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IRENE CAESAR, PH.D. / ИРИНА ЦЕЗАРЬ, ДОКТ. ФИЛОСОФ. НАУК

~ https://www.wavegenome.com

IRENE CAESAR, PH.D. / ИРИНА ЦЕЗАРЬ, ДОКТ. ФИЛОСОФ. НАУК

Tag Archives: SARS-CoV-2

DR. IRENE CAESAR ON DR. ROBERT MALONE, DR. JENNIFER DOUDNA AND DR. GEORGE CHURCH OR THE TALE OF THREE PIGS

18 Tuesday Jan 2022

Posted by Irene Caesar, Ph.D. / Ирина Цезарь, Доктор Философских Наук in NEGROID BLOODLINE OF THE QUEEN OF ENGLAND

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adenovirus-vector vaccine, binary biological weapon, biohacking, crispr/cas9, digital currnecy, DURC, effect of the destructive rna interference, experimental genetic drug, gain of function, gene silencing, genetically modified humans, gmo humans, implants, internet of boides, irene caesar, jennifer doudna, joe rogan interview of Dr. Robert Malone, miRNA, mRNA, mRNA vaccine, ralph baric, reverse transcriptase, robert malone, SARS-CoV-2, sterilization, sterilization via vaccination, wave genome

DR. JEKYLL CLUMPING ON THE BLOOD VESSELS

Dr. Robert Malone’s (inventor of mRNA reverse transcriptase gene delivery) Twitter account was permanently deleted, when he voiced protest against vaccinating children with his mRNA experimental genetic drug aka “COVID-19 vaccine” — that he, Dr. Robert Malone, had proudly created. The pride is all his, since Dr. Robert Malone repeats in his every interview that it was he, Dr. Robert Malone, who had created the genetic drug aka “mRNA vaccine” that now causes the organ failures all over the world and en masse. Let the psychiatrists decide what kind of psychiatric deviation is that.

Dr. Robert Malone also says in his every interview that he himself got brain fog after his “mRNA vaccine” was administered to him. (Now, THIS explains why Dr. Robert Malone says what he says). I would have felt sorry for him if not for horror I feel every time I recall that the US hospital has forced Dr. Robert Malone’s experimental genetic drug on my son — every time I see how people, “vaccinated” by Dr. Robert Malone, get convulsions when they drive, or when tennis stars, vaccinated by Dr. Robert Malone, are shattered from chest pain right during the tournament.

Dr Robert Malone’s interview with Joe Rogan is now the #1 podcast episode in America. The only thing I do not understand is: why Dr. Robert Malone calls himself “the inventor of mRNA vaccines”, and why, in all his interviews, he conceals that he invented, instead, the “gene therapy” technology, which is alike CRISPR/CAS9, and is nothing else, but the gene silencing and sterilization method, which ruins the Wave Optics in chromosomes and makes humans into GMOs (genetically modified organisms) or “transhumans” who will not be able to have children?

For example, in one of his most recent interviews, he denied that mRNA “vaccine” gets into nucleus, though it is already proven by the peer-reviewed journal on biology. Here is this very important recent article “SARS-CoV-2 Spike Impairs DNA Damage Repair and Inhibits V(D)J Recombination In Vitro” – PubMed, proving that SARS-CoV-2, indeed, PENETRATES into nucleus, and, indeed, changes human DNA, what is denied by criminals in Russian and American State National Health Institutions:

https://pubmed.ncbi.nlm.nih.gov/34696485/

My question to Dr. Robert Malone: do you, Dr. Robert Malone, seek to escape the coming criminal prosecution at the Nuremberg Trials #2 for your crime against humanity, which consists in the deliberate creation of the binary biological weapon for the sterilization of humanity, and, thus, committing the most horrific genocide of making humankind extinct?

Here are some thoughts of mine on Dr. Robert Malone’s Podcast Number One in the US.

The action of mRNA vaccines consists, besides other things, in inducing microRNAs for gene silencing. This is their TRUE meaning.

MicroRNA (micronome) interaction with the messenger RNA for gene silencing is how the Effect of the Destructive RNA Interference manifests itself. Hence, Dr. Robert Malone lies to the public concealing he has invented the effective mechanism of gene silencing. In this sense, Dr. Robert Malone is a bigger criminal than Tony Faux-chi.

