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Persuasive Essay On Gene Therapy

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Another huge part of medicine is expected to involve genes sequencing, or in other words: genetic screening. Originally, it cost several million dollars to sequence all the genes in a single human body. Today, because of improved technologies, it would cost $50,000. But in the future Moore’s law going to drive down the price of genetic scanning and make it possible even for an average person to get their full “gene portfolio”. In within 10 years scientist expecting the price of it be a $1,000. Which means that one day everyone might have a CD or chip with his or her genes described on it. It would open an entirely new branch of medicine, called bioinformatics, or using a computers to rapidly scan and analyze the genome of thousands of organisms. …show more content…

In the future, gene therapy may be able to cure many of the 5,000 known genetic diseases. There are two types of gene therapy: somatic and germ line. Somatic gene therapy involves fixing the broken genes of a single individual and germ-line gene therapy fixes the genes of the sex cells, so that the repaired gene can be passed on to the next generation. The process of curing genetic diseases has two main steps. First is analyzing the genes of the individual and tracing family tree, going back many generation, in order to find the precise location of the gene that may be damaged. Second: taking the healthy version of the gene, inserted into harmless virus, and then injection it into the patient. The virus quickly inserts the “good gene” into the cells, potentially curing the disease. So far the progress in the field of genetic medicine has been slow and the results mixed. There are some problems, that scientist are looking forward to solve in the near future. One of them is: the body often confuses injected harmless virus, containing the “good gene” with a dangerous virus and begins to attack it. Despite it, Michio Kaku has a positive prediction that “by midcentury, gene therapy will be a standard method of treating a variety of genetic diseases”

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Green briefly touches on gene therapy that aims to cure diseases in an individual. He also considers the fact that this is therapy is particularly risky and dangerous, he holds strong with his idea that, “if the disease is serious enough […] it is usually worth trying.” (pg. 56). Green then moves onto the second ‘square’ of this chapter-germline gene therapy. Green goes much more deeply into this section, mostly because this subject often

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It is like a “potential medical miracle worker.” Gene therapy will produce a good gene for a person and control the bad gene. There are two main types of gene therapy. The first gene therapy is called “Somatic gene therapy.” Somatic gene therapy will treat the patient by using a good gene and putting it in the person’s cells.

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“Recently developed techniques for modifying genes are often called “gene editing ("Human Genetic Modification | Center for Genetics and Society").” Genetic modification can be applied in two very different ways: “somatic genetic modification” and “germline genetic modification. Somatic genetic modification adds, cuts, or changes the genes in some of the cells of an existing person, typically to alleviate a medical condition. These gene therapy techniques are approaching clinical practice, but only for a few conditions, and at a very high

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Then we can build more accurate models for the risk management and the process of new drug discovery and clinical trials. Also, we can know better the relationship between genome and phenotypes/diseases. Based on my experience, I firmly believe that machine learning will play as a core component of biotechnology. I definitely want to act

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Human genetic modification is the manipulation of genes in human DNA so that defective genes don’t obstruct proper functioning, and so that inherited diseases are not passed on. Those against it may argue that genetic modification is simply unnecessary, immoral, or interferes with nature’s course. However, genetic modification overall is and will continue to be beneficial to the mental and physical health of the entire human species. Falling under the umbrella of biology, it is sensible to consider the studying of genes as a significant aspect of the biological sciences because it’s learning how to manipulate them in order to progress preventative medicine and create the possibility of a healthier future. One method of genetic modification

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In addition, it is a costly procedure so there is limited access to this treatment. Ethical issues: Offspring of germ line gene therapy have not provided their consent for the procedure. This process can also be used to enhance offspring i.e.. their genetic and physical features, leaving the patient with unfair advantages in certain situations. STEM CELL THERAPY Principles: Stem cells can be used to generate new cells that can develop into functional cells/tissues/organs and it is therefore introduced in the patients body for this purpose.

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I want you all to imagine a world with no diseases and maybe even no cancer. Seems pretty impossible right? Well, with gene therapy that could all change. B. Background and Audience Relevance: Gene therapy is essentially using genes as drugs for the treatment of human disease. In the future, this experimental technique may allow doctors to treat a disorder by inserting a gene into a patient’s cells instead of using medicine or surgery.

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Gene Therapy is an experimental technique that involves altering genes inside the body in order to treat or prevent disease. Since the understanding of the flow of genetic materials in organisms is established, the cause of disease has been linked to the abnormal expression of genetic information. It is believed that diseases are treatable by correcting such defects; hence gene therapy evolves as an active field of research. The first clinical trial of gene therapy was started at NIH Clinical Center in 1990 (National Institute of Health, 2005-2014). However, it is not until 2012 that Glybera appeared as the first gene therapy to be approved in European Union (EU).

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Just as with germ-line gene therapy, there are risks with implementing any developing medical, surgical or pharmaceutical treatment. However, it is argued that the advantages outweigh any negative consequences. If germ-line gene therapy is performed well, there is the potential to eliminate diseases that, as of now, are considered irremediable. An example of such idea observed in the present is the administering of chemotherapy to treat different kinds of cancer.

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The 21st century is the time that full of the opportunities of science and technology, and genetic engineering is one of most significant fields. We have experienced how powerful that our the daily technology have been affecting us since Nikola Tesla began the modern technology by his great inventions. Nowadays, we are living in a life that much better than our fathers, and we will live better than now. But humans are not only satisfied in improving our living goods anymore, because no matter how well we live, we still have to face diseases and death one day. So genetic engineering is the way to solve those problems.

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The researchers then combine the broken gene with a healthy gene. This new healthy gene is now modified and free from the mutation it had before. Although many individuals’ ethics and morals stand in the way of gene editing, this technology affects society in many different

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Science has enabled us to thrive in a world where change is a must if an organism wishes to live. It has allowed for us to bend and twist the world at our feet, even having enough strength to repel the touch of death. Genetic engineering is the next scientific advancement that will stand close in the near future. It has the capability of modifying the food production process, elimination of diseases and disorders, and the guarantation of the best traits in an organism.

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Gene editing is the alteration of a person’s genetic material to delete undesirable traits or to create desirable new ones. Scientists can identify a defective DNA strand to be cut out and changed, then they use a protein that acts like scissors to cut out the improper gene and cells, then a healthy strand of DNA is inserted at the cut site and enzymes repair it (Crow). The goal of gene editing is to treat genetic disorders. Gene editing could potentially decrease or even

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