DR. IRENE CAESAR: GLOBAL BINARY BIOLOGICAL WAR WAS STARTED BY THE GLOBAL ORGANIZED CRIME “NEW JERUSALEM” / “CYBER ZION”

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AD-5, adenovirus, andrew fire, binary biological war, binary biological weapon, COVID-19, COVID-19 origin, craig mello, cyber zion, depopulation, destructive RNA interfernece, DURC, gain of function, gmo, GMO virus, HIV, irene caesar, mRNA, new jerusalem, pirbright institute, prion disease, ralph baric, rna, SARS-CoV-2, sterilization, wave genome, wave optics in chromosomes, zombi apocalypse

English text is beneath Russian text.

Выводы слушаний в Конгрессе США о происхождении COVID-19 (опубликованы 29 июня 2021 г. – слушания, проведенные членами Республиканской партии Подкомитета Палаты представителей по надзору и реформе по вопросу о кризисе, вызванном коронавирусом) следующие:

(1) SARS-CoV- 2 – это бинарное биологическое оружие, химерный вирус (ретровирус под прикрытием коронавируса), созданный в результате «исследования по добавлению функций» (“gain of function”), или «DURC» – «исследование двойного назначения, вызывающее озабоченность». Этот вирус был создан в лаборатории и НЕ является результатом естественной мутации.

(2) SARS-CoV-2 был создан таким образом, что его функции были «приобретены», включая (а) подавление интерферонного иммунного ответа, так что инфицированные люди остаются бессимптомными достаточно долго, чтобы заразить как можно больше людей, (b) наличие нуклеотидной последовательности CGG CGG, которая не присутствует в классе коронавирусов, но присутствует в вирусах ВИЧ, ZIKA и EBOLA, то есть в ретровирусах, которые вставляют свои гены в ДНК человека, вызывая аутоиммунитет, т. е., СПИД, когда иммунная система атакует сама себя; (c) эта последовательность модифицировала S-белок (белок поверхностного шипа) таким образом, что был преодолён межвидовой барьер, и вирус приобрел функцию заражения людей; (г) эта модификация не может быть получена коронавирусом в ходе естественной мутации, поскольку в природе нет нуклеотидной гомологичности (сопоставимости) между классом коронавирусов и этой нуклеотидной модификацией.

(3) Это усиление функции было достигнуто за счет длительного заражения искусственной генетической линии гуманизированных мышей (ГМО-мышей с искусственно встроенными человеческими генами). Такое усиление функции стало возможным после открытия обратной транскрипции (обратной транскриптазы), которая сделала возможным искусственное создание ВИЧ. Косвенным доказательством того, что SARS-CoV-2 представляет собой ГМО-вирус, искусственно созданный в качестве бинарного биологического оружия, является тот факт, что китайцы не смогли найти промежуточное животное, и что не было представлено случаев передачи вируса от животного человеку. Были представлены только случаи передачи вируса от человека к человеку.

(4) SARS-CoV-2 запатентован Институтом Пирбрайта в Лондоне и, таким образом, был создан по заказу британской элиты в сотрудничестве с американцами и французами. Крупнейший американский специалист по коронавирусам Ральф Барик, проф. из Университета Северной Каролины, непосредственно отвечал за тестирование модели, созданной британцами с помощью вычислительной биологии. А Французы отправили в Ухань 50 специалистов и оборудование, чтобы научить китайцев создавать бинарное биологическое оружие под названием SARS-CoV-2.

Их цель состояла в том, чтобы подтолкнуть китайцев к созданию «этнического генетического биологического оружия», основанного на мРНК, специально нацеленного против русских, посредством таргетирования российской РНК, которую американцы закупили в больших количествах в течение двух предыдущих лет. Вариант Дельта в Индии – это генетическое биологическое оружие, нацеленное на гаплогруппу R1a1, которую русские разделяют с высшей кастой брахманов в Индии и евреями-ашкеназами в Израиле.

В заключение, можно сказать, что COVID-19 был актом государственного биотерроризма Великобритании, специально направленным против американцев и русских и, как следствие, против китайцев, которых обвинят, а точнее, с целью уничтожить американскую республику и её президента Дональда Трампа, для возвращения Соединенным Штатам их колониального статуса как колонии Великобритании, и для уничтожения России ради захвата российских природных ресурсов. Французы играли привычную роль проститутки. https://m.youtube.com/watch?v=B3LuOhtrq4M

Итак, на Россию было произведено нападение бинарным биологическим оружием, распространяемым аэрозольно, как это было заявлено на заседании конгресса США. И мы должны говорить НЕ о естественно развивающейся пандемии на территории России, а о защитных мерах в условиях биологической войны. Мы должны оценивать эффективность нашей биологической защиты в условиях биологической войны с точки зрения, насколько наше правительство адекватно оценивает цели и методы противника, развязавшего против России биологическую войну.

Цели и методы нашего противника — изменить наше ДНК за счёт обратной транскрипции и сделать население России стерильным. Заявление Гинзбурга о том, что ни SARS-CoV-2, ни вакцины НЕ меняют человеческий Геном являются ЛОЖЬЮ, что доказано уже исследованиями MIT (самого крупного научного института США); и тем, что все протеины в SARS-CoV-2 гомологичны человеческим протеинам, кроме одного — так что, нуклеотиды вируса, за счёт комплиментарности, встраиваются в наше ДНК. Поэтому Гинзбург является либо профессионально непригодным, либо преступником.

На данный момент, населению России вводятся белки вируса, у которого все белки гомологичны человеческим белкам, кроме одного, что вызывает эффект Деструктивной Интерференции РНК (Нобелевская премия 2006 год, Эндрю Файер и Крэг Мелло – Andrew Fire and Craig Mello: они брали РНК у червя c.elegans, и обратно вводили в червя — и червь умирал). То есть, вакцина Гинзбурга продолжают и расширяет нападение врага биологическим оружием. Враг напал аэрозольным вирусом. А Гинзбург вводит данный вирус прямо в кровь.

Против гомологичных вирусов, то есть, ретровирусов, не может быть вакцин, в принципе. Так, до сих пор, нет вакцины от ВИЧа. На сегодняшний момент, вакцина Гинзбурга — это заражение граждан России слабой дозой ВИЧ инфекции (Индусы обнаружили в SARS-CoV-2 четыре вставки ВИЧа). Технология аденовирусного вектора (Ad-5) — это старая и устаревшая технология, созданная американцами очень давно, когда они пытались создать вакцину против ВИЧа. Американцы провели два клинических испытания, которые показали, что, если у человека есть иммунитет против аденовируса, то, в таком случае, вакцина заражает человека ВИЧ вирусом, вместо создания иммунитета против ВИЧ вируса. А аденовирус — это чрезвычайно распространённая инфекция. Именно поэтому Американцы отказались от данной технологии. А Гинзбург получил за эту провальную и ошибочную технологию государственную премию.

Именно предшествующий аденовирусный иммунитет обьясняет случаи заражения коронавирусом после инъекции вакциной Гинзбурга. В заключение, мы можем констатировать, что биологическая зашита России от нападения бинарным биологическим оружием является неадекватной. Более того, без всякого сомнения, мы можем заявить, что подобная «зашита» является продолжением, и даже усилением нападения врага. Насильственная вакцинация гомологичными белками — это ГЕНОЦИД. Чиновников, которые навязывают насильственную “вакцинацию” “экспериментальными генными препаратами” будут НЕИЗБЕЖНО судить новым Нюрнбергским трибуналом — за ПРЕСТУПЛЕНИЕ ПРОТИВ ЧЕЛОВЕЧЕСТВА.

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The conclusions of the US Congress hearing on the origin of COVID-19 (Published on Jun 29, 2021 — Hearing by GOP members of the House Oversight and Reform Subcommittee on Select Coronavirus Crisis) are as following:

(1) the SARS-CoV-2 is a binary biological weapon, a chimerical virus (retrovirus under the cover of coronavirus) as the result of the “gain of function research”, or “DURC” — “dual-use research of concern”. This virus was created in the laboratory, and is NOT the result of the natural mutation.

(2) SARS-CoV-2 was created in such a way that its function was “gained”, including (a) the interferon immune response suppression, so that, the infected people are asymptomatic long enough to infect as many people as possible, (b) the presence of CGG CGG nucleotide sequence that is not present in the class of the coronaviruses but is present in HIV, ZIKA and EBOLA, that is, in retroviruses, which insert their genes into human DNA, causing the autoimmunity, i.e., AIDS, when the immune system attacks itself; (c) this sequence had modified the S-protein (surface spike protein) in such a way that the interspecies barrier was surpassed, and the virus gained the function of infecting humans; (d) this modification cannot be gained by the coronavirus in the course of natural mutation, since there is no nucleotide homogeneity (comparability) between the class of coronaviruses and this nucleotide modification in nature.

