Someone created you first human and then quite possible you were turned to hybrid. By syncytia the mark of the beast. You would do well to seek out your creator by your heart before it’s too late for repentance from the mark of the beast and deliverance by His Mercy and Grace.
The book said they would not repent of taking the m.o.t.b.
THE MARK OF THE BEAST/cellular chimerism
What did the [back scene] do to those who took it? It desecrated the human body. The “body is the temple”. Desecrated by adding beast gnome to the cellular structure building blocks. The immune system command centers natural bio-changes affected the spiritual condition in more ways than one. Chimp to be precise. With help from Cancer (immortalized cell lines) and a few toxic inflammatory agents from hell like PEG. In turn the eternal gift from God of Hope and possibly Love/Faith eternal were also waivered. Why? Chimps are not privy to God’s spiritual gifts.
Yes God’s gifts are without repentance. The mark of the beast had to be taken of free will to be effective in desecrating mankind. It had to be a choice of free will. Even if pressured into that choice by loss of job or social constructs of oppression.
Syn-cytia (excisited sin?) are multinucleated cells formed from the fusion of multiple individual cells, and their use in genome therapy involves creating a viral or genetic vector that induces syncytia to promote viral spread, enhance the bystander effect, or deliver genetic material to target cells more efficiently. In oncolytic (cancer-fighting) virotherapy, for example, viruses are engineered to express fusogenic proteins, which trigger syncytia formation and facilitate the spread of the virus throughout a tumor. This process can also be leveraged in gene therapy to improve the delivery and efficiency of gene transfer by creating syncytia from recipient cells.
How it works
1. Cell Fusion:
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The core of syncytia genome therapy is inducing cell-to-cell fusion. This is achieved by introducing genes for fusogenic proteins into the viral vector or the target cells.
2. Syncytia Formation:
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These fusogenic proteins, often viral membrane glycoproteins, are expressed on the surface of infected or transduced cells, causing them to fuse with neighboring cells.
3. Multinucleated Cells:
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The result is the formation of syncytia, large single cells containing thousands of nuclei from the fused cells.
Applications in Genome Therapy
Oncolytic Virotherapy:
Enhanced Viral Spread: Syncytia can help spread oncolytic viruses more efficiently throughout the tumor microenvironment, reaching more cancer cells.
Increased Bystander Killing: As viruses spread and induce syncytia, the resulting multinucleated cells can undergo a type of immunogenic cell death, releasing more tumor antigens and activating the immune system to target surrounding cancer cells.
Gene Delivery:
Efficient Gene Transfer: Viral vectors, particularly those pseudotyped with envelopes like the RD114 envelope, can induce syncytia to enhance the efficiency of gene transfer into target cells, especially difficult-to-transfect cells like hematopoietic cells.
Examples and Research
Recombinant Fusogenic Viruses:
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Researchers have created recombinant viruses, such as Vesicular Stomatitis Virus (VSV) vectors, by inserting genes for fusogenic proteins (like FAST or F-proteins) from other viruses.
Targeted Tumor Therapy:
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Fusogenic VSV vectors have shown promise in targeting and destroying liver cancer cells by forming syncytia exclusively within the tumors, without harming healthy liver tissue.
Immune Activation:
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Studies have shown that syncytia formation and subsequent immunogenic cell death by oncolytic viruses can boost the adaptive immune response, leading to an increase in activated CD8+ and CD4+ T cells that can target cancer cells.
Right. Cause they always claim to be working science for good. Good for who? Not the slaves of course. The slaves get the shit end of the science stick. Science used to desecrate or science used to potentate (aids in a means of ruling over the slaves).
BAD NEWS (one source) https://www.biorxiv.org/content/10.1101/2021.02.05.429860v1.full
“Migration of human cells to chimpanzees, or interspecies cellular migration, is a form of xenotransplantation that is scientifically possible but raises significant ethical and biological concerns. Research in this field is extremely limited and heavily restricted, though experiments involving combining human and non-human primate cells for scientific study have been reported.
Interspecies vs. intraspecies migration
Interspecies cellular migration: This term refers to the movement of cells between two different species, such as a human and a chimpanzee. This is the correct term for what you are asking about.
Intraspecies cellular migration: This describes cell movement within a single species. An example would be the migration of neural progenitor cells within a developing human embryo, or comparing migration patterns of neural cells between humans and chimpanzees in a lab setting.
Scientific and ethical considerations
Creating chimeras (organisms with cells from two different species) or transplanting human cells into a non-human primate is a deeply controversial topic. Key issues include:
Cognitive and emotional status: The most significant ethical concern is the potential to “humanize” a non-human primate by introducing human brain cells. This could cause the animal to develop human-like cognitive abilities, self-awareness, or emotional states, raising major questions about its welfare and moral status.
Safety and disease transmission: There are risks of cross-species transmission of viruses, such as porcine endogenous retrovirus (PERV) from pigs to humans, that could cause epidemics.
Biological incompatibility: As with any xenotransplantation, there are issues of immune rejection, inflammation, and blood clotting from the host’s body attacking the foreign tissue.
Key research and related concepts
Cell fusion studies: Scientists have successfully created hybrid human-chimpanzee induced pluripotent stem cells (iPSCs) in a laboratory dish. This allows for studying the evolutionary differences in gene regulation by fusing the cells and letting them divide in a controlled environment.
Brain organoid research: Researchers have compared the development of brain organoids (mini-brains grown in a lab) derived from human and chimpanzee stem cells. This has revealed differences in developmental timing, such as human neural progenitor cells taking longer to complete a crucial stage of cell division. This allows for comparative studies without risking the health of living primates.
Human-monkey chimeras: In 2021, scientists reported injecting human stem cells into monkey embryos and allowing them to develop for a short period before being destroyed. This research was conducted to better understand developmental biology, but it highlighted the serious ethical concerns of creating human-non-human primate chimeras.
Transgenic animals: A separate 2019 study involved inserting human brain genes into monkeys to study the evolution of”