Article IV) The application: Medical

Veterans Of Foreign Wars (VFW) International
Departments Of Defense (DOD) International
(Article IV) The application: Medical
''The logical scientific answer and action to cure human medical ailments, including pathogens such as Sars-2 linked to Covid-19.''

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Article IV) The application: Medical Since the human body is a composition of atoms and a form of energy, then the MEC and the Extraordinarily Fast Computer version Five (C1V5) The major components of the C1V5.

CPU at One Thousand & Twenty Four-Core

ROM ~ 10E12 (10,000,000,000,000 Bits, Bytes of Data.)

BIOS 10E18 [10,000,000,000,000,000,000
Bits, Bytes of Data.]

INTERFACE-CHIPS

@ Storage capability of
10E+73 x 10E+73 x 10E+73
bits/bytes of data.

5V 10W 2 Ma Energy Cell

The Medical Converter, MC, is 2.133607 M (7 ft) long, by 1.5 M (4.9212495 Ft. square.

Internal is,
A 1 Quatilliondecillion (10E73 1.00E+73) CPS CPU,+ ROM +, RAM, 1 Quatilliondecillion RAM capacity.

A CPU with a 1,024 core processor, ROM of 10E12 (10,000,000,000,000 Bits, Bytes of Data, RAM @ 1 Quatilliondecillion, a Solid State Hard Drive Storage Cube Operating at 1 Quatilliondecillion CPS with storage capability of 10E+73 x 10E+73 x 10E+73 bits/bytes of data AS powered by the energy cell and specialized TPEOM OS that can accept the human body as an item to be converted into energy, stored within the EFCV5 and then reassembled as the same physical physique of matter/energy and inclusive of all the original human brain neuron energy patterns (memories) as it was before the C1V5 and the MC converted it and then stored it within the C1V5.

After the Matter to Energy conversion and data bits storage of the, C1V5, its OS will medically examine that human bodies current medical condition against the original DNA architecture at birth and then return it back to that original of atomic particulars of it at birth architecture, with consideration to that moment of time passed.(age factor) wrinkles removal, skin flexibility restored, excessive body fat gone.

Then within 5 minutes after the process of the converter was initiated, the C1V5 & the MC will bring back that human body fully functional while excluding such cells as tumors of cancer or whatever else was not originally specified within the chromosomes or Genome of the DNA, RNA of the original architecture of that human body.

A certified MD medical professional experienced in genetics will be present to operate this medical orientated (MEC) converter unit by utilizing the MC converters holographic screen selection to function as a Matter to Energy Converter particularly selected via the C1V5 selection as ‘medical’ OS for its action of conversion. (OS = Operating System software, TPEOM Soft.)

The unit is operated via a projected holographic screen menu that operates as a holographic touch screen to call forth the index of selections to do the physiology and genetic DNA, RNA selections to be done by the C1V5 and the medical converter (MC) unit as powered by the Energy Cell.

The implementation of the C1V5 with its extensive specialized OS software and the variable capable power of the Energy Cell and the six internal atomic Element plates that are the inner walls, floor and ceiling of the MC converter.

The C1V5 and energy cell are housed in the base of the MC. That Energy Cell is for the full supply of all energies the C1V5 needs to perform as the MEC function. The converter system will convert the human body and its DNA, RNA into atomic energy conversion particles and be the production of stored bits//bytes of recoverable data as the full living, thinking alive architecture of the medically converted human and its ‘body’.

“The final exact, answer to the ongoing human medical condition. The Complete Medical cure at the highest, purest and most immediate level.”

Chemical / Atomic Elements Composition of the Human Body Major Classes of Compounds in the Human Body Most of the elements are found within compounds. Water and minerals are inorganic compounds.

Organic compounds include fat, protein, carbohydrates, and nucleic acids.

Water: Water is the most abundant chemical compound in living human cells, accounting for 65 percent to 90 percent of each cell.
It's also present between cells. For example, blood and cerebrospinal fluid are mostly water.

Fat: The percentage of fat varies from person to person, but even an obese person has more water than fat.

