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Gene therapy and gene-based drugs are two ways we could benefit from our growing mastery o

f genetic science. But there will be others as well. Here is one of the remarkable therapies on the cutting edge of genetic research that could make their way into mainstream medicine in the coming years.

While it's true that just about every cell in the body has the instructions to make a complete human, most of those instructions are inactivated, and with good reason: the last thing you want for your brain cells is to start churning out stomach acid or your nose to turn into a kidney. The only time cells truly have the potential to turn into any and all body parts is very early in a pregnancy, when so-called stem cells haven't begun to specialize.

Yet this untapped potential could be a terrific boon to medicine. Most diseases involve the death of healthy cells-brain cells in Alzheimer's, cardiac cells in heart disease, pancreatic cells in diabetes, to name a few. If doctors could isolate stem cells, then direct their growth, they might be able to furnish patients with healthy replacement tissue.

It was incredibly difficult, but last fall scientists at the University of Wisconsin managed to isolate stem ceils and get them to grow into neural, gut, muscle and bone cells. The process still can't be controlled, and may have unforeseen limitations; but if efforts to understand and master stem-cell development prove successful, doctors will have a therapeutic tool of incredible power.

The same applies to cloning, which is really just the other side of the coin; true cloning, as first shown with the sheep Dolly two years ago, involves taking a developed cell and reactivating the genome within, resetting its developmental instructions to a pristine state. Once that happens, the rejuvenated cell can develop into a full-fledged animal, genetically identical to its parent.

For agriculture, in which purely physical characteristics like milk production in a cow or low fat in a hog have real market value, biological carbon copies could become routine within a few years. This past year scientists have done for mice and cows what Ian Wilmut did for Dolly, and other creatures are bound to join the cloned menagerie in the coming year.

Human cloning, on the other hand, may be technically feasible but legally and emotionally more difficult. Still, one day it will happen. The ability to reset body cells to a pristine, undeveloped state could give doctors exactly the same advantages they would get from stem cells., the potential to make healthy body tissues of all sorts, and thus to cure disease. That could prove to be a true "miracle cure."

The writer holds that the potential to make healthy body tissues will ______.

A.aggravate moral issues of human cloning

B.bring great benefits to human beings

C.help scientists decode body instructions

D.involve employing surgical instruments

答案
B
解析:题干问:“作者认为制造健康的身体组织的这种潜能将会……”。文章开宗明义,在第一段讲述到,如果我们掌握了基因科学,将会对人类有极大的好处,此外第三段的第一句“然而这种没被开发的潜能对医学有极大的好处”,以及全文的最后一句都呼应了这一观点,因此B“给人类带来极大的好处”为正确选项。而选项A“使人类克隆的道德问题变得更为严重”,选项C“帮助科学家们解码身体指令”和选项D“涉及使用外科仪器”都是与题干不相关的。
更多“Gene therapy and gene-based drugs are two ways we could benefit from our growing mastery o”相关的问题

第1题

A gene that takes part in the synthesis of polypeptide is

A.Structural gene

B.Regulator gene

C.Operator gene

D.Promoter gen

E.Noncoding region

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第2题

基因治疗(gene therapy) 名词解释

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第3题

Fatal enzyme deficiencies may be treated by _______.

A.X-ray therapy

B.chemotherapy

C.immunotherapy

D.gene therapy

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第4题

The usual therapies for cancer treatment are ________.

A.surgery, radiotherapy and chemotherapy

B.surgery

C.gene therapy

D.food therapy

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第5题

Gene therapy offers unique possibilities to treat the _______ causes of diseases.

A.genetic

B.environmental

C.emotional

D.dietary

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第6题

The use of gene therapy as a supportive method along with traditional treatments has
点击查看答案

第7题

Gene therapy offers unique possibilities to treat the _______ causes of diseases, su
ch as fatal enzyme deficiencies.

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第8题

课程中颈腰痛的常用治疗方法没有(Common treatments for neck and back pain mentioned in the course include)

A.生物治疗 (Biotherapy )

B.基因治疗 (Gene therapy )

C.手术治疗 (Operation treatment )

D.冷敷治疗 (Cold compress treatment)

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第9题

课程中颈腰痛的常用治疗方法没有(Common treatments for neck and back pain mentioned in the course include)

A.生物治疗 (Biotherapy )

B.基因治疗 (Gene therapy )

C.手术治疗 (Operation treatment )

D.冷敷治疗 (Cold compress treatment)

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第10题

听力原文:There are two primary ways that genes can be used to treat disease. The first is
gene therapy, in which one or more genes are injected into the patient to replace those that are absent or not working properly. This approach has been used to treat heart disease and many forms of cancer. The second way to exploit genes to treat disease is known as small-molecule therapy. In this approach, a small-molecule (that is a drug) is given to the patient to modify the function of one or more genes in the body.

According to the speaker, small-molecule therapy can be used to ______.

A.replace genes not functioning properly in the body

B.increase the number of genes working properly in the body

C.modify the function of some genes in the body

D.replace genes absent in the body

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第11题

"Before the operation, I would look at someone and all I could see for their face was jell
y," says Jonathan Wyatt "Now, I can see peoples faces." The 65-year-old is one of six people in the world to receive gene therapy for a【C1】______type of inherited eye disease【C2】______choroideremia(an eye disease). The first published【C3】______of the trial, released today, suggest that【C4】______peoples genes can stop the disease from causing blindness—and【C5】______sight in those whose vision has become【C6】______. Choroideremia is caused by【C7】______in the CHM gene. In those who have the disease, a【C8】______of REP-1 means that cells in the eyes stop working and slowly begin to【C9】______causing blindness. Enter gene therapy, which uses a virus to insert a【C10】______copy of a gene into cells with a gene defect and could【C11】______be used to treat many genetic conditions. Robert MacLaren of the University of Oxford and his colleagues decided to see if it could【C12】______choroideremia. Starting two years ago with Wyatt, they【C13】______a virus carrying a corrective copy of the CHM gene into the eyes of people with choroideremia. Today the team【C14】______that of the six people who received the treatment six months【C15】______or longer, all have described【C16】______in their vision. Still, the long-lasting effects of the treatment remain【C17】______Wyatt had the treatment first, so can【C18】______that the benefits seem to last two years,【C19】______hes just one case. The treatment also cant replace cells that have been【C20】______destroyed.

【C1】

A.common

B.ambiguous

C.rare

D.simple

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