[HTML][HTML] Fundamental elements in autism: from neurogenesis and neurite growth to synaptic plasticity

J Gilbert, HY Man - Frontiers in cellular neuroscience, 2017 - frontiersin.org
Autism spectrum disorder (ASD) is a set of neurodevelopmental disorders with a high
prevalence and impact on society. ASDs are characterized by deficits in both social behavior …

Pushing the limits of the scanning mechanism for initiation of translation

M Kozak - Gene, 2002 - Elsevier
Selection of the translational initiation site in most eukaryotic mRNAs appears to occur via a
scanning mechanism which predicts that proximity to the 5′ end plays a dominant role in …

Cell migration in the forebrain

O Marín, JLR Rubenstein - Annual review of neuroscience, 2003 - annualreviews.org
▪ Abstract The forebrain comprises an intricate set of structures that are required for some of
the most complex and evolved functions of the mammalian brain. As a reflection of its …

Modes of neuronal migration in the developing cerebral cortex

B Nadarajah, JG Parnavelas - Nature Reviews Neuroscience, 2002 - nature.com
The conventional scheme of cortical formation shows that postmitotic neurons migrate away
from the germinal ventricular zone to their positions in the developing cortex, guided by the …

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

K Kitamura, M Yanazawa, N Sugiyama, H Miura… - Nature …, 2002 - nature.com
Male embryonic mice with mutations in the X-linked aristaless-related homeobox gene (Arx)
developed with small brains due to suppressed proliferation and regional deficiencies in the …

[HTML][HTML] Accelerated evolution of nervous system genes in the origin of Homo sapiens

S Dorus, EJ Vallender, PD Evans, JR Anderson… - Cell, 2004 - cell.com
Human evolution is characterized by a dramatic increase in brain size and complexity. To
probe its genetic basis, we examined the evolution of genes involved in diverse aspects of …

14-3-3ε is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller–Dieker syndrome

K Toyo-Oka, A Shionoya, MJ Gambello, C Cardoso… - Nature …, 2003 - nature.com
Abstract Heterozygous deletions of 17p13. 3 result in the human neuronal migration
disorders isolated lissencephaly sequence (ILS) and the more severe Miller–Dieker …

LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages

JW Tsai, Y Chen, AR Kriegstein, RB Vallee - The Journal of cell biology, 2005 - rupress.org
Mutations in the human LIS1 gene cause the smooth brain disease classical lissencephaly.
To understand the underlying mechanisms, we conducted in situ live cell imaging analysis …

[HTML][HTML] 14-3-3 proteins in brain development: neurogenesis, neuronal migration and neuromorphogenesis

B Cornell, K Toyo-Oka - Frontiers in molecular neuroscience, 2017 - frontiersin.org
The 14-3-3 proteins are a family of highly conserved, multifunctional proteins that are highly
expressed in the brain during development. Cumulatively, the seven 14-3-3 isoforms make …

[PDF][PDF] Genetic mosaic dissection of Lis1 and Ndel1 in neuronal migration

S Hippenmeyer, YH Youn, HM Moon, K Miyamichi… - Neuron, 2010 - cell.com
Coordinated migration of newly born neurons to their prospective target laminae is a
prerequisite for neural circuit assembly in the developing brain. The evolutionarily …