(3) This gain of function was achieved by the long-term infection of the artificial genetic line of humanized mice (GMO mice with the artificially inserted human genes). This gain of function became possible after the discovery of the reserve transcription (reverse transcriptase), which made possible the artificial creation of HIV. The indirect proof that SARS-CoV-2 is the GMO virus, artificially created as the binary biological weapon, is the fact that Chinese could not find the intermediary animal, and that there were no cases of animal to human transmission presented. Only the cases of human to human transmission were presented.

(4) SARS-CoV-2 is patented by Pirbright Institute in London, and, so, was created at the order of the British elites in collaboration with Americans and French. The major American specialist in coronaviruses Ralph Baric, Prof. of the North Carolina University, was immediately responsible for testing the model that the British had created with the computational biology. And French had sent 50 specialists and equipment to Wuhan to teach the Chinese how to create the binary biological weapon called SARS-CoV-2.

Their goal was to push Chinese towards the creation of the “ethnic genetic bioweapon”, based upon mRNA, specifically targeted against Russians, via targeting Russian RNA, which Americans had bought in large quantities during the two preceding years. The Delta variant in India is, precisely, the genetic bioweapon which is targeting the R1a1 haplogroup, which is shared by Russians with the highest caste of Brahmans in India and with the Ashkenazi Jews in Israel.

To conclude, the COVID-19 was the act of the state bioterrorism by the United Kingdom specifically aimed against Americans and Russians, and, by complication, against Chinese, who would be blamed, and, more precisely, with the goal of destroying the American Republic and its president Donald Trump, and returning the United States into its colonial status as a colony of the United Kingdom, and destroying Russia for the sake of grabbing Russian natural resources. French played the customary role of a hooker. https://m.youtube.com/watch?v=B3LuOhtrq4M

So, Russia was attacked by a binary biological weapon distributed by aerosol, as it was stated at a meeting of the US Senate. And we should NOT talk about a naturally developing pandemic on the territory of Russia, but about protective measures in the conditions of biological warfare. We must evaluate the effectiveness of our biological defense in the conditions of biological warfare from the point of view of how our government adequately assesses the goals and methods of the enemy who unleashed a biological war against Russia.

The goals and methods of our enemy are to change our DNA through reverse transcription and make the population of Russia sterile. Ginsburg’s statement that neither SARS-CoV-2 nor vaccines change the human Genome is a LIE, which has already been proven by research at MIT (the largest scientific institute in the United States); and by the fact that all the proteins in SARS-CoV-2 are homologous to human proteins, except for one, so that the nucleotides of the virus, due to complementarity, are embedded in our DNA. Therefore, Ginsburg is either professionally unfit or a criminal.

At the moment, the population of Russia is injected with proteins of a virus, in which all proteins are homologous to human proteins, except for one, which causes the effect of the Destructive RNA Interference (Nobel Prize 2006, Andrew Fire and Craig Mello: they took RNA from the c.elegans worm, and injected it back into the worm — and the worm died). That is, the Ginzburg vaccine continues and expands the enemy’s attack with biological weapons. The enemy attacked with an aerosol virus. And Ginsburg introduces this virus directly into the blood.

There can be no vaccines against homologous viruses, that is, retroviruses, in principle. So, so far, there is no vaccine for HIV. At the moment, the Ginzburg vaccine is an infection of Russian citizens with a weak dose of HIV infection (the Indians found four HIV inserts in SARS-CoV-2). The technology of the adenovirus vector (Ad-5) is an old and outdated technology created by the Americans a long time ago when they were trying to create a vaccine against HIV. The Americans conducted two clinical trials that showed that if a person has immunity against the adenovirus, then, in this case, the vaccine infects a person with the HIV virus, instead of creating immunity against the HIV virus. And adenovirus is an extremely common infection. That is why the Americans abandoned this technology. And Ginsburg received a Russian State prize for this failed and erroneous technology.

It is the previous adenovirus immunity that explains cases of coronavirus infection after injection with the Ginzburg vaccine. In conclusion, we can state that Russia’s biological defense against an attack with binary biological weapons is inadequate. Moreover, without any doubt, we can say that such “protection” is a continuation, and even an increase of the enemy’s attack. Forced vaccination with homologous proteins is GENOCIDE. Officials who impose forced “vaccination” with an “experimental gene drug” will INEVITABLY be tried by the new Nuremberg Tribunal – for A CRIME AGAINST HUMANITY.

SARS-CoV-19 is the Resurrected, SARS-Camouflaged, GOF HIV Airborne, 100-Anniversary Deadliest H1N1 Spanish Flu Pandemics of 2019-2020

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1918 pandemics, accelerated virus evolution, ACE2, airborne hiv, atlanta airport blackout, barack obama, betacoronaviruses, bill gates, binary biological war, burin-like cleavage site, cdc, coronavirus, coronavirus pandemics, cover-19, depopulation, dis biological weapons drill, ecocide, Edward Holmes, Fang Li, furin, gain of function, gain of function virus, genocide, glycoprotein, GOF, H1N1, haemagglutinin, haemagglutinin identity between SARS and H1N1, hemagglutinin, hiv keys, influenza, irene caesar, Judy Mikovits, MERS, mosaicism, National Institute of Health, NIH, Nikolai Petrovsky, philip berman, pre-pandemic vaccines, RBD, retroviridae, retrovirus, rna virus, s protein, SARS, SARS spike protein identical to H1N1 with HIV inserts, sars-1, sars-2, SARS-CoV-2, Simon Wain-Hobson, spanish flu, Stephen C. Harrison, sterilization, vaccine, who, world health organization, wuhan, wuhan virus

WARNING TO THE US INTELLIGENCE СOMMUNITY. ILLICIT ISRAELI WAR AGAINST UNITED STATES THROUGH THE MOSSAD SHILLS IN CIA

SARS-2 (COVID-19) pandemic is a camouflaged — resurrected and recombinant — 1918 flu virus (H1N1) that caused the deadliest pandemic in the history of humankind (“Spanish Flu” killed an estimated 50 million people worldwide, including an estimated 675,000 people in the United States). The aggressive virulence factors (sustained human to human transmission), characteristic of 1918 virus, were specifically extracted from the 1918 virus and combined with various forms of human influenza and coronavirus. The 2009 H1N1 pandemic and COVID-19 pandemic (1918 virus camouflaged as “Coronavirus”) were meant to “celebrate” the 10th “anniversary” and the 100-year “anniversary” of the 1918 pandemic respectively.

It is established that the emergence of the 1957 H2N2 and 1968 H3N2 influenza A pandemic viruses was caused by the RECOMBINATION where new avian genome segments were imported into the backbone of 1918-descended H1N1 viruses (137), as well as the 2003 emergence of the pathogenic Fujian H3N2 influenza strain by interclade reassortment. Source:
Webby, R. J., and R. G. Webster. 2001. Emergence of influenza A viruses. Philos. Trans. R. Soc. Lond. B 3561817-1828
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546865/

This means that the 1918 flu virus (H1N1) samples were carefully preserved and kept all these years, whatever CDC says about its recent digging out from the Alaska permafrost.

“Avian” or “swine” or “dogs” (coronavirus) specifics of the pandemics is explained by the biomaterial, in which the 1918 virus is grown. Coronavirus was specifically used to conceal that the SARS-1 and SARS-2 (COVID-19) pandemics were simply the heavily recombinant 1918 virus. I emphasize, specifically the 1918 virus had provided the sustained human to human transmission, i.e., high virulence of SARS-CoV-19 virus. This is called “GAIN OF FUNCTION” (GOF). The recombinant (man-made) nature of all the recent pandemics explains why CDC has “pre-pandemic vaccines”. Of course, if you make viruses (Pathogen) yourself, you have the vaccine (Antigen) automatically.

