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An Entity of Type : owl:Class, within Data Space : covidontheweb.inria.fr associated with source document(s)

AttributesValues
type
label
  • Gene Therapy
subClassOf
topic
http://purl.obolibrary.org/obo/NCIT_NHC0
  • C15238
http://purl.obolibrary.org/obo/NCIT_P106
  • Therapeutic or Preventive Procedure
http://purl.obolibrary.org/obo/NCIT_P108
  • Gene Therapy
http://purl.obolibrary.org/obo/NCIT_P207
  • C0017296
http://purl.obolibrary.org/obo/NCIT_P322
  • CDISC
  • CDISC-GLOSS
  • CTRP
http://purl.obolibrary.org/obo/NCIT_P325
  • Treatment of human disease by gene transfer.
  • Treatment that alters a gene. In studies of gene therapy for cancer, researchers are trying to improve the body's natural ability to fight the disease or to make the cancer cells more sensitive to other kinds of therapy.
  • Introduction of genetic material into cells in order to correct or treat an inherited or acquired disease.
  • Therapy based on ex vivo or in vivo gene modification of cells using specific technologies, e.g., viral vectors and direct genome editing technologies. NOTE: A particular example of this is the therapy with gene-modified T cells (chimeric antigen receptor (CAR) T-cell therapies) used as immunotherapy in oncology. [After Natalie Mount, et al. Cell-based therapy technology classifications and translational challenge. Philos Trans R Soc Lond B Biol Sci. 2015 Oct 19; 370(1680): 20150017.] See also cell therapy, regenerative medicine therapy, regenerative medicine advanced therapy, biological product.
http://purl.obolibrary.org/obo/NCIT_P366
  • Gene_Therapy
definition
  • Application of genetic material (usually DNA) into cells in order to permanently correct an inherited disease or acquired disease.
has_exact_synonym
  • DNA Therapy
  • GENETIC
  • Gene Therapy
  • Gene Transfer Procedure
  • Gene transfer
  • Intervention, Genetic
  • Molecular Biology, Gene Therapy
  • gene therapy
in_subset
http://purl.obolibrary.org/obo/NCIT_P107
  • Gene Therapy
http://purl.obolibrary.org/obo/NCIT_P98
  • Gene therapy techniques attempt to replace a faulty or missing gene associated with a particular disease, mediate localized delivery of a protein producing specified therapeutic effects, or introduce new cellular functions.
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