The war on human genes, Cholesterol, LNPs and Covid genetically modifying injections, now also in the CRISPED patients.

Update 2/9/25: C15:0 (pentadecanoic acid) is a healthy and essential odd-chain saturated fatty acid, a ‘new’ healthy saturated fat for long-term metabolic, heart, immune, and liver health ,i.e. or healthy aging, for lowering cholesterol level, to be only in milk and its products, yogurt, butter => fight for healthy cows!:) ^18.

Update 9/27/2024:

USRTK FOIAs: Links File #1 (embeds)

Update 10/1/2024: Reminder, Mod-E-RNA and Pfizer covid injections contain CHOLESTEROL. Here some knowledge by Robertson and Burnett in experimenting with tumour-grafted rats, who showed that intravenous injections of cholesterol in sodium oleate cause the tumours in the injected animals to grow twice as fast as in the controls, all the rats having been grafted at the same time and with the same tumour (ROBERTSON, T. B. and BURNETT, T. C. “The influence of lecithin and cholesterin upon the growth of tumours.” Jour. Exper. Med., 1913, xvii, 344-352.)^17

---

With so many critical hot summer ‘24 events, drops in, drops out, official lack of proof for women identification (according to the Olympics organizer Thomas Bach), with contradictory news everywhere, maybe the few left out tired readers show some interest in that tiny, so sticky innocent, cholesterol..? THANK YOU for choosing this sub-stack, even after a very LONG pause, which now will be substituted with a long post;). Before anything else though, just want to remind everyone this speech, which was suppressed on every single MSM, a speech very similar to the one RFK Jr. gave few weeks before that Aug 2020, in Sacramento CA, a speech you won’t find anymore, anywhere, so lets go back at least to the Berlin 2020 speech:

If people had listened to it, or read the book ‘The Real Anthony Fauci‘ by RFK Jr., and took into their hearts all the contents, we wouldn’t be here, where we are today…

Some history first. Julian Huxley, British evolutionary biologist, eugenicist and director of the International Union for Conservation of Nature/Unesco(United Nations Educational, Scientific and Cultural Organization), aligned with Rockefeller Foundation, said in 1947:

‘we’ll be improving the genetic quality of the human population through selective breeding, the population has to be controlled and the unfit have to go’, which partly explains where we are today:

On July 22nd ‘24, an email send out by MIT Technology Review announces a Roundtable titled: “CRISPR Babies: Six years later“ with a short introduction, quote:

”Gene-editing can correct or improve the DNA of human embryos, essentially opening the door to ‘technological evolution’ of our species. But in 2018, a premature attempt to use gene-editing led to a prison term for the researcher involved.”

Where do the gene therapies stand today? There are many, many extremely rich people, who finance the Creators Overwrite, while changing and mixing up the genetic footprint of what was given to us by God, so let’s take the recent actor on the political scene, JD Vance. Thanks to the illegal gene therapies of the War(p) S(p)eed, the amount of ‘those in need’ (injured) raises with every day, and here is where some of Vance’s endeavors come in: “Kriya Announces Exclusive License and Collaboration Agreement with Everads to Advance Gene Therapies for Prevalent Diseases in Ophthalmology Including Geographic Atrophy“ and from its CEO quote: ”We are excited about the potential to advance a gene therapy that blocks both complement C3 and C5, which are validated biological targets for the treatment of geographic atrophy,” said Shankar Ramaswamy, M.D., Co-Founder and CEO of Kriya.” And no, geographic atrophy is not loosing weight depending on where you stand on the planet earth… And who is the gene specialist Shankar? A younger brother from Vivek, friend of JD Vance. Half a year after introduction of the illegally ‘approved’ genetically modifying covid injections:”Battelle (please remember that, or read Leonard G. Horowitz books), investors including J.D. Vance, launch gene therapy startup, AmplifyBio” (https://www.dispatch.com/story/business/2021/05/05/battelle-investors-including-j-d-vance-launch-gene-therapy-startup/4935970001/). What does the AmplifyBio do? The answer is in the title of this link, https://www.amplify-bio.com/amplifybio-and-rnav8-bio-announce-strategic-partnership-to-support-mrna-therapeutic-developers-from-sequence-design-to-gmp-manufacture/ . Two important quotes from it:

-”Together (AmplifyBio+RNAV8), this partnership creates a one-stop shop for mRNA sequence/chemistry engineering, in vitro performance screening, in vivo (diseased vs. healthy) model data generation, and mRNA production volumes ranging from micrograms to 100+ grams.”

