Area of research
Cell Biology · Oncology
Research interest
Research interests include Cell biology, Microtubule, Biology, Axon, Kinesin, and Microtubule nucleation.
CAMSAPs and nucleation-promoting factors control microtubule release from γ-TuRC
Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions
Combined kinesin-1 and kinesin-3 activity drives axonal trafficking of TrkB receptors in Rab6 carriers
WDR47 protects neuronal microtubule minus ends from katanin-mediated severing
Centrosome‐mediated microtubule remodeling during axon formation in human iPSC‐derived neurons
Arginine π-stacking drives binding to fibrils of the Alzheimer protein Tau
Cortical anchoring of the microtubule cytoskeleton is essential for neuron polarity
Microtubule Minus-End Binding Protein CAMSAP2 and Kinesin-14 Motor KIFC3 Control Dendritic Microtubule Organization
Quantitative mapping of transcriptome and proteome dynamics during polarization of human iPSC-derived neurons
MAP7 family proteins regulate kinesin-1 recruitment and activation
Feedback-Driven Mechanisms between Microtubules and the Endoplasmic Reticulum Instruct Neuronal Polarity
Feedback-Driven Assembly of the Axon Initial Segment
VAP‐SCRN1 interaction regulates dynamic endoplasmic reticulum remodeling and presynaptic function
MAP7D2 Localizes to the Proximal Axon and Locally Promotes Kinesin-1-Mediated Cargo Transport into the Axon
The HAUS Complex Is a Key Regulator of Non-centrosomal Microtubule Organization during Neuronal Development
Regulation of KIF1A-Driven Dense Core Vesicle Transport: Ca2+/CaM Controls DCV Binding and Liprin-α/TANC2 Recruits DCVs to Postsynaptic Sites
Quantitative Map of Proteome Dynamics during Neuronal Differentiation
TRIM46 Controls Neuronal Polarity and Axon Specification by Driving the Formation of Parallel Microtubule Arrays