“The 2019 novel coronavirus, or “SARS-CoV-2″, was discovered because of Wuhan virus pneumonia cases in 2019, and was named by the World Health Organization on January 12, 2020. It belongs to the beta genera of the Coronaviridae family, together with SARS coronavirus in 2003 and MERS coronavirus in 2012. The alignment between SARS-CoV-2 and 2003 SARS CoV has about 70% sequence (some say 86%) similarity and 40% sequence similarity with MERS CoV. The coronavirus genome encodes a spike protein, an envelope protein, a membrane protein, and a nucleoprotein. Among them, spike protein is the most important surface membrane protein of coronavirus.” (source: https://sars-cov-2.creative-biolabs.com/sars-cov-2-2019-ncov-spike-protein-elisa-kit-329.htm). Remark: 70% sequence similarity and 40% sequence similarity with SARS-1 and MERS is a proof of itself for the intentional “accelerated virus evolution”. “SARS-CoV-2 has all the same genetic equipment as the original SARS-CoV, which caused a global outbreak in 2003, but with around 6,000 mutations sprinkled around in the usual places where coronaviruses change. Think whole milk versus skim milk.” Source: https://www.snopes.com/news/2020/04/02/what-the-coronavirus-does-to-your-body-that-makes-it-so-deadly/

In the SARS-CoV-1 outbreak, the first Coronavirus virus, that was synthesized by CDC, was inefficiently transmitted by most infected people, so that, quarantine allowed the epidemic to be stopped before the virus could become fully established in humans. Now, its variation in the SARS-CoV-2, the second Coronavirus was artificially made to gain the ability to spread “efficiently”. The fairytale that this virus had “emerged naturally” is laughable, because the second version of SARS-CoV had suddenly emerged with GOF – GAIN OF FUNCTION. Evidently, somebody in CDC had worked hard to make the virus “spread more efficiently”. See: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546865/#r137

This statement is confirmed by Dr. Fang Li of the Minnesota University in the important paper on the artificially GAINED OF FUNCTION SARS-CoV-1, analyzed below.

“Gain of Function” was objected by French scientist Dr. Simon Wain-Hobson of Pasteur Institute in Paris in 2014. He pointed that GOF is clearly the DURC = “Dual-Use Research of Concern”, i.e., the bioweapons:
https://www.ncbi.nlm.nih.gov/pubmed/25077136

In October 2014 the administration of US President Barack Obama banned GOF research on influenza, SARS, and MERS. Concerns over so-called “gain-of-function” (GOF) studies that make pathogens more potent or likely to spread in people erupted in 2011, when Kawaoka’s team and Ron Fouchier’s lab at Erasmus Medical Center in Rotterdam, the Netherlands, announced that they had modified the H5N1 bird flu virus to enable it to spread between ferrets (that is, to cross the barrier between species). The ban was lifted on December 19 2017, according to Science:
https://www.sciencemag.org/news/2017/12/nih-lifts-3-year-ban-funding-risky-virus-studies

Importantly, there should be “an intermediate host” for the Coronavirus to hop from snakes or bats to humans. Notably, the paper published by the US Federal government-funded researchers in the Nature Medicine on November 15, 2015 had proven that only the CHIMERIC SARS-like virus out of the surface spike protein of a coronavirus found in horseshoe bats, called SHC014, and the backbone of a SARS virus that could be grown in mice, CERTAINLY WITH OTHER ADDITIONS, can infect humans. See: “A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence” by Vineet D Menachery, Boyd L Yount Jr, Kari Debbink, Sudhakar Agnihothram, Lisa E Gralinski, Jessica A Plante, Rachel L Graham, Trevor Scobey, Xing-Yi Ge, Eric F Donaldson, Scott H Randell, Antonio Lanzavecchia, Wayne A Marasco, Zhengli-Li Shi & Ralph S Baric. The research was jointly done by the University of North Carolina at Chapel Hill, USA; the Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA; and the Chinese Academy of Sciences, Wuhan, China:
https://www.nature.com/articles/nm.3985.pdf?origin=ppub
https://www.nature.com/news/engineered-bat-virus-stirs-debate-over-risky-research-1.18787

Notably, “these certain other additions’ were made earlier, now forgotten in the public eye. In the paper “Structural Analysis of Major Species Barriers between Humans and Palm Civets for Severe Acute Respiratory Syndrome Coronavirus Infections” by Fang Li, published in J Virol. 2008 Jul, it is claimed that (1) “The major species barriers between humans and civets for SARS-CoV infections are the specific interactions between a defined receptor-binding domain (RBD) on a viral spike protein and its host receptor, angiotensin-converting enzyme 2 (ACE2); (2) to cross this inter-species barrier, “a chimeric ACE2 bearing the critical N-terminal helix from civet and the remaining peptidase domain from human was constructed, and it was shown that this construct has the same receptor activity as civet ACE2”. (3) Furthermore, “crystal structures of the chimeric ACE2 complexed with RBDs from various human and civet SARS-CoV strains were synthesized”. This means that the CROSS-SPECIES LINK was artificially synthesized to transmit SARS-CoV from a civet to a human. While a civet was a link from a bat to a human. Dr. Fang Li says that “the major species barrier for the transmission of SARS-CoV from a civet to a human WAS IN NATURE the INCOMPATIBILITY between four ACE2 residues (residues 31, 35, 38, and 353) in humans and two RBD residues (residues 479 and 487) in civets. That is why the NATURALLY-OCCURRING civet (animal) SARS-CoV virus was prevented from infecting humans due to “incompatible salt bridges at the hydrophobic virus/receptor interface”. Dr. Fang Li claims that after his manipulations with the SARS-CoV virus of civets, he was a success of trespassing this incompatibility “by eliminating unfavorable free charges at the interface through stepwise mutations at positions 479 and 487”. As the result, Dr. Fang Li says, the SARS-CoV virus of civets had gained “the sustained infectivity for human cells”. The newly SYNTHESIZED GOF SARS-CoV was submitted to the Protein Data Bank under accession numbers 3D0G (complex of chimeric ACE2 and hTor02 RBD), 3D0H (complex of chimeric ACE2 and cSz02 RBD), and 3D0I (complex of chimeric ACE2 and cGd05 RBD). Dr. Fang Li works for the Department of Pharmacology at the University of Minnesota Medical School, Minneapolis, Minnesota. Though the data on the Gained of Function SARS-CoV was filed by the University of Minnesota in July 2008 after the epidemic of SARS in 2002-2003, we can definitely claim that this 2002-2003 pandemic was itself a synthesized GOF binary biological warfare, though that time, the SARS-CoV-1 did not have enough human to human virulence. This was precisely corrected by the joint forces at the University of Minnesota. And, so, Dr. Fang Li says that SARS-CoV-1 had “reemerged in Guangdong in 2003 to 2004, with four sporadic infections, no fatalities, and no subsequent human-to-human transmission. SARS has been absent in humans ever since”. This makes it clear that if not for the University of Minnesota efforts to keep SARS-CoV-1 highly virulent in the human-to-human transmission, we would not have gotten the present SARS-CoV-2 pandemic:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2446986/

Dr. Fang Li is a front man for Dr. Stephen C. Harrison who evidently wanted to stay in shadows for this controversial research. The research on the GAINED IN FUNCTION SARS-CoV-1 by Dr. Fang Li was funded by NIH (US National Institute of Health) grant CA-13202 to Stephen C. Harrison of Harvard. Dr. Stephen C. Harrison is the director of the Center for Molecular and Cellular Dynamics of Harvard Medical School, head of the Laboratory of Molecular Medicine at Boston Children’s Hospital, and investigator of the Howard Hughes Medical Institute. Remarkably, Stephen C. Harrison led the Structural Biology team at the Center for HIV/AIDS Vaccine Immunology (CHAVI) when it received National Institute of Allergy and Infectious Diseases (NIAID) funding of around $300 million to design and test the HIV vaccine. As is seen below, the HIV inserts play the major role in the GAINED OF FUNCTION SARS-CoV-2.

The research by Fang Li proves that there can be no direct transmission of SARS-CoV between bats and humans without an intermediate host. The argument that the closely related viruses in human can be a bridge for the SARS-CoV transmission from bats to humans does not hold, according to Dr. Fang Li research.

The Wuhan lab worked with the CLOSEST known relative of SARS-CoV-2, which is a bat coronavirus called RaTG13. The evolutionary virologist Edward Holmes, of the Charles Perkins Center and the Marie Bashir Institute for Infectious Diseases and Biosecurity at the University of Sydney, said in a statement from the Australian Media Center that “the level of genome sequence divergence between SARS-CoV-2 and RaTG13 is equivalent to an average of 50 years (and at least 20 years) of evolutionary change.” That means that in the wild, it would take about 50 years for these viruses to evolve to be as different as they are. Thus, we have a clear “accelerated virus evolution”. Nikolai Petrovsky of the College of Medicine and Public Health at Flinders claims that Bat coronaviruses can be cultured in lab dishes with cells that have the human ACE2 receptor, so that, over time, the virus will gain adaptations that let it efficiently bind to human receptors. Source: https://www.msn.com/en-us/health/medical/does-the-novel-coronavirus-have-any-links-to-a-high-security-lab-in-wuhan/ar-BB12QiM3

For recombination to occur, the two divergent viruses are made to infect the same organism simultaneously. So, SARS-CoV-2 has HIV inserts. The genetic mosaicism exists not only between divergent viruses, but also between viruses and bacteria. Thus, there certainly can be the recombination between the influenza virus H1N1 1918 and the SARS-CoV-2. That is why the Flu Vaccine Increases Coronavirus Risk 36% Says Military:

Flu Vaccine Increases Coronavirus Risk 36% Says Military Study

https://www.sciencedirect.com/science/article/pii/S0264410X19313647?via%3Dihub

And, in fact, CDC had published in its Volume 26, Number 6—June 2020 (retrieved on May 15^th, 2020) the Research Letter “Co-infection with SARS-CoV-2 and Influenza A Virus in Patient with Pneumonia, China” by Xiaojing Wu, Ying Cai, Xu Huang, Xin Yu, Li Zhao, Fan Wang, Quanguo Li, Sichao Gu, Teng Xu, Yongjun Li, Binghuai Lu, and Qingyuan Zhan of China-Japan Friendship Hospital, Beijing; The Sixth Medical Center of PLA General Hospital, Beijing; Weifang No. 2 People’s Hospital, Weifang; Vision Medicals Co., Ltd., Guangzhou, all in China: https://wwwnc.cdc.gov/eid/article/26/6/20-0299_article

The coinfection, and, thus, mosaicism between SARS-CoV-2 and H1N1 (Spanish Flu 1918) is also confirmed by Dr. Judy Mikovits for the SARS-CoV-2 pandemic in the North Italy, please, see below.

