Gene and Cell Therapy

Gene and Cell Therapy focuses on innovative treatments aimed at correcting genetic defects and repairing damaged cells to address Neurological disorders. This field includes gene editing techniques like CRISPR-Cas9, which are used to target and modify faulty genes associated with conditions such as Huntington’s disease and spinal muscular atrophy. Gene therapy also involves delivering therapeutic genes into patients' cells to produce missing or dysfunctional proteins.

  • Track 22-1: Gene Editing Techniques in neurology: Current Applications.
  • Track 22-2: Stem Cell Therapy for Neurological Regeneration
  • Track 22-3: CRISPR-Cas9 Gene Editing
  • Track 22-4: Induced Pluripotent Stem Cells (iPSCs) Applications
  • Track 22-5: Combination Therapies in Neurodegenerative Diseases
  • Track 22-6: Safety and Efficacy of Gene and Cell Therapies

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