Area of research
Cellular and Molecular Neuroscience · Developmental Neuroscience
Research interest
Research interests include Neurogenesis and neuroplasticity mechanisms, Neuroscience and Neuropharmacology Research, Genetics and Neurodevelopmental Disorders, and Axon Guidance and Neuronal Signaling.
Glial reactivity and cognitive decline follow chronic heterochromatin loss in neurons
Author Correction: A critical period of translational control during brain development at codon resolution
Protein translation rate determines neocortical neuron fate
Semaphorin heterodimerization in cis regulates membrane targeting and neocortical wiring
The murine ortholog of Kaufman oculocerebrofacial syndrome gene Ube3b is crucial for the maintenance of the excitatory synapses in the young adult stage
A critical period of translational control during brain development at codon resolution
The Role of Neurod Genes in Brain Development, Function, and Disease
Ablation of Vti1a/1b Triggers Neural Progenitor Pool Depletion and Cortical Layer 5 Malformation in Late-embryonic Mouse Cortex
Adhesion dynamics in the neocortex determine the start of migration and the post-migratory orientation of neurons
Split Chloramphenicol Acetyl-Transferase Assay Reveals Self-Ubiquitylation-Dependent Regulation of UBE3B
TrkC-T1, the Non-Catalytic Isoform of TrkC, Governs Neocortical Progenitor Fate Specification by Inhibition of MAP Kinase Signaling
Human endogenous retrovirus HERV-K(HML-2) RNA causes neurodegeneration through Toll-like receptors
Protein Synthesis in the Developing Neocortex at Near-Atomic Resolution Reveals Ebp1-Mediated Neuronal Proteostasis at the 60S Tunnel Exit
The murine ortholog of Kaufman oculocerebrofacial syndrome protein Ube3b regulates synapse number by ubiquitinating Ppp3cc
Srsf10 and the minor spliceosome control tissue-specific and dynamic SR protein expression
Molecular Evolution, Neurodevelopmental Roles and Clinical Significance of HECT-Type UBE3 E3 Ubiquitin Ligases
Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy Loss
mTORC1 and mTORC2 Differentially Regulate Cell Fate Programs to Coordinate Osteoblastic Differentiation in Mesenchymal Stromal Cells
Polarity Acquisition in Cortical Neurons Is Driven by Synergistic Action of Sox9-Regulated Wwp1 and Wwp2 E3 Ubiquitin Ligases and Intronic miR-140
Satb2 Cre/+ mouse as a tool to investigate cell fate determination in the developing neocortex
Zeb2 is essential for Schwann cell differentiation, myelination and nerve repair
NOMA-GAP/ARHGAP33 regulates synapse development and autistic-like behavior in the mouse
Unc5C and DCC act downstream of Ctip2 and Satb2 and contribute to corpus callosum formation