In fact, “H” in H1N1 stands for haemagglutinin.  The “H” in the Betacoronaviruses (like SARS-CoV-19) also stands for haemagglutinin. But in the case of H1N1, the hAEmagglutinin is written down as “HA” gene, while in the case of Betacoronviruses, the hAEmagglutinin is written down as “HE”.  I claim that this confusion is intentional to hide the fact that SARS-CoV-19 is a cover up for the global biowar via the resurrected and GOF H1N1 Spanish Flu 2018 virus.

And, indeed, “researchers have drawn parallels between SARS-CoV-2 and the avian influenza viruses, noting that a protein called haemagglutinin in influenza is the equivalent of the SARS-CoV-2 spike protein and that furin activation sites may make these viruses so highly pathogenic”, — says Ana Sandoiu in “Medical News Today” on March 17, 2020: https://www.medicalnewstoday.com/articles/why-does-sars-cov-2-spread-so-easily

Ana Sandoiu emphasizes that SARS-CoV-2 is spreading much faster than SARS-CoV-1 of the 2002-2003 pandemic. In 2003, 8,098 SARS cases, with 774 deaths, occurred within 8 months. By contrast, within 2 months of the start of the SARS-CoV-2 outbreak, the new coronavirus infected more than 82,000 people, causing more than 2,800 deaths. And Ana Sandoiu claims that precisely the fact that SARS-CoV-2 has the SAME haemagglutinin, as in H1N1, makes SARS-CoV-2 much more contagious than SARS-CoV-1. Thus, we have the crucial evidence of mosaicism between SARS-CoV-2 and H1N1 that goes beyond the mosaicism between SARS-CoV-2 and HIV, which both belong to the retroviruses.  The stable mosaicism between SARS-CoV-2 and H1N1 is a conclusive evidence of engineering the SARS-CoV-2 as “GAIN OF FUNCTION” virus.

Ana Sandoiu continues: “Spike proteins are what coronaviruses use to bind to the membrane of the human cells that they infect. The binding process is activated by certain cell enzymes.  SARS-CoV-2, however, has a specific structure that allows it to bind “at least 10 times more tightly than the corresponding spike protein of SARS-CoV-1 to their common host cell receptor.  This is due to the fact that the spike protein contains a site that recognizes and becomes activated by an enzyme called furin.” The “furin-like cleavage site” recently discovered in SARS-CoV-2 spike proteins may explain the viral life cycle and pathogenicity of the virus”.  Moreover, “furin is a host-cell enzyme in various human organs, such as the liver, the lungs, and the small intestines.  The fact that this enzyme resides in all of these human tissues means that the virus can potentially attack several organs at once.”

The furin recognition ability in SARS-CoV-2, absent in SARS-CoV-1, is also emphasized by  Prof. Gary Whittaker at Cornell University, in Ithaca, New York, in the paper “Structural modeling of 2019-novel coronavirus (nCoV) spike protein reveals a proteolytically-sensitive activation loop as a distinguishing feature compared to SARS-CoV and related SARS-like coronaviruses” by Javier A. Jaimes, Nicole M. André, Jean K. Millet, Gary R. Whittaker. Prof. Gary Whittaker et al. says that the furin activation site sets the SARS-CoV-2 up very differently to SARS-CoV-1, in terms of its entry into cells, that effects the stability and virulence of SARS-CoV-2. Authors also confirm that, “since furin is highly expressed in lungs, an enveloped virus that infects the respiratory tract may successfully exploit this convertase to activate its surface glycoprotein”.

https://www.biorxiv.org/content/10.1101/2020.02.10.942185v1

This conclusion is confirmed by the paper “The spike glycoprotein of the new coronavirus 2019-nCoV contains a furin-like cleavage site absent in CoV of the same clade” by B.Coutarda C., VallebX.de Lamballeriea, B.Canardb, N.G.Seidahc, E.Decrolyb, published in Antiviral Research, Volume 176, April 2020. Paper also claims that the anti-2019-nCoV therapeutics should include the furin inhibitors.  The authors specifically state that, that it is the specific form of hemagglutinin with the furin cleavage site that makes both the Influenza virus and the SARS-CoV-2 virus most virulent.  Alike SARS-CoV-2, the highly pathogenic forms of influenza have a furin cleavage site, namely, the H5N1 hemagglutinin HA cleavage site, e.g., causing the hyper-virulence of the virus during the Hong Kong 1997 outbreak.  Authors continue that the 2019-nCoV (SARS-CoV-2) S-protein sequence contains 12 additional nucleotides, which correspond to a canonical furin-like cleavage site. Authors specifically point out that this is the gain-of-function to the 2019-nCoV for efficient spreading in the human population compared to other lineage b betacoronaviruses.

https://www.sciencedirect.com/science/article/pii/S0166354220300528

Thus, the S protein in the SARS-CoV-2 was artificially generated, so that SARS-CoV-2 is a chimeric virus modified from the original SARS-CoV, with the addition of the desired S protein to make them more easily bind to human cells, thus amplifying their virulence and transmissibility. Also, SARS-CoV-2 exhibited an “uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag.” The Indians discovered the 2019-nCoV (SARS-CoV-2) has four new sequences inserted — all of which can be found in HIV genetic sequences. The supposed HIV genetic insertions on SARS-CoV-2 gene are:
Insert 1: TNGTKR
Insert 2: HKNNKS
Insert 3: RYSL—TPGDSSG
Insert 4: QTNSPRRA: https://www.researchgate.net/publication/338957445_Uncanny_similarity_of_unique_inserts_in_the_2019-nCoV_spike_protein_to_HIV-1_gp120_and_Gag

Notably, the adaptation of HIV-1 to humans from chimpanzees was associated with a change in the p17 Gag protein, which may be involved in the specific targeting of the protein within the host cell cytoplasm. If SARS-CoV-2 virus has the Gag HIV insert, it might mean that precisely the Gag HIV insert is responsible for the adaptation of the highly contagious coronavirus from bats to civets and to humans.

Also, it is clear that HIV itself is a synthetic GOF virus, since its transfer from chimpanzees to humans had definitely happened through an intermediate host, which is “yet to be identified”, as it is claimed by the paper “Cross-Species Virus Transmission and the Emergence of New Epidemic Diseases” by
Colin R. Parrish, Edward C. Holmes, David M. Morens, Eun-Chung Park, Donald S. Burke, Charles H. Calisher, Catherine A. Laughlin, Linda J. Saif, and Peter Daszak, in Microbiol Mol Biol Rev. 2008 Sep. I bet that this “intermediate host yet to be identified” is CDC itself:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546865/#r137

Analogously, “despite several proposed candidates, from snakes to pangolins to dogs, researchers have failed to find a clear “intermediate host” — an animal that would have served as a springboard for SARS-CoV-2 to jump from bats to humans”. The reason of why researchers have failed to find an “intermediate host” between bats and humans for SARS-CoV-2 is precisely the fact that SARS-CoV-2 was artificially synthesized, including by the efforts of Dr. Stephen C. Harrison of Harvard University and his protégé Dr. Fang Li of the Minnesota University.

