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ra1l [238]
2 years ago
8

I need help finding a good college. I am only 17 almost 18 in 5 months. I graduate next year and I want to be either a Pediatric

Nurse or a Travel Nurse. I want one that will be close to me so I chose either UACCB in Batesville AR, Lyons college in Batesville AR or ASU Heber Springs AR. Please I need some advice I don't know which one to chose. I came down to 2 which are UACCB & Lyons college but I need one that will help me to toward my dreams.
Please I need help choosing a college can y'all give me some advice on what to do
Medicine
1 answer:
ehidna [41]2 years ago
4 0

Answer:

If you have the money then Lyons is a good choice since it's private, but if you don't then UACCB is a great pick as well because it's a public university. I don't know much about these types of colleges since they aren't in my general area of interests but that is some of the advice I could give.

Don't stress too much though, you'll be okay no matter where you go :)

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Okay

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Human topoisomerase I plays an important role in removing positive DNA supercoils that accumulate ahead of replication forks. It also is the target for camptothecin-based anticancer drugs that act by increasing levels of topoisomerase I-mediated DNA scission. Evidence suggests that cleavage events most likely to generate permanent genomic damage are those that occur ahead of DNA tracking systems. Therefore, it is important to characterize the ability of topoisomerase I to cleave positively supercoiled DNA. Results confirm that the human enzyme maintains higher levels of cleavage with positively as opposed to negatively supercoiled substrates in the absence or presence of anticancer drugs. Enhanced drug efficacy on positively supercoiled DNA is due primarily to an increase in baseline levels of cleavage. Sites of topoisomerase I-mediated DNA cleavage do not appear to be affected by supercoil geometry. However, rates of ligation are slower with positively supercoiled substrates. Finally, intercalators enhance topoisomerase I-mediated cleavage of negatively supercoiled substrates but not positively supercoiled or linear DNA. We suggest that these compounds act by altering the perceived topological state of the double helix, making underwound DNA appear to be overwound to the enzyme, and propose that these compounds be referred to as ‘topological poisons of topoisomerase I’

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