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

Vaz, Fiona, Hanenberg, Helmut, Schuster, Beatrice, Barker, Karen, Wiek, Constanze, Erven, Verena, Neveling, Kornelia, Endt, Daniela +12 more·2010·Nature Genetics

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  10. Diagnosis of Fanconi's Anemia by Diepoxybutane Analysis in Children from Serbia
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  13. Regulated Expression of a FANCL Splicing Variant as a Potential Modifier of DNA Repair Activity
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  17. Structural peculiarities of the (MHF1–MHF2)4 octamer provide a long DNA binding patch to anchor the MHF–FANCM complex to chromatin: A solution SAXS study
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  20. SNV/indel hypermutator phenotype in biallelic RAD51C variant: Fanconi anemia
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    Pietro G. A. Aronica, Chandra Shekhar Verma, Bojana Popovic, Robin J. Leatherbarrow, Ian R. Gould · 2016 · Protein Engineering Design and Selection
  22. Investigation of mutations in Fanconi anemia genes and malignancy predisposition in Brazilian patients
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  23. Effect of RAD51C expression on the chemosensitivity of Eμ-Myc p19Arf‑/‑ cells and its clinical significance in breast cancer
    Shao‐Guang Liao, Lu Liu, Yajie Wang · 2018 · Oncology Letters
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  28. Genetic diagnosis of Fanconi anemia. Literature review
    Агнеса Владимировна Панферова, N. M. Timofeeva, Yulia V Olshanskaya · 2016 · Oncohematology
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  30. Fanconi Anemia: A Pathway of Hematopoiesis and Cancer Predisposition
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  31. Identification of new RAD51D-regulating microRNAs that also emerge as potent inhibitors of the Fanconi anemia/homologous recombination pathways
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  37. Correspondence
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  39. Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancer
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  41. Clastogen-Induced Chromosomal Breakage Analysis of Suspected Fanconis Anemia Cases of Kashmir, North India
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  42. The FANCA to FANCZ of DNA interstrand crosslink repair: Lessons from Fanconi anemia
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  44. Genetics
    Ian S. Fentiman · 2017 · Springer eBooks
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  46. RAD51C and MYST3 Mutations in a Case of Desmoid-Type Fibromatosis With No Mutation in CTNNB1 or APC
    Keith M. Skubitz, Paari J Murugan · 2024 · Cureus
  47. Investigating the effects of the ARG258HIS mutation on RAD51C in inherited Fanconi Anemia and cancer disease
    Sara Seifeldin, Mοhd Saeed, Khalid Alshaghdali, Elgeli Yousif, Amal Abu Sabaa, Hatem Rabie, Samra Siddiqui, Amir Saeed · 2024 · Journal of Biomolecular Structure and Dynamics
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    Alix Eden Seif, Beverly J. Lange, Jaclyn A. Biegel, Kim E. Nichols · 2012 · Cambridge University Press eBooks
  49. DNA Repair: Disorders
    Alan R. Lehmann, Mark O’Driscoll · 2010 · Wiley eBooks
  50. Faculty Opinions recommendation of A dominant mutation in human RAD51 reveals its function in DNA interstrand crosslink repair independent of homologous recombination.
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  52. RAD51C als weiteres Hochrisiko-Gen für familiären Brust- und Eierstockkrebs identifiziert
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  53. Germline Mutations in CHEK1 and CHEK2 in Women with Ovarian, Peritoneal, or Fallopian Tube Cancer
    Maria I. Harrell · 2015 · ScholarWorks (Walden University)
  54. Bone Marrow Microenvironment defects in Fanconi AnemiaBone Marrow Microenvironment Defects in Fanconi Anemia
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    Florêncio Porto Freitas · 2014 · Digital Library of Theses and Dissertations (Universidade de São Paulo)
  57. Mutaciones del gen RAD51 en el cáncer familiar de ovario: revisión de la literatura
    Alexandra Madariaga L, Daniel E Sanabria S, Luz Dary Gutiérrez C · 2015 · Revista chilena de obstetricia y ginecología
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    Mohamed E. Ashour, Lamia El-Shafie, Sherif F. El‐Khamisy · 2014 · Cancer metastasis
  59. RAD51C IS A TUMOR SUPPRESSOR IN MAMMARY AND SEBACEOUS GLANDS
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  61. Fanconi anemia: in all its glory
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    Aline Cristina Zandoná Teixeira · 2013