Protein: In a lean male, the percentages of protein and water are comparable. It's about 16 percent by mass. Muscles, including the heart, contain a lot of muscle. Hair and fingernails are protein.

Skin contains a large amount of protein as are the fingernails, toenails, also.

Minerals: Minerals account for about 6 percent of the body.

They include salts and metals. Common minerals as including sodium, chlorine, calcium, potassium, and iron.

Carbohydrates: Although humans use the sugar glucose as an energy source, there isn't that much of it free in the bloodstream at any given time. Sugar and other carbohydrates only account for about 1% of body mass.

Six elements account for 99% of the mass of the human body.
Elements in the Human Body

The acronym CHNOPS may be used to help remember the six key chemical elements that are used in biological molecules. C is carbon, H is hydrogen, N is nitrogen, O is oxygen, P is phosphorus, and S is sulfur. While the acronym is a good way to remember the identities of the elements it doesn't reflect their abundance.

Oxygen is the most abundant element in the human body accounting for approximately 65% of a person's mass. Each water molecule consists of two hydrogen atoms bonded to one oxygen atom, but the mass of each oxygen atom is much higher than the combined mass of the hydrogen. In addition to being a component of water, oxygen is essential for cellular respiration.

Carbon is contained in all organic compounds, which is why carbon is the second most abundant element in the body, accounting for about 18% of body mass. Carbon is found in proteins, carbohydrates, lipids, and nucleic acids. It's also found in carbon dioxide.

Hydrogen atoms are the most numerous type of atom in a human, but because they are so light, they only make up around 10% of the mass. Hydrogen is in water, plus it's an important electron carrier.

Nitrogen is about 3.3% of body mass,It's found in proteins and nucleic acids.
Calcium accounts for 1.5% of body mass. It's used to build bones and teeth, plus it's important for muscle contraction

Phosphorus is about 1% of body mass. This element is found in nucleic acids, Breaking bonds connecting phosphate molecules is a major component of energy transfer.

Potassium is around 0.2-0.4% of the mass of a person. It's used in nerve conduction, Potassium is a key cation or positively-charged ion in the body.

Sulfur is found in some amino acids and proteins. It's about 0.2-0.3% of body mass. Sodium, like potassium, is a positively-charged ion.
It's about 0.1-0.2% of body mass.

Sodium helps regulate the electrolyte balance in the body and maintain homeostasis with respect to the volume of water in the blood and cells.

Although aluminum and silicon are abundant in the earth's crust, they are found in trace amounts in the human body.

Other trace elements include metals, which are often cofactors for enzymes.

Trace elements include iron, cobalt, zinc, iodine, selenium, and fluorine.

The human brain has 100 billion neurons, each neuron connected to 10 thousand other neurons. Sitting on your neck and shoulders is the most complicated computational object in the known universe. [1,000,000,000,000,000] 1E+5 neurons of the human brain.

There are 71027E+39 = Calculated Atoms of the human body of an average 70 kg adult human male 18939 = powers of ten in scientific notation of large numbers to say 189E + 39 sets of 3 zeros = 1 duodecillion 10E+39 1.00E+39. Atoms for the MC converter to assimilate into its RAM & solid state storage cube capable of storing 1 Quadrilliondecillion x 1 Quadrilliondecillion x 1 Quadrilliondecillion or 10E+48 x 10E+48 x 10E+48 bits of data that equals a grand exception of much more bit data than any Number of atoms of any size of human body.

The EFCV5 ~ OS will implement its medical OS specifically for human body DNA RNA configuration recognition as it was originally at birth 'architecturally' configured, then at the instruction of the attending Geneticist the converter medical OS will heal the body's differential back to its original DNA RNA profile with no ailments of any sort.

The below chart is a simplified exemplification of the Elemental Composition of the human body that can easily be assimilated by the MC EMC ~ MEC converter system.