Andrew Fire and Craig Mello received a Noble Prize in 2006 for the discovery of the Effect of the Destructive RNA Interference. They took RNA from a c.elegans worm, and gave it back to the worm, and the worm died.

The miRNA interaction with mRNA is based on complementarity of nucleotides. And since all proteins in SARS-CoV-2 are homologous to human proteins except for one, both the SARS-CoV-2 as the binary biological weapon by Dr. Ralph S. Baric and mRNA “vaccine” by Innovio’s Dr. Robert Malone are inducing the effective gene silencing.

Dr. Robert Malone is grossly mistaken on almost everything he reveals to the public. Again, he said that the SARS-CoV-2 and his “vaccine” does NOT enter the nucleus with the DNA packed in the nucleus, and, he said, does not downgrade the DNA transcription. At the moment he said this there was already a paper published in the peer-reviewed journal which has proven that both Dr. Baric’s SARS-CoV-2 and Dr. Malone’s gene-silencing drug aka “mRNA vaccine” do indeed enter the nucleus and effect the DNA replication and repair.

Also, Dr. Malone is unprofessionally mistaken on the safety of the adenovirus-vector “vaccines”.

The two clinical trials of the adenovirus-vector vaccine against HIV had demonstrated that if a patient has the prior immunity to adenovirus, the adenovirus-vector vaccine infects the patient with HIV instead of giving him immunity against HIV. That is why the adenovirus-vector based HIV “vaccines” technology was abandoned. Since Dr. Baric’s DURC SARS-CoV-2 is a mutated HIV, it is clear that Great Britain and Russia, which use this technology, are effectively infecting their population en masse with HIV, because the adenovirus is a very wide spread infection, and the adenovirus immunity is almost universal.

Hence, Dr. Robert Malone’s fixation on S-protein is either his criminal conspiracy or professional impotence of the deliberate or unprofessional attempt to hide the fact that the real result of his experimental genetic drug is gene silencing, which is the true reason for organ failures.

Dr. Robert Malone tries to conceal the devastating Effect of the Destructive RNA Interference by appealing to the peristalsis of the blood vessels caused by S-protein. So, we can define the pseudo-Samaritan public appearances of Dr. Malone as the criminal attempt to conceal the crucial scientific evidence from the humanity.

“Clamping down on blood vessels” is the best Dr. Malone can do in explaining organ failures.

Dr. Malone explains the risk of the brain fog, and prion disease in the “long Covid” cases also by the blood vessels clamping, again, hiding the real reason — the gene silencing by the miRNA Destructive Interference.

The entire public discussion of whether the SARS-CoV-2 was isolated or not, or whether S-protein is a toxin or not is meant to conceal the crime of the global gene silencing committed by Pentagon and DARPA officers anticipating to buck-in big time on the implantable Digital currency which will be based upon the programmable gene silencing, i.e., the AI protocols for the Global Gene Silencing with genes being turned-on or silenced by the long-range wireless and NFC networks and smart dust.

The same way Dr. Malone had erroneously denied that SARS-CoV-2 and his experimental gene-silencing drug aka “mRNA vaccine” goes into the nucleus (via reverse transcriptase), Dr. Malone denies that his genetic drug goes into ovaries causing sterilization. He argues that only the liposome envelope “goes” into ovaries causing harm.

In the same line, Dr. Malone explains the “Denmark data” on the Omicron infection and COVID in the fully vaccinated by the “risky behavior”. To conclude, we can characterize Dr. Malone’s “US number One podcast” as a gross psyop.

PS In his Joe Rogan’s interview, Dr. Robert Malone has also said that the “mRNA vaccine” of his concoction causes hallucinations in the “vaccinated” victims. I hope we will not be forced to contemplate how Dr. Robert Malone will be hallucinating.

ON THE CRIMINAL NATURE OF THE CRISPR/Cas9 “GENE EDITING” OR JENNIFER WITH A GENETICALLY COMPROMISED BRAIN AND GEORGE WITH A PIG’S HEART

As we say in Russia: to break is not to create.

