Med Sci (Paris)
Volume 29, Number 8-9, Août–Septembre 2013
L’oncogénomique : chroniques d’un avènement
Page(s) 807 - 810
Section Repères
Published online 05 September 2013
  1. Lengauer C, Kinzler KW, Vogelstein B. Genetic instabilities in human cancers. Nature 1998 ; 396 : 643–649. [CrossRef] [PubMed] [Google Scholar]
  2. Kops GJPL, Weaver BAA, Cleveland DW. On the road to cancer: aneuploidy and the mitotic checkpoint. Nat Rev Cancer 2005 ; 5 : 773–785. [CrossRef] [PubMed] [Google Scholar]
  3. Burrell RA, McClelland SE, Endesfelder D, et al. Replication stress links structural and numerical cancer chromosomal instability. Nature 2013 ; 494 : 492–496. [CrossRef] [PubMed] [Google Scholar]
  4. Bartkhova J, Rezaei N, Liontos M, et al. Oncogene-induced senescence is part of the tumorigenesis barrier imposed by DNA damage checkpoints. Nature 2006 ; 444 : 633–637. [CrossRef] [PubMed] [Google Scholar]
  5. Bunz F, Fauth C, Speicher MR, et al. Targeted inactivation of p53 in human cells does not result in aneuploidy. Cancer Res 2002 ; 62 : 1129–1133. [PubMed] [Google Scholar]
  6. Anglana M, Apiou F, Bensimon A, Debatisse M. Dynamics of DNA replication in mammalian somatic cells : nucleotide pool modulates origin choice and interorigin spacing. Cell 2003 ; 114 : 385–394. [CrossRef] [PubMed] [Google Scholar]
  7. Bester AC, Roniger M, Oren YS, et al. Nucleotide deficiency promotes genomic instability in early stages of cancer development. Cell 2011 ; 145 : 435–446. [CrossRef] [PubMed] [Google Scholar]
  8. Billaud M. L’hétérogénéité intratumorale, un obstacle darwinien à la médecine personnalisée ? Med Sci (Paris) 2012 ; 12 : 1116–1119. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  9. Maydan G, Noyman I, Har-Zahav A, et al. Multiple congenital anomalies-hypotonia seizures syndrome is caused by a mutation in PIGN. J Med Genet 2011 ; 48 : 383–389. [CrossRef] [PubMed] [Google Scholar]
  10. Krawitz PM, Schweiger MR, Rödelsperger C, et al. Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nat Genet 2010 ; 42 : 827–829. [CrossRef] [PubMed] [Google Scholar]
  11. Krawitz PM, Murakami Y, Hecht Y, et al. Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation. Am J Hum Genet 2012 ; 91 : 146–151. [CrossRef] [PubMed] [Google Scholar]
  12. Buchet-Poyau H, Courchet J, Le Hir H, et al. Identification and characterization of human Mex-3 proteins, a novel family of evolutionarily conserved RNA-binding proteins differentially localized to processing bodies. Nucleic Acids Res 2007 ; 35 : 1289–1300. [CrossRef] [PubMed] [Google Scholar]
  13. Topol E. The creative destruction of medicine. New York : Basic Books, 2012. [Google Scholar]

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