Hmm, I wonder if there will be wonder when it happens then..
Pretty sure they do, but I'm no expert. They have ATC: https://www.rad.com/resources/Application-Briefs/ATC-communications-application-brief
AI governance
It's about access and increase, not information
You can access the 28 pg pdf from the link.
Yeah I think that would qualify. There have been many small steps in this transhumanism direction, boiling frog type stuff maybe. They've normalized things that should never have been up for negotiation, I think.
It really is mind boggling.. I wish I knew what to say, it's all a terrible mess. I think it goes into transhumanism stuff too.
Abstract
Therapeutic applications of synthetic mRNA were proposed more than 30 years ago, and are currently the basis of one of the vaccine platforms used at a massive scale as part of the public health strategy to get COVID-19 under control. To date, there are no published studies on the biodistribution, cellular uptake, endosomal escape, translation rates, functional half-life and inactivation kinetics of synthetic mRNA, rates and duration of vaccine-induced antigen expression in different cell types. Furthermore, despite the assumption that there is no possibility of genomic integration of therapeutic synthetic mRNA, only one recent study has examined interactions between vaccine mRNA and the genome of transfected cells, and reported that an endogenous retrotransposon, LINE-1 is unsilenced following mRNA entry to the cell, leading to reverse transcription of full length vaccine mRNA sequences, and nuclear entry. This finding should be a major safety concern, given the possibility of synthetic mRNA-driven epigenetic and genomic modifications arising. We propose that in susceptible individuals, cytosolic clearance of nucleotide modified synthetic (nms-mRNAs) is impeded. Sustained presence of nms-mRNA in the cytoplasm deregulates and activates endogenous transposable elements (TEs), causing some of the mRNA copies to be reverse transcribed. The cytosolic accumulation of the nms-mRNA and the reverse transcribed cDNA molecules activates RNA and DNA sensory pathways. Their concurrent activation initiates a synchronized innate response against non-self nucleic acids, prompting type-I interferon and pro-inflammatory cytokine production which, if unregulated, leads to autoinflammatory and autoimmune conditions, while activated TEs increase the risk of insertional mutagenesis of the reverse transcribed molecules, which can disrupt coding regions, enhance the risk of mutations in tumour suppressor genes, and lead to sustained DNA damage. Susceptible individuals would then expectedly have an increased risk of DNA damage, chronic autoinflammation, autoimmunity and cancer. In light of the current mass administration of nms-mRNA vaccines, it is essential and urgent to fully understand the intracellular cascades initiated by cellular uptake of synthetic mRNA and the consequences of these molecular events.
That is wild.. found the show: https://archive.org/details/childhoods-end-miniseries
I'm not afraid of et, I'm afraid of people worshipping et, that to me is truly terrifying.
Links to the 3 part film in description
I might check that out, thanks
Are your blue beamy senses tingling? Edit: https://www.frontnieuws.com/cia-directeur-geeft-toe-dat-uaps-niet-menselijke-technologie-bezitten-waartegen-we-ons-niet-kunnen-verdedigen/
Po tay toes, boil'em, mash'em, stick'em inna stew! And a bit of ol' toby, eh?
Plants! Tending ground, that's not lame like dead flowers.
I was just thinking this, men probably want a garden or something.
They will lose, have lost already really, regardless of literally anything. At some point in time, that I think is close or soon, this world will end and the waking up that needs to happen, now, like right now, everywhere, is for people to find their salvation through the Savior/Messiah Jesus Christ, there is no other way and there is no other plan to be had, for me. (Edit: Remember we're frens and I say this with much love)
Yes, a few times, I've also copied them here on scored by chapter for discussions.
Love that my literary heroes fought the good fight!
Hybrid nucleic acid-nanoparticles combine molecular recognition and programmability features of DNA with the efficient properties of nanoparticles. Different hybrid DNA nanostructures have emerged depending on the types of nanoparticles, including DNA-inorganic nanoparticles, DNA-lipid, and DNA- polymer hybrid nanosystems [41]. DNA-gold nanoparticles complex combines the high affinity and specificity of the DNA for a specific ligand with the optical features of the gold nanoparticles in biosensor development and drug delivery [42]. For instance, hybrid DNA-gold nanoparticles functionalized with human epidermal growth factor receptor 2 antibodies specifically target the breast cancer cells for co- delivery of the doxorubicin and 5-fluorouracil anticancer drugs [43]. DNA-calcium phosphate nanoparticles are biocompatible structures with high cellular uptake. These hybrid structures have shown strong immunological response, high transfection efficiency, and immunomodulatory function [44,45].
Improvements in computational tools, design strategies, and control over the structure’s functionality enable the creation of more intricate 2D and 3D DNA nanostructures, translating the technology toward nanofabrication and biomedical applications [11]. DNA honeycombs [12], DNA origami polyhedrons in tripods [13], barcoded DNA origami [14], self-folding amphiphilic DNA origami [15], and many Programmable cage-like structures with molecular gates [16,17] are some examples of DNA nanostructures. The artificially designed DNA nanostructures with sophisticated surface features provide a robust and versatile framework for functionalization with various drugs, imaging dyes, probes, and chemicals [18]. The convenience of DNA functionalization makes DNA nanostructures one of the most favorable candidates with therapeutic and diagnostic potential.
Although recent progress in design, fabrication, and functionalization strategies have greatly expanded the efficacy of DNA nanostructures for diverse applications, the transition from bench to bedside still requires many improvements. The limits are primarily due to the vulnerability of DNA nanostructures to heat denaturation, enzymatic degradation, and structural disassembly in biological environments [19]. Therefore, the biostability and structural integrity of the DNA nanostructures should be the main concerns in biomedical research.
I wonder if they are actively building some private, off the grid type infastructure, hmm 🤔