Junk DNA

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出版者:Columbia University Press
作者:Nessa Carey
出品人:
页数:224
译者:
出版时间:2015-3
价格:USD 29.95
装帧:Hardcover
isbn号码:9780231170840
丛书系列:
图书标签:
  • 科普
  • 生物学
  • 生物
  • 表观遗传学
  • 英文原版
  • 科学和心理学
  • Non-Fiction
  • JunkDNA
  • 基因组学
  • 非编码DNA
  • 遗传学
  • 分子生物学
  • 科学普及
  • DNA
  • 基因
  • 进化
  • 生物学
  • 生命科学
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具体描述

For decades after identifying the structure of DNA, scientists focused only on genes, the regions of the genome that contain codes for the production of proteins. Other regions that make up 98% of the human genome were dismissed as "junk," sequences that serve no purpose. Yet recently researchers have discovered variations and modulations in this junk DNA that underwrite a number of intractable diseases. This knowledge has led to innovative research and treatment approaches that may finally control these conditions.

Junk DNA can play vital and unanticipated roles in the control of gene expression, from fine-tuning individual genes to switching off entire chromosomes. Its function has forced scientists to revisit the very meaning of the word "gene" and has engendered a bitter battle over whether or not this genomic "nonsense" is the source of human biological complexity. Drawing on her experience with leading investigators in Europe and North America, Nessa Carey provides a clear and compelling introduction to junk DNA and its critical involvement in phenomena as diverse as genetic diseases, viral infections, sex determination in mammals, disease treatments, and evolution. We are only now unlocking the secrets of junk DNA, and Carey's book is an indispensable resource for navigating the codes and controversies of this fast-growing and hotly disputed field.

作者简介

Nessa Carey is a visiting professor at Imperial College, London, and earned her Ph.D. in virology from the University of Edinburgh. Having worked in the biotech and pharma industries for more than a decade, she maintains strong relationships with leading researchers in Europe and across the United States, at such institutions as the Harvard Medical School, the University of Pennsylvania, the Wistar Institute, MD Anderson Cancer Center, and the University of Southern California. Carey is also the author of The Epigenetics Revolution: How Modern Biology Is Rewriting Our Understanding of Genetics, Disease, and Inheritance.

目录信息

Acknowledgments
Notes on Nomenclature
An Introduction to Genomic Dark Matter
1. Why Dark Matter Matters
2. When Dark Matter Turns Very Dark Indeed
3. Where Did All the Genes Go?
4. Outstaying an Invitation
5. Everything Shrinks When We Get Old
6. Two Is the Perfect Number
7. Painting with Junk
8. Playing the Long Game
9. Adding Colour to the Dark Matter
10. Why Parents Love Junk
11. Junk with a Mission
12. Switching It On, Turning It Up
13. No Man's Land
14. Project ENCODE - Big Science Comes to Junk DNA
15. Headless Queens, Strange Cats, and Portly Mice
16. Lost in Untranslation
17. Why LEGO is Better Than Airfix
18. Mini Can Be Mighty
19. The Drugs Do Work (Sometimes)
20. Some Light in the Darkness
Notes
Appendix: Human Diseases in Which Junk DNA Has Been ImplicatedIndex
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读后感

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通俗易懂的介绍了非编码基因的研究历史,功能,病例,以及医药公司开发针对不同基因表达的药物的难度。感觉很受用,作者语言幽默,举例接地气,很容易读下去。推荐。

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很具有科普性质的一本书,Nesaa Carey用了很多简单易懂的例子来阐述,即便不是生物专业的人也能读懂。

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对于人类还是不完全清楚的领域,这种科普书籍的确难写。专业的读者读觉得太浅显,非专业的读者又有可能完全看不懂。我的感受是,“存在即合理”,我们现有的科学探索能力把non-codingDNA为Junk,但是所有事物不都是:风光的(显著表达)就那么1-2%,其他的都是作为系统,提供平台滋养“精英”的吗?

评分

通俗易懂的介绍了非编码基因的研究历史,功能,病例,以及医药公司开发针对不同基因表达的药物的难度。感觉很受用,作者语言幽默,举例接地气,很容易读下去。推荐。

评分

对于人类还是不完全清楚的领域,这种科普书籍的确难写。专业的读者读觉得太浅显,非专业的读者又有可能完全看不懂。我的感受是,“存在即合理”,我们现有的科学探索能力把non-codingDNA为Junk,但是所有事物不都是:风光的(显著表达)就那么1-2%,其他的都是作为系统,提供平台滋养“精英”的吗?

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