The invention involves the development of vectors for somatic gene therapy.
Adenoviruses (Ads) and vectors derived thereof have been used for somatic gene therapy, gene therapy of cancer and gene therapy of infectious diseases/vaccination.
The invention relates to transposon Hsmar2 and to the use thereof in the generation of vectors that can be used in somatic gene therapy.
[4] CRISPR and somatic gene therapy: an initial human clinical trial in China
How should the arrest of a clinical research protocol for somatic gene therapy be regulated?
Somatic human gene therapy is expected to correct or improve treatments for inherited diseases.
It said somatic cell gene therapy "seeks to eliminate or reduce genetic defects on the level of somatic cells" (DP 25).
It said somatic cell gene therapy "seeks to eliminate or reduce genetic defects on the level of somatic cells" (DP 25).
It said somatic cell gene therapy "seeks to eliminate or reduce genetic defects on the level of somatic cells" (DP 25).
Human genome modifications using genome editing aiming at developing a therapy will have to bend to the established laws concerning somatic cell gene therapy.
In somatic gene therapy, a virus is typically used as a vector to insert genetic material into the cells of the recipient’s body.
Somatic gene therapy alters or eliminates genes that cause disease in a patient without imparting these changes to future generations.
Somatic gene therapy alters or eliminates genes that cause disease in a patient without imparting these changes to future generations.
This type of research must first aim at treating and preventing diseases and disabilities, i.e., in priority somatic cell gene therapy for certain hereditary diseases.
This type of research must first aim at treating and preventing diseases and disabilities, i.e., in priority somatic cell gene therapy for certain hereditary diseases.
Somatic gene therapy has been developed to treat inherited and acquired diseases, for which there are currently no or only limited other treatment options.
By inhibiting this defective gene, the other gene can then express itself normally, eliminating or mitigating the genetic disease of which the defective gene was the source.
Somatic cell gene therapy seeks to eliminate or reduce genetic defects on the level of somatic cells, that is, cells other than the reproductive cells, but which make up the tissue and organs of the body.
Somatic cell gene therapy that seeks to eliminate or reduce genetic defects on the level of somatic cells, that is, cells other than the reproductive cells, but which make up the tissue and organs of the body.
Somatic cell gene therapy seeks to eliminate or reduce genetic defects on the level of somatic cells, that is, cells other than the reproductive cells, but which make up the tissue and organs of the body.
Somatic cell gene therapy that seeks to eliminate or reduce genetic defects on the level of somatic cells, that is, cells other than the reproductive cells, but which make up the tissue and organs of the body.
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