Abstract
Using the “Bi-Digital O-Ring Test Molecular Identification Method” based on the resonance phenomenon existing between 2 identical substances originally discovered by Y. Omura, the author was able to develop the following methods which may have profound implications for both clinical and basic medical science, as additional useful techniques to compliment the powerful basic diagnostic “Bi-Digital O-Ring Test.”:
Imaging of the outline of any internal organ is possible with the use of a reference control substance which is identical to the organ to be imaged (i.e., microscopic slide of the organ to be imaged). When the outline of the internal organ is imaged by the Bi-Digital O-Ring Test Imaging Method using a microscopic slide of that organ as a reference control substance, it was also found that from the outline of the image of the internal organ lines were coming out towards upwards and downwards directions. When these lines were followed, it formed an ancient Chinese meridian-like network of that particular internal organ. Along this meridian-like network, the line bulged at certain locations. These bulges corresponded to the well-known acupuncture points. Using this imaging method, the ancient Chinese acupuncture meridian-like network and its acupuncture points of specific internal organs can be accurately and individually localized. Errors in many acupuncture meridian charts can thus be corrected and the effects of giving acupuncture on the real acupuncture points as well as the presumed acupuncture points (which may not be real acupuncture points) can be studied. In diseased areas, diameters of acupuncture points are usually enlarged significantly compared with acupuncture points at normal parts of the body. When an acupuncture needle was inserted on these enlarged acupuncture points, the diameter of these acupuncture points was reduced rapidly towards the normal small size. Simple and quick screening for the presence or absence of antigen or antibody against certain microorganisms, including viruses, bacteria, and fungi is possible. Using microscopic slides of pure micro-organisms or their pure antibodies (monoclonal antibody is most desirable) as a reference control substance, one can localize positive areas of the antigen or antibody. With non-invasive early screening of specific types of cancer of specific internal organs such as adenocarcinoma of the stomach, colon, head of the pancreas, etc., detection of even a small group of cancer cells or a monolayer of the cancer cells is possible as long as a microscopic slide of the specific cancer cells of a specific tissue is available as a control reference substance. These usually cannot be detected by X-Ray, CAT-Scan, or MRI unless the thickness reaches more than a few millimeters and often more than 5 mm. Often in cancer or precancer tissue, HTLV-III or HTLV-I, or a combination of the two were positive, limited to cancer tissue with or without positive responses to these viruses at the thymus gland (localized immune deficiency in cancer or precancer tissue with or without involvement of the thymus gland without having generalized infection in the rest of the body). Normally existing neuro-transmitters (such as serotonin, dopamine, norepinephrine, acetylcholine, endorphins, GABA, as well as some of their precursors) in Using part of a specific internal organ, such as a piece of the organ or a microscopic slide of the organ, one can localize the representation area of that organ (e.g. organ representation areas of different parts of the body represented in certain areas of the body such as the brain, ear, hand, and feet, etc.) accurately for each individual. For example, more accurate representation areas of different internal organs represented in different parts of the ears can be localized and accuracy of the currently available auricular organ representation chart can be evaluated for each individual. Similarly, representation areas of different internal organs of the entire body can be accurately localized at the hands, as well as the feet (hand or foot reflexology charts) for each individual. Any light beam can carry molecular information of specific molecules or substances placed on the pathway of the beam or near the pathway of the beam, and the molecular information will be carried bi-directionally, in the direction the light is travelling in any distance where the light beam can reach as well as towards the source of emission of the light. Monochromatic light beams, such as various laser beams, can carry the information more effectively over long distances. This phenomenon was originally discovered in 1983 by the author and it is possible to apply this phenomenon to various applications including:
We were able to localize various neurotransmitters of small animal tissue (such as a microscopic slide of a cross-section of the small brain of mice, rats, or guinea pigs) by magnifying it through an enlarger and projecting the microscopic slide of small brain to a large area onto a piece of white paper and first tracing outlines of the entire cross-section of the brain tissue as well as the visually identifiable landmarks of the brain. Using the “Bi-Digital O-Ring Test”, a resonance phenomenon exists between two identical substances, and it is possible to localize the exact location of the distribution of various neurotransmitters in detail in a very small section of the brain or other tissues in a matter of a few hours instead of several days or several weeks usually required with standard histo-chemical methods. Neurotransmitters magnified in the optically enlarged area of a slice of a small animal's brain was compared with the results of histo-chemical localization of neurotransmitters, and they both had a very similar distribution. The electro-magnetic field from drugs was projected through space as a narrow beam or it was carried to a long distance by a monochromatic light beam such as a helium-neon laser beam, and this field can influence living human beings as well as tissue cultured cells (e.g. affecting norepinephrine uptake by pheochromocytoma in tissue culture by the projection of the electro-magnetic drug field of desipramine).
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