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#1
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Who would you suggest?
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"Have the clean racing people run any ads explaining that giving a horse a Starbucks and a chocolate poppyseed muffin for breakfast would likely result in a ten year suspension for the trainer?" - Dr. Andrew Roberts |
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#2
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"Always be yourself...unless you suck!" |
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#3
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Long way to go on this.
The stem cells made by using no fetal tissue (skin connective cells called fibroblasts which I worked 3 years with, only in chickens) dont necessarily give rise to organs they might want to clone. It is exciting that they can use nonembryonic cells to make what behave like stem cells early on, but later, when the important differentiation occurs... not even close. Im going to make a prediction. This is going to be very difficult. I think these genes they put in to cause these cells to revert to the stem cell stage do not change already altered crucial genes important in producing, for example, a fully functional liver. I believe that as cells differentiate, some very significant changes occur in the genome that will be very difficult to fix. Lots of splicing and dicing goes on. Very difficult stuff. |
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#4
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You may be entirely correct with your prediction. There's a long way to go with producing replacement organs (such as a liver as you suggest). We can discuss matrix and regeneration techniques some other time. I think that the use of four protien transcriptors using retroviruses that express as pluripotent stem cells (as the Nature article states) and the transfer of iPS DNA to progeny are quite interesting. Watson was recently given his personal genome and within a short time, all of us will have access to our own for a very modest price (1K). I agree with you that this is "difficult", but not out of reach. DTS |
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#5
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For a long time we had no idea how our bodies could make antibodies to chocolate, diff types of perfume, and bacteria and viruses. We now know. Alteration of coding sequences in a random way to produce a huge array of cells that can recognize the most unique conformation of chemicals in invading organisms. Quite a hit and miss way, but a beautiful way to cover the bases given the very basic genetic code. This last example was given to show the tremendous alteration that can occur in the genomes of certain cell lines, never to come back home to a stem cell. Last edited by pgardn : 06-07-2007 at 04:19 PM. |
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#6
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You put out a lot of different ideas in this thread. Yes, cells are preprogammed to die. It varies but mitosis is limited. White cells (immune system) are still a puzzle. If we could understand T connects, HIV-Aids would have a cure. We're not there yet. Anti bodies and encoding for them is something I don't know much about. My interest is in "triggering" genes like fgf 15, fgf 8, and others that program the cell for development after the stem stage. White cells are much further along, like other differentiated cells. It's interesting to me that some of the same triggering genes play a role in cancers (retinal, and neural) as cardio. At this point, it's good that the markers exist to track them. Beyond that, it's a long way to organ production. Imagine if one's own skin cells could be used to regenerate a heart or liver, or any diseased organ. There would be no need for anti-immune therapy. One's replacement organ could be grown and implanted without the risk of rejection. We have a long way to go. Seems to me that creating stem cells from skin cells is a huge step forward. New findings will be realized soon. |
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#7
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Part of the reason I decided to teach classical Physics. Biology is so damned hard. Its is so incredibly complicated. One really has to make it a thematic class, or take the easy way out and just have kids memorize a whole new vocabulary and pretend like you have taught them something. Classical Physics is as beautiful and clean as it gets. |
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