Source: https://www.msn.com/en-us/health/medical/does-the-novel-coronavirus-have-any-links-to-a-high-security-lab-in-wuhan/ar-BB12QiM3

Dr. Judy Mikovits told The Epoch Times in her analysis and comparison of the virus of the SARS-Cov-2 (the virus that causes the COVID-19): “(it) apparently has genes that come from human and other species including some envelope—the one from HIV.” Source: https://gulfnews.com/world/coronavirus-did-not-jump-from-wuhans-seafood-market-heres-the-evidence-1.1586936434717

In 2004, virologists demonstrated how retroviruses (specifically, immunodeficiency virus), pseudotyped with the SARS coronavirus spike protein, efficiently infect cells expressing angiotensin-converting enzyme 2 (ACE2) in humans. This research had demonstrated that “when using S-protein-pseudotyped SIV (in animals, similar to human HIV), the enzymatic activity of ACE2 made no contribution to S-protein-mediated infection”, meaning that ACE2 human receptors are not the main pathway. This means that HIV inserts in SARS-CoV-2 are the main pathway of infection.  This paper “Retroviruses pseudotyped with the severe acute respiratory syndrome coronavirus spike protein efficiently infect cells expressing angiotensin-converting enzyme 2”  in J Virol. 2004 Oct. by Moore MJ1, Dorfman T, Li W, Wong SK, Li Y, Kuhn JH, Coderre J, Vasilieva N, Han Z, Greenough TC, Farzan M, Choe H. had in fact demonstrated that SARS-CoV is a CHIMERA of Coronavirus and HIV virus in animals (SIV). This combination, as the authors demonstrated, is “the codon optimization of the SARS-CoV S-protein gene” that “substantially enhanced S-protein expression”, that is, the virulence of SARS-CoV virus. They say: “Infection mediated by an S-protein variant whose cytoplasmic domain had been truncated and altered to include a fragment of the cytoplasmic tail of the human immunodeficiency virus type 1 envelope glycoprotein was, in both cases, substantially more efficient than that mediated by wild-type S protein.” The authors also stated that this was the additional “codon enhancement” to the in-itself enhancement of SARS-CoV virus to make it more virulent.

https://www.ncbi.nlm.nih.gov/pubmed/15367630

Also, this research had shown that a soluble and catalytically inactive form of ACE2 potently blocked infection by S-protein-pseudotyped retrovirus and by SARS-CoV. These results permit studies of SARS-CoV entry inhibitors without the use of live virus and suggest a candidate therapy for SARS.  This statement is a proof that we deal with the “pseudotyped” or “recombinant” virus in COVID-19 pandemic.  “Pseudotyping” means precisely the ARTIFICIAL recombination, thus proving that SARS-CoV-2 is the artificially created bioweapon.  Source: https://www.ncbi.nlm.nih.gov/pubmed/15367630

A soluble and catalytically inactive form of ACE2 is sold at the moment by Creative Biolabs in the US, for example: https://sars-cov-2.creative-biolabs.com/stable-cell-line-ace2-cho-for-sars-cov-2-study.htm But this company grows ACE2 in the Chinese hamster ovary (CHO) cells, thus, destroying the Wave Optics of human chromosomes. Growing the ACE2 in the hamster’s ovary (CHO) cells also means that hamster might become an “intermediary host” for transmitting the “pseudotyped” HIV/SIV between humans, camouflaged as a “novel” SARS-3 for the yet-coming global pandemic.

Recombination between Coronavirus and HIV (lentivirus) occurs since both of these viruses belong to the family of Retroviruses (Retroviridae) — single-stranded RNA viruses that produce reverse transcriptase by means of which DNA is produced using their RNA as a template and incorporated into the genome of infected cells, that are often tumorigenic.

Gp41 and gp120, the transmembrane glycoproteins, are the HIV “keys” to infecting human cells. Consequently, the recombinant-gp120-based vaccines were offered to the HIV-infected humans in 1990 by Philip Berman and colleagues in Nature. Again, If SARS-CoV-19 infects the host cell via the HIV mechanism of infection, then the ACE2 research is irrelevant for the possible cure:
https://www.nature.com/articles/d42859-018-00010-y

 

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I refer to the blackop SARS-CoV-2 State Terrorism Global biowarfare in my article “WARNING TO THE US INTELLIGENCE СOMMUNITY. ILLICIT ISRAELI WAR AGAINST UNITED STATES THROUGH THE MOSSAD SHILLS IN CIA” on January 21, 2018:

https://irenecaesar.wordpress.com/2018/01/21/warning-to-the-us-intelligence-сommunity-illicit-israeli-war-against-united-states-through-the-mossad-shills-in-cia/

and in my February 25, 2018 article “THE BINARY BIOLOGICAL WAR APPROACHING”, published in March and April 2018 issues of the “Socialist Factor” Magazine, a glossy Indian magazine, printed in Lucknow and London in 50,000 copies, and distributed to 240 embassies.

https://irenecaesar.wordpress.com/tag/bioelectronic-war/

It looks like that Mossad played the same role in the SARS-CoV-2 global bioware strike, as it played in 9/11. The Gained of Function SARS-CoV-2 was secretly flown from the major CDC Influenza / SARS Biolab in Atlanta by the SINGLE Israeli plane through the Atlanta airport during the intentional Airport blackout, on December 20^th 2017.  In January 2018, DHS conducted the Biological Weapons drill, marking the beginning of preparations for the global biowarfare strike.

Those idiots and criminals, who had resurrected H1N1 most deadly 1918-19 Spanish Flu virus, took their number of 60 millions killed worldwide by SARS-CoV-2 precisely from 50 millions killed by H1N1 1918-19 Spanish Flu Virus, in their mathematical model presented at the October 19, 2019 “201 Event” “Pandemic Exercise” in NYC.

 

MAN BEHIND CORONAVIRUS PANDEMIC 2019

 

The man behind the SARS-2 (Covid-19) pandemic is the same as behind the Blue Plague in the Mexican Gulf. And his name is …. Craig Venter. The present pandemic is the result of the fallacious theory of computational biology, when the Wave Geometry / Wave Optics of DNA is written down by the binary computer code.

Novartis together with Craig Center are now creating the synthetic viruses and synthetic vaccines. He says the vaccine for the HIV virus is not possible due to the high rate of the HIV virus mutation. Venter assumes he can win the race with a mutating virus. But, instead, he released into the world the airborne HIV.

Our other hero of the computational biology is Dr. D.E.Shaw. I bet his project for the synthetic American super soldier had completely failed by now — soldiers as DNA computers. He started at the same time as Craig Venter – both with the project of the “synthetic life”. Ten years ago.

Alas, the lobby of Big Pharma desires to pull now the so-called “biotech revolution”, which, they hope, will be analogous to the Bill Gates and dot.com revolution in the 1990s – both making huge fortunes in a matter of two years or so. For the prospect of this monetary gain, the Big Pharma and their lobbyists in DC had conspired to release the synthetic virus onto the global scene, killing people by thousands.

But this time, as with the Blue Plague in the Mexican Gulf, instead of monetary gain, they got the national and global catastrophe that would endanger the very survival of our species, if they will be allowed to continue.

So, you might say, the present COVID-19 pandemic, caused by SARS-2 (SARS-CoV-19) was announced by Craig Venter exactly ten years ago. He directly said: I will produce synthetic viruses and synthetic vaccines. Noticeably, he mentioned the HIV virus, as an example. It is widely known by now that SARS-2 is an artificially-made virus with the HIV inserts.

At that moment, 10 years ago, Craig Venter’s computational biology became the Federal classified biotech program. And the guy capitalized on killing tens of thousands of his fellow Americans by his false theory and erroneous technology.

Noticeably, Craig Venter openly hints in his speeches that depopulation is legit.

Before the Feds in the US picked up on his research, Craig Venter was mostly sponsored by BP (British Petroleum) – the British anti-American colonial force. That is why the present virus SARS-2 is patented by the British — the London-based Pirbright Institute.

British Petroleum had themselves exploded their rig in the Mexican Gulf in 2010 – in order to release Craig Venter’s synthetic bacteria Cynthia that eats now human flesh in the Mexican Gulf. It was supposed that this artificial algae (that does not need sun light) will soften the huge deposits of crude oil on the bottom of the Mexican Gulf. But in addition, the Cynthia is now eating the arms and leggs off the bodies of local folks.

The Mother Lodge / MI6 / British colonialists had now repeated the same crime. They artificially released their man-made synthetic virus in order to profit from the global sales of their man-made synthetic vaccine.

The major problem with the flu vaccines lies in the issue of the flu virus high mutation rate, so that every new flu season makes the flu vaccine obsolete.

The US Feds hope that they will catch up with the flu virus mutation with the help of Craig Venter’s computational biology. But, alas, their hopes are futile. Since the synthetic vaccine by Dr. Craig Venter et al. will sterilize them.

I think that, at least, Bill Gates deserves sterilization!

Bill Gates and Ray Kurzweil plan to obtain “the enhanced genetics” for the elites only.  “Gain of Function” Bill Gates and Ray Kurzweil hope that they and their families will escape death and suffering caused by the COVID-19 pandemics thanks to the GMO bioscience. But the “special” “for elite only” vaccine will not save, or enhance Bill Gates and Ray Kurzweil, since the GMO technology is wrong and destructive, and makes the genetically modified organisms sterile.  “Genetic enhancement for elites” will sterilize the elites as effectively as the “weaponized sterilization Flu and SARS vaccine” for ghettos.

