Sridharan, D., & Lambert, M. W. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25352 · Cited by 10

Assembling an orchestra: Fanconi anemia pathway of repair

Yuan, F. (2010) · Frontiers in bioscience · doi:10.2741/3666 · Cited by 10

Nuclear alpha spectrin: Critical roles in DNA interstrand cross-link repair and genomic stability

Lambert, M. W. (2016) · Experimental Biology and Medicine · doi:10.1177/1535370216662714 · Cited by 10

Inherited Bone Marrow Failure Syndromes

Canham, L. E., & de Jong, J. L. O. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15717-2.00131-1 · Cited by 10

Stabilizing and Remodeling the Blocked DNA Replication Fork: Anchoring FANCM and the Fanconi Anemia Damage Response

Thompson, L. H., & Jones, N. J. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.03.003 · Cited by 10

The Fanconi anemia pathway is downregulated upon macrophage differentiation through two distinct mechanisms

Lu, W.-T., Lemonidis, K., Drayton, R. M., & Nouspikel, T. (2011) · Cell Cycle · doi:10.4161/cc.10.19.17178 · Cited by 10

Identification of Novel Susceptibility Genes for Breast Cancer – Genome-Wide Association Studies or Evaluation of Candidate Genes?

Meindl, A. (2009) · Breast Care · doi:10.1159/000211991 · Cited by 9

Use of DNA–Damaging Agents and RNA Pooling to Assess Expression Profiles Associated with BRCA1 and BRCA2 Mutation Status in Familial Breast Cancer Patients

Walker, L. C., Thompson, B. A., Waddell, N., kConFab Investigators, Grimmond, S. M., & Spurdle, A. B. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000850 · Cited by 9

Monoubiquitination-dependent chromatin loading of FancD2 in silkworms, a species lacking the FA core complex

Sugahara, R., Mon, H., Lee, J. M., & Kusakabe, T. (2012) · Gene · doi:10.1016/j.gene.2012.03.071 · Cited by 9

A Protein Prioritization Approach Tailored for the FA/BRCA Pathway

Haitjema, A., Brandt, B. W., Ameziane, N., May, P., Heringa, J., de Winter, J. P., Joenje, H., & Dorsman, J. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062017 · Cited by 9

Differential roles for Chk1 and FANCD2 in ATR-mediated signalling for psoralen photoactivation-induced senescence

Hovest, M. G., Krieg, T. M., & Herrmann, G. (2011) · Experimental Dermatology · doi:10.1111/j.1600-0625.2011.01365.x · Cited by 9

Preparation of N3-thymidine–butylene–N3-thymidine interstrand cross-linked DNA via an orthogonal deprotection strategy

Sun, G. Z., Noronha, A. M., & Wilds, C. J. (2012) · Tetrahedron · doi:10.1016/j.tet.2012.07.043 · Cited by 9

Embryonic Lethality after Combined Inactivation of Fancd2 and Mlh1 in Mice

van de Vrugt, H. J., Eaton, L., Newell, A. H., Al-Dhalimy, M., Liskay, R. M., Olson, S. B., & Grompe, M. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-2452 · Cited by 9

A FANCD2 domain activates Tip60‐dependent apoptosis

Hejna, J., Bruun, D. A., Pauw, D., & Moses, R. E. (2010) · Cell Biology International · doi:10.1042/cbi20090251 · Cited by 9

Family History of Cancer Rather Than p53 Status Predicts Efficacy of Pegylated Liposomal Doxorubicin and Oxaliplatin in Relapsed Ovarian Cancer

Nicoletto, M. O., Bertorelle, R., Borgato, L., Salvo, G. L. D., Artioli, G., Lombardi, G., Zustovich, F., Marcato, R., Parenti, A. R., Montagna, M., et al. (2009) · International Journal of Gynecological Cancer · doi:10.1111/igc.0b013e3181a83cb5 · Cited by 9

TOPBP1 , CLSPN and PALB2 genes in familial breast cancer susceptibility

Erkko, H. (2008) · Cited by 9

Bloom Syndrome Radials Are Predominantly Non-Homologous and Are Suppressed by Phosphorylated BLM

Owen, N. M., Hejna, J., Rennie, S., Mitchell, A., Newell, A. H., Ziaie, N., Moses, R. E., & Olson, S. B. (2014) · Cytogenetic and Genome Research · doi:10.1159/000375247 · Cited by 8

Signalling DNA Damage

Joaquin, A., & Fernández-Capetillo, Ó. (2012) · InTech eBooks · doi:10.5772/50863 · Cited by 14

New features on Pso2 protein family in DNA interstrand cross-link repair and in the maintenance of genomic integrity in Saccharomyces cerevisiae

Munari, F. M., Guecheva, T. N., Bonatto, D., & Henriques, J. A. P. (2013) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2013.09.003 · Cited by 8

Identification of FANCA as a protein interacting with centromere-associated protein E

Du, J., Chen, L., & Shen, J. (2009) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmp074 · Cited by 9

Control of the Cell Cycle

Malumbres, M. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-47674-4.00004-9 · Cited by 10

Correction of mutant Fanconi anemia gene by homologous recombination in human hematopoietic cells using adeno‐associated virus vector

Paiboonsukwong, K., Ohbayashi, F., Shiiba, H., Aizawa, E., Yamashita, T., & Mitani, K. (2009) · The Journal of Gene Medicine · doi:10.1002/jgm.1382 · Cited by 8

A Complex Involved in the DNA Damage Response Network of Fanconi Anemia and Breast Cancer

Yan, Z., Xu, D., Guo, R., Xue, Y., Chen, L., Li, Y., & Wang, W. (2009) · The FASEB Journal · doi:10.1096/fasebj.23.1_supplement.429.2

New Advances in the DNA Damage Response Network of Fanconi Anemia and BRCA proteins: FAAP95 Replaces BRCA2 as the True FANCB Protein

Fei, P., Yin, J., & Wang, W. (2004) · Cell Cycle · doi:10.4161/cc.4.1.1358 · Cited by 43

The Fanconi anaemia genome stability and tumour suppressor network

Bogliolo, M. (2002) · Mutagenesis · doi:10.1093/mutage/17.6.529 · Cited by 56

The Fanconi anaemia genome stability and tumour suppressor network. Mutagenesis

Bogliolo, M., Cabré, O., Callén, E., Castillo, V., Creus, A., Marcos, R., & Surrallés, J. (2013)

The interplay of Fanconi anemia proteins in the DNA damage response

Wang, X., & D’Andrea, A. D. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.04.005 · Cited by 72