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Table of contents

Neuron 63, — Evsyukova, I. Integrative mechanisms of oriented neuronal migration in the developing brain. Cell Dev. Fleck, M.


Hippocampal abnormalities and enhanced excitability in a murine model of human lissencephaly. Reelin, Disabled 1, and beta 1 integrins are required for the formation of the radial glial scaffold in the hippocampus. Frantz, G. Gleeson, J. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 92, 63— Harrison, P. The hippocampus in schizophrenia: a review of the neuropathological evidence and its pathophysiological implications.

Psychopharmacology Berl. Hattori, M. Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]. Hiesberger, T. Hirotsune, S. Graded reduction of Pafah1b1 Lis1 activity results in neuronal migration defects and early embryonic lethality. The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons. Honda, T. Regulation of cortical neuron migration by the Reelin signaling pathway. Howell, B. Neuronal position in the developing brain is regulated by mouse disabled Keays, D.

Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell , 45— Kerjan, G. Mice lacking doublecortin and doublecortin-like kinase 2 display altered hippocampal neuronal maturation and spontaneous seizures. Kim, J.

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Kitazawa, A. Klein, R. SDF-1 alpha induces chemotaxis and enhances Sonic hedgehog-induced proliferation of cerebellar granule cells. La Fata, G. FMRP regulates multipolar to bipolar transition affecting neuronal migration and cortical circuitry. Li, G.

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Identification of a transient subpial neurogenic zone in the developing dentate gyrus and its regulation by Cxcl12 and reelin signaling. The development of hippocampal cellular assemblies. Wiley Interdiscip. Lo Nigro, C. Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome.

Lu, M. Abnormal development of the hippocampal dentate gyrus in mice lacking the CXCR4 chemokine receptor. Ma, Q. Meyer, K. Disc1 regulates granule cell migration in the developing hippocampus. Miyata, T. Asymmetric inheritance of radial glial fibers by cortical neurons.

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Neuron 31, — Mizuseki, K. Hippocampal CA1 pyramidal cells form functionally distinct sublayers. Montenegro, M. Patterns of hippocampal abnormalities in malformations of cortical development. Psychiatry 77, — Morest, D. A study of neurogenesis in the forebrain of opossum pouch young.

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Nadarajah, B. Two modes of radial migration in early development of the cerebral cortex. Nakahira, E. Neuronal generation, migration, and differentiation in the mouse hippocampal primoridium as revealed by enhanced green fluorescent protein gene transfer by means of in utero electroporation. Nakajima, K. Disruption of hippocampal development in vivo by CR mAb against reelin.

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Niethammer, M. Neuron 28, — Niu, S.

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Neuron 41, 71— Noctor, S. Neurons derived from radial glial cells establish radial units in neocortex. Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases. Nowakowski, R. The mode of migration of neurons to the hippocampus: a Golgi and electron microscopic analysis in foetal rhesus monkey. The site of origin and route and rate of migration of neurons to the hippocampal region of the rhesus monkey. Ogawa, M.

Cellular Dynamics of the Neuron

The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons. Neuron 14, — Ohshima, T. Cdk5 is required for multipolar-to-bipolar transition during radial neuronal migration and proper dendrite development of pyramidal neurons in the cerebral cortex. Impairment of hippocampal long-term depression and defective spatial learning and memory in p35 mice.

Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death. Pleasure, S.

Unique expression patterns of cell fate molecules delineate sequential stages of dentate gyrus development. Rakic, P. Mode of cell migration to the superficial layers of fetal monkey neocortex. The time of origin of neurons in the hippocampal region of the rhesus monkey. Reiner, O. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Sasaki, S. Seki, T. Seki, K. Sawamoto, J. Parent, and A.

Alvarez-Buylla Tokyo: Springer , — Google Scholar. Distinctive population of Gfap-expressing neural progenitors arising around the dentate notch migrate and form the granule cell layer in the developing hippocampus. Sekine, K. How does Reelin control neuronal migration and layer formation in the developing mammalian neocortex? Shitamukai, A.