My question is: snakes use poison to kill their enemies. A simple question is: can a human incorporate inside his body a snake’s poison to fight his viruses and bacteria? The answer is: EVIDENTLY NOT. Streptococcus pyogenes uses its own poison (so-called CAS9) to cut viruses in pieces and “kill” them. So, another simple question is: can a human incorporate inside his body a CAS9 protein in order to satisfy Jennifer Doudna and to successfully fight his viruses? The answer is: EVIDENTLY NOT. CAS9 is simply a very dangerous TOXIN, specific for Streptococcus pyogenes. And calling the very pathogenic bacteria Streptococcus pyogenes with a fancy word ‘CAS9’ does not change the matter at hand.

CAS9 used the way Jennifer Doudna offered is a biological weapon for silencing genes, and also with a high percentage of missing the mark. The third simple question is: does bacteria Streptococcus pyogenes itself use its toxin CAS9 to self-engineer itself genetically? The answer is also: NO. Bacterial-viral mosaicism (verbosely called by Jennifer Doudna as “Clustered regularly-interspaced short polindromic repeats” [CRISPR] evidently to obscure the matter) does not change functionality of Streptococcus pyogenes’ genome, and Streptococcus pyogenes does NOT produce a virus which it is killing with its CAS9 toxin.

ERGO: Streptococcus pyogenes is homogenous with CAS9, since CAS9 is its own component. But humans are evidently not the Streptococcus pyogenes, and CAS9 is NOT a human inherent component. The idea to apply the highly pathogenic Streptococcus pyogenes to “genetically enhance humans” could have come only to a sociopath… or to a criminal. It is the same as to say: “OK, pals, we are going to use the bacteria of Tuberculosis to “genetically enhance humans”, since the toxins of this bacterium will surely damage the human DNA!”

Criminal negligence demonstrated by Jennifer Doudna reminds me of George Church with his “xenotransplantation” of pig’s organs into humans. Looks like Dr. George Church is completely unaware of the structural difference between humans and pigs. And this was even before taking Dr. Robert Malone’s hallucinogenic jab. We can only guess what hallucinogenic heights will be taken on by Dr. George Church now, after the pig’s jab… It is I think also a psychiatric case that Dr. George Church cannot tell pigs from people. I only wish Jennifer Doudna eats only GMO, and all her own treatments are CRISPR/Cas9, while George Church will sooner or later receive pig’s heart! They deserve this, for sure!

CONCLUSION: PIGS OUT OF FOCUS

The main problem with genetic modification (including through vaccines) is not genetic discrimination. The main problem is that genetically modified organisms are sterile. That is, genetic modification is a sterilization mechanism.

Thus, Robert Malone, Jennifer Doudna and George Church are CRIMINALS. There can be no second opinion on this. All three of them are completely identical to criminals in the 15th century Europe who, during the Great Black Plague, were throwing the infected clothes into the water wells. Also, all three of them demonstrate complete lunacy, because they are throwing the infected clothes into the water wells, while yelling loud that they benefit humanity in this way.

Jennifer Doudna said that this is not the genetic modification, if she uses client’s own genetic material for the modification. She does not evidently know of the Effect of the Destructive RNA Interference (Noble Prize 2006). Again, Andrew Fire and Craig Mello took RNA from the c.elegans worm, and gave it back to the worm. And the worm died. This happened because any genetic modification (via addiing or subtracting) destroys the precisely calibrated Wave Optics in Chromosomes (© Dr. Irene Caesar 1985-2014).

George Church does not see any problem in introducing animal proteins directly into human blood stream. He does not evidently know of the Translational Spatial Symmetry Principle, which is the cause for the prion disease – infective proteins with the destroyed crystalline structure, i.e., with the structural damage, which cause the extreme case of encephalopathy (“mad cow disease” or “mad man disease”). Also, he is not aware of the Holographic Principle, which states that the whole is entirely in its every part. According to the Holographic Principle, human liver or human heart will be structurally different on the molecular (chromosomal), atomic, and subatomic levels from a pig’s liver and pig’s heart. If pig’s chromosomes have less structural coherence than human chromosomes, then, the introduction of pig’s genetic material straight into human blood stream will cause the degradation of structural coherence in human chromosomes, on the way to the prion disease. Indeed, the same gene gets expressed in the functional species and individuals by the metacentric chromosome, which is analogous to a well-centered and well-focused eye crystal. And the same gene gets expressed in the dysfunctional species and individuals by the acrocentric chromosome, which is analogous to a farsighted or a nearsighted eye, out of focus. For example, the same gene gets expressed in an ape via the acrocentric chromosome, and in a man via the metacentric chromosome. But George Church is unaware of this. Maybe, he is already structurally and intellectually on the level of an ape or a pig.