That action by the `converter `components of the C1V5 & MC converter units then reconfigures that human body back to its original DNA RNA before conversion and with the cure of;
• A loss of Asthma.
• A loss of Rheumatoid Arthritis.
• A loss of kidney stones.
• Regain your eye sight.
• Be with normal hearing.
• Reconfigured broken bones.
• Cured Athletic Injuries
• The answer to polio
• The final cure for cancer
• The full cure for HIV.
• The full cure for any sexually transmitted disease.
• The answer to hair loss.
• The answer to wrinkly skin. • The full repair of bullet wounds.
• The end of osteoporosis.
• The end of Tuberculosis
• The end of Covid -19. The absolute DNA RNA Chromosome locking, blocking of these keys to life within the Covid-19 as enabling it productivity as growth continuance. The Dead End of Covid-19 in all of humanity as being absolutely immune to any further pathogens of infectious effect.
• Inclusive of any additional microbe or pathogenic biological’s!

The end of VFW soldiers medical needs of any country on Earth.
And the medical list of ailments curable by the Medical Converter (MC) goes into the total inclusive encompassment of all the human medical conditions ailments.
The final exact, answer to the ongoing human medical condition.
The Complete Medical cure at the highest, purest and most immediate level.
A medical professional experienced in genetics will be present to operate this medical orientated converter (MC) unit.

The unit is operated via a projected holographic screen menu that operates as a holographic touch screen to call forth the index of selections to do the physiology and genetic DNA RNA Selections to be done by the C1V5 and the MC EMC ~ MEC medical converter (MC) unit as powered by the Energy Cell.

Veterans of Foreign Wars (VFW) International.
Departments of Defense (DOD) International.
With concern for military veterans.

You as a soldier that was involved in a military confrontation operation with a military opponent that cost you the loss of one or more of your much needed appendages such as an arm or hand or a leg or foot or some other physiological body part and you now consider yourself as physiologically incomplete and are not now as fully as you were genetically physically birthed to be, and that is the MISSING part of your body modality has sincerity depressed your lifestyle while you are being aware and knowing that the missing part of your body is now only a prosthetic that was put to your body by the VFW clinic or physical therapy center that you attend that is near your current residence. Even though you now have, or may have, a prosthetic you remain with the physical feeling that the original appendage that is now missing is still being with you.
HARKEN TO THIS SOLDIERR:

By way of this TPEOM Medical Converter (TPEOM MC) as a scientific technology of a TPEOM Medical Matter to Energy Converter ~ Energy to Matter Converter (TPEOM MC MEC ~ EMC) unit you can have your missing appendage, body part returned to you as Genetically as correct as per the original DNA RNA Genome architecture of your body as it was originally birthed to be.

This action is by way of the TPEOM Medical converter (TPEOM MC).
This reinstatement process of your missing limb or other body appendage part(s) happens only within a time line of five (5) minutes after your entry into the TPEOM MC and the TPEOM MC unit is activated by the attending medical geneticist that is responsible for its application.

You whom are a VFW soldier attending a veteran’s hospital or physical therapy center and have concisely read this VFW section of TPEOM with comprehension and then became imbued with determination to be physiologically complete again and thereafter with that reinstated physical completion you will continue onward with your life and your body as being physiologically correctly complete.

So then, and therefore, you can or will only as yourself, or as a group of veterans determinably go and approach the VFW HQ nearest you and only you, or as a group will strongly or diplomatically state your collective desire to meet with the head administrator and you or your group will comprehensively make your statement to that VFW administrator for the VFW to do all within their governmental and military power to insure that the needed TPEOM MC MEC ~ EMC units are forthwith acquired by the VFW or military DOD from TPEOM and then installed at the VFW hospital or physical therapy center that you and your VFW colleagues ~ fellow soldiers attend for their VFW medical care that is nearest your collective residences.

