AbstractLIS1 is a product of the causative gene for type I lissencephaly characterized by a smooth brain surface due to a defect in neuronal migration during brain development and a regulatory subunit of platelet-activating factor acetylhydrolase (PAF-AH). It is also a mammalian homologue of the fungal nuclear distribution (nud) gene, nudF, which controls the migration of fungal nuclei. Using the two-hybrid system, we identified a novel LIS1-interacting protein, rat NUDE (rNUDE), and found that it is a mammalian homologue of another fungal nud gene product, NUDE, and Xenopus mitotic phosphoprotein 43 which is phosphorylated in a cell cycle-dependent manner. rNUDE and the catalytic subunits of PAF-AH interact with the N- and C-termini of LIS...
Nuclear migration depends on microtubules, the dynein motor complex, and regulatory components like ...
AbstractMutations in the Lis1 gene result in lissencephaly (smooth brain), a debilitating developmen...
AbstractNudC is a highly conserved protein necessary for cytoplasmic dynein-mediated nuclear migrati...
AbstractLIS1 is a product of the causative gene for type I lissencephaly characterized by a smooth b...
AbstractImportant clues to how the mammalian cerebral cortex develops are provided by the analysis o...
Important clues to how the mammalian cerebral cortex develops are provided by the analysis of geneti...
The LISI-encoded protein (Lis 1) plays a role in brain development because a hemizygous deletion or ...
AbstractLissencephaly is a brain developmental disorder characterized by disorganization of the cort...
AbstractLIS1, a microtubule-associated protein, is required for neuronal migration, but the precise ...
Lissencephaly is a brain developmental disorder characterized by disorganization of the cortical reg...
Miller-Dieker lissencephaly syndrome (MDS) is a human developmental brain malformation caused by neu...
AbstractMutations in the LIS1 gene cause lissencephaly, a human neuronal migration disorder. LIS1 bi...
AbstractDisruption of one allele of the LIS1 gene causes a severe developmental brain abnormality, t...
Mutations in the LIS1 gene cause lissencephaly, a human neuronal migration disorder. LIS1 binds dyne...
Brain development is severely defective in children with lissencephaly. The highly organized distrib...
Nuclear migration depends on microtubules, the dynein motor complex, and regulatory components like ...
AbstractMutations in the Lis1 gene result in lissencephaly (smooth brain), a debilitating developmen...
AbstractNudC is a highly conserved protein necessary for cytoplasmic dynein-mediated nuclear migrati...
AbstractLIS1 is a product of the causative gene for type I lissencephaly characterized by a smooth b...
AbstractImportant clues to how the mammalian cerebral cortex develops are provided by the analysis o...
Important clues to how the mammalian cerebral cortex develops are provided by the analysis of geneti...
The LISI-encoded protein (Lis 1) plays a role in brain development because a hemizygous deletion or ...
AbstractLissencephaly is a brain developmental disorder characterized by disorganization of the cort...
AbstractLIS1, a microtubule-associated protein, is required for neuronal migration, but the precise ...
Lissencephaly is a brain developmental disorder characterized by disorganization of the cortical reg...
Miller-Dieker lissencephaly syndrome (MDS) is a human developmental brain malformation caused by neu...
AbstractMutations in the LIS1 gene cause lissencephaly, a human neuronal migration disorder. LIS1 bi...
AbstractDisruption of one allele of the LIS1 gene causes a severe developmental brain abnormality, t...
Mutations in the LIS1 gene cause lissencephaly, a human neuronal migration disorder. LIS1 binds dyne...
Brain development is severely defective in children with lissencephaly. The highly organized distrib...
Nuclear migration depends on microtubules, the dynein motor complex, and regulatory components like ...
AbstractMutations in the Lis1 gene result in lissencephaly (smooth brain), a debilitating developmen...
AbstractNudC is a highly conserved protein necessary for cytoplasmic dynein-mediated nuclear migrati...