Gene therapy is a method of treatment. It is specifically used to treat patients who are suffering from diseases due to defective genes. Essentially, the treatment involves researchers replacing the defective or faulty genes with a normal functioning gene.
It involves:
1) Detection of gene
2)Determination & its role
3)Isolation & cloning
4)Introducing the gene by proper way. This is either germline gene therapy (done in germ cells) or somatic gene therapy (done in somatic cells).
in 1989 us approve gene therapy exprement on human
Gebe theroij
Yes, cystic fibrosis is a candidate for gene therapy. Gene therapy offers the potential to correct the underlying genetic cause of the disease, which is a mutation in the CFTR gene. While there have been some promising developments in gene therapy for cystic fibrosis, further research and clinical trials are needed to fully assess its effectiveness.
Gene therapy involves inserting a healthy copy of a gene into cells that have a defective copy. This can potentially correct the genetic mutation causing the disease and restore normal cell function. The goal is to treat or prevent genetic disorders by replacing or supplementing missing or defective genes.
Gene therapy usually seeks to replace a defective gene in a cell with the correct one using a vector for delivery, often a virus. The result is the transformed cells will product the correct protein. Protein therapy usually refers to injecting a functional protein into a patient to compensate for its absence.
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
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.
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.
Cosmetic gene therapy is a branch of medicine that deals with the maintenance and cure of the body disease.
Dongsheng Duan has written: 'Muscle gene therapy' -- subject(s): Duchenne Muscular Dystrophy, Laboratory Manuals, Muscles, Genetics, Diseases, Gene Therapy, Gene therapy, Therapy, Laboratory manuals, Methods
somatic gene
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.