What do loss of function alleles tell us about normal gene function? Why would a researcher be interested in over- or mis-expression phenotypes?
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What do loss of function alleles tell us about normal gene function? Why would a researcher be interested in over- or mis-expression |
Why are genetic screens useful? Why do biologists do screens? What are we trying to do? What is the Big Picture purpose? |
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- fueled.brightspace.com/d2l/le/enhancedSequenceViewer/3300467?url=https%3A%2F%2Ff59af8a9-95f5-419c-a486-a A rdschools.com bookmarks Drive Classes B Login Page Sign In Education and Lear... Content = 1.08 Unit Test: Gene Expression - Part 1 Which statement is most accurate? Hair is different from kidneys because the cells that make up hair and kidneys have different genes All cells have the same genes, but different genes are active in different cells. As cells and tissues differentiate, they produce new genes. All cells have the same genes, and all of a cell's genes are active at the same time. #m C $ J лае 1 2 3 4 5 & 7 8Give a schematic diagram of how we can Treatment Down's syndrome by using gene therapy? Please answer at your own words,please..What are the ethical issues associated with gene and cell therapy? What are stem cells? Why are stem cells so important in gene and cell therapy?
- How gene therapy or cell therapy can help cure diseases? What kinds of diseases do gene and cell therapy treat? What is the difference between gene therapy and cell therapy? What are the different approaches to gene and cell therapy? What risks are associated with gene and cell therapy? What are the ethical issues associated with gene and cell therapy? What are stem cells? Why are stem cells so important in gene and cell therapy?A) Ensuring Equal Access to Customized Medicine How can healthcare providers ensure equitable access to expensive technologies that not only treat illnesses but also promise to promote longevity and enhance patients’ quality of life? What are the ethics of cost/benefit analyses when human lives are at stake? What policies could help avoid “genetic discrimination” when medical test results reveal conditions or genetic susceptibilities to specific diseases that weren’t the subject of the original tests?LO 71- Explain why studying the epigenome is harder than studying the genome of an organism. Select all of the factors that make studying the epigenome more difficult than studying the genome: epigenetic changes are unstable and not heritable epigenome is bigger than the genome the epigenome cannot be 'sequenced' as the genome can the epigenome is variable across different types of cells epigenetic changes produce unobservable nucleotide sequence changes
- What is preimplantation genetic testing? Give an example of a condition screened for? Do you agree with preimplantation screening and what are some of the ethical concerns surrounding the practice?Topic: Recombinant pharmaceuticals (for the production of insulin, human growth hormone or blood clotting factors) Question What are the drawbacks/disadvantages/unknowns associated with this genetic process?Please Write a Brief Note on "Treatment for the genetic disorders by using gene therapy " Please write at your own words, please...
- This is a blank question. Thank you in advance, Bloom Syndrome Bloom syndrome is a rare genetic disorder. It is characterized by short stature and a long narrow face with prominent nose and ears. There is also increased sensitivity to light. People who have the disorder often develop rashes on their face, forearms, and hands when they have been exposed to the sun. In addition, these people often suffer from chronic obstructive pulmonary disorder (COPD) and have a higher chance of developing cancer. The cause of this genetic disorder is a mutation in the BLM gene located on chromosome 15. The immediate effect of this mutation is that there is a defect in the functioning of the DNA helicase enzyme. What would be the effect of this mutation on DNA replication? What stage of the cell cycle would be most affected?You are a genetic counselor, and your patient has asked to be tested to determine if she carries a gene that predisposes her to early-onset cancer. If your patient has this gene, there is a 50/50 chance that all of her siblings inherited the gene as well; there is also a 50/50 chance that it will be passed on to their offspring. Your patient is concerned about confidentiality and does not want anyone in her family to know she is being tested, including her identical twin sister. Your patient is tested and found to carry a mutant allele that gives her an 85% lifetime risk of developing breast cancer and a 60% lifetime risk of developing ovarian cancer. At the result-disclosure session, she once again reiterates that she does not want anyone in her family to know her test results. a. Knowing that a familial mutation is occurring in this family, what would be your next course of action in this case? b. Is it your duty to contact members of this family despite the request of your patient? Where do your obligations lie: with your patient or with the patients family? Would it be inappropriate to try to persuade the patient to share her results with her family members?How can you treatment for the genetic disorders by using gene therapy? Please answer at your own words, please..