Gene therapy is an experimental technique that uses genes to treat or prevent disease. In the future, this technique may allow doctors to treat a disorder by inserting a gene into a patient’s cells instead of using drugs or surgery. Researchers are testing several approaches to gene therapy, including:
Replacing a mutated gene that causes disease with a healthy copy of the gene.
Inactivating, or “knocking out,” a mutated gene that is functioning improperly.
Introducing a new gene into the body to help fight a disease.
That process is called gene therapy. It involves inserting functional copies of a gene into the cells of a person with a genetic disorder to correct the genetic mutation causing the disorder.
Gene therapy is not always successful. Sometimes when inserting genes into the chromosome, we misplace them, and the original problem is aggravated. Gene therapy can be somewhat effective at reducing symptoms of genetic diseases though.
building muscle and increase stamina through gene therapy
Gene therapy is not practiced frequently. It is still in a clinical trial level. Though just temporary results are got often using gene therapy. In 2011 a person has been completely cured of hiv by gene therapy. But still it is a very difficult process since the man's entire bone marrow had to be removed and replaced!
Gene therapy for cystic fibrosis involves delivering a functional copy of the CFTR gene to affected cells in order to restore normal function of the protein. This can be achieved by using viral vectors to deliver the gene into the cells and allow it to produce normal CFTR protein. By correcting the underlying genetic defect, gene therapy holds promise for treating cystic fibrosis at the molecular level.
Application of bitech is that it is used in Biorobotics, Gene therapy and ‎Bioengineering.
Gene Therapy
at the gene level gene therapy is done and at the the protein level protein therapy is done
That process is called gene therapy. It involves inserting functional copies of a gene into the cells of a person with a genetic disorder to correct the genetic mutation causing the disorder.
With the help of Gene therapy we can replace or supress the cancer gene
a new gene which codes for the protein that can repair defective genes is introduced.
in 1989 us approve gene therapy exprement on human
Gene therapy effects children by helping to cure disease and to lengthen lives. Gene therapy can also be used to eliminate diseases that are inherited.
Though the application of gene therapy at clinical level is at its primary stage it appears promising. Mostly till date it has given only temporary cure. It needs more experimenting and further bloom in technology can help it grow into a promising method.
Gene therapy is a method that aims to cure inherited diseases by providing the patient with correct copy of the defective gene. There are four potential approaches to gene therapy:1)Addition of normal gene to replace the function of defective gene. This is gene replacement orgene augmentation therapy.2)Replacing the defective gene with the correct gene. This isCorrective gene therapy.3)Establishment of alternative pathways that bypass mutant genes function4)Change in regulation of normal or mutant genesThe first two are the basic approaches in gene therapy
not so positive, but it does depend on what kind of gene therapy and for what purpose
Gene therapy is shown promise in controlling Cystic Fibrosis.