PS Real help is offered by my company Wave Genome LLC that had just released a new revolutionary product to address COVID-19 pandemic:

http://wavegenome.com/ra_shield.html

RA SHIELD PRESS RELEASE

Tags

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PRESS RELEASE: RA SHIELD BY WAVE GENOME LLC

http://wavegenome.com/ra_shield.html

On March 18th, 2020, Wave Genome LLC has released a new product to address the COVID19 pandemics: RA SHIELD. The device is the paradigmatic device for the personalized, addressed and preventive treatment. The technology is based upon recording client’s Holographic Signal, for example, from his saliva or mucus, and, then, reversing or inverting this signal. The inverted signal is also subjected to the generator of the scalar wave (patented), and, after this, applied via two electrodes to client’s skull, and, alternatively, via an electrode to water for treatment. The client can have his or her own individualized treatment in the privacy of their homes. An extended electrode to program the large quantities of water is provided.

The principle of inversion is used very successfully for a long time in Russia, and device is proven to be very efficient.  The same is true of the generator of scalar waves, which effectiveness can be demonstrated by the special technical device.

This device is very important since the Wuhan Coronavirus is a single strand RNA virus. The only way to fight it is to create its negative invert via the scalar wave. In the scalar wave, the peak of the forward-going wave is annulled by the trough of the same wave, when it is reflected back upon itself.

Bill Gates had created the machine for the «vaccine» injection «Cellectra». Its design is wrong and destructive. It is analogous to electrophoresis used for destroying DNA for making GMO (sterile biological organisms). The machine consists of two electrodes for one-way induced electrical current. In principle, there should be FOUR electrodes. And the two anti-parallel currents in a scalar way, or the other way for inverting the signal of the virus. It should be even better if electrodes will be shaped as induction coils.

Because the Wuhan Coronavirus is a single strand wave structure, analogous to the spiral antenna, the Wuhan virus is incurable by any chemical substance, analogous to the Lyme disease, caused by the spirochete (single spiral antennae) bacteria; and analogous to the HIV retrovirus, which components are artificially inserted into the Wuhan Coronavirus. This is, in fact, already confirmed by the Chinese biologists. The Wuhan Coronavirus returns to the cured patients. Chinese claim that no immunity can be produced to the Wuhan Coronavirus. This means that no vaccine can be produced. Moreover, the “maybe”-vaccine will be disseminating the virus instead of protecting from the virus.

That is why the RA SHIELD is the device that has crucial importance in fighting the global pandemic.

We actually can cure AIDS and cancer with RA SHIELD, since these two diseases are caused by the failure in crystallization of Chromosomes due to failure of Wave Optics during cell division (so-called translocation, transposition, deletions, and other structural defects of chromosomes). So there is hope! And we will claim it now! Enough is enough!

The promotional price for the times of pandemic is $2500.

www.wavegenome.com

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THE RA SHIELD

1. NEED FOR THE RA SHIELD

The RA SHIELD was released by Wave Genome LLC to help its clients restore the Wave Optics of chromosomes under the condition of the SARS-CoV-19 pandemic. SARS-Cov-19 has the artificial HIV inserts, so that the HIV retrovirus has now become airborne. HIV retrovirus, alike the spirochete bacteria causing the Lyme disease, are considered to be incurable. SARS-Cov-19 as the airborne HIV retrovirus constitutes great danger since (1) its risk lies not in the short-term pandemic with high mortality, but in the slow shut-down of the structural genes across the wide human populations via the recombinant RNA of the retrovirus, causing the slow degeneration with the resultant sterilization of human populations; (2) the airborne HIV can spread over the borders and to any rank of society, demobilizing the working force, the elites, government, army, and intelligence; (3) no immunity is produced by the human body, and, so, no vaccine can be provided by FDA due to the nature of SARS-Cov-19 as the airborne HIV retrovirus. The pandemic of SARS-CoV-19 will end up not in the elimination and control of the infection, but in the mutation of the virus, so that it will weaken and become less noticeable in the public eye, though preserving all its disastrous impact on human genome. Since no immunity is formed, any attempt at vaccine will be the spread of the virus, instead of its elimination. This is besides the factor of the seasonal mutations of the virus, which makes any vaccine obsolete with a new flu season. The RA SHIELD by Wave Genome LLC addresses these risks, offering the personalized on-the-spot treatment of client’s Wave Optics of chromosomes.

2. DESCRIPTION OF THE RA SHIELD

The RA SHIELD device, hereinafter referred to as the device, is intended for restoring the Wave Optics in chromosomes during cell division via the technology of Bioholography. The technology of Bioholography is based upon Dr. Irene Caesar’s fundamental theory of Wave Optics in Chromosomes (1985-2014). The device produces Bioholograms for the Bioholographic treatment. Client is able to create his/her own Personalized Bioholographic Pharmacies in the privacy of their homes. For personalization of Bioholographic drugs, client uses his/her own biological material (saliva, mucus, blood, urine, etc.). Client can modulate his/her own Biohologram with any Biomodulator, e.g., the immunomodulator.

The RA SHIELD produces a Biohologram via the generator of the form, which creates the scalar wave when the trigger of the certain signal is present, which is impulse, coherent (with the stable frequency), and having the low-high range of frequencies. The generator of the form provides the reflection of the wave back upon itself. The scalar wave is created by the superposition of the two waves-components of the original trigger-wave in the opposite phases. These two components of the scalar wave are described as an Object Beam and a Reference Beam modulated by the Refraction Code of Object’s Modulating Wave.

The RA SHIELD uses the three-level mechanism for creating a Biohologram. The first-level is the electro-magnetic induction method for transferring the electric potential into the magnetic potential. The second level is the generator of the scalar waves as the electret-based chip produced as a microprocessor. And the third level is the multi-step repetition of the two modes of involution of the resultant signal for increasing the density of the scalar wave diffraction grating for the sake of the more precision of Refraction towards the Zero Center / Focus of client’s Biohologram. Client can initiate the third level him/herself.

The produced Bioholograms are intended for the use (1) via electrodes directly onto the skull; and (2) via recording the Biohologram onto the various media, including in big quantities. Client increases the density of the scalar wave diffraction grating due to the needs of his/her health condition.

3. THEORY BEHIND THE RA SHIELD

Dr. Irene Caesar had developed her fundamental theory of Wave Optics in Chromosomes (2010-2014) based upon her theory of Wave Crystals or the wave crystal media (© Dr. Irene Caesar – Wave Crystallography, 1985).

During cell division, the Chromatin forms two chromatids. And two chromatids form an x-shaped chromosome. So, the liquid crystal media of your body literally crystallizes during cell division. The universe is 93% energy, and only 7% particles, which are also only the concentrated energy. So, the wave crystallization comes first, and, then, the crystallization of the liquid crystal media of our bodies (we are water for 95%). Wave crystal media demonstrates the same structure as solid crystals, and is characterized by the fractal centering and focusing of the systematic whole, based upon the Wave Optics within the scalar wave diffraction grating. Thus, treatment should be based upon addressing the 93% wave nature of the living matter.

For example, the electronic microscopy demonstrates that RNA is the nonlocal torsion splashes simultaneously lighting up around the cell. Since RNA infections are the wave forms of life for 93%, and the biochemical matter only for 7%, it is possible to fight against the RNA viral infections, like SARS-Cov-19, only via Wave Genome’s LLC technology of Bioholography, based upon Dr. Irene Caesar’s fundamental theory of Wave Optics in chromosomes. It is precisely because retroviruses are the nonlocal simultaneous wave forms within the cell, the human immune system has difficulty in localizing them, and building the defense. The immune system responds with the inadequate response, attacking client’s own bodily organs and physiological systems, causing organ failure, and death from the autoimmune disease. That is why, the Hydroxychloroquine is used for the SARS-Cov-19 cases, since the Hydroxychloroquine is an immune modulator used for the autoimmune diseases, like AIDS and Rheumatoid Arthritis. But the Hydroxychloroquine does not treat the virus itself, and its side effect is the total suppression and the resultant failure of the immune system. Therefore, the Hydroxychloroquine should not be in any case considered as a treatment (and, of course, not a cure) for the SARS-Cov-19.

All dysfunctions and diseases are caused by the destruction of Wave Optics in chromosomes (transposition, deletion, etc., as the structural defects of chromosomes) — failure in centering and focusing of Wave Crystals (wave crystal media). The same gene gets expressed in the functional individuals and species by the metacentric chromosome, which is analogous to a well-centered and well-focused eye. And the same gene gets expressed in the dysfunctional individuals and species by the acrocentric chromosome, which is analogous to a near-sighted or far-sighted eye, out of focus. The RA SHIELD by Wave Genome LLC creates Wave Lenses that assist your chromosomes in crystallization, so that you get your Wave Matrix / Biohologram most centered and most focused.

