Area of research
Molecular Biology · Developmental Neuroscience
Research interest
Research interests include Neurogenesis and neuroplasticity mechanisms, Pluripotent Stem Cells Research, MicroRNA in disease regulation, and Epigenetics and DNA Methylation.
Skin-derived α-synuclein strains from PD, DLB, and MSA induce distinct intracellular pathology and neurodegeneration
Phosphorylation and DNA damage resolution coordinate SOX2-mediated reprogramming in vivo.
Dysregulated nuclear Lamin B1 in DYT1 dystonia thickens nuclear lamina and disrupts 14-3-3 proteins.
Atto 643 Carboxy Selectively Labels Astrocytes with Minimal Oligodendrocyte Cross-Reactivity
In vivo reprogramming of NG2 glia improves bladder function after spinal cord injury
GADD45G operates as a pathological sensor orchestrating reactive gliosis and neurodegeneration.
Phosphorylation and DNA Damage Resolution Coordinate SOX2-Mediated Reprogramming in vivo
Unbiased Quantification of Persistent Postural and Motor Deficits Following Spinal Cord Injury in Mice
in vivo Reprogramming of NG2 Glia Improves Bladder Function After Spinal Cord Injury
Dysregulated nuclear Lamin B1 in DYT1 dystonia thickens the nuclear lamina and disrupts 14-3-3 proteins
The Citron homology domain of MAP4Ks improves outcomes of traumatic brain injury.
Distinct alpha-synuclein strains derived from Parkinson’s disease patient tissues trigger differential inclusion pathology in a novel biosensor cell model
Simple and highly specific targeting of resident microglia with adeno-associated virus.
Screens in aging-relevant human ALS-motor neurons identify MAP4Ks as therapeutic targets for the disease.
NG2 glia reprogramming induces robust axonal regeneration after spinal cord injury.
MAP4K inhibition as a potential therapy for amyotrophic lateral sclerosis.
In vivo cell fate reprogramming for spinal cord repair.
Simple and Highly Specific Targeting of Resident Microglia with Adeno-Associated Virus
NG2 Glia Reprogramming Induces Robust Axonal Regeneration After Spinal Cord Injury
Chemical screens in aging-relevant human motor neurons identify MAP4Ks as therapeutic targets for amyotrophic lateral sclerosis
Resolution doubling in light-sheet microscopy via oblique plane structured illumination.
In vivo glia-to-neuron conversion: pitfalls and solutions.
NEK6 is an injury-responsive kinase cooperating with STAT3 in regulation of reactive astrogliosis.
Reply to In vivo confusion over in vivo conversion.
Resolution doubling in light-sheet microscopy via oblique plane structured illumination
Revisiting astrocyte to neuron conversion with lineage tracing in vivo.
Disease Modeling with Human Neurons Reveals LMNB1 Dysregulation Underlying DYT1 Dystonia.
Aging-relevant human basal forebrain cholinergic neurons as a cell model for Alzheimer's disease.
Therapeutic Nanomaterials for Neurological Diseases and Cancer Therapy
Rapid and efficient <i>in vivo</i> astrocyte-to-neuron conversion with regional identity and connectivity?