Nothing. The patent is hard to enforce (no enablement for majority of the systems). You can try to shrink the size requirement for things that needs to be transduced in the cells and improve target specificity. However, it is still far away from anything useful for disease therapeutics. Just think it is a better version of zinc-finger protease and we have that technology for longtime.
: Nothing. The patent is hard to enforce (no enablement for majority of the
: systems). You can try to shrink the size requirement for things that needs
: to be transduced in the cells and improve target specificity. However , it
: is still far away from anything useful for disease therapeutics. Just think
: it is a better version of zinc-finger protease and we have that technology
: for longtime.
【在 A******y 的大作中提到】 : Nothing. The patent is hard to enforce (no enablement for majority of the : systems). You can try to shrink the size requirement for things that needs : to be transduced in the cells and improve target specificity. However, it : is still far away from anything useful for disease therapeutics. Just think : it is a better version of zinc-finger protease and we have that technology : for longtime.
A*y
14 楼
It is about hype...CNS is very good at doing that. Very good for academia, but poorly for industry. When Gleevec was first discovered, the guy cannot get it published in CNS at all (including sub-journal) and finally settled for Cancer Research (its crystal structure with Bcr-Abl was first, it published in a IF 2 journal).
of that However Just
【在 h*****s 的大作中提到】 : 还是应该有意义的 否则你看cns怎么铺天盖地的发表crispor的文章 : : : Nothing. The patent is hard to enforce (no enablement for majority of : the : : systems). You can try to shrink the size requirement for things that : needs : : to be transduced in the cells and improve target specificity. However : , it : : is still far away from anything useful for disease therapeutics. Just : think