-”Comprising a team of experts hailing from prominent backgrounds at Moderna, Pfizer, and Resilience, the company stands at the forefront of innovation in this field.”

Isn’t that a continuation of Warp Speed sickening the entire humanity? Check out this, to see the real truth of what happened in the last 4.5 years(!!!): https://www.brighteon.com/a5b31f9e-b523-4171-b875-1d795cbfbcbb

or this professional collection of major political facts, can equally help in understanding the bigger picture:

Resilience, the manufacturer of Mod-E-RNA shots was covered here:

All what one needs to know, are the CIA ties in all of it, extremely well covered in the mentioned RF Kennedy’s Jr. book, and also covered in this post:

How does the cholesterol fit into that GMO’s covid crime scene?

One would think, the so demonized cholesterol, the biggest enemy of all, not a protein, not a genetic material would escape all of the above. Since it is synthesized enzymatically by >20 enzymes in the liver (diet delivers ~20% of daily cholesterol needs), with each of them expressed by a GENE, it does not escape anything. Cholesterol as the most vital rigid membrane lipid of all (https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2013.00031/full), ~(25-30)% of which builds the dry mass of the brain, serves as precursor for sex hormones, for all fat soluble vitamins, Vit D including (this implying everything related to the immune defense of the human body), it is located in every single cell membrane, and all of it is genetically driven (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474947/). That does not even include all the genes involved in cholesterol transportation and degradation (https://www.pnas.org/doi/epdf/10.1073/pnas.96.20.11041). How to find all those involved genes??? By genetic screening of specific cells and later on targeted controlling and monitoring the levels of specific short length RNA types (https://www.cell.com/action/showPdf?pii=S1550-4131%2809%2900157-0). If you monitor RNA’s, because they imply, influence and result in genetic control, can those short internal HUMAN mRNA signals be affected by the CDC/FDA/Fauci et al. mandatory injected covid19 Spike synthetic mod mRNA? What will happen when you CHANGE these RNA’s? The entire information of the genetic control is a ‘reset’, a ‘great’ one indeed….

Cholesterol can do so much more. It binds to bacterial toxin’s via just single dipeptide Thr-Leu (TL) capable of lysing an entire cell, all described in article titled “Only two amino acids are essential for cytolytic toxin recognition of cholesterol at the membrane surface“ (https://www.pnas.org/doi/10.1073/pnas.0911581107 ). How many of the TL-dipeptides are embedded in the synthetic, patented Spike sequence? SIX, which makes the impression of Spike being a well designed cholesterol catcher, similar to the HIV-1 envelope glycoprotein precursor gp160, with equally SIX ‘TL’ dipeptides.

There is a link between heat shock proteins (HPSs) and cholesterol. HSPs affect folding of many other proteins in a temperature dependent manner affecting cancer, neurodegenerative, cardiovascular, and autoimmune diseases. Everyone has some antibodies to some of the HSPs, like to Hsp60, Hsp70, but we also have some antibodies to cholesterol (https://pubmed.ncbi.nlm.nih.gov/15488946/). Strangely, during HIV-1 infection the Hsp70 and cholesterol antibodies go over the roof (https://pubmed.ncbi.nlm.nih.gov/15488946/). The same Hsp70 has a strong affinity towards negatively charged phosphatidyl serine lipids, but only on membranes of cancer cells, not the normal ones (https://www.nature.com/articles/s41598-023-46131-x). And all of it is cholesterol dependent. Despite of all of this, cholesterol is an ‘evil doer’, which the Global Center for Health (In?)Security at: https://www.unmc.edu/healthsecurity/transmission/2023/05/30/covid-19-can-cause-new-cholesterol-problems-what-to-know/

decided to connect with a ‘global warning style’ message, quote: “They found that unvaccinated people who had been infected with SARS-CoV-2 were significantly more likely to develop high cholesterol and other unhealthy levels of blood fats than people who had not been infected.“??? It almost sounds like the SARS-CoV-2 virus could be put on the McDonald’s menu list…

It is also the very first time, that ‘disease preventing injections’ of covid19 Pfizer and Mod-E-RNA genetically modifying concoctions, have cholesterol^3 on their ingredients list. The only other injecrtion material with cholesterol in it is Shingrix, which replaced Zostavax in Nov 2020 ( https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf)... So ‘somehow’ the new covid mod mRNA based injections now suppose to protect from high cholesterol, by not giving you covid19, while having the cholesterol in them..? Imagine the despair of those cardiologists who might need to end their statins prescriptions. And let’s not mention here EU’s established guidelines for statin drugs, which the Germans ‘HEaLth minister’ now intends to put on drugs list of 5 years old children. There is no mention that sugar consumption correlates with heart diseases more than cholesterol, that smoking chemicals (NOT nicotine though…) and high blood pressure does the same. Just insane, and evil.

Are there maybe other connections between the universally injected synthetic Spike genes embedded into a matrix of novel lipid-nanoparticles and cholesterol?? The Sep 2021^2 study, titled “Cholesterol Hinders the Passive Uptake of Amphiphilic Nanoparticles into Fluid Lipid Membranes“, stated: ”membrane cholesterol, at biologically relevant concentrations, hinders the molecular mechanism for passive NP penetration within fluid bilayers, resulting in a dramatic reduction in the amount of NP incorporated.”, where NP stands for synthetic engineered nanoparticles… Doesn’t it indicate, maybe, that the more cholesterol the better protection from nano’s? Thus, could we say, human body essential building block, cholesterol, is not so good for the gene therapies to work optimally because it functions as a stronger barrier against the nanos cell membrane penetration and thus gene delivery? At least this one is sure, cholesterol modulates the NPs abilities (https://www.nature.com/articles/s41565-023-01455-7) thus looking into ‘cholesterol business’ makes sense.

Let’s switch for a moment to N. Harraris’ way of thinking, so to make the universal illegal covid gene therapy more effective, let’s give the foreign non-human Spike genes, we’ll inject into everyone, some cholesterol, and take it away from the real humans… That’s absurd (!), yet countless scientific groups, claim that statin drugs, that usually block the cholesterol production in the liver, thus represent neurotoxins due to prevention of continuation of brain regeneration, were beneficial for ‘covid19’ disease! Just few examples, out of many: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233054/ and one more with only ‘in-hospital conditions’: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463212/ and one group with ‘yes but no’ strategy: https://www.nejm.org/doi/full/10.1056/NEJMoa2309995. Countless publications link covid19 with acetylcholine and its related enzymes and many confirm the protective role of choline (eggs as the no 1 source) during covid-19 disease (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532804/ or https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775685/), and yet, the statins, essential in affecting neurotransmission, are the everydays’ bread of ‘health care’ system, in particular in covid times... There are many health professionals who question ‘cholesterol hysteria’, among them is a danish researcher Uffe Ravnskov, who says ““The cholesterol campaign is the greatest medical scandal in modern time“. His lifelong work with lot of precious resources is summarized at http://www.ravnskov.nu/uffe/ and it only confirms what was just recently published by Dr. Mercola at: https://articles.mercola.com/sites/articles/archive/2023/05/27/just-say-no-to-statins.aspx

Linus Pauling was known for his unified theory of cardio-diseases in which vitamin C deficiency leads to body using cholesterol taking over the role of collagen, normally used to heal the blood vessels. There is another great resource going more in depth on the VitC/statins/cholesterol topic: https://jeffreydachmd.com/2016/12/linus-pauling-heart-disease-prevention-with-vitamin-c/ , and it describes the NIH role in this coverup… Little shorter version of the link between lipoprotein A and VitC, challenging the ‘cholesterol theories’ of heart diseases by Pauling, can be found at: https://www2.lbl.gov/Science-Articles/Archive/pauling-and-vitamin-c.html

Cholesterol suppose to be involved in prion disease while playing a role as cofactor in the conversion of the naturally present in brain prion protein (PrP) into its pathogenic form (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871914/). With that 2022 study, here comes a new solution, in 2024 (https://www.science.org/doi/10.1126/science.ado7082): “Brainwide silencing of prion protein by AAV-mediated delivery of an engineered compact epigenetic editor“ with the following quote:”This study represents the first demonstration of AAV-mediated delivery of an epigenetic editor that can programmably methylate DNA in the brain for durable, potent silencing of a target gene”. Further “When coupled to a prion protein–targeting zinc finger domain and delivered to the mouse brain through AAV, CHARM methylates the prion gene promoter and achieves up to 80% brainwide reduction in neuronal prion protein, far exceeding the minimal reduction required for therapeutic benefit.“ The CHARM stands for Coupled Histone tail for Autoinhibition Release of Methyltransferase, and AAV for Adeno-Associated Virus. While cutting and pasting the major DNA ‘editor’ histone H3, the science geniuses actually reduced only the NATURAL PrP protein without indicating the mental/emotional/ status of their experimental molestation object, the mouse… The ‘epigenetic editor’ is a new name, again, like covid ‘vaccines’, for GENE THERAPY…

Who has this key to GENETICALLY get rid of prions? BROAD Institute and MIT, the main players in covid genetically modifying injections, i.e. the ones, who contributed to the problem in the first place.

The many faces of cholesterol and the covid thrill do not end here, ~10 years ago chinese scientists found out that ivermectin binds to the Farnesoid X receptor (FXR) responsible for cholesterol homeostasis (https://www.nature.com/articles/ncomms2924). Ivermectin decreased serum glucose and cholesterol levels. And in 2023 the beloved Welcome Trust and Oxford Uni members determined that FXR controls the ACE2 transcription thus must have direct effect on SARS-CoV-2 infection (https://www.nature.com/articles/s41586-022-05594-0). What a cascade of events, ivermectin controls FXR, FXR controls ACE2, SARS-CoV-2 depends on them all, and now we got the metabolism-modulating drugs repurposed for COVID-19, like statins and metformin (https://www.nature.com/articles/s41392-023-01510-8), without ever mentioning the universal cure for it all, ivermectin:

Ivermectin for Parkinson's Disease - MS, Stroke, Chronic Pain, Anxiety, Depression, and Schizophrenia? Modulated through P2X4 Receptors

In the meantime we find that “Serious errors plague DNA tool that’s a workhorse of biology“ (https://www.nature.com/articles/d41586-024-02280-1) and everything else related to Gene Therapies applied without human consent, being dangerously redirected towards a new phenomenon, birds with no symptoms of coughing or sneezing, landing on cows, later on humans giving rise to the new covid-2.0: https://expose-news.com/2024/07/11/is-another-pandemic-is-being-orchestrated/. This time it is equally serious: BARDA gives Mod-E-RNA $176 million to support late-stage development for an mRNA-based influenza vaccine (https://investors.modernatx.com/news/news-details/2024/Moderna-Receives-Project-Award-through-BARDAs-Rapid-Response-Partnership-Vehicle-Consortium-to-Accelerate-Development-of-mRNA-based-Pandemic-Influenza-Vaccine/default.aspx), Nature article announces that EU bought already 700,000 doses of a flu vaccine manufactured by UK biotech CSL Seqirus, with the option to buy another 40 million (https://www.nature.com/articles/d41586-024-02237-4), and then there is that very questionable member of the birdflusummit who in a phone request for more information, shows, that she knows nothing about the bird flu: https://birdflusummit.com/ in Oct24. The old CSL news from 2022 which describe their product: https://newsroom.csl.com/2022-10-05-CSL-Announces-Positive-Preclinical-Data-for-Self-Amplifying-Messenger-RNA-sa-mRNA-Influenza-Vaccine-Candidates might point to the smiling Bill Gates face while talking about the next one… Is that what EU bought already, self amplifying mRNA? The covid19 story of the last 4.5 years indicated that the real issues started AFTER starting the applications of covid genetically modifying injections, and this time, it shall never end..? Just in case the science geniuses will come out with SELF-amplifying mRