I was just thinking that aging was a function of life, and life was an
ongoing set of interrelated chemical reactions. At that point, I could see
the Venn diagram:
The big box - the universe, set of all sets.
The box inside the big box - set of all ongoing interrelated chemical
reactions.
The box inside that box - eukaryotic life. (This box is divided into 4
separate boxes).
The 4 separate boxes - lipids (fats), proteins, carbohydrates (sugars), and
nucleic acids.
The nucleic acid box, divided into 4 separate boxes - in terms of the
chromosomes: 1 bond, the other bond, both bonds, and no bonds.
Life is an ongoing set of interrelated chemical reactions. Chemical
reactions require chemicals. In Biochemistry there are 4 choices: lipids,
proteins, carbohydrates, and nucleic acids. Whatever causes aging must be a
nucleic acid (because we live longer than dogs and cats). What determines
whether we are human, a dog or a cat, are the nucleic acids. In terms of
the chromosomes, there are 4 possibilities: that whatever causes aging is
bonded by the phosphate-sugar bond, the hydrogen bonding, both the
phosphate-sugar bond and the hydrogen bonding, or no bonds at all. The
human genome has been sequenced, and aging has not been found, so the cause
of aging is not both bonds. The phosphate-sugar bond would be repaired in a
few hours or less by the repair mechanism, so the cause of aging is not the
phosphate-sugar bond. The possibility that aging is caused by no bonds to
the chromosome does not work because no cytoplasmic factor has been found
for aging. Also, if the aging factors were cytoplasmic, one might expect to
see somatic segregation (when a cell divides - 1 cell getting more aging
factors, and the other cell getting less aging factors). Therefore, aging
is caused by something bonding through hydrogen bonding to the chromosomes.
There is a reason why I could see this, whereas no one else could see this.
Back in 1974, when my professors asked me what I wanted as my research
question for my Master's thesis, I said, "How does DNA add to DNA". In
doing research on this subject, I found that there was a class of molecules
which were bonded to the chromosome only through hydrogen bonding. The
molecules are short sequences of RNA and short sequences of DNA.
For years I have done pure research, however in seeing the obvious
application, I started to look into how to remove the short bits of RNA and
DNA from the chromosomes to reset the age of the cells.
I received 2 patents on the process from the U.S. government.
You might think that the U.S. government would like to know the cause of
aging. This is not the case. The problem is that there were (at least) 2
assumptions (that were false) about the structure of DNA. One assumption
was that DNA would have the same structure in water as it does in a salt
crystal. The other assumption was that our DNA has one structure.
Another problem is that they totally missed the major system of our
inheritance. If I told you that you had inherited money, you would most
likely want to know who died and why they left it to you. After the shock
wore off, you most likely would ask, "How much?". We not only inherit the
proteins, we inherit the "how much" of the proteins separately. I call the
system that calibrates how much of a protein is inherited the "encoding
system". I call the system that codes for the protein the "encryption
system".
In March of 2020, I contacted the CDC. I told them that I had come up with
a physical process to drop the kill-rate of COVID-19. Of course, the
information was disregarded and over a million Americans have died of
COVID-19. I estimate we could have dropped the kill-rate by 90%.
How does the physical process work? When someone goes to the hospital with
a case of COVID-19, they put a nebulizer mask on the patient and hook the
mask to hospital air, and put a solution of mostly water and a very small
amount of nuclease (the enzyme that breaks down RNA and DNA) in the
nebulizer chamber, and turn the air on. The mist containing the enzyme
lands on the surface of the lungs. The enzyme degrades RNA and DNA until a
protease enzyme breaks down the nuclease enzyme. As the RNA and DNA are
broken down on the surface of the lungs, the concentration of RNA and DNA
in the water on the surface of the lungs drops. This gradient causes more
short bits of RNA and DNA to exit the cells near the surface of the lungs
and get degraded. The short bits of RNA and DNA inside the lung cells are
in equilibrium with the short bits of RNA and DNA bonded to the chromosome
through hydrogen bonding. As the concentration of the short bits of RNA and
DNA drop inside the lung cells, some of the short bits of RNA and DNA
bonded to the chromosomes of the lung cells come off the chromosomes. This
in turn, resets the protein levels in the lung cells to an earlier point in
time.