D. it has the power to interpret laws
Answer:
The Monroe Doctrine was to prevent further European colonization in the Western Hemisphere.
Explanation:
Monroe Doctrine, (December 2, 1823), cornerstone of U.S. foreign policy enunciated by Pres. James Monroe in his annual message to Congress. Declaring that the Old World and New World had different systems and must remain distinct spheres, Monroe made four basic points: (1) the United States would not interfere in the internal affairs of or the wars between European powers; (2) the United States recognized and would not interfere with existing colonies and dependencies in the Western Hemisphere; (3) the Western Hemisphere was closed to future colonization; and (4) any attempt by a European power to oppress or control any nation in the Western Hemisphere would be viewed as a hostile act against the United States.
In declaring separate spheres of influence and a policy of non-intervention in the foreign affairs of Europe, the Monroe Doctrine drew on past statements of American diplomatic ideals, including George Washington’s Farewell Address in 1796, and James Madison’s declaration of war with Britain in 1812.
That statement is true
This result can be used as proof that certain type of genotype among humans are not affected by environmental factors. (some of us are born to be physically stronger or intellectually inferior without making any effort, environmental factors could only resulted in very little deviation.)
In 1890, Captain Alfred Thayer Mahan, a lecturer in naval history and the president of the United States Naval War College, published The Influence of Sea Power upon History, 1660–1783, a revolutionary analysis of the importance of naval power as a factor in the rise of the British Empire.
Mahan became the college's president in 1886 and held that post until 1889. In 1890 Mahan published his college lectures as The Influence of Sea Power upon History, 1660–1783. ... Before his death in December 1914, Mahan foretold the defeat of the Central Powers and of the German navy in World War I.
Answer:
Following are the responses to the given points:
Explanation:
For point a:
In the management of bipolar type 2 disorder, its genetics play an important role. Bipolar may evolve genetically engineering or to be inherited. Bipolar type 2 diseases are believed to be impossible to be caused by a genetic mutation, however, the development is related to numerous gene mutations. All those genetic changes render no commitment to the growth of bipolar disease by other factors such as intense lifestyle habits and rest. Prevalence of bipolar may be transmitted through bipolar type 2, although genetic factors things practically 60-80 percent.
For point b:
Hypothalamus-pituitary impairment and stress impairment have an important role in the development of mental mania. The etiology of term thinking and mood disorders of bipolar disorder plays a significant part. hypercortisolism Such symptoms arise caused by elevated Cortisol causing neuro-cytotoxicity. Manic episodes of mental mania have followed elevated levels of ACTH or cortisol in the head due to HPA axis dysfunction. All such high ACTH and Cortisol levels cause brain defects and vital influence in bipolar hypertension.
For point c:
Its elevated oxidative stress style is concerned with Type 2 bipolar. The peripheral rates of pro-inflammatory cytokines are markedly increased in bipolar Type 2 disorder. Its increase in pro-inflammatory during depressive symptoms is aggravated. Its cytokines cause immediate proteins like haptoglobin and C reactive proteins to be generated. Those same acute proteins are associated with bipolar disorders together with an increase in plasma supplement rates.
Through activating the HPA-axis, macrophages will raise the ACTH and Cortisol levels, exacerbating the bipolar of type 2. These cytokines also interact with the neurotransmitter synthesis including serotonin and dopamine that control functions of the mood, cognition, and psychomotor. Dopamine and SEROTONIN synthesis can exacerbate the effects of bipolar Type 2 syndrome.
