Shenfeng Qiu

Modulation of synaptic plasticity and memory by Reelin involves differential splicing of the lipoprotein receptor Apoer2.

A fresh look at an ancient receptor family: emerging roles for low density lipoprotein receptors in synaptic plasticity and memory formation.

Sequential involvement of distinct glutamate receptors in domoic acid-induced neurotoxicity in rat mixed cortical cultures: effect of multiple dose/duration paradigms, chronological age, and repeated exposure.

Cognitive disruption and altered hippocampus synaptic function in Reelin haploinsufficient mice.

Histopathological and molecular changes produced by hippocampal microinjection of domoic acid.

Differential reelin-induced enhancement of NMDA and AMPA receptor activity in the adult hippocampus.

Associative and spatial learning and memory deficits in transgenic mice overexpressing the RNA-binding protein HuD.

Reelin signaling facilitates maturation of CA1 glutamatergic synapses.

Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation.

Ascorbate transport by primary cultured neurons and its role in neuronal function and protection against excitotoxicity.

Impaired secretion of apolipoprotein E2 from macrophages.

Self-association of human PCSK9 correlates with its LDLR-degrading activity.

The role of reelin in adult synaptic function and the genetic and epigenetic regulation of the reelin gene.

Alterations in mossy fiber physiology and GAP-43 expression and function in transgenic mice overexpressing HuD.

Domoic acid induces a long-lasting enhancement of CA1 field responses and impairs tetanus-induced long-term potentiation in rat hippocampal slices.

New mouse genetic model duplicates human 15q11-13 autistic phenotypes, or does it?

Loss of limbic system-associated membrane protein leads to reduced hippocampal mineralocorticoid receptor expression, impaired synaptic plasticity, and spatial memory deficit.

Circuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinase.

SnapShot: genetics of autism.

Modeling of autism genetic variations in mice: focusing on synaptic and microcircuit dysfunctions.

Single-neuron RNA-Seq: technical feasibility and reproducibility.

Induced neural stem cells generated from rat fibroblasts.

MET receptor tyrosine kinase as an autism genetic risk factor.

Convergent synaptic and circuit substrates underlying autism genetic risks.

Plasticity of binocularity and visual acuity are differentially limited by nogo receptor.

MET receptor tyrosine kinase controls dendritic complexity, spine morphogenesis, and glutamatergic synapse maturation in the hippocampus.

Neurodevelopmental Underpinnings of Angelman Syndrome.