about
Pathophysiological power of improper tonic GABA(A) conductances in mature and immature models.Allelic diversity in human developmental neurogenetics: insights into biology and diseaseThe LIS1-related NUDF protein of Aspergillus nidulans interacts with the coiled-coil domain of the NUDE/RO11 proteinCerebral cortex expansion and folding: what have we learned?Toward developmental models of psychiatric disorders in zebrafishTwo modes of radial migration in early development of the cerebral cortexLis1 is necessary for normal non-radial migration of inhibitory interneuronsLoss of cell polarity causes severe brain dysplasia in Lgl1 knockout miceGrowth and folding of the mammalian cerebral cortex: from molecules to malformationsNeurotoxic autoantibodies mediate congenital cortical impairment of offspring in maternal lupus.Magnetic resonance imaging features of lissencephaly in 2 Lhasa Apsos.MCPH1: a window into brain development and evolution.Differential modulation of proliferation in the neocortical ventricular and subventricular zones.Neocortical malformation as consequence of nonadaptive regulation of neuronogenetic sequence.Mechanisms and disturbances of neuronal migration.Cell migration and cerebral cortical development.Human neocortical development: the importance of embryonic and early fetal events.Epilepsy and genetic malformations of the cerebral cortex.Apoptosis and brain development.Hereditary lissencephaly and cerebellar hypoplasia in Churra lambsIdentification of a 31-bp deletion in the RELN gene causing lissencephaly with cerebellar hypoplasia in sheep.Reelin' in Genes for Cortical Dysplasia.MEKK4 signaling regulates filamin expression and neuronal migration.The centrosome in human genetic disease.Brain size is controlled by the mammalian target of rapamycin (mTOR) in miceCortical malformation and pediatric epilepsy: a molecular genetic approach.Developmental differences of the major forebrain commissures in lissencephalies.Critical role of integrin-linked kinase in granule cell precursor proliferation and cerebellar development.Accumulation of GABAergic neurons, causing a focal ambient GABA gradient, and downregulation of KCC2 are induced during microgyrus formation in a mouse model of polymicrogyria.Emerging roles of neural stem cells in cerebral cortex development and evolution.From genes to folds: a review of cortical gyrification theory.Improving treatment of neurodevelopmental disorders: recommendations based on preclinical studies.YAP regulates neural progenitor cell number via the TEA domain transcription factor.A JIP3-regulated GSK3β/DCX signaling pathway restricts axon branching.Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15.A perturbation of multimodal GABA functions underlying the formation of focal cortical malformations: assessments by using animal models.Characterization of inhibitory circuits in the malformed hippocampus of Lis1 mutant mice.VIP and PACAP 38 modulate ibotenate-induced neuronal heterotopias in the newborn hamster neocortex.A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex.Expression and role of sulfoglucuronyl (HNK-1) carbohydrate and its binding protein SBP-1 in developing rat cerebral cortex.
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
name
Genetic malformations of the human cerebral cortex.
@ast
Genetic malformations of the human cerebral cortex.
@en
type
label
Genetic malformations of the human cerebral cortex.
@ast
Genetic malformations of the human cerebral cortex.
@en
prefLabel
Genetic malformations of the human cerebral cortex.
@ast
Genetic malformations of the human cerebral cortex.
@en
P1433
P1476
Genetic malformations of the human cerebral cortex.
@en
P2093
P356
10.1016/S0896-6273(00)80749-7
P407
P577
1999-05-01T00:00:00Z