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

14 Wednesday Jul 2021

Posted by Irene Caesar, Ph.D. / Ирина Цезарь, Доктор Философских Наук in NEGROID BLOODLINE OF THE QUEEN OF ENGLAND

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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.


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.

DR. IRENE CAESAR – “REMOTE BIOHOLOGRAPHY FOR RESTORING THE WAVE OPTICS OF CHROMOSOMES DAMAGED BY SARS-COV-2-CAUSED AUTOIMMUNITY”, SPEECH AT BIOST 2021

26 Saturday Jun 2021

Posted by Irene Caesar, Ph.D. / Ирина Цезарь, Доктор Философских Наук in NEGROID BLOODLINE OF THE QUEEN OF ENGLAND

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autoimmunity, bioholography, chromosome refraction code, COVID-19, irene caesar, mRNA vaccine, mRNA vaccine prion disease, prion disease, remote bioholography, SARS-CoV-2, sterilization, wave genome, wave optics of chromosomes

I gave a keynote speech at the plenary session at the World Biological Science and Technology Conference 2021, August 25 2021. The Honorary Chairperson is Prof. Mary Elizabeth Anne Sunday, Duke University, USA.

The other two speakers, who gave Keynote Speeches at the Plenary Forum, were Dr. Hiroshi Kida, Hokkaido University, Japan, and Dr. Bo Liang, IVIEW Therapeutics, Inc., USA. In my speech, I have explained why the mRNA “vaccines” and mRNA “boosters” will cause the Effect of the Destructive RNA Interference with the resultant AIDS, and, finally, the prion disease (“Mad Man Disease”). The next day after my speech, Japan suspended 1.63 million doses of the Moderna mRNA vaccine.

Other renowned speakers are Prof. Robin Ketteler, University College, London, UK; Prof. Hiroshi Kida, Hokkaido University, Japan; Prof. Jingjun Hong, University of Science and Technology of China, China; Dr. Maliha Zahid, University of Pittsburgh School of Medicine, USA; Prof. Pranela Rameshwar, Rutgers New Jersey Medical School, USA; Prof. Rajendra Badgaiyan, University of Minnesota, USA; Prof. Stephane Dedieu, University of Reims Champagne-Ardenne, France; Prof. Glenda M. Davidson, Cape Peninsula University of Technology, South Africa; Dr. Julie Ledford, University of Arizona, USA; Dr. Wei Guo, University of Wisconsin-Madison, USA; Dr. Changning Wang, Massachusetts General Hospital, Harvard Medical School, USA; Prof. Suzana Yusup, University Teknologi Petronas, Malaysia; Asst. Prof. Dr. Emin Taner Elmas, Igdir University, Turkey.

https://www.biostvirtual.org

Title: «Remote Bioholography for Restoring the Wave Optics of Chromosomes damaged by the SARS-CoV-2-caused autoimmunity».

