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
DOI 10.1038/ng.570
Cited by (408)
Items 301–400 of 408
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- Genetic diagnosis of Fanconi anemia. Literature reviewАгнеса Владимировна Панферова, N. M. Timofeeva, Yulia V Olshanskaya · 2016 · Oncohematology
- Distinct cellular phenotype linked to defective DNA interstrand crosslink repair and homologous recombinationAleksandra M. Gorniewska, Katarzyna Kluzek, Lidia Gackowska, Izabela Kubiszewska, Małgorzata Z. Zdzienicka, Aneta Bialkowska · 2017 · Molecular Medicine Reports
- Fanconi Anemia: A Pathway of Hematopoiesis and Cancer PredispositionAli Y Suliman, Franklin O. Smith, Gary M. Kupfer · 2018 · Pediatric oncology
- Identification of new RAD51D-regulating microRNAs that also emerge as potent inhibitors of the Fanconi anemia/homologous recombination pathwaysNina Hater, Katharina M Iwaniuk, Carina Leifeld, Pia Grüten, Constanze Wiek, Katharina Raba, Fan Zhang, Johannes Fischer, Paul R. Andreassen, Helmut Hanenberg et al. · 2022 · Human Molecular Genetics
- Hot on RAD51C: structure and functions of RAD51C‐XRCC3Barnabás Szakál, Dana Branzei · 2023 · Molecular Oncology
- The Fanconi Anemia Pathway and Interstrand Cross-Link RepairMasamichi Ishiai, Junya Tomida, Akiko Itaya, James Hejna, Minoru Takata · 2016 · Springer eBooks
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- Correction: A Protein Prioritization Approach Tailored for the FA/BRCA PathwayAnneke Haitjema, Bernd Willem Brandt, Najim Ameziane, Patrick May, Jaap Heringa, Johan P. de Winter, Hans Joenje, Josephine C. Dorsman · 2013 · PLoS ONE
- CorrespondenceSukanta Nandi, Arnab Biswas, Sriram Krishnamurthy, Subramanian Mahadevan, H. P. Singh, Avani Solanki, Babu Rao Vundinti, Kamlesh Harish, Karanveer Singh, Prakash Gambhir et al. · 2014 · Indian Pediatrics
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- Integration of tumour sequencing and case–control data to assess pathogenicity of RAD51C missense variants in familial breast cancerBelle W.X. Lim, Na Li, Simone M. Rowley, Ella R. Thompson, Simone McInerny, Magnus Zethoven, Rodney John Scott, Lisa Devereux, Erica K. Sloan, Paul Andrew James et al. · 2022 · npj Breast Cancer
- From the Molecular Biology to the Gene Therapy of a DNA Repair Syndrome: Fanconi AnemiaPaula Rı́o, Susana Navarro, A. De Juan · 2011 · InTech eBooks
- Clastogen-Induced Chromosomal Breakage Analysis of Suspected Fanconis Anemia Cases of Kashmir, North IndiaTahir Mohiuddin Malla, Mahrukh Hameed Zargar, Fayaz Ahmad Dar · 2016 · Journal of Genetic Syndromes & Gene Therapy
- The FANCA to FANCZ of DNA interstrand crosslink repair: Lessons from Fanconi anemiaJulienne J. O’Rourke, Andrew J. Deans · 2016 · Elsevier eBooks
- FANCF hypomethylation is associated with colorectal cancer in Han ChineseHang Yu, Ranran Pan, Tong Gao, Dongping Wu, Jieer Ying, Shiwei Duan · 2020 · The Turkish Journal of Gastroenterology
- GeneticsIan S. Fentiman · 2017 · Springer eBooks
- Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from PakistanMuhammad Usman Rashid, Noor Muhammad, Umara Shehzad, Faiz Ali Khan, Asif Loya, Ute Hamann · 2022 · Familial Cancer
- RAD51C and MYST3 Mutations in a Case of Desmoid-Type Fibromatosis With No Mutation in CTNNB1 or APCKeith M. Skubitz, Paari J Murugan · 2024 · Cureus
- Investigating the effects of the ARG258HIS mutation on RAD51C in inherited Fanconi Anemia and cancer diseaseSara Seifeldin, Mοhd Saeed, Khalid Alshaghdali, Elgeli Yousif, Amal Abu Sabaa, Hatem Rabie, Samra Siddiqui, Amir Saeed · 2024 · Journal of Biomolecular Structure and Dynamics
- Heritable predisposition to childhood hematologic malignanciesAlix Eden Seif, Beverly J. Lange, Jaclyn A. Biegel, Kim E. Nichols · 2012 · Cambridge University Press eBooks
- DNA Repair: DisordersAlan R. Lehmann, Mark O’Driscoll · 2010 · Wiley eBooks
- Faculty Opinions recommendation of A dominant mutation in human RAD51 reveals its function in DNA interstrand crosslink repair independent of homologous recombination.Claire Wyman · 2018 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Distinct complexes of RAD51 paralogs participate in different fork protection pathwaysDebanjali Bhattacharya, Harsh Kumar Dwivedi, Satyaranjan Sahoo, Shariva Kadupatil, Ganesh Nagaraju · 2026 · bioRxiv (Cold Spring Harbor Laboratory)
- RAD51C als weiteres Hochrisiko-Gen für familiären Brust- und Eierstockkrebs identifiziertK. Bosse · 2011 · Der Onkologe
- Germline Mutations in CHEK1 and CHEK2 in Women with Ovarian, Peritoneal, or Fallopian Tube CancerMaria I. Harrell · 2015 · ScholarWorks (Walden University)
- Bone Marrow Microenvironment defects in Fanconi AnemiaBone Marrow Microenvironment Defects in Fanconi AnemiaWen Xing, Mingjiang Xu, Feng‐Chun Yang · 2013 · InTech eBooks
- IDENTIFICATION OF NOVEL FANCD2 INTERACTING PROTEINS VIA IMMUNOPRECIPITATION AND MASS SPECTROMETRYPaul A. Azzinaro · 2014
- Investigação de potenciais biomarcadores redox - um enfoque em aldeídos e seus produtosFlorêncio Porto Freitas · 2014 · Digital Library of Theses and Dissertations (Universidade de São Paulo)
- Mutaciones del gen RAD51 en el cáncer familiar de ovario: revisión de la literaturaAlexandra Madariaga L, Daniel E Sanabria S, Luz Dary Gutiérrez C · 2015 · Revista chilena de obstetricia y ginecología
- DNA Damage Response Pathways in Cancer Predisposition and ProgressionMohamed E. Ashour, Lamia El-Shafie, Sherif F. El‐Khamisy · 2014 · Cancer metastasis
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