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수명이 다한 서버 환경의 레거시 웹 응용 프로그램에 대한 책임 귀하는 현재 응용 프로그램 환경에 다음과 같은 제한 사항이 있으므로이 응용 프로그램을 최대한 빨리 AWS로 마이그레이션하려고합니다.
The VM's single 10GB VMDK is almost full Me virtual network interface still uses the 10Mbps driver, which leaves your 100Mbps WAN connection completely underutilized It is currently running on a highly customized. VMware 환경 내의 Windows VM :
You do not have me installation media
이것은 RTO (Recovery Time Objective)가 8 시간 인 미션 크리티컬 애플리케이션입니다. RPO (Recovery Point Objective)가 1 시간입니다. 비즈니스 연속성 요구 사항을 충족하면서이 애플리케이션을 AWS로 가장 잘 마이그레이션 할 수 있습니까?
A. ec2-bundle-instance API를 사용하여 VM의 이미지를 EC2로 가져 오기
B. Use 53 to create a backup of the VM and restore the data into EC2.
C. 가져 오기 / 내보내기를 사용하여 VM을 ESS 스냅 샷으로 가져 와서 EC2에 첨부합니다.
D. vCenter의 EC2 VM 가져 오기 커넥터를 사용하여 VM을 EC2로 가져옵니다.
Answer: D
別の国から情報を取得するために、どのゲートウェイで委員会のレゴトリが使用されますか?
A. エグモントの原則に基づくFIUリクエスト
B. MLATリクエスト
C. バーゼル委員会との監督チャネル要求
D. FATFリクエスト
Answer: B
Gene therapy offers a new treatment paradigm for curing human disease. Rather than altering the disease phenotype by using agents that interact with gene products, or are themselves gene products, gene therapy can theoretically modify specific genes resulting in disease cure following a single administration.
Initially gene therapy was envisioned for the treatment of genetic disorders, but is currently being studied for use with a wide range of diseases, including cancer, peripheral vascular disease, arthritis, Neurodegenerative disorders and other acquired diseases.
Certain key elements are required for a successful gene therapy strategy. The most elementary of these is that the relevant gene be identified and cloned. Upon completion of the Human Genome Project, gene availability will be unlimited. Once identified and cloned, the next consideration must be expression of the gene. Questions pertaining to the efficiency of gene transfer and gene expression remain at the forefront of gene therapy research, with current debates revolving around the transfer of desired genes to appropriate cells, and then to obtaining sufficient levels of expression for disease treatment. With luck, future research on gene transfer and tissue-specific gene expression will resolve these issues for the majority of gene therapy protocols.
Other important considerations for a gene therapy strategy include a sufficient understanding of the pathogenesis of the targeted disorder, potential side effects of the gene therapy treatment, and a more in depth understanding of the target cells which are to receive gene therapy.
Gene transfer vector is the mechanism by which the gene is transferred into a cell. Currently there are at least 150 clinical gene therapy protocols worldwide. Since the approval process for these protocols is not as public outside the U.S., it is difficult to ascertain the exact number of worldwide protocols. As of December 1995, 1024 patients had been treated with either a gene transfer or gene therapy protocol.
Much controversy exists regarding how many of these patients have benefited from their gene therapy, and no one has yet been cured.
Public controversy in the field of human gene therapy is driven by several factors. Ordinary citizens as well as scientists easily understand the enormous potential of gene therapy, but the former may not appreciate all the pitfalls and uncertainly that lie in the immediate future. The financial interests of biotechnology firms and, some have asserted the career interests of some gene therapists have encouraged extravagant, or at least verily optimistic public statements about contemporary gene therapy. In spite of the proliferation of protocols, the actual number of patients treated remains small, and only one genuinely controlled study of human gene therapy has been published as of this date The author's attitude toward the gene therapy as a future cure for cancer, peripheral vascular disease, arthritis, Neurodegenerative disorders and other acquired diseases is
A. Amusement
B. Indifference
C. Cautious optimism
D. Censure
E. Disapproval
Answer: C
Explanation:
Explanation/Reference:
Explanation:
The best answer is D.
In the opening sentence, the author optimistically states that gene therapy offers a new treatment paradigm for curing human disease. However, in the fifth paragraph the author mentions some of the problems.
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