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Dysregulation of the balance between the proliferation and the cell cycle exit in neural progenitors is one of the major causes of microcephaly (small brain). Recent studies indicate that cell cycle machinery influences not only the proliferation but also <jats:styled-content style=\"fixed-case\">INM<\/jats:styled-content> in neural progenitors. Furthermore, several cell cycle\u2010related proteins, including p27<jats:sup>kip1<\/jats:sup>, p57<jats:sup>kip2<\/jats:sup>, Cdk5, and Rb, regulate the migration of neurons in the postmitotic state, suggesting that the growth arrest confers dual functions on cell cycle regulators. Consistently, several types of microcephaly occur in conjunction with neuronal migration disorders, such as periventricular heterotopia and lissencephaly. However, cell cycle re\u2010entry by disturbance of growth arrest in mature neurons is thought to trigger neuronal cell death in Alzheimer's disease. In this review, we introduce the cell cycle protein\u2010mediated regulation of two types of nuclear movement, <jats:styled-content style=\"fixed-case\">INM<\/jats:styled-content> and neuronal migration, during cerebral cortical development, and discuss the roles of growth arrest in cortical development and neurological disorders.<\/jats:p>","DOI":"10.1111\/gtc.12029","type":"journal-article","created":{"date-parts":[[2013,1,7]],"date-time":"2013-01-07T14:42:46Z","timestamp":1357569766000},"page":"176-194","source":"Crossref","is-referenced-by-count":45,"title":["Extra\u2010cell cycle regulatory functions of cyclin\u2010dependent kinases (<scp>CDK<\/scp>) and <scp>CDK<\/scp> inhibitor proteins contribute to brain development and neurological disorders"],"prefix":"10.1111","volume":"18","author":[{"given":"Takeshi","family":"Kawauchi","sequence":"first","affiliation":[{"name":"Precursory Research for Embryonic Science and Technology (PRESTO) Japan Science and Technology Agency (JST) 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