4.8 Review

Brains, Genes, and Primates

期刊

NEURON
卷 86, 期 3, 页码 617-631

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2015.03.021

关键词

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资金

  1. Gatsby Charitable Foundation
  2. Crick Jacobs Center of the Salk Institute
  3. Salk Innovation Award
  4. National Institutes of Health [R01 EY021827, R01-HD063276, R01-HD057121, R01-HD059946, R01-EY021214, P51-OD011092]
  5. Brain Mapping by Integrated Neurotechnologies for Disease Studies (Brain/MINDS)
  6. Ministry of Education, Culture, Sports, Science, and Technology of Japan (MEXT)
  7. U.S. National Institutes of Health, NINDS
  8. NIMH
  9. G. Harlod and Leila Y. Mathers Charitable Foundation
  10. Leona M. and Harry B. Helmsley Charitable Trust [2012-PG-MED002]
  11. Poitras Center for Affective Disorders Research at McGovern Institute for Brain Research at MIT
  12. Stanley Center for Psychiatric Research at Broad Institute of MIT and Harvard
  13. Science Innovation Award from Brain Research Foundation
  14. Salk Innovation Grant
  15. Clayton Foundation
  16. National Institute of Aging
  17. National Institute of Neurological Disorders and Stokes
  18. NSF-IDBR
  19. NIDCD
  20. Leducq Foundation
  21. OHSU institutional funds
  22. NIH Director's New Innovator Award Program [1-DP2-OD006495-01]
  23. NARSAD Independent Investigator Grant
  24. NEI
  25. Howard Hughes Medical Institute
  26. Office of Naval Research
  27. NINDS, NIH
  28. National Institutes of Health (through NIMH) [5DP1-MH100706]
  29. National Institutes of Health (through NIDDK) [5R01-DK097768]
  30. National Science Foundation
  31. Keck, New York Stem Cell
  32. Damon Runyon Foundation
  33. Searle Scholars Foundation
  34. Merkin Foundation
  35. Vallee Foundation
  36. Bob Metcalfe
  37. San Bio Co. Ltd.

向作者/读者索取更多资源

One of the great strengths of the mouse model is the wide array of genetic tools that have been developed. Striking examples include methods for directed modification of the genome, and for regulated expression or inactivation of genes. Within neuroscience, it is now routine to express reporter genes, neuronal activity indicators, and opsins in specific neuronal types in the mouse. However, there are considerable anatomical, physiological, cognitive, and behavioral differences between the mouse and the human that, in some areas of inquiry, limit the degree to which insights derived from the mouse can be applied to understanding human neurobiology. Several recent advances have now brought into reach the goal of applying these tools to understanding the primate brain. Here we describe these advances, consider their potential to advance our understanding of the human brain and brain disorders, discuss bioethical considerations, and describe what will be needed to move forward.

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