Researchers replace a mutated gene with a healthy copy of the gene. The healthy gene must first attach to a chromosome within a patient's cells. Then the gene needs to make the correct type and amount of protein. These techniques are still experimental at this time.
1.
Gene therapy research uses _______ to alter defective hereditary material. (1 point)
Correct answer: cells
Cells
gene therapy.
Because scientists want to see what they can do to help people in need of medical attention because of the hereditary diseases they may have. Gene therapy also has the potential to provide permanent cures for diseases as opposed to temporary alleviations of the symptoms or deficiencies.
Cell salt therapy, like homeopathy, is not based on scientific research but on provings. Provings are basically anecdotal evidence gathered from volunteers.
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).
Cells
Enclosing normal hereditary material in a virus and allowing it to move into cells to replace defective hereditary material in the treatment of genetic disorder is a form of gene therapy. A cell in which a virus multiplies itself in a host.
gene therapy, in which defective gene is replaced by correct gene with help of virus which work as vechicle for viruses
gene therapy
It depends which research you read.
Gene therapy is an experimental treatment in which genetic material is introduced into a person's cells to cure disease. Because it is still experimental it is being done at research hospitals.
gene therapy.
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
Because scientists want to see what they can do to help people in need of medical attention because of the hereditary diseases they may have. Gene therapy also has the potential to provide permanent cures for diseases as opposed to temporary alleviations of the symptoms or deficiencies.
applications of cell therapy in the United States are still in the research, experimental, and clinical trial stages.
Behaviour Research and Therapy
Christopher E. Bork has written: 'Research in physical therapy' -- subject(s): Physical therapy, Research