Philadelphia University + Thomas Jefferson University

Zhou, Hongxia

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Hongxia Zhou, PhD

Hongxia Zhou, PhD

Contact Dr. Zhou

1020 Locust Street
Jefferson Alumni Hall, Suite 506
Philadelphia, PA 19107

(215) 503-1037


Most Recent Peer-Reviewed Publications

  1. Increased Ubqln2 expression causes neuron death in transgenic rats
  2. Heat transfer and flow characteristics during the formation of TBAB hydrate slurry in a coil heat exchanger
  3. TBAB hydrate slurry based latent heat thermal storage system
  4. Modelling and experimental validation of a fluidized bed based CO2 hydrate cold storage system
  5. The evolutionary landscape of intergenic trans-splicing events in insects
  6. Heat transfer and flow characteristics during the formation of TBAB hydrate slurry
  7. Pathogenic Ubqln2 gains toxic properties to induce neuron death
  8. Profiling the genes affected by pathogenic TDP-43 in astrocytes
  9. Expression of ALS-linked TDP-43 mutant in astrocytes causes non-cell-autonomous motor neuron death in rats
  10. Reactive astrocytes secrete lcn2 to promote neuron death
  11. Pathogenic mutation in VPS35 impairs its protection against MPP+ cytotoxicity
  12. XBP1 depletion precedes ubiquitin aggregation and Golgi fragmentation in TDP-43 transgenic rats
  13. Entorhinal cortical neurons are the primary targets of FUS mislocalization and ubiquitin aggregation in FUS transgenic rats
  14. Mutant TDP-43 in motor neurons promotes the onset and progression of ALS in rats
  15. Early exposure to paraquat sensitizes dopaminergic neurons to subsequent silencing of PINK1 gene expression in mice
  16. Temporal expression of mutant LRRK2 in adult rats impairs dopamine reuptake
  17. TDP-43 potentiates alpha-synuclein toxicity to dopaminergic neurons in transgenic mice
  18. FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration
  19. Sustained Expression of TDP-43 and FUS in Motor Neurons in Rodent's Lifetime
  20. Transgenic rat model of neurodegeneration caused by mutation in the TDP gene