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NEW QUESTION: 1
必要に応じて、次のログイン資格情報を使用します。
Azureユーザー名：xxxxx
Azureパスワード：xxxxx
次の情報は、テクニカルサポートのみを目的としています。
ラボインスタンス：10543936

データが削除されてから最大10日以内に、storage10543936という名前のAzure Storageアカウントからblobデータを復元できることを確認する必要があります。
このタスクを完了するには、Azureポータルにサインインします。
Answer:
Explanation:
See the explanation below.
Explanation
Enable soft delete for blobs on your storage account by using Azure portal:
1. In the Azure portal, select your storage account.
2. Navigate to the Data Protection option under Blob Service.
3. Click Enabled under Blob soft delete

4. Enter the number of days you want to retain for under Retention policies. Here enter 10.
5. Choose the Save button to confirm your Data Protection settings
Note: Azure Storage now offers soft delete for blob objects so that you can more easily recover your data when it is erroneously modified or deleted by an application or other storage account user. Currently you can retain soft deleted data for between 1 and 365 days.
Reference:
https://docs.microsoft.com/en-us/azure/storage/blobs/storage-blob-soft-delete

NEW QUESTION: 2
There is a simple view SCOTT.DEPT_VIEW on the table SCOTT.DEPT.
This insert fails with an error:
SQL> insert into dept_view values('SUPPORT','OXFORD'); insert into dept_view values('SUPPORT','OXFORD')
* ERROR at line 1:
ORA-01400: cannot insert NULL into ("SCOTT"."DEPT"."DEPTNO")
What might be the problem?
A. The INSERT violates a constraint on the detail table.
B. The view was created as WITH READ ONLY.
C. The view was created as WITH CHECK OPTION.
D. The INSERT violates a constraint on the view.
Answer: A
Explanation:
B is incorrect because constraints are enforced on detail tables, not on views. C and D are incorrect because the error message would be different.

NEW QUESTION: 3
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 All of the following are mentioned in the passage as elements that are required for a successful gene therapy strategy EXCEPT:
A. Identifying the relevant gene
B. Expressing the relevant gene
C. Understanding of the pathogenesis of the targeted disorder
D. Determining the side effects of the relevant gene
E. Gaining and a more in depth understanding of the target cells which are to receive gene therapy.
Answer: D
Explanation:
Explanation/Reference:
Explanation:
The best answer is C.
One must determine the side effects of the relevant gene therapy treatment, and not of the relevant gene itself

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