What make leaders successful or unsuccessful change agents

 

You will put well-known personalities and yourself under the microscope to learn what makes you and the individuals you select not only leaders but also what it takes for leaders to be change agents.

Choose any two leaders who you consider to have been very successful change agents and two who you believe have been unsuccessful change agents.

Write a brief biography of each of the leaders you selected.
What were the leaders’ bases of power? How was it gained? What was their reach or influence?
How did the leaders find themselves in the position to serve as change agents? Describe the situation, including the need for a change agent.
Were the leaders successful change agents?
What made the leaders successful or unsuccessful change agents?

 

Sample Solution

to recognize potential antimutagens and anticarcinogens giving open doors to the advancement of new medications to be utilized in the avoidance and treatment of neoplasies (Gebhart, 1992). Among the bioassays to evaluate DNA harm in mammalian cells in vivo, the chromosomal variation test is a powerful transient measure on the grounds that the occurance of the chromosomal deviations is one of the main natural outcome of openness of an organic entity to the genotoxic specialist. In vivo mammalian chromosomal distortion test has been effectively utilized for the identification of underlying variations prompted by the test substance in the bone marrow cells of creatures, typically rodents (Preston et al., 1987; Amer et al., 2002; Patlolla and Tchounwou, 2005). The benefits of the CA measure are connected with the phone by cell approach, a precise distinguishing proof of all the different chromosome transformation types, a potential co-discovery of mitotic lists and the semi robotized scoring by picture examination.

In late many years, upgrades in disease treatment have emphatically expanded the endurance rates among patients (UNSCEAR, 2000). However, the therapies like radiotherapy and chemotherapy are possibly genotoxic and mutagenic which can prompt the improvement of optional, therapy related conditions, including further tumors, as well as incline survivors toward different non-harmful illnesses that can frequently appear in the posterity (Glades et al., 2009). Present chemotherapy disease medicines have ended up being insufficient because of their poisonousness as well as for the cells creating opposition (Mc Whirter et al., 1996). Concentrates on carried on mice have likewise demonstrated the way that openness to anticancer medications can result in transgenerational genomic shakiness (Glen and Dubrova, 2012). Chemotherapy malignant growth treatment cases include perpetual use of antineoplastic specialists which kill neoplastic tissue as they are poisonous to quickly multiplying cells. Anyway all the while, they can harm ordinary multiplying cells too. This brings down their remedial record. In this manner long haul utilization of these antineoplastic specialists has turned into a subject of expanding concern (Arif et al., 2009).

In excess of 100 chemotherapy drugs are utilized in disease treatment, either alone or in blend with different medications or medicines. One such medication is Cyclophosphamide. Cyclophosphamide (CPA) which has a place with the class of oxazaphosphorines is an alkylating specialist. It had been recorded as one of the best chemotherapy drugs on the World Wellbeing Associations Rundown of Fundamental Meds. Cyclophosphamide has stamped immunosuppressant properties against both humoral and cell resistance due to which it has been widely used to treat various youth and grown-up malignancies (Thomson et al., 2002; Colvin, 1999; Triphaty et al., 2008) including bosom disease, lymphomas and leukemias, retinoblastoma, little cell cellular breakdown in the lungs, ovarian malignant growth, sarcomas and numerous myeloma (Fleming, 1997), since its underlying amalgamation in 1958. In any case, throughout the time its utilization has been declining a result of it making unfriendly hereditary impacts. The synthetic is initiated by t

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