Cdk5rap2 exposes the centrosomal root of microcephaly syndromes

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WDR62 is associated with the spindle pole and is mutated in human microcephaly

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Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

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CDK5RAP2 Is a Pericentriolar Protein That Functions in Centrosomal Attachment of the γ-Tubulin Ring Complex

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Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome

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CDK5RAP2 stimulates microtubule nucleation by the γ-tubulin ring complex

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Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

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Control of planar divisions by the G-protein regulator LGN maintains progenitors in the chick neuroepithelium

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Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly

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CEP152 is a genome maintenance protein disrupted in Seckel syndrome

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Zygotic development without functional mitotic centrosomes

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Many roads lead to primary autosomal recessive microcephaly

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Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

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Drosophila neuroblasts retain the daughter centrosome

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Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline

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Cdk5rap2 Interacts with Pericentrin to Maintain the Neural Progenitor Pool in the Developing Neocortex

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Ab ovo or de novo? Mechanisms of Centriole Duplication

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Distinct BRCT domains in Mcph1/Brit1 mediate ionizing radiation-induced focus formation and centrosomal localization

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Interaction of CDK5RAP2 with EB1 to Track Growing Microtubule Tips and to Regulate Microtubule Dynamics

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Emerging Connection Between Centrosome and DNA Repair Machinery

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A Tale of Too Many Centrosomes

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