PCP4 (PEP19) overexpression induces premature neuronal differentiation associated with Ca2+/Calmodulin-Dependent kinase II-δ activation in mouse models of down syndrome

Molecular analysis of neocortical layer structure in the ferret

(2010) Joanna J. Rowell et al.   JOURNAL OF COMPARATIVE NEUROLOGY

eIF2  Phosphorylation-Dependent Translation in CA1 Pyramidal Cells Impairs Hippocampal Memory Consolidation without Affecting General Translation

(2010) Z. Jiang et al.   JOURNAL OF NEUROSCIENCE

Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development

(2009) Julien Laffaire et al.   BMC GENOMICS

Brca1 is required for embryonic development of the mouse cerebral cortex to normal size by preventing apoptosis of early neural progenitors

(2009) J. N. Pulvers et al.   DEVELOPMENT

The "Down Syndrome Critical Region" Is Sufficient in the Mouse Model to Confer Behavioral, Neurophysiological, and Synaptic Phenotypes Characteristic of Down Syndrome

(2009) N. P. Belichenko et al.   JOURNAL OF NEUROSCIENCE

A PKC-Dependent Recruitment of MMP-2 Controls Semaphorin-3A Growth-Promoting Effect in Cortical Dendrites

(2009) Bertrand Gonthier et al.   PLoS One

δ Ca2+/Calmodulin-Dependent Protein Kinase IIIsozyme-Specific Induction of Neurite Outgrowth in P19 Embryonal Carcinoma Cells

(2003) Lesley D. Johnson et al.   JOURNAL OF NEUROCHEMISTRY