This is your life, so now that you know of this TPEOM MC unit you are aware of a way to make better of your life at your will as you will for your physiological life to be fully complete again -

Regards;
TPEOM

Prof. Dr. Yoshida, Mike Kazuo PhD. Prof, BA, Bsc, MBA, MD GP, CNC.
Environmental Science Physicist
Practical & Theoretical Physics Science Researcher R & D (ESPPTPSRRD)
The Pyran Environmental Organization Malaysia (TPEOM) (TEP) (NPO ~ NGO)
http://www.tgmncsb.com
donate@tpeom.org +6017-292-4072
Jalan Pasir Puteh, Ipoh, Darul Ridzuan, Perak, 31450, Malaysia
ORCHID ID: 0000-0003-3394-9135795
https://orcid.org/0000-0003-3394-9135
DUNS # 659308259
DOI: 10.13140/RG.2.2.14518.63044 >Research Gate: https://www.researchgate.net/profile/Mike-Yoshida

*** Should you be a medical specialist, hospital (Cedars-Sinai Medical Center) a private party deeply interested in performing the above as stated, or a government of a country then you are welcome to contact me for considerations of your having such a tool as you will, to make good for the citizens of your country and expat visitors for medical service.
I am sure we can or you can and will settle the financial modality of this to make it a special implementation.
(****>>>) Or you are a great Humanitarian that deeply desires to know and see the great health of all of humanity by not being infected by any form of pathogen, virus. Then you can make it your true reality by Sponsoring TPEOM’s Destined absolute focus to make available to all medical facilities the MC system unit ASAP while owning a good portion of interest into the TPEOM MC (Medical Converter) unit.

Below is an exemplification of DNA, nucleic acid,RNA, Nucleotides Nitrogenous base Adenine Guanine Cytosine Thymine and more...

The image above contains image of nucleic acid structure (primary, secondary, tertiary, and quaternary) using DNA helices and examples from the VS ribozyme and telomerase and nucleosome. (PDB: ADNA, 1BNA, 4OCB, 4R4V, 1YMO, 1EQZ) Nucleic acid structure refers to the structure of nucleic acids such as DNA and RNA. Chemically speaking, DNA and RNA are very similar. Nucleic acid structure is often divided into four different levels: primary, secondary, tertiary, and quaternary.

Contents 1 Primary structure 1.1 Complexes with alkali metal ions 2 Secondary structure 3 Tertiary structure 4 Quaternary structure

Primary structure
Nucleic acid sequence

Chemical structure of DNA Primary structure consists of a linear sequence of nucleotides that are linked together by phosphoresced bond. It is this linear sequence of nucleotides that make up the primary structure of DNA or RNA. Nucleotides consist of 3 components:

Nitrogenous base Adenine Guanine Cytosine Thymine (present in DNA only) Uracil (present in RNA only) 5-carbon sugar which is called deoxyribose (found in DNA) and ribose (found in RNA). One or more phosphate groups. The nitrogen bases adenine and guanine are purine in structure and form a glycogenic bond between their 9 nitrogen and the 1' -OH group of the deoxyribose. Cytosine, thymine, and uracil are pyrimidine's, hence the glycogenic bonds form between their 1 nitrogen and the 1' -OH of the deoxyribose. For both the purine and pyrimidine bases, the phosphate group forms a bond with the deoxyribose sugar through an ester bond between one of its negatively charged oxygen groups and the 5' -OH of the sugar.

The polarity in DNA and RNA is derived from the oxygen and nitrogen atoms in the backbone.

Nucleic acids are formed when nucleotides come together through phosphoresced linkages between the 5' and 3' carbon atoms.

A nucleic acid sequence is the order of nucleotides within a DNA (ACT) or RNA (GA CU) molecule that is determined by a series of letters.

Sequences are presented from the 5' to 3' end and determine the covalent structure of the entire molecule. Sequences can be complementary to another sequence in that the base on each position is complementary as well as in the reverse order. An example of a complementary sequence to ACT is TOGA. DNA is double-stranded containing both a sense strand and an anti sense strand.

Therefore, the complementary sequence will be to the sense strand.

Nucleic acid design can be used to create nucleic acid complexes with complicated secondary structures such as this four-arm junction.
These four strands associate into this structure because it maximizes the number of correct base pairs, with As matched to as and as matched to GS.

Complexes with alkali metal ions There are three potential metal binding groups on nucleic acids: phosphate, sugar, and base moieties. Solid-state structure of complexes with alkali metal ions.

