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Essay on gene patenting
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Gene Patenting
What is gene patenting? Before you can investigate into gene patenting, one must understand what genes are and what the importance of genes. Genes are proteins and molecules that make up the DNA of everything around us. In essence, they are ingredients that complete everything we touch, feel, or see. We recognize genes as a part of the human DNA. Genes can determine a person’s race, sex, and even how healthy we are. Genetics have multiple purposes. The main purposes of commonly recognized genes are human genetics. Yet, we all do not know the facts about human genetics. The Health Research Funding Organization published a study in 2014 in where “99.5% of all humans do not know that we share a percent of each other’s DNA.”
Not all genes are the same, in fact, some human genetics are remarkable. So much so, that we have instituted research into our lives. The timeline presented by Kenneth Jost of the CQ Researcher suggests we have been discovering and patenting specific genetic discoveries since 1911 with the first patenting being the discovery of adrenaline and reproduction of the cells for the general public. Although we share different genes within our species, there are so many separate genetic markers that create our specific identity as humans. Within the research, we are also finding cures to cancers and diseases that have been due to the genetic research. Biotech companies have creating vaccines and medicine with these genetic discoveries. Shouldn’t they be entitled to patenting their discovery and product? Why would there be a problem with patenting these markers discovered for cures?
There is great controversy and debate on whether or not gene patenting should be allowed to anyone. The purpose of this pap...
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...to work around. In a 2002 case, Madey v. Duke, the Court of Appeals for the Federal Circuit made it clear that academic institutions could be held liable for patent infringement even in a nonprofit research.
In practice, however, no research institution has been sued for studying a gene or using it in academic research. This is partly because the patent holders are more than likely to benefit from research that reveals how their patented genes work. The other reason is partly due to the difficulty in proving damages from mere use in research. One gray zone is the use of materials or processes with gene patents in clinical research, such as genetic testing in the context of a clinical trial. Laboratories offering patented genetic tests for research studies have been asked to “cease and desist” unless they refer materials to or get a license from the patent holder.
...hich inherited traits, such as those for genetic disease, can be tracked over generations. Throughout out the course of human development, scientists will continue to find new new ways to help the human race through the discovery of the human gene inside of each of us, its uses, as well as complications, that can help the survival of our species.
The first case of Cananvan disease was described in 1931 by Myrtelle Canavan who was one of the first female pathologists. In 1987 a family with two children with Canavan disease sent tissue samples to Reuben Matalon who was a researcher looking for the gene. With those samples he was able to identify the gene 1993. He was able to make a test to help at risk couples that might have a child with the disease. The test was free but in 1997 the Miami Children’s Hospital, which was Dr. Matalon’s employer, patented the gene and claimed everything received from testing. This resulted in the Canavan Foundation withdrawing their testing. The Canavan Foundation later sued the Hospital and the lawsuit was resolved in a sealed out of court session. This case raised the issue of how suitable it is to patent genes.
The age of genetic technology has arrived. Thanks to genetic technological advancements, medical practitioners, with the help of genetic profiling, will be able to better diagnose patients and design individual tailored treatments; doctors will be able to discern which medications and treatments will be most beneficial and produce the fewest adverse side effects. Rationally designed vaccines have been created to provide optimal protection against infections. Food scientists have hopes of genetically altering crops to increase food production, and therefore mitigate global hunger. Law enforcement officers find that their job is made easier through the advancement of forensics; forensics is yet another contribution of genetic technology. Doctors have the ability to identify “high-risk” babies before they are born, which enables them to be better prepared in the delivery room. Additionally, oncologists are able to improve survival rates of cancer patients by administering genetically engineered changes in malignant tumors; these changes result in an increased immune response by the individual. With more than fifty years of research, and billions of dollars, scientists have uncovered methods to improve and prolong human life and the possibilities offered by gene therapy and genetic technology are increasing daily.
... fight the disease. It is crucial that regulation be a necessary component of gene therapy research and applications. In hopes that the government can regulate and can receive this treatment, not restricting it to people that has serious genetic diseases. Gene therapy will change the field of medicine from what it is today. As scientist discovers more genes and their functions, the potential of this treatment is limitless. Though gene therapy is an auspicious treatment choice for numerous diseases (including inherited disorders, some types of cancer, and certain viral infections), the procedure remains precarious and is still under study to make sure that it will be safe and effective. Thus government regulators and scientist must take a lead role in adopting a practical approach to address these issues and determining the correct procedures for dealing with them.
Over 40 years ago, two men by the names of James Watson and Francis Crick discovered deoxyribonucleic acid, or DNA. DNA is hereditary material in humans and almost all other organisms (What is DNA?). From this finding, gene therapy evolved. Today, researchers are able to isolate certain specific genes, repair them, and use them to help cure diseases such as cystic fibrosis and hemophilia. However, as great as this sounds, there are numerous ethical and scientific issues that will arise because of religion and safety.
