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Q: Epigenetics (epigenomics) refers to changes in the _______.
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- Fragile X syndrome, caused by a change in the FMR1 gene, is the most common form of intellectual disability. In patients with this syndrome, a small part of the gene is repeated several times in one area of the chromosome. This defect in the gene makes the body unable to produce adequate amounts of a protein needed for normal brain functioning. In males, this syndrome causes a moderate intellectual disability, and in females, a mild intellectual disability. A family that exhibits Fragile X syndrome is shown in the pedigree. In the pedigree, squares represent males and circles represent females. Shaded symbols represent a person with the disorder. Which of the following correctly predicts the outcome if offspring 11 mated with a homozygous normal female, based on the inheritance pattern shown in the pedigree? The male offspring would exhibit Fragile X syndrome because Fragile X is an X-linked recessive trait. The female offspring would exhibit Fragile X syndrome because Fragile X…With regard to human cancer cells, which of the following statements is true? A. Cancer cells within one tumor usually do not share common mutations B. Cancer cells generally have lost the ability to divide C. Oncogenes are non-human genes not related to normal genes in the human genome D. Mutations in DNA repair genes result in an increased chance of getting cancer.A disease "D" is caused by a combination of genetic and environmental factors. Polymorphisms in multiple genes can make an individual susceptible to this disease. Can gene therapy be a feasible therapeutic option to treat "D"? Why or why not?
- Studies have shown that there are significant differences in cancer rates among different ethnic groups. For example, the Japanese have very high rates of colon cancer but very low rates of breast cancer. It has also been demonstrated that when members of low-risk ethnic groups move to high-risk areas, their cancer risks rise to those of the high-risk area. For example, Japanese who live in the United States, where the risk of breast cancer is high, have higher rates of breast cancer than do Japanese who live in Japan. What are some of the possible explanations for this phenomenon? What factors may explain why the Japanese have higher rates of colon cancer than do other ethnic groups?Our understanding of the molecular biology of cancer formation has been greatly enhanced by studying oncogenic viruses. Answer the following questions regarding oncogenic retroviruses? Explain how a gain of function mutation in the Ras protein caused by a retrovirus might lead to cancer formation.differentiate the structure of the gene or genes of a genetically inherited disease to the one that just mutated caused by environmental factors
- "Genome-Wide Association Studies Identify Genome Variations That Contribute to Disease" Explain this ?people with osteogenesis imperfecta have a dominant mutation in one of the two genes that produce type 1 collagen. people with OI have weak bones, bkuish color in teh whites of eyes, and a variety of afflictions that cause weakness in their joint and teeth. However, some people can carry the mutation but have no symptoms. Thus, families can unknowingly transmit the mutation but does not express the OI phenotype. This is an example of which of the following? a. incomplete penetrance b. variable expressivity c. epistasis d. incomplete dominanceDespite the failure to date of gene therapy, identification of the gene responsible for cystic fibrosis has very recently led to effective treatments for the disease in patients with particular mutant alleles. Give an example?
- Which ONE of the following genetic patterns defines a patient with acute myeloid leukaemia with the most favourable prognosis? Select one: A.Deletion of chromosome 5 B.Normal karyotype with FLT3 tyrosine kinase domain mutation C.t(8;21) translocation D.Deletion of chromosome 7Go to the NCBI’s website at https://ncbi.nlm.nih.gov On the database dropdown menu, select “Gene” and search for “RB1.” The first entry should be on the Homo sapiens version; click the gene name. Use the information to answer the following: What is the chromosomal location of RB1? Scroll down to the “Expression” data. List 2-3 examples of normal tissues that typically express the RB1 gene. Would you say that RB1 expression is very specific or general within tissues? Scroll down to the “NCBI Reference Sequences (RefSeq)” section. Click on the “GenBank” link under NG_009009.1 RefSeqGene. This will take you to the genomic sequence of RB1. How many nucleotides long is the full-length RB1 gene? Return to the RefSeq section in the Gene Database for RB1 (back click once from where you were for part c). Click on the link under “mRNA and Protein(s)” listed as NM_000321.3. This will take you to the mature mRNA sequence data: How many bases long is the full-length RB1 mRNA transcript? Scroll…Genetic Diseasesa. List the differences between infectious and genetic diseases.b. Discuss the reasons why genetic diseases could hardly be diagnosed in fish.c. Describe the how albinism occur in fish and why it is considered a disease.d. List other fish species, documented to exhibit albinism.e. Elucidate the process by which melanoma or skin cancer-prone sword tail develops. Describethe genetic mechanism involved.f. Describe how domestication can lead to genetic problems in aquaculture.