Secondary structure Main article: Nucleic acid secondary structure Secondary structure is the set of interactions between bases, i.e., which parts of strands are bound to each other.

In DNA double helix, the two strands of DNA are held together by hydrogen bonds. The nucleotides on one strand base pairs with the nucleotide on the other strand.

The secondary structure is responsible for the shape that the nucleic acid assumes.

The bases in the DNA are classified as purine's and pyrimidine's.

The purine's are adenine and guanine. Purine's consist of a double ring structure, a six-metered and a five-metered ring containing nitrogen.

The pyrimidine's are cytosine and thymine.

It has a single ring structure, a six-metered ring containing nitrogen.

A purine base always pairs with a pyrimidine base (guanine (G) pairs with cytosine (C) and adenine (A) pairs with thymine (T) or uracil (U)).

DNA's secondary structure is predominantly determined by base-pairing of the two poly nucleotide strands wrapped around each other to form a double helix. Although the two strands are aligned by hydrogen bonds in base pairs, the stronger forces holding the two strands together are stacking interactions between the bases.

These stacking interactions are stabilized by Van dear Wails forces and hydrophobic interactions, and show a large amount of local structural variability.

There are also two grooves in the double helix, which are called major groove and minor groove based on their relative size.

The secondary structure of RNA consists of a single poly nucleotide. Base pairing in RNA occurs when RNA folds between complementarity regions.

Both single- and double- stranded regions are often found in RNA molecules.

The anti parallel strands form a helical shape. The four basic elements in the secondary structure of RNA are helices, loops, bulges, and junctions.

Stem-loop or hairpin loop is the most common element of RNA secondary structure.

Stem-loop is formed when the RNA chains fold back on themselves to form a double helical tract called the stem, the unpaired nucleotides forms single stranded region called the loop.

Secondary structure of RNA can be predicted by experimental data on the secondary structure elements, helices, loops, and bulges. Bulges and internal loops are formed by separation of the double helical tract on either one strand (bulge) or on both strands (internal loops) by unpaired nucleotides. A tetra loop is a four-base pairs hairpin RNA structure.

There are three common families of tetra loop in ribosome RNA: Unix, GNRA, and CHUG (N is one of the four nucleotides and R is a purine).Unix is the most stable tetra loop.

Pseudo knot is a RNA secondary structure first identified in turnip yellow mosaic virus. Pseudo knots are formed when nucleotides from the hairpin loop pair with a single stranded region outside of the hairpin to form a helical segment.

H-type fold pseudo knots are best characterized. In H-type fold, nucleotides in the hairpin loop pair with the bases outside the hairpin stem forming second stem and loop.

This causes formation of pseudo knots with two stems and two loops. Pseudo knots are functional elements in RNA structure having diverse function and found in most classes of RNA. DotKnot-PW method is used for comparative pseudoknots prediction. The main points in the DotKnot-PW method is scoring the similarities found in stems, secondary elements and H-type pseudoknots.

Tertiary structure
Nucleic acid tertiary structure

DNA structure and bases

A-B-Z-DNA Side View Tertiary structure refers to the locations of the atoms in three-dimensional space, taking into consideration geometrical and steric constraints. It is a higher order than the secondary structure, in which large-scale folding in a linear polymer occurs and the entire chain is folded into a specific 3-dimensional shape. There are 4 areas in which the structural forms of DNA can differ.

Handedness – right or left [auto minded physiological selection] Length of the helix turn Number of base pairs per turn Difference in size between the major and minor grooves.

The tertiary arrangement of DNA's double helix in space includes B-DNA, A-DNA, and Z- DNA.

B-DNA is the most common form of DNA in vivo and is a more narrow, elongated helix than A-DNA.

Its wide major groove makes it more accessible to proteins. On the other hand, it has a narrow minor groove. B-DNA's favored conformations occur at high water concentrations; the hydration of the minor groove appears to favor B-DNA. B- DNA base pairs are nearly perpendicular to the helix axis.

The sugar pucker which determines the shape of the a-helix, whether the helix will exist in the A-form or in the B-form, occurs at the C2'-endo.