In September 14, 1990, an operation, which is called gene therapy, was performed successfully at the National Institutes of Health in the United States. The operation was only a temporary success because many problems have emerged since then. Gene therapy is a remedy that introduces genes to target cells and replaces defective genes in order to cure the diseases which cannot be cured by traditional medicines. Although gene therapy gives someone who is born with a genetic disease or who suffers cancer a permanent chance of being cured, it is high-risk and sometimes unethical because the failure rate is extremely high and issues like how “good” and “bad” uses of gene therapy can be distinguished still haven’t been answered satisfactorily.
The genetic technology revolution has proved to be both a blessing and a blight. The Human Genome Project is aimed at mapping and sequencing the entire human genome. DNA chips are loaded with information about human genes. The chip reveals specific information about the individuals’ health and genetic makeup (Richmond & Germov 2009).The technology has been described as a milestone by many in that it facilitates research, screening, and treatment of genetic conditions. However, there have been fears that the technology permits a reduction in privacy when the information is disclosed. Many argue that genetic information can also be used unfairly to discriminate against or stigmatize individuals (Willis 2009).
Genetic engineering depends on the location and analysis of genes on chromosomes and ultimately DNA sequencing. The early cartography of the genes used the principles of Mendelian genetics . It is assumed that alleles that are transmitted together side by side are located on the same chromosome : it is said that are connected or linkage . These genes form a bridging group - linkage group : are the same for gametes and are usually transmitted together , so they do not have independent distribution. Crossing-over occurring during meiosis may cause these alleles can be exchanged between the chromosomes of a homologous pair .
The Human Genome Project is the largest scientific endeavor undertaken since the Manhattan Project, and, as with the Manhattan Project, the completion of the Human Genome Project has brought to surface many moral and ethical issues concerning the use of the knowledge gained from the project. Although genetic tests for certain diseases have been available for 15 years (Ridley, 1999), the completion of the Human Genome Project will certainly lead to an exponential increase in the number of genetic tests available. Therefore, before genetic testing becomes a routine part of a visit to a doctor's office, the two main questions at the heart of the controversy surrounding genetic testing must be addressed: When should genetic testing be used? And who should have access to the results of genetic tests? As I intend to show, genetic tests should only be used for treatable diseases, and individuals should have the freedom to decide who has access to their test results.
"The aim is to decrease the fear of a brave new world and to encourage people to be more proactive about their health. It [Gene therapy] will help humans become better physically and even mentally and extend human life. It is the future” (Hulbert). Dr. Hulbert, a genetic engineer, couldn’t be anymore right; more time, money, and research needs to be put into gene therapy and genetic engineering, since it can cure certain illness and diseases that are incurable with modern medicine, has fewer side-effects than conventional drugs or surgery, and allows humans to be stronger physically and mentally at birth. Gene therapy or genetic engineering is the development and application of scientific methods, procedures, and technologies that permit direct manipulation of genetic material in order to alter the hereditary traits of a cell, organism, or population (NIH). It essentially means that we can change DNA to make an organism better. Genetic engineering is used with animals and plants every day; for example with genetic...
Over the past few decades, advances in technology have allowed scientists to actively manipulate the genetic sequence of an organism through a process called 'genetic engineering'. Many believe that this is a technique which we should exploit and take full advantage of as, after all, it may be the key to curing many hereditary diseases such as heart disease and cancer. It may very well be the solution to overcoming evolutionary barriers and allow us to breed new species. However, if you consider the unknown consequences we may have to face as a result of our futile experimenting, you would find that messing with a system as intricate as nature for curiosity's sake is hardly justifiable.
Another area of medical advancement is genetic engineering. Genetic engineering will detect and possibly stop diseases before birth. Many diseases are associated with specific genes that can be checked for disease and replaced if dysfunctional. Genetic testing has already revealed genetic mutations that cause hypertension, heart disease, diabetes, osteoporosis, colon cancer, polycystic kidney disease, Alzheimers disease, and others. (5) Replacing missing, altered, inactive, or dysfunctional genes will prevent diseases or even death. Also, progression of a disease can be monitored, and
Due to the fact that the field of biotechnology is very serious and potentially dangerous, rules must be set down in order to keep the research in check. The high risk research of genetic therapy needs guidelines that have to be followed in order to keep the study just. The articles that are discussed in this essay focus on ethical issues and ideas that should be followed in the field in order to keep research safe and valid.
The topic of gene therapy in humans is one that is highly debated due to the ethical implications connected to the science. Both sides of the debate have various reasons for their position, but the main factors come down to the ethics of changing someone’s genome and the consequences that accompany the altercations. The two types of gene therapy, somatic and germ-line, are seen in different light. There is more debate over germ-line therapy because the alterations have more consequences than somatic gene therapy. There are many moral and ethical decisions that need to be considered before gene therapy can be widely accepted.
Genetic engineering seems decades away, but through modern technology, it has recently entered the human realm. Some believe genetic engineering will bring forth great advancements in the human brain and body, but instead some believe one mistake creates a world where every child will be genetically engineered just to keep up with the rest of society. Many times, the media plays a very strong role in the image of this issue, and masks the true identity of this social injustice. However, what forms of genetic engineering can be done in humans today? What is in store for the future? What are the risks and what could be the possible benefits? Currently gene therapy is one of the only ways to change the genetic makeup of an animal or human. Also,