Mutation of the RAD51C gene in a Fanconi anemia–like disorder

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   B. Wappenschmidt, J. Hauke, U. Faust, D. Niederacher, L. Wiesmüller, G. Schmidt, E. Groß, A. Gehrig, C. Sutter, J. Ramser et al. · 2020 · Geburtshilfe und Frauenheilkunde
2. Assessment of FANCD2 nuclear foci formation in paraffin-embedded tumors: a potential patient-enrichment strategy for treatment with DNA interstrand crosslinking agents
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4. Gene Silencing of FANCF Potentiates the Sensitivity to Mitoxantrone through Activation of JNK and p38 Signal Pathways in Breast Cancer Cells
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5. The HsRAD51B–HsRAD51C stabilizes the HsRAD51 nucleoprotein filament
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6. Mutation screening of RAD51C in high-risk breast and ovarian cancer families
   Wenping Lü, Xianshu Wang, Hongsheng Lin, Noralane M. Lindor, Fergus J. Couch · 2012 · Familial Cancer
7. Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma
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8. The homologous recombination protein RAD51D protects the genome from large deletions
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10. Genetics of gastrointestinal atresias
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11. A decade of RAD51C and RAD51D germline variants in cancer
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12. Veliparib Alone or in Combination with Mitomycin C in Patients with Solid Tumors With Functional Deficiency in Homologous Recombination Repair
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13. A Hypomorphic PALB2 Allele Gives Rise to an Unusual Form of FA-N Associated with Lymphoid Tumour Development
    Philip J. Byrd, Grant S. Stewart, Anna Jo Bodurtha Smith, Charlotte D. Eaton, Alexander J. Taylor, Chloe Guy, Ieva Eringyte, Peggy Fooks, James I. K. Last, Robert Horsley et al. · 2016 · PLoS Genetics
14. Coordinated action of the Fanconi anemia and ataxia telangiectasia pathways in response to oxidative damage
    Pau Castillo Bosch, Massimo Bogliolo, Jordi Surrallés · 2011 · DNA repair
15. Konsensusempfehlung des Deutschen Konsortiums Familiärer Brust- und Eierstockkrebs zum Umgang mit Ergebnissen der Multigenanalyse
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16. Testis-expressed gene 11 inhibits cisplatin-induced DNA damage and contributes to chemoresistance in testicular germ cell tumor
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17. Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair
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18. High expression of Rad51c predicts poor prognostic outcome and induces cell resistance to cisplatin and radiation in non-small cell lung cancer
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19. Targeting Homologous Recombination Repair in Cancer
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20. Disrupted Signaling through the Fanconi Anemia Pathway Leads to Dysfunctional Hematopoietic Stem Cell Biology: Underlying Mechanisms and Potential Therapeutic Strategies
    Anja Geiselhart, Amelie Lier, Dagmar Walter, Michael D. Milsom · 2012 · Anemia
21. The stem cell fitness landscape and pathways of molecular leukemogenesis
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22. Comprehensive Functional Characterization and Clinical Interpretation of 20 Splice-Site Variants of the RAD51C Gene
    Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, Elena Bueno-Martínez, P. Llovet, Beatriz Díez-Gómez, M. J. Caloca, P. Pérez-Segura, Eugenia Fraile-Bethencourt, Marta Colmena, S. Carvalho et al. · 2020 · Cancers
23. Mutational analysis of RAD51C and RAD51D genes in hereditary breast and ovarian cancer families from Murcia (southeastern Spain)
    Ana Isabel Sánchez-Bermúdez, María Desamparados Sarabia-Meseguer, Ángeles García-Aliaga, Miguel Marín-Vera, José Antonio Macías Cerrolaza, Pilar Sánchez Henaréjos, Verónica Castillo Guardiola, Francisco Ayala de la Peña, José Luis Alonso-Romero, José Antonio Noguera Velasco et al. · 2018 · European Journal of Medical Genetics
24. Fanconi anaemia: from a monogenic disease to sporadic cancer
    Antonio Valeri, Sandra Luz Martinez, José Antonio Casado, Juan Antonio Bueren · 2011 · Clinical & Translational Oncology
25. Molecular defects identified by whole exome sequencing in a child with Fanconi anemia
    Zhaojing Zheng, Juan Geng, Ruen Yao, Caihua Li, Daming Ying, Yongnian Shen, Lei Ying, Yongguo Yu, Qihua Fu · 2013 · Gene
26. Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic
    Markéta Janatová, Jana Soukupová, Jana Stribrna, Petra Kleiblová, Michal Vočka, Petra Boudova, Zdeněk Kleibl, Petr Pohlreich · 2015 · PLoS ONE
27. Chronic treatment with cisplatin induces chemoresistance through the TIP60-mediated Fanconi anemia and homologous recombination repair pathways
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28. DNA polymerase ι compensates for Fanconi anemia pathway deficiency by countering DNA replication stress
    Rui Wang, W. Frank Lenoir, Chao Wang, Dan Su, Megan E. McLaughlin, Qianghua Hu, Xi Hua Shen, Yanyan Tian, Naeh L. Klages-Mundt, Erica J. Lynn et al. · 2020 · Proceedings of the National Academy of Sciences
29. Treatment of ovarian cancer: From the past to the new era (Review)
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30. RAD51 paralogs synergize with RAD51 to protect reversed forks from cellular nucleases
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31. Genetic Counseling for Fanconi Anemia: Crosslinking Disciplines
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32. Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process
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33. A Dutch Fanconi AnemiaFANCCFounder Mutation in Canadian Manitoba Mennonites
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34. The ubiquitin family meets the Fanconi anemia proteins
    Xavier Renaudin, Letícia Koch Lerner, Carlos Frederico Martins Menck, Filippo Rosselli · 2016 · Mutation Research/Reviews in Mutation Research
35. Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes
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36. Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients
    Lixian Chang, Weiping Yuan, Huimin Zeng, Quanquan Zhou, Wei Wei, Jianfeng Zhou, Miaomiao Li, Xiaomin Wang, Mingjiang Xu, Feng‐Chun Yang et al. · 2014 · BMC Medical Genomics
37. Fanconi Anemia Proteins and Their Interacting Partners: A Molecular Puzzle
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38. Expanding the FANCO/RAD51C associated phenotype: Cleft lip and palate and lobar holoprosencephaly, two rare findings in Fanconi anemia
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39. FANCD2 but not FANCA promotes cellular resistance to type II topoisomerase poisons
    Lisa Ann Kachnic, Li Li, Loreen Fournier, Natalie Ferraiolo, Jochen Dahm‐Daphi, Kerstin Borgmann, Henning Willers · 2011 · Cancer Letters
40. Cytoplasmic FANCA-FANCC Complex Interacts and Stabilizes the Cytoplasm-dislocalized Leukemic Nucleophosmin Protein (NPMc)
    Wei Du, Jie Li, Jared Sipple, Jianjun Chen, Qishen Pang · 2010 · Journal of Biological Chemistry
41. Cryo–electron microscopic visualization of RAD51 filament assembly and end-capping by XRCC3-RAD51C-RAD51D-XRCC2
    Luke A. Greenhough, Lorenzo Galanti, Chih‐Chao Liang, Simon J. Boulton, Stephen Craig West · 2025 · Science
42. Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families
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43. A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients
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44. Cytogenetics in Fanconi Anemia: The Importance of Follow-Up and the Search for New Biomarkers of Genomic Instability
    Lismeri Wuicik Merfort, Mateus de Oliveira Lisboa, Luciane R. Cavalli, Carmem Bonfim · 2022 · International Journal of Molecular Sciences
45. Heterozygous Mutations in DNA Repair Genes and Hereditary Breast Cancer: A Question of Power
    Nathan A. Ellis, Kenneth Offit · 2012 · PLoS Genetics
46. A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH)
    Luis Alfredo Umaña, Pilar L. Magoulas, Weimin Bi, Carlos A. Bacino · 2011 · American Journal of Medical Genetics Part A
47. The FANC pathway is activated by adenovirus infection and promotes viral replication-dependent recombination
    Gioia Cherubini, Valeria Naim, Paola Caruso, Romina Burla, Massimo Bogliolo, Enrico Cundari, Karim Benihoud, Isabella Saggio, Filippo Rosselli · 2011 · Nucleic Acids Research
48. The phenotype of FancB-mutant mouse embryonic stem cells
    Tae Moon Kim, Jun Ho Ko, Yong Jun Choi, Lingchuan Hu, Paul Hasty · 2011 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
49. C. elegans Ring Finger Protein RNF-113 Is Involved in Interstrand DNA Crosslink Repair and Interacts with a RAD51C Homolog
    Hyojin Lee, Arno F. Alpi, Mi So Park, Ann M. Rose, Hyeon‐Sook Koo · 2013 · PLoS ONE
50. Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations
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51. Replication Protein A (RPA) deficiency activates the Fanconi anemia DNA repair pathway
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52. Differentially expressed miRNAs in oxygen-induced retinopathy newborn mouse models
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53. MicroRNAs that affect the Fanconi Anemia/BRCA pathway are downregulated in imatinib-resistant chronic myeloid leukemia patients without detectable BCR-ABL kinase domain mutations
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54. Germline mutations in RAD51C in Jewish high cancer risk families
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55. The ubiquitination machinery of the Fanconi Anemia DNA repair pathway
    Winnie Tan, Andrew J. Deans · 2020 · Progress in Biophysics and Molecular Biology
56. RNAi-mediated knockdown of FANCF suppresses cell proliferation, migration, invasion, and drug resistance potential of breast cancer cells
    Li Zhao, N. Li, Juan‐Han Yu, Hongtao Tang, Y.L. Li, Miao He, Zhaojin Yu, Xue‐Feng Bai, Zhaohui Zheng, E.H. Wang et al. · 2013 · Brazilian Journal of Medical and Biological Research
57. A Case Report of Fanconi Anemia Diagnosed by Genetic Testing Followed by Prenatal Diagnosis
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58. Estrogen induces RAD51C expression and localization to sites of DNA damage
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59. The DNA-binding activity of USP1-associated factor 1 is required for efficient RAD51-mediated homologous DNA pairing and homology-directed DNA repair
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60. Using mouse models to investigate the biological and physiological consequences of defects in the Fanconi anaemia/breast cancer DNA repair signalling pathway
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61. XRCC2 (X-ray repair cross complementing 2)
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62. Impaired function of Fanconi anemia type C-deficient macrophages
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65. Hypomorphic Brca2 and Rad51c double mutant mice display Fanconi anemia, cancer and polygenic replication stress
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66. Screening of Finnish RAD51Cfounder mutations in prostate and colorectal cancer patients
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68. Minigene Splicing Assays Identify 20 Spliceogenic Variants of the Breast/Ovarian Cancer Susceptibility Gene RAD51C
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71. The role of USP 1 autocleavage in DNA interstrand crosslink repair
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72. Mechanism of BCDX2-mediated RAD51 nucleation on short ssDNA stretches and fork DNA
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74. Familial Breast Cancer Risk
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75. Nucleotide proofreading functions by nematode RAD51 paralogs facilitate optimal RAD51 filament function
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76. The Fanconi anemia pathway is downregulated upon macrophage differentiation through two distinct mechanisms
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99. BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer
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