With an “anti-ca” FITC we detected the small bacteria in freeze sectioned cancer tissue and in blood smears of cancer patients but rarely in the control group (Ruzicka,1983). Ciftcioglu and Kajander, 1998 showed that many malignant cells have receptors for “nanobacterial” adherence.
An animal experiment showed that from 18 mice with subcutaneous injection of 0,1ml particle (“basoplasmas”) suspension 28% fall ill with cancer. 39% had chronic inflammations and 67% had granulocytosis. One mouse from the control had an adenoma of the lung and one an osteoma that are 17%, the other mice were healthy (Ruzicka,1983).
As a conclusion of our results we think that these small bacteria are a cofactor of oncogenesis and not a commensal. Our supposition is that these facultative alkaliphilic and hemotrophic 0,25µm bacteria called by us (Ruzicka, 1983) “basoplasmas” or “Basoplasma sanguineum sp. nov.” first infects erythrocytes. A possible pathway of infection are ticks. Erythrocytes have no nucleus and therefore their transformation is not possible. If the number of “basoplasmas” after their multiplication within erythrocytes is high enough they infects other human tissues. Infection is directed by a tumour inducing (Ti) plasmid, by the insertion of specific genes (T-DNA) into the genome of infected human cells.
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Many claims are being made about what one can do with Live Blood Analysis and this course will blow the trumpet of caution on several popular assumptions. That way you are going to end up with 1) a balanced view and 2) greater clinical confidence. By examining this topic in an comparative way from several angles you will get an excellent grasp of what is reasonable and above all what works in clinical practice!!
Wednesday, July 05, 2006
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