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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.

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10y ago
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11y ago

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Gene therapy research uses _______ to alter defective hereditary material. (1 point)

  • bacteria
  • cells
  • interferons
  • viruses

Correct answer: cells

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Q: What does Gene therapy research use to alter defective hereditary material?
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What do Gene therapy researchers use to alter defective hereditary material?

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 disorders is a form of?

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.


Enclosing mornal hereditary material in a virus and allowing it to move into cells to replace defective hereditary material in the treatment of genetic disorders is a form of?

gene therapy, in which defective gene is replaced by correct gene with help of virus which work as vechicle for viruses


What is the name for replacement of a defective gene with a healthy one?

gene therapy


What does research suggest about the impact of free therapy preparation on therapy?

It depends which research you read.


Where does one go to get gene therapy?

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.


A technique that involves putting a healthy copy of a gene into cells that have a defective copy of the same gene?

gene therapy.


How is genetic therapy used to treat genetic disorders?

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


Why is gene therapy being researched?

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.


What research has been done on cell therapy?

applications of cell therapy in the United States are still in the research, experimental, and clinical trial stages.


What does BRAT stand for?

Behaviour Research and Therapy


What has the author Christopher E Bork written?

Christopher E. Bork has written: 'Research in physical therapy' -- subject(s): Physical therapy, Research