The Holographic Principle states that the Universe is entirely in its every Matrix Point. This means that every Wave Matrix / Biohologram has the infinite number of waves, particles and fields, i.e., it is nonlocal in the Quantum Biononlocality. Therefore, it is impossible to correct and enhance the functionality of chromosomes just by one frequency or the set of frequencies. So, the Digital Homeopathy with its simple inversion of the signal, recorded from the client, is insufficient for the treatment.

The implication of the Holographic Principle (© Dr. Irene Caesar, 2012) states that, if the Universe is entirely in its every Matrix Point, then, every Matrix Point is not simply different from any other Matrix Point, but is unique. Every Matrix has its own Wave Optics with its own unique Refraction Code. Wave Matrices / Bioholograms differ from each other by one’s own unique Refraction Code towards one and only Zero Center / Focus, shared by all the Wave Matrices from galaxy to chromosome. This means that any treatment should be personalized. The treatment should be based upon the procedure of extracting client’s own biological material (blood, saliva, mucus, urine, etc.) and subjecting it to the protocol of Bioholography for correcting client’s Wave Optics in chromosomes. Biohologram is not “an image”, but the structural nature of the signal. To correct the structural abnormalities in chromosomes on the biochemical level, we need to correct the structural abnormalities in client’s Wave Optics of chromosomes.

Wave Genome LLC is the first biotechnology company in the world to encode the electret-based chips (“Psi-generators”) with client’s unique Biohologram (Refraction Code of Wave Optics) via laser on nanolevel, recorded from client’s childhood or adult photograph; and from client’s biomaterial. Wave Genome LLC is the first biotechnology company in the world to create the Bioholographic Stem Cell treatment, based upon client’s own stem cells extracted from client’s epithelial cells, in collaboration with the Bauman Russian State Technology University in Moscow, the largest and most important science University in Russia, of MIT level.

The protocol of the Bioholography consists of three stages. The first stage is for the neutralizing all the external linear signals via reflecting them back upon themselves (inverting) within the scalar wave. Scalar wave annuls any external linear signal, when the peak of the forward-going wave is nullified by the trough of the same wave reflected back upon itself. The second stage is the creation of the scalar wave diffraction grating (wave media crystallization), and the emergence of Refraction, so that the next external linear signal is refracted towards the Zero Center / Focus of the emerged Wave Crystal (wave crystal media). And the third stage is the scaling of Refraction, so that every segment of the scalar wave diffraction grating becomes itself the scalar wave, from the bodily organ level, to the cellular level, to the molecular level, to the atomic level, and to the subatomic levels, ad infinitum.

The Zero Center / Focus of the Wave Crystal is the access to the Quantum Biononlocality. Every Biohologram is unique and nonlocal, and has its own Refraction Code for accessing the Quantum Biononlocality. Disease is the loss of client’s access to the Quantum Biononlocality. Treatment should consist in deciphering client’s unique Refraction Code of his/her nonlocal Wave Optics (from direct recording the wave activity of the brain; from client’s childhood photograph; from client’s preserved placenta, etc.), then, in enhancing client’s Refraction Code via the scalar waves, and, finally, in applying client’s enhanced Refraction Code in treatment.

Since the universe is holographic, the signals, that are not holographic, are harmful to us. Especially harmful are the one-strand spiral antenna wave forms of viruses and bacteria, like spirochete bacteria that causes Lyme disease, and retroviruses, like HIV, which causes AIDS. There are no vaccines possible for these viruses and bacteria, and diseases caused by them are considered to be incurable due to the fact that they are simply the antenna-plug-ins of the nonlocal planetary wave forms of life. Viruses and bacteria are the binary biological matter, meaning that viruses (microphages) and bacteria are coupled in ecosphere, with their genes interchanged (genetic mosaicism). Therefore, in the ecosphere, as a whole, they exist as the planetary scalar wave, but in our bodies, they manifest themselves as the linear signal plug-ins. It is possible to counter these wave plug-ins only via the Scalar Wave Inversion and Refraction in Bioholography.

The process of the Bioholography is initiated by the scalar wave created by an Object Beam and a Reference Beam modulated by the Refraction Code of Object’s Modulating Wave. Further on, the process of the Bioholography allows for adding more wave modulations, as the additional Refraction Codes, e.g., the immunomodulators. Bioholograms can be recorded (and, then, transferred) in any spectrum of the electro-magnetic range via recreating the Refraction Code of object’s Wave Optics. The Bioholographic treatment is in principle nonlocal at the close and long range through the Quantum Biononlocality.

4. TECHNOLOGY BEHIND THE RA SHIELD

Technology of Bioholography is based upon the Refraction Codes in the scalar wave diffraction grating. Let us analyze the three stages of the Bioholography in detail. At the first stage of restoring client’s Wave Optics in chromosomes, the RA SHIELD creates the scalar wave to nullify the external linear signals, alien to client’s intrinsic Wave Optics calibrated to precision. In the scalar wave, the peak of the forward-going wave is annulled by the trough of the same wave when it is reflected back upon itself. Specifically, the RA SHIELD is capable to nullify, via the scalar wave, the one-strand spiral antenna wave forms of viruses and bacteria, which are otherwise considered to be incurable.

The device uses the new technology of the scalar inversion, i.e., the electret-based generator of the scalar waves (patented), which provides the more efficient scalar wave diffraction grating. Being a microprocessor, this generator of the scalar waves gets directly and faster to the micro cellular and molecular levels, than any induction coil generator. As a result, the RA SHIELD creates the much more dense scalar wave diffraction grating, and, thus, the much more precise refraction of Wave Optics. The main problem with the Digital Homeopathy and its protocol of inversion lies in its inability to sustain the coherence of the signal (stable frequency) for creating the stable scalar wave diffraction grating. That is why, the Digital Homeopathy, either via shaking, or via the induction coil inversion, cannot provide the sizeable and scalable results.

Via the mechanism of scalar waves, the External Linear Signals are transformed in our bodies into our unique Holographic Signals. Our metabolism and cell division are running on the constant transformation back and forth between the single-strand torsion-shaped Linear Signals and the double-strand torsion-shaped Holographic Signals. These two kinds of signals are produced by the bioantennas of the different form: the single-strand spiral antenna of RNA and the double-strand spiral antenna of DNA. These two kinds of antennas have different mechanisms of receiving and transmitting the signals.

The single-strand antenna of RNA operates based upon the mechanism of destructive and constructive wave interference. Destructive interference leads to nullifying the signal in the scalar wave, and, so, to the transformation of RNA into DNA (transcription). Constructive interference, when the same wave is overlaid with itself, increases the amplitude of this wave, leading, for example, to infection in the case of SARS-Cov-19.

DNA, as the double-strand antenna, is a paradigmatic scalar wave: in DNA, one strand has signal going in one direction, and the second strand has signal going in the opposite direction, thus, creating the scalar wave. Thus, DNA is protected by its scalar wave against the external Linear Signals, specifically, of the single-strand spiral antenna wave forms of retroviruses and spirochete bacteria. Failure of DNA in protecting itself against such viruses and bacteria is caused by the structural defects of chromosomes. Restoration of DNA is possible only via the restoration of the Wave Optics in chromosomes.

DNA operates based upon the Wave Optics, as the scalar wave diffraction grating, which is a certain wave crystal media, aka “Wave Crystal”. The Wave Crystal of DNA receives and transmits information through its Zero Center / Focus. This information is received from the Quantum Biononlocality, or the Zero Field.

The Scalar Principle is not understood by the leading companies in biotechnology. For example, Inovio Pharmaceuticals Inc., backed by Bill Gates, had created «Cellectra», the device for the SARS-CoV-19 «vaccine». Its design is wrong and destructive. It is analogous to electrophoresis used for destroying DNA for making GMO (sterile biological organisms). The machine consists of two electrodes for one-way induced electrical current. In principle, there should be FOUR electrodes. And the two anti-parallel currents in a scalar way, or the other way for inverting the signal of the virus. It should be even better if electrodes will be shaped as induction coils. The harm from using the “Cellectra” will be bigger than from the SARS-CoV-19 itself.

At the second stage, the device creates a Biohologram or a “Wave Lens” (scalar wave diffraction grating), which is beneficial on its own, for centering and focusing our chromosomes during cell division.

At the third stage, the device modulates the emerged Wave Crystal (wave crystal lens) with the desirable modulations (Refraction Codes), e.g., an immunomodulator.

5. OPERATION OF THE RA SHIELD

The RA SHIELD creates and transfers the Bioholograms.

The RA SHIELD creates and transfers client’s Biohologram from the direct brain output; from the bodily liquids (saliva, mucus, urine, blood, placenta, etc.); from the digital input.

