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Updated: May 2, 2026

Quantitative Immunofluorescence Assay to Measure the Variation in Protein Levels at Centrosomes
Published on: December 20, 2014
Microcephaly: STIL(l) a tale of too many centrosomes
Véronique Marthiens1, Renata Basto1
1UMR144, CNRS- Institut Curie, 12 rue Lhomond, 75005, Paris, France.
Abstract:
Centrosome mutations associated with microcephaly are normally thought to result in loss-of-function phenotypes. A new study shows, however, that mutations found in the human microcephaly STIL gene cause centrosome amplification, suggesting a direct link between the presence of extra centrosomes and the establishment of this disease.
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