Dr. Irene Caesar, President, Wave Genome LLC

Abstract

All proteins in SARS-CoV-2 are homologous to human proteins, except for one, and, that is why, COVID-19 causes the Destructive RNA Interference, with the resultant autoimmunity and sterilization. Even more, COVID-19 mRNA vaccines are proven to cause the prion disease, when proteins lose their crystalline structure, acquiring a sponge-like shape, as the result of the structural damage in chromosomes. It is proven that SARS-CoV-2 is capable of inserting its genetic material into human DNA, so that SARS-CoV-2 is a chimerical virus with the gain of function – a retrovirus under the disguise of a coronavirus. The world is on the verge of the global health system collapse due to the impending global prion disease after the eight-year incubation period. Wave Genome LLC found a technological solution – the Remote Holographic Drug Delivery — for reversal of the structural damage in chromosomes, and, so, the reversal of the structural damage in proteins. Humans are water for 85%. But the Universe is energy for 93%, and particles for only 7%. So, humans are the liquid crystal media for 7%, and the wave crystal media for 93%. In order to restore the structural coherence in the liquid crystal media, we need, first, to restore the structural coherence in the wave crystal media. The notion of the wave crystal media or Wave Crystal (a crystal consisting of waves) was created by Dr. Irene Caesar in 1985, long before anybody in the field of Bioholography, in her fundamental theory of Wave Optics in Chromosomes. Wave Crystal is a Refractive Lens, built up by the coherent impulse wave fronts of the scalar nature, with the trigger-signal having its wave length equal to the size of the resonator. Chromosome as a Wave Crystal changes its bioinformation due to the change in its Refraction Mode towards one and only Zero Center / Focus, the same for chromosome and galaxy, so that DNA communication occur not through chemical or electro-chemical exchange between living cells, but via the Quantum Nonlocality, remotely and instantaneously. The same gene is expressed in the functional individuals by metacentric chromosome, and in dysfunctional individuals via acrocentric chromosome. Metacentric chromosome is analogous to a well-centered and focused eye crystal, while acrocentric chromosome is analogous to a myopic or farsighted eye. Wave Genome LLC, founded by Dr. Irene Caesar, was the first company in the world to develop Bioholography as the Remote Wave Optics based upon Refraction Codes in the scaled scalar wave diffraction grating, with Refraction Codes being the wave modulations of the scalar nature, as client’s unique and nonlocal Biohologram, immune system modulation Biohologram, stem cell modulation Biohologram, etc.

Biography

Irene Caesar, Ph.D., is the Founder and President of Wave Genome LLC, company who has pioneered Bioholography, producing Bioholograms for the remote management of biosystems in the form of electret applicators (Wave Genome LLC was the first company in the world to code electrets with client’s unique Bioholograms); bioelectronic devices; digital files; and software for the Holographic Drug Delivery for rejuvenation only (founded 2010); Co-founder of “Matrix City” Consortium with the Institute for National Security in Moscow for building self-sufficient human settlements based upon the remote management of biosystems, climate and geophysical processes for the first time in the history of humankind (founded 2012), presented in the Honorary Lecture at the Harriman Institute of the Columbia University in September 2012; Co-founder of the Quantum Biointernet for the remote rejuvenation via distant laser signal, commercially offered for the first time in the history of humankind by Irene Caesar’s company Wave Genome LLC in May 2013; Colonel of Irkutsk Cossack Military, awarded the Medal of Faith and Service to Russia (2014). Dr. Irene Caesar received her doctoral degree from the Graduate Center of the City University in New York.

Kind regards,
Irene Caesar, Ph.D.
President
Wave Genome LLC

Dr. Irene Caesar on danger of contracting AIDS through SARS-CoV-2 vaccination

13 Wednesday Jan 2021

Posted by Irene Caesar, Ph.D. / Ирина Цезарь, Доктор Философских Наук in NEGROID BLOODLINE OF THE QUEEN OF ENGLAND

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AIDS, airborne aids, airborne hiv, biohologram, bioholographic drug, bioholography, chimeric retrovirus, coronavirus, COVID-19, danger of vaccination, HIV, HIV inserts in SARS-CoV-2, irene caesar, moderna vaccine danger, mRNA, mRNA vaccine, pfizer vaccine danger, plandemic, pseudotyped retrovirus, retrovirus, SARS-CoV-2, scalar wave, socialist factor magazine, vaccination, wave genome, wave genome llc, wave optics, wave optics of chromosomes

Article by Dr. Irene Caesar for the large Indian glossy magazine “Socialist Factor” on the danger of contracting AIDS through SARS-CoV-2 vaccination.

Scientists at the Massachusetts Institute of Technology have discovered that SARS-CoV-2 can insert its genes into the human genome.

By Irene Caesar

January 5, 2021

Thus, it has been proven that SARS-CoV-2, presented as a vaccine into the bloodstream, will cause AIDS (autoimmunity) when the immune system attacks itself. These findings are in response to virologists who classify SARS-CoV-2 as a common coronavirus and not as a “pseudotyped (chimeric) retrovirus”.