The RA SHIELD creates and transfers the Bioholograms of drugs to various carriers: water, alcohol, saline, sugar, etc., which are later used instead of the original drugs.

The RA SHIELD creates and transfers the Bioholograms via an attached electrode, including directly to the brain, and to water in large quantities.

The RA SHIELD uses the direct scalar inversion, and involuted scalar inversion (double, triple, etc., inversion), applied in stages and degrees.

The Potency of the Biohologram is defined by the density of its scalar wave diffraction grating. The increased Bioholographic Potency is achieved by the increase of degrees in the direct and the involuted scalar inversion.

The value of the Bioholographic Potency is indicated in decimal: D1, D2, D3, … or hundredth: C1, C2, SZ, … system. The corresponding value shows the degree of the scalar inversion, i.e., the number of the direct scalar inversions and the involuted scalar inversions, which must be made at each stage of producing the Biohologram.

For simplicity, the mode of the direct scalar inversion is called “without inversion”. And the mode of the involuted scalar inversion is called “with inversion”. For clarification, the direct scalar inversion can be compared to the induction coil with one strand, which makes turns for 180 grades thus reflecting the trigger-wave back upon itself. And the involuted scalar inversion can be compared to the double-wired induction coil, and the induction coil with the antiparallel wiring.

The RA SHIELD offers a completely new model of treatment: instead of stockpiling the substances, the client can produce and scale any treatment from the preparation of certain potency. This is specifically important in the times of shortages in the wellness substances during pandemics.

6. DEVICE DESIGN

The device is produced in a rectangular small-sized plastic case, inside of which there are the electronic components that produce and transfer the Biohologram; the timer; the triggering and enhancing signal for creating the scalar wave diffraction grating; the electret-based generator of the scalar waves; and a power source.

The interface of the device has the following components:

1. Button for changing the scalar wave trigger-signal.
2. The knob for adjusting the potency of the Bioholographic preparations when it is recorded onto the “receiver” cup.
3. A cup for placing the “source” of information (substances), from which information is transferred.
4. A socket for connecting an electrode used for recording onto liquids in large (up to 100 ml) quantities, with inversion.
5. A cup for placing the substances (water, sugar, alcohol, saline, etc.), onto which information is transferred with inversion.
6. A cup for placing the substances (water, sugar, alcohol, saline, etc.), onto which information is transferred without inversion.
7. Socket for connecting an electrode used for recording onto liquids in large (up to 100 ml) quantities without inversion.
8. A socket for connecting a “source” of information (liquids located in large [up to 100 ml] vessels, medical cartridges with the Bioholographic preparations, etc.), from which information is transferred.
9. The reset button (erase) of the information stored in the device from the previous substance.
10. Button to start the procedure for recording the information.

7. ORDER OF WORK WITH THE DEVICE FOR PRODUCING THE BIOHOLOGRAPHIC PREPARATIONS

1. Prepare the workplace, ensuring maximum cleanliness: remove other devices and disturbing substances that can lead to distortion of the recording process – sources of electromagnetic radiation (television sets, VHF transmitting equipment, satellite receiving equipment, etc.), active solvents, esters, acetones, gasolines, etc.
2. Place the source (substance), from which information is transferred, to cup 3 or connect the source of information to socket 8.
3. Place the carrier (substance) onto which the information is transferred, onto the cup 6.  Liquefy the carrier or moisten it with 30% alcohol solution or vodka.

For liquid carriers (distillate water, alcohol, saline, etc.), a cylindrical vessel of appropriate sizes (for example, a burette) is used, which is placed on the cup 6.

When using water as a carrier, it is desirable to prepare it in a special way for recording by irradiation with laser, ultraviolet light, etc.

When recording to liquids placed in large (up to 100 ml) vessels, the latter are connected using a special electrode to socket 7.

To obtain an inverse recording of the substance, it is necessary to use a cup 5 for solid substances, and socket 4 for liquid substances.

4. To carry out the process of transferring information, press the 10 button twice. The recording process occurs during the two-time sounding of the triggering signal, and stops automatically after the last sound.
5. After completing the recording process, first remove the “copy” from cup 6, and then the “original” from cup 3.
6. In subsequent recording of substances, the information is saved by the device. To erase the information, and restart the process, press the reset button 9.

Note: Consume the Bioholographic Preparations three times a day half an hour before the food intake.

8. ORDER OF WORK WITH THE DEVICE FOR PRODUCING THE BIOHOLOGRAPHIC PREPARATIONS USING CLIENT’S BIOMATERIAL

STEP ONE: Recording the information of the therapeutic substance onto the carrier.

 Perform the steps in Section 7. 

STEP TWO: Recording client’s Refraction Code onto the carrier.

1. Continue in the same workplace and with the same carrier.
2. Place the source (substance, i.e., client’s saliva, mucus, blood, urine, placenta, etc.), from which information is transferred, to cup 3 or connect the source of information to socket 8 (electrode connected to client’s skull).
3. Place the carrier (substance) onto which the information is transferred, onto the cup 6.   Liquefy the carrier or moisten it with 30% alcohol solution or vodka.

For liquid carriers (distillate water, alcohol, saline, etc.), a cylindrical vessel of appropriate sizes (for example, a burette) is used, which is placed on the cup 6.

When using water as a carrier, it is desirable to prepare it in a special way for recording by irradiation with laser, ultraviolet light, etc.

When recording to liquids placed in large (up to 100 ml) vessels, the latter are connected using a special electrode to socket 7.

To obtain an inverse recording of the substance, it is necessary to use a cup 5 for solid substances, and socket 4 for liquid substances.

4. To carry out the process of transferring information, press the 10 button twice. The recording process occurs during the two-time sounding of the triggering signal, and stops automatically after the last sound.
5. After completing the recording process, first remove the “copy” from cup 6, and then the “original” from cup 3.
6. In subsequent recording of substances, the information is saved by the device. To erase the information, and restart the process, press the reset button 9.

Note: Consume the Bioholographic Preparations, modulated by your Refraction Code, three times a day half an hour before the food intake.

STEP THREE: Recording client’s corrected and enhanced Refraction Code back upon client’s biomaterial.

1. Continue in the same workplace, but with the change of a carrier. Now, the carrier is client’s biomaterial.
2. Place the source (the Bioholographic Preparation), from which information is transferred, to cup 3 or connect the source of information to socket 8 (the digital input).
3. Place the carrier (substance – client’s biomaterial) onto which the information is transferred, onto the cup 6.   Liquefy the carrier or moisten it with 30% alcohol solution or vodka.

For liquid carriers, a cylindrical vessel of appropriate sizes (for example, a burette) is used, which is placed on the cup 6.

When using bodily liquid as a carrier, it is desirable to prepare it in a special way for recording by irradiation with laser, ultraviolet light, etc.

When recording to liquids placed in large (up to 100 ml) vessels, the latter are connected using a special electrode to socket 7.

To obtain an inverse recording of the substance, it is necessary to use a cup 5 for solid substances, and socket 4 for liquid substances.

4. To carry out the process of transferring information, press the 10 button twice. The recording process occurs during the two-time sounding of the triggering signal, and stops automatically after the last sound.
5. After completing the recording process, first remove the “copy” from cup 6, and then the “original” from cup 3.
6. In subsequent recording of substances, the information is saved by the device. To erase the information, and restart the process, press the reset button 9.

Note: Client’s biomaterial as a carrier is not consumed as a substance by the client. The Bioholographic treatment is applied remotely at the close and long range via the Quantum Biononlocality.

9. CHANGE OF POTENCY OF THE BIOHOLOGRAPHIC PREPARATIONS

1. The maximum change in potency depends on the type of substance, its place of manufacture and storage time, and can reach 200-500 times at the extreme right position of the potency adjustment knob 2 (position 10).
2. It is recommended that when recording from cup 3 to cups 5 or 6, the selection of potency is carried out according to the following procedure:

— record when the adjustment knob is in position from 9 to 10 (recording 1:1);

— test the Bioholographic Preparation;

— if it is necessary to increase the scalar inversion, you should record when the adjustment knob 2 is in the position lower than 9.

3. Table 1 shows the conversion factors and the resulting potency for the Bioholographic recording of the original substance, depending on the position of the adjustment knob 2:

10. REPLACING THE POWER SUPPLY

The RA SHIELD uses the AA batteries as its power source.

To replace the battery, open the device case by unscrewing the fixing screw and insert the battery observing its polarity.

 

11. INSIDE THE BOX

1. The device “RA SHIELD” ………………………….. 1 piece.
2. Electrode for recording onto liquid ……………. 1 piece.

 

12. WARRANTY

The manufacturer guarantees the operational characteristics of the device for 6 months from the date of purchase, subject to non-violation of the exploitation rules.