Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1

@inproceedings{Tibelius2009MicrocephalinAP,
  title={Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1},
  author={Alexandra Tibelius and Joachim Marhold and H. Zentgraf and Christoph E Heilig and Heidemarie Neitzel and Bernard Ducommun and Anita Rauch and Anthony D. Ho and Jiri Bartek and Alwin Kraemer},
  booktitle={The Journal of cell biology},
  year={2009}
}
Primary microcephaly, Seckel syndrome, and microcephalic osteodysplastic primordial dwarfism type II (MOPD II) are disorders exhibiting marked microcephaly, with small brain sizes reflecting reduced neuron production during fetal life. Although primary microcephaly can be caused by mutations in microcephalin (MCPH1), cells from patients with Seckel syndrome and MOPD II harbor mutations in ataxia telangiectasia and Rad3 related (ATR) or pericentrin (PCNT), leading to disturbed ATR signaling. In… CONTINUE READING

Citations

Publications citing this paper.
SHOWING 1-10 OF 58 CITATIONS, ESTIMATED 28% COVERAGE

FILTER CITATIONS BY YEAR

2010
2018

CITATION STATISTICS

  • 10 Highly Influenced Citations

  • Averaged 2 Citations per year over the last 3 years

References

Publications referenced by this paper.
SHOWING 1-10 OF 32 REFERENCES

Similar Papers

Loading similar papers…