Research Grant: AFM Lettre d'engagement. Hepatic gene therapy for hemophilia using integration-defective lentiviral vectors: effects of miRNA regulation on induction of immune tolerance.

Project Details

Description

Hepatic gene therapy for hemophilia using integration-defective lentiviral vectors: effects of miRNA regulation on induction of immune tolerance.

The ultimate goal of gene therapy is the replacement of a defective gene sequence with a corrected version to eliminate disease for the lifetime of the patient
AcronymAII100
StatusFinished
Effective start/end date1/10/1331/03/15

Keywords

  • Fibrosis
  • Hepatic Stellate Cells
  • Histon (de)acetylation
  • Stellate cell activation
  • Liver Cell Transplantation
  • Liver Sinusoidal Cells
  • Portal hypertension
  • Sinusoidal Cells
  • cirrhosis
  • Cytoskeleton
  • Cell Biology
  • Fat-Storing Cells
  • NASH / NAFLD
  • Intermediate Filaments
  • liver stem / progenitor cells
  • autophagy
  • Flow Cytometry
  • Metabolic Syndrome

Flemish discipline codes in use since 2023

  • Biological sciences
  • Electrical and electronic engineering
  • Basic sciences

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