Based on the classical classification of coronaviruses, they say that SARS-CoV-2 is not a retrovirus and cannot be incorporated into the human genome. But SARS-CoV-2 is called a “pseudotyped retrovirus” because HIV receptors have been incorporated into its surface spike protein receptors (S-protein).

This is exactly what the virologist is talking about in “The Bourne Legacy” 2012 movie. The virologist says: “The virus is a kind of suitcase that delivers the right genes to chromosomes.” “The Bourne Legacy” movie simply explains to the general public that the current so-called pandemic is not a pandemic per se, but an attempt to change the genetics of target nations, making them dysfunctional and sterile.

The insertion of HIV into the spikes (surface protein) of the coronavirus allowed the coronavirus (1) to cross the interspecies barrier between animals and humans; (2) make the coronavirus much more infectious (the surface protein hemaglutinin is also present in the influenza A virus derived from the Spanish Flu 1918 virus preserved by the Rockefellers); (3) make the coronavirus much more harmful.

Adding the four inserts of the HIV virus to the spikes of the coronavirus is exactly the “map” of the attachment of the virus receptors to the human receptors, which allows one to deliver, like a “suitcase”, harmful genes to destroy the genetics of an entire nation. This viral “suitcase” is called a “viral vector”.

Only products of my company Wave Genome LLC allow to restore Wave Optics in chromosomes in the case of autoimmune diseases. Please, read below.

All products by my company Wave Genome LLC work for restoring the Wave Optics of Chromosomes as proven for decades of usage, first, in the military hospitals, and, then, in the civilian hospitals. Price increases with effectiveness: the complexity / density of the scalar wave diffraction grating (the scalar wave interference grid) and the complexity of wave modulation. Wave Genome LLC provides the protocol for restoring the Wave Optics of Chromosomes in the case of vaccine damage.

DNA is a liquid crystal media, since we are 95% water. You can see on YouTube videos on how water gets structured by waves. Universe is 93% energy and only 7% particles. So, our DNA is the liquid crystal media for 7%; and our DNA is the wave crystal media for the 93%. That is why water is so responsive to the waves.

The same gene gets expressed in the functional species and individuals via the metacentric chromosome, which is analogous to the well-centered and well-focused eye. And the same very gene gets expressed in the dysfunctional species and individuals via the acrocentric chromosome, which is analogous to the farsighted or nearsighted eye out of focus.

Between cell division cycles, chromatin is not crystallized. During the cell division cycle, the chromatin gets literally crystallized, forming two chromatids, which, in turn, form a chromosome. The Geometical Wave Optics of the chromosome is the basis of the successful cell division.

Cancer and other degenerative processes are caused by the structural damage in chromosomes, that is, the destruction of chromosome’s shape — deletions, translocations, duplications, inversions, etc.

This structural damage of chromosome is in fact the destruction in coherence of the scalar wave diffraction grating in chromosome. Chromosome is a scalar wave during the cell division. Moreover, the DNA as such is a scalar wave: the first strain has its signal going in one way, and the second strain has its signal in the opposite way.

That is why DNA is inherently protected from mutations, since the scalar wave annuls any external linear signal, when the forward-wave is annulled by the trough of the same wave, when this wave is reflected back upon itself.

To the contrary, RNA is a one-strain induction coil spiral antenna, which receives and transmits linear external signal. RNA is renewed on the constant basis to provide that its Wave Optics corresponds to client’s Wave Optics of DNA.

If DNA has mutations as the result of the structural damage of chromosomes, only the scalar wave modulated by the unique Refraction Code of client’s Wave Optics of Chromosomes can restore client’s DNA to its initial state.

(© Dr. Irene Caesar, Founder & President of Wave Genome LLC).

Scientists at the Massachusetts Institute of Technology have discovered that SARS-CoV-2 can insert its genes into the human genome.

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

17 Sunday May 2020

Posted by Irene Caesar, Ph.D. / Ирина Цезарь, Доктор Философских Наук in NEGROID BLOODLINE OF THE QUEEN OF ENGLAND

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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 15th, 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

 


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 20th 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

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