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1.How were researchers able to get the anti-thrombin gene intothe goat?

2.How were they able to have the anti-thrombin gene expressedonly in mammary tissues?

3. What types of diseases have the potential to be cured bystem cell technology?

4. Are any stem cell treatment currently approved or inclinical trials?

5. What is the difference between an embryonic stemcell and an adult stem cell? What are thechanges that occur in a cell as itdifferentiates?

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Beverley Smith
Beverley SmithLv2
28 Sep 2019
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Related questions

1.What types of diseases have the potential to be cured bystem cell technology?

2. Are any stem cell treatment currently approved or inclinical trials?

3. What is the difference between an embryonic stemcell and an adult stem cell? What are thechanges that occur in a cell asitdifferentiates?

4. How are stem cells and cancer cells similar?

5. What are the ethical issues surrounding the use of embryonicstem cells? Can any of these issues be avoided using technologysuch as somatic cell transfer or inducedpluripotent stem cells, explain why or why not?

6. What are the potential dangers of stem cell technology?

Can you help me with these questions? Thank you!

5. What basic principle of biology makes it possible to placegenes from one organism into another? In chapter 8, the productionof a transgenic goat is described. How were researchers able to getthe anti-thrombin gene into the goat?

6. How were they able to have the anti-thrombin gene expressedonly in mammary tissues?

1. What is the greatest benefit of GMF’s and conversely thegreatest danger? Develop your own opinion and be able to support itwith your own reliable research.

2. How were they able to have the anti-thrombin gene expressedonly in mammary tissues?

3. What basic principle of biology makes it possible to placegenes from one organism into another? In chapter 8, the productionof a transgenic goat is described. How were researchers able to getthe anti-thrombin gene into the goat?

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