The video Naomi did with her guest has some misunderstandings in it on both of their parts. I made a post on this days ago that explains it clearly. The EUA was granted based on trials that used modRNA created by the clean but more expensive PCR method. After they got the EUA, they switched to the cheaper method using E Coli and DNA plasmids. They did not filter out the DNA when they put the modRNA in the vials. This latter dirty method is the way they made the modRNA that got injected into the arms of the more than one billion people in the US and the world. The body doesn't "clean up the DNA" as was suggested in the video. If the body could do that, there would be no DNA in our bodies and then where would we be? DNA is not like RNA which does get degraded in minutes or hours (except the pseudouridine-modified type). It will be in the nucleus forever getting transcribed into mRNA which will go into the cytoplasm and get translated into spike protein forever in the usual fashion. There is also an SV40 promoter in the DNA plasmid code which will also get made. I explained all of this in clear, simple steps in this post from a few days ago: https://drreidsheftall.substack.com/p/a-crime-of-monumental-significance
I thought the DNA fragments randomly added to the blood stream would NOT get to cell nuclei and into the human genome nor even into cells. By what mechanism would DNA junk in the blood get into cell nuclei? Unless it was somehow incased in the lipid nanotech along with the mod/synthetic mRNA. Lipid nano can, of course, get into any cell and nuclei, too..
Is that what you are saying? The Dr. in video mentioned that but didn't think that would be likely.
Believe it or not, the spike protein can act as a carrier and get nucleic acids across cell and nuclear membranes. But remember, not all of the material injected into a person's deltoid gets to the bloodstream; only some of it.
As you point out, we know well how lipid nanos deliver their contents into the cytoplasm of cells and cross the blood/brain barrier- by a fusion mechanism because "like dissoloves like". We know generally how hydrophilic substances get across lipid membranes- with the use of a carrier or receptor on the surface of the cell- but we don't know everything in every case.
The spike protein itself is hydrophilic yet it gets from the interstitial space into a cell's cytoplasm and then into its nucleus to disrupt DNA repair. This is well known and one of the proposed mechanisms to explain the cancer increases people are seeing in the data.
How does the mRNA transcribed from DNA get from the nucleus into the cytoplasm where it will get translated into proteins? Probably by the vague but ubiquitous carrier system that always seems to come to the rescue.
Are you familiar with introns in our DNA; inactive sequences that don't get transcribed? Many scientists believe these sequences started out as part of viral genomes. How did they get in our genomes? There things we don't have a good explanation for yet must be occurring because these hydrophilic polymers are getting where they are appearing on the other side of lipophilic membranes. Examples of this are everywhere.
The video Naomi did with her guest has some misunderstandings in it on both of their parts. I made a post on this days ago that explains it clearly. The EUA was granted based on trials that used modRNA created by the clean but more expensive PCR method. After they got the EUA, they switched to the cheaper method using E Coli and DNA plasmids. They did not filter out the DNA when they put the modRNA in the vials. This latter dirty method is the way they made the modRNA that got injected into the arms of the more than one billion people in the US and the world. The body doesn't "clean up the DNA" as was suggested in the video. If the body could do that, there would be no DNA in our bodies and then where would we be? DNA is not like RNA which does get degraded in minutes or hours (except the pseudouridine-modified type). It will be in the nucleus forever getting transcribed into mRNA which will go into the cytoplasm and get translated into spike protein forever in the usual fashion. There is also an SV40 promoter in the DNA plasmid code which will also get made. I explained all of this in clear, simple steps in this post from a few days ago: https://drreidsheftall.substack.com/p/a-crime-of-monumental-significance
I thought the DNA fragments randomly added to the blood stream would NOT get to cell nuclei and into the human genome nor even into cells. By what mechanism would DNA junk in the blood get into cell nuclei? Unless it was somehow incased in the lipid nanotech along with the mod/synthetic mRNA. Lipid nano can, of course, get into any cell and nuclei, too..
Is that what you are saying? The Dr. in video mentioned that but didn't think that would be likely.
Believe it or not, the spike protein can act as a carrier and get nucleic acids across cell and nuclear membranes. But remember, not all of the material injected into a person's deltoid gets to the bloodstream; only some of it.
As you point out, we know well how lipid nanos deliver their contents into the cytoplasm of cells and cross the blood/brain barrier- by a fusion mechanism because "like dissoloves like". We know generally how hydrophilic substances get across lipid membranes- with the use of a carrier or receptor on the surface of the cell- but we don't know everything in every case.
The spike protein itself is hydrophilic yet it gets from the interstitial space into a cell's cytoplasm and then into its nucleus to disrupt DNA repair. This is well known and one of the proposed mechanisms to explain the cancer increases people are seeing in the data.
How does the mRNA transcribed from DNA get from the nucleus into the cytoplasm where it will get translated into proteins? Probably by the vague but ubiquitous carrier system that always seems to come to the rescue.
Are you familiar with introns in our DNA; inactive sequences that don't get transcribed? Many scientists believe these sequences started out as part of viral genomes. How did they get in our genomes? There things we don't have a good explanation for yet must be occurring because these hydrophilic polymers are getting where they are appearing on the other side of lipophilic membranes. Examples of this are everywhere.