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Volume 2012, Article ID 425814, 11 pages
Review Article

Fanconi Anemia Proteins and Their Interacting Partners: A Molecular Puzzle

1Department of Pediatrics, Université Laval, Cité Universitaire, Québec, QC, Canada G1K 7P4
2Reproduction, Perinatal Health and Child Health, Centre de Recherche du CHUQ-CHUL, 2705 Boul Laurier, Québec, QC, Canada G1V 4G2

Received 9 December 2011; Accepted 13 March 2012

Academic Editor: Henri J. van de Vrugt

Copyright © 2012 Tagrid Kaddar and Madeleine Carreau. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [11 citations]

The following is the list of published articles that have cited the current article.

  • Lindsey E. Romick-Rosendale, Vivian W.Y. Lui, Jennifer R. Grandis, and Susanne I. Wells, “The Fanconi anemia pathway: Repairing the link between DNA damage and squamous cell carcinoma,” Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, vol. 743-744, pp. 78–88, 2013. View at Publisher · View at Google Scholar
  • Paolo Degan, Carlo Dufour, Silvia Ravera, Daniele Vaccaro, Paola Cuccarolo, Martina Bartolucci, Alessandro Morelli, Marta Columbaro, Cristina Capanni, Enrico Cappelli, and Isabella Panfoli, “Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A,” Biochimie, vol. 95, no. 10, pp. 1828–1837, 2013. View at Publisher · View at Google Scholar
  • Anneke Haitjema, Berber M. Mol, Irsan E. Kooi, Maarten P. G. Massink, Jens A. L. Jorgensen, Davy A. P. Rockx, Martin A. Rooimans, Johan P. de Winter, Hanne Meijers-Heijboer, Hans Joenje, and Josephine C. Dorsman, “Coregulation of FANCA and BRCA1 in human cells,” Springerplus, vol. 3, 2014. View at Publisher · View at Google Scholar
  • Helen Walden, and Andrew J. Deans, “The Fanconi Anemia DNA Repair Pathway: Structural and Functional Insights into a Complex Disorder,” Annual Review of Biophysics, vol. 43, no. 1, pp. 257–278, 2014. View at Publisher · View at Google Scholar
  • Reinhart Speeckaert, Mireille Van Gele, Marijn M. Speeckaert, Jo Lambert, and Nanja van Geel, “The biology of hyperpigmentation syndromes,” Pigment Cell & Melanoma Research, 2014. View at Publisher · View at Google Scholar
  • FengFei Huang, Manel Ben Aissa, Audrey Magron, Caroline C. Huard, Chantal Godin, Georges Levesque, and Madeleine Carreau, “The Fanconi Anemia Group C Protein Interacts with Uncoordinated 5A and Delays Apoptosis,” Plos One, vol. 9, no. 3, 2014. View at Publisher · View at Google Scholar
  • C. C. Huard, C. S. Tremblay, A. Magron, G. Levesque, and M. Carreau, “The Fanconi anemia pathway has a dual function in Dickkopf-1 transcriptional repression,” Proceedings of the National Academy of Sciences, vol. 111, no. 6, pp. 2152–2157, 2014. View at Publisher · View at Google Scholar
  • Aleksandra M. Koczorowska, Aneta Bialkowska, Malgorzata Z. Zdzienicka, and Katarzyna Kluzek, “The role of the Fanconi anemia pathway in DNA repair and maintenance of genome stability,” Postepy Higieny i Medycyny Doswiadczalnej, vol. 68, pp. 459–472, 2014. View at Publisher · View at Google Scholar
  • Audrey Magron, Sabine Elowe, and Madeleine Carreau, “The Fanconi anemia C protein binds to and regulates stathmin-1 phosphorylation,” PLoS ONE, vol. 10, no. 10, 2015. View at Publisher · View at Google Scholar
  • Bong Sub Kim, Hae In Choi, Jong Heon Kim, Sung Ho Goh, Chang-Hun Lee, Min Jeong Chun, Sunshin Kim, Soo Kyung Hwang, and Hyoun Geun Kim, “AMP-activated protein kinase is involved in the activation of the Fanconi anemia/BRCA pathway in response to DNA interstrand crosslinks,” Oncotarget, vol. 7, no. 33, pp. 53642–53653, 2016. View at Publisher · View at Google Scholar
  • Julia Hess, Kristian Unger, Michael Orth, Ulrike Schötz, Lars Schüttrumpf, Verena Zangen, Igor Gimenez-Aznar, Agata Michna, Ludmila Schneider, Ramona Stamp, Martin Selmansberger, Herbert Braselmann, Ludwig Hieber, Guido A. Drexler, Sebastian Kuger, Diana Klein, Verena Jendrossek, Anna A. Friedl, Claus Belka, Horst Zitzelsberger, and Kirsten Lauber, “Genomic amplification of Fanconi anemia complementation group A (FancA) in head and neck squamous cell carcinoma (HNSCC): Cellular mechanisms of radioresistance and clinical relevance,” Cancer Letters, 2016. View at Publisher · View at Google Scholar