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Genes and brain malformations associated with abnormal neuron positioningNeurological aspects of human glycosylation disordersMyocardin-related transcription factors regulate the Cdk5/Pctaire1 kinase cascade to control neurite outgrowth, neuronal migration and brain developmentBilateral subcortical heterotopia with partial callosal agenesis in a mouse mutantAbsent cavum septum pellucidum: a review with emphasis on associated commissural abnormalities.Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration.miR-139-5p modulates cortical neuronal migration by targeting Lis1 in a rat model of focal cortical dysplasiaGenesis of teratogen-induced holoprosencephaly in mice.Brainstem respiratory oscillators develop independently of neuronal migration defects in the Wnt/PCP mouse mutant looptail.Populations of radial glial cells respond differently to reelin and neuregulin1 in a ferret model of cortical dysplasia.Liquid-diet with alcohol alters maternal, fetal and placental weights and the expression of molecules involved in integrin signaling in the fetal cerebral cortex.Nischarin is differentially expressed in rat brain and regulates neuronal migration.Impaired Reelin-Dab1 Signaling Contributes to Neuronal Migration Deficits of Tuberous Sclerosis ComplexMagnetic resonance microscopy-based analyses of the brains of normal and ethanol-exposed fetal mice.Magnetic resonance microscopy defines ethanol-induced brain abnormalities in prenatal mice: effects of acute insult on gestational day 7Kinesin-1 acts with netrin and DCC to maintain sensory neuron position in Caenorhabditis elegans.Enhanced Burst-Suppression and Disruption of Local Field Potential Synchrony in a Mouse Model of Focal Cortical Dysplasia Exhibiting Spike-Wave Seizures.Genetic testing in patients with global developmental delay / intellectual disabilities. A review.Antenatal diagnosis of alobar holoprosencephaly.Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy.KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis.Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.Subcortical band heterotopia in rat offspring following maternal hypothyroxinaemia: structural and functional characteristics.Nijmegen breakage syndrome with macrocephaly, schizencephaly and large CSF spaces—extended spectrum of the condition.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
New trends in neuronal migration disorders.
@ast
New trends in neuronal migration disorders.
@en
type
label
New trends in neuronal migration disorders.
@ast
New trends in neuronal migration disorders.
@en
prefLabel
New trends in neuronal migration disorders.
@ast
New trends in neuronal migration disorders.
@en
P2093
P1476
New trends in neuronal migration disorders.
@en
P2093
Alberto Spalice
Alberto Verrotti
Antonella Castronovo
Fabiana Ursitti
Laura Papetti
Paola Iannetti
Rosanna Mariani
P356
10.1016/J.EJPN.2009.01.005
P577
2009-03-04T00:00:00Z