Leadership Legacy

 

 

 

1. Does the monopoly power wielded by professional sports leagues hurt the fans, players, citizens, local economies, or the sport?
2. What solutions could be used?
Q12
This discussion is a two-parter. Complete the Your Leadership Legacy assessment http://www.yourleadershiplegacy.com/assessment/assessment.php
Discuss your assessment results for the leadership styles: Ambassador, Advocate, People Mover, Truth-Seeker, Creative Builder, and Experienced Guide.
• What scores surprised you the most? Why were you surprised?
• Which style(s) are most helpful to you now and how will this information be helpful for your business venture?
• Incorporate information from the readings such as leadership power to support your discussion.

 

Sample Solution

Monopoly sports leagues grant fewer franchises than would exist in a competitive market. To hold salary levels below the competitive level, leagues adopt restrictions on the mobility of players that limit the efficient allocation of players among teams.” On the horizon, the distinct possibility exists that sportscasts will shift from free television to cable, forcing fans to pay for what they now receive for free. Finally, monopoly sports leagues tolerate inefficient and wasteful management practices by franchise owners that leagues facing the pressure of competition could not endure.

There are more than 30 million single-nucleotide polymorphisms that are like a finger print of genetic code in human genome(37). International Haplotype Mapping Project characterizes these SNPs in variety of population for public usage(38). Researchers can use these databases to identify association between disease risk .disease studies and genome- wide association studies linked by commercially available microarrays (SNP chips)(39). When specific allele of a SNP is present , a fluorescent signal is produced by using allele specific oligonucleotide probes for SNP arrays and array have skill of analyzing up to 1 million SNPs in a single sample(40). Also allelic imbalance, copy number variation, or loss of heterozygosity of cancer genome can be screened by SNP array.

Microarray analysis

Expression levels of thousand gene in cancer is analyzed with single experiment of microarray. Microarrays that are chips have immobilized capture molecules serve as probes to bind fluorescently labeled targets prepared from the two samples for comparing (41). These capture molecules can be oligonucleotides or cDNA. MRNA, miRNA, DNA and protein microarrays are most popular analysis. Gene expression profiling has been used for catogarizing unique subtypes of cancer, identifying invasive and non invasive cancer type’s phenotype, forecasting prognosis and response to treatment and risk of recurrence(42). New miRNA microarray platform data’s can be used as a cancer biomarker. To classify patients prognostic groups and treatment subgroups, miRNA signatures is used. Also misroarray is used to determine epigectic alteration that is contributed to tumorigenesis and direct to manage patient(43).

Proteomics by mass spectrometry

Changing of protein profiles in cancer cell is important to determine new biomarker and might help to classify of tumors subtypes(44). Proteomic analysis have more advantage than measurement of mRNA. Because protein is the final effector molecule and their level can not overlap the level of mRNA due to the posttranscriptional modifications(45). In addition to that , protein-protein interactions contribute to cellular pathways and carcinogenesis. Proteins are quanrified in mass spectrometry according to their mass to

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