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  64. DNA Methylierung ausgewählter BRCA- und Fanconi Anämie-Gene beim familiären Mammakarzinom
    Robin Zazoff · 2014 · MACAU: Open Access Repository of Kiel University (University Library Kiel)
  65. High-, Moderate-, and Low-Penetrance Genes Involved in the Pathogenesis of a Hereditary Predisposition to Breast Cancer
    Larissa A. Korde, Stacey Shiovitz · 2013
  66. Hereditäres Mamma- und Ovarialkarzinom: BRCA1, BRCA2 und BRCA3
    Marion B. Kiechle · 2011 · Springer eBooks
  67. Disorders of DNA Repair and Metabolism
    Sharon E. Plon · 2013 · Elsevier eBooks
  68. Genome sensitivity in patients with chromosomal instability disorders
    Sanja Cirković · 2012
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    Andrew S. Holpuch, Susan R. Mallery · 2016 · Springer eBooks
  70. The Shu complex is a conserved regulator of Rad51 filament formation
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  73. Genetic Counseling
    Hema Purandarey · 2009 · Jaypee Brothers Medical Publishers (P) Ltd. eBooks
  74. SURVEY AND SUMMARY Homologous recombination and its regulation
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  77. Identifizierung von Patientinnen und Patienten mit der hereditären Form des Mamma- und Ovarialkarzinoms mittels Next-Generation-Sequencing-(NGS)-Technologie
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  78. Polymorphic Variants of Genes RAD51B and XRCC1 Influence on Breast Cancer Development
    З. И. Бисултанова, М М Биттуева, П. М. Джамбетова, L. M. Dzhambetova, E. Machogov · 2019 · International Conference on Health and Wellbeing in Modern Society (ICHW)
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    Ana Isabel Sánchez Bermúdez, M.a Desamparados Sarabia Meseguer, Verónica Castillo Guardiola, Francisco Ruiz Espejo, José Antonio Noguera Velasco · 2020 · Revista de Medicina de Laboratorio
  81. IONIZING RADIATION
    2013 · CRC Press eBooks
  82. Fanconi Anemia
    Richa Saxena, Mampi Debnath, Sudha Chamoli · 2018
  83. Five Novel Deleterious Variants in FANCA, FANCF and FANCG Identified in Pakistani Fanconi Anemia Families Using Exome Sequencing
    Ashley S. Thompson, Nusrat Saba, Lisa J. McReynolds, Saeeda Munir, Parvez Ahmed, Sumaira Sajjad, Kristine M. Jones, Meredith Yeager, Frank X. Donovan, Settara C. Chandrasekharappa et al. · 2020
  84. Faculty Opinions recommendation of Novel insights into RAD51 activity and regulation during homologous recombination and DNA replication.
    Roland Kanaar · 2018 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
  85. Pembrolizumab activity in patients with Fanconi anemia repair pathway competent and deficient tumors
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  86. Identifying Novel Candidate Biomarkers of Early Epithelial Ovarian Cancer
    Sarah Sczelecki · 2023
  87. Varianten im FANCA-Gen bei Fanconi-Anämie-Patienten aus Pakistan im internationalen Vergleich
    David Alexander Ziegler · 2023
  88. Alteración de los patrones de splicing en genes de susceptibilidad a cáncer de mama: análisis funcional mediante minigenes híbridos.
    Lara Sanoguera‐Miralles · 2024
  89. A practice changing paper: biallelic inactivation of BRCA2 in Fanconi anaemia
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  90. Diet induced mitochondrial DNA replication instability in Rad51c mutant mice drives sex-bias in anemia of inflammation
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  92. Hematologic Problems
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    Rochelle R. Maxwell, Tamar Berger, Caroline S. Jiang, Allana Rosenberg, Ashlyn-Maree Gonzalez, Jodie Odame, Yu-Chien Lin, Francis P. Lach, Jennifer A. Kennedy, Rebecca K. Tryon et al. · 2025 · medRxiv
  94. Fanconi anemia: mechanistic insights into a phenotypically diverse disease using divers model systems
    Sandra Segura‐Bayona · 2013 · Utrecht University Repository (Utrecht University)
  95. Cap a un model complet de la xarxa molecular alterada en l’anèmia de Fanconi i el càncer de mama
    Griselda Martrat Sànchez · 2012 · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
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  97. Insights and modulation of RNA polymerase–dependent R-loop and dsRNA in Fanconi anemia hematopoietic stem cells
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  99. Prédispositions génétiques au cancer du sein et de l'ovaire dans la population suisse entre 1996 et 2009 : bilan de l'activité oncogénétique et du dépistage de mutations constitutionnelles dans les gènes BRCA1/BRCA2
    Aurélie Ayme · 2013
  100. Mechanistic Study of D-loop Formation during Homologous Recombination by Molecular Microscopy
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