A-DNA, is a form of the DNA duplex observed under dehydrating conditions.

It is shorter and wider than B-DNA.

RNA adopts this double helical form, and RNA-DNA duplexes are mostly A-form, but B-form RNA-DNA duplexes have been observed.

In localized single strand dinucleotide contexts, RNA can also adopt the B-form without pairing to DNA.

A-DNA has a deep, narrow major groove which does not make it easily accessible to proteins.

On the other hand, its wide, shallow minor groove makes it accessible to proteins but with lower information content than the major groove.
< br> Its favored conformation is at low water concentrations.

A-DNAs base pairs are tilted relative to the helix axis, and are displaced from the axis.

The sugar pucker occurs at the C3'-endo and in RNA 2'-OH inhibits C2'-endo conformation.

Long considered little more than a laboratory artifice, A-DNA is now known to have several biological functions.

Z-DNA is a relatively rare left-handed double-helix. Given the proper sequence and super helical tension, it can be formed in vivo but its function is unclear.

It has a more narrow, more elongated helix than A or B. Z-DNA's major groove is not really a groove, and it has a narrow minor groove.

The most favored conformation occurs when there are high salt concentrations.

There are some base substitutions but they require an alternating purine-pyrimidine sequence.

The N2-amino of G H-bonds to 5' PO, which explains the slow exchange of protons and the need for the G purine. Z-DNA base pairs are nearly perpendicular to the helix axis.

Z-DNA does not contain single base-pairs but rather a GpC repeat with P-P distances varying for GpC and CpG.

On the GpC stack there is good base overlap, whereas on the CpG stack there is less overlap. Z-DNA's zigzag backbone is due to the C sugar conformation compensating for G glycosidic bond conformation.

The conformation of G is syn, C2'-endo; for C it is anti, C3'-endo.

A linear DNA molecule having free ends can rotate, to adjust to changes of various dynamic processes in the cell, by changing how many times the two chains of its double helix twist around each other.

Some DNA molecules are circular and are topologically constrained.

More recently circular RNA was described as well to be a natural pervasive class of nucleic acids, expressed in many organisms

A covalently closed, circular DNA (also known as cccDNA) is topologically constrained as the number of times the chains coiled around one other cannot change.< br>
This cccDNA can be super coiled, which is the tertiary structure of DNA. Super coiling is characterized by the linking number, twist and writhe.

The linking number (Lk) for circular DNA is defined as the number of times one strand would have to pass through the other strand to completely separate the two strands.

The linking number for circular DNA can only be changed by breaking of a covalent bond in one of the two strands.

Always an integer, the linking number of a cccDNA is the sum of two components: twists (Tw) and writhes (Wr).

{\displaystyle Lk=Tw+Wr}Lk=Tw+Wr Twists are the number of times the two strands of DNA are twisted around each other. Writhes are number of times the DNA helix crosses over itself. DNA in cells is negatively super coiled and has the tendency to unwind.

Hence the separation of strands is easier in negatively super coiled DNA than in relaxed DNA.

The two components of super coiled DNA are solenoid and plectonemic.

The plectonemic super coil is found in prokaryotes, while the solenoidal super coiling is mostly seen in eukaryotes.

Quaternary structure Nucleic acid quaternary structure The quaternary structure of nucleic acids is similar to that of protein quaternary structure.

Although some of the concepts are not exactly the same, the quaternary structure refers to a higher-level of organization of nucleic acids.

Moreover, it refers to interactions of the nucleic acids with other molecules.

The most commonly seen form of higher-level organization of nucleic acids is seen in the form of chromatin which leads to its interactions with the small proteins histones.

Also, the quaternary structure refers to the interactions between separate RNA units in the ribosome or spliceosome.

With all due concern with care I say to you whom is viewing this document with the focused interest to be from the beginning of this document to these words of saying to you that you are appreciated for having found this, then continued with this to be encompassed within your mind, with my hope that you find inspiration to fulfill the spirit of the why this is here for you and for all the individuals of this world planet Earth, Our graciously beautiful home of planet Earth amongst the stars of this universe.

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