Eran Perlson

Dynein tethers and stabilizes dynamic microtubule plus ends.

Dynein interacts with the neural cell adhesion molecule (NCAM180) to tether dynamic microtubules and maintain synaptic density in cortical neurons.

Long-distance axonal transport of AAV9 is driven by dynein and kinesin-2 and is trafficked in a highly motile Rab7-positive compartment.

Real-time sensing of enteropathogenic E. coli-induced effects on epithelial host cell height, cell-substrate interactions, and endocytic processes by infrared surface plasmon spectroscopy.

Rabies Virus Hijacks and accelerates the p75NTR retrograde axonal transport machinery.

Anterograde glycoprotein-dependent transport of newly generated rabies virus in dorsal root ganglion neurons.

A compartmentalized microfluidic neuromuscular co-culture system reveals spatial aspects of GDNF functions.

Amyotrophic lateral sclerosis as a spatiotemporal mislocalization disease: location, location, location.

A Dynein Light Chain 1 Binding Motif in Rabies Virus Polymerase L Protein Plays a Role in Microtubule Reorganization and Viral Primary Transcription.

Receptor-mediated increase in rabies virus axonal transport.

Developmental Axon Pruning Requires Destabilization of Cell Adhesion by JNK Signaling.

Proteomic Analysis of Dynein-Interacting Proteins in Amyotrophic Lateral Sclerosis Synaptosomes Reveals Alterations in the RNA-Binding Protein Staufen1.

Neurodegeneration and Alzheimer's disease (AD). What Can Proteomics Tell Us About the Alzheimer's Brain?

Compartmental microfluidic system for studying muscle-neuron communication and neuromuscular junction maintenance.

Tracking Quantum-Dot labeled neurotropic factors transport along primary neuronal axons in compartmental microfluidic chambers.

Phosphatidylserine Ameliorates Neurodegenerative Symptoms and Enhances Axonal Transport in a Mouse Model of Familial Dysautonomia.

ALS Along the Axons - Expression of Coding and Noncoding RNA Differs in Axons of ALS models.

Spatial-specific functions in retrograde neuronal signalling.

Phosphatidylserine improves axonal transport by inhibition of HDAC and has potential in treatment of neurodegenerative diseases.

High content image analysis reveals function of miR-124 upstream of Vimentin in regulating motor neuron mitochondria.

The receptor tyrosine kinase TrkB signals without dimerization at the plasma membrane.

miR126-5p Downregulation Facilitates Axon Degeneration and NMJ Disruption via a Non-Cell-Autonomous Mechanism in ALS.

Retrograde Degenerative Signaling Mediated by the p75 Neurotrophin Receptor Requires p150 Deacetylation by Axonal HDAC1.

Localization of RNAi Machinery to Axonal Branch Points and Growth Cones Is Facilitated by Mitochondria and Is Disrupted in ALS.

Muscle secretion of toxic factors, regulated by miR126-5p, facilitates motor neuron degeneration in amyotrophic lateral sclerosis.

Targeting the Sigma-1 Receptor via Pridopidine Ameliorates Central Features of ALS Pathology in a SOD1 Model.

Structural Principles in Robo Activation and Auto-inhibition.

Patient-derived co-cultures for studying ALS.

Efficient gene transfer into primary muscle cells to analyze nerve-independent postsynaptic organization in vitro.

Single-Particle Diffusion Characterization by Deep Learning.

Flow Arrest in the Plasma Membrane.

An compartmental system underlines the contribution of mitochondrial immobility to the ATP supply in the NMJ.

CRMP2 mediates Sema3F-dependent axon pruning and dendritic spine remodeling.