After I have earned my Bachelor’s degree in Texas A&M University, I immediately ventured into the professional world. I started my career by working as Sanderson Farms in Bryan, Texas as a line supervisor. In this job, my principal task is to supervise the activities of over 50 employees and to learn about the various operations involved in the poultry processing industry.
After only 8 months, I was straight away promoted as a customer service and sales representative. This job entailed working with the sales accounts of grocery giants such as HEB. This positive outcome would have not happened if it were not for my continuous hard work and perseverance to excel in my chosen field.
Despite this success, I still feel the need to gain more knowledge about my profession in order to be highly competitive and profitable in the world of agriculture and science. Because of this, I decided to pursue a master’s degree in veterinary at Texas A&M University. For me, this academic institution has helped me immensely in being who I am now. It has equipped me with the necessary knowledge and training that I utilized when I worked for Sanderson Farms.
Through this, I know that Texas A&M University can provide the necessary education I needed in order to fulfill my lifelong dreams and goals. I know that the road to success and contentment will not be easy. There will be instances when I will be tempted to give up or to question if I have the ability to fulfill my dreams.
But due to my experiences when I was an undergraduate and working for Sanderson Farms, I have become more mature and goal-oriented. These events in my life taught me not to dwell on the past and to be more optimistic about my future. With this attitude and determination, I know that I will eventually reach my dream and I can be the best person that I want to be.
P53 and the future for cancer treatments
P53 and the future for cancer treatments.
Research paper that examines a debatable topic. It also needs to have a clear thesis. Your paper has neither of these traits. You need a clear thesis. What one thing are you trying to say here? What are you trying to argue? It cannot be just telling the reader about P53. Think of a controversial issue related to its potential future use. Is there a specific form of cancer that could be your focus? For example, cancers caused by a virus. Are you arguing that it is the most viable option for cancer treatment? Are you arguing that it is the future direction for cancer treatment? If so, you need to say that outright and then develop points to convince the reader. Think of 2-4 points that you could make here. Or you could focus on the P53 gene and cancers caused by a virus. You need a better opening or lead paragraph, one that really grabs the reader’s attention and makes them want to continue reading. You could do that with an anecdote or story related to genetic research or a specific patient. Draw them into the subject. After your initial paragraph in which you grab the readers’ attention. Set the stage for your thesis statement. Then state it as well as how you are going to argue it in the paper. Follow this with a couple pages of background information on how cancer is typically treated. Then give background information on P53. Lay your ideas out in an outline and email it to me. Build your argument.Watch some videos. Connect the scholarly and nonscholarly sources into a paper for your peers that argues a specific point. As you revise your thesis, you may need additional scholarly sources that match it better. Come to class on Wednesday with a revised paper. Professor Shumway Example: YouTube video on P53 – https://www.youtube.com/watch?v=8Mp7D7qWxG4 Citations for the attached articles: Trafton, Anne. “Closing a Back Door for Cancer.” MIT Technology Review, vol. 117, no. 1, Jan. 2014, p. 7. EBSCOhost, search.ebscohost.com/login.aspx?direct=true&AuthType=cookie,ip,url,cpid&custid=s9004980&db=aph&AN=93251064&site=ehost-live&scope=site. Markx, Jean. “Recruiting the Cell’s Own Guardian for Cancer Therapy.” Science, vol. 315, no. 5816, 2 March 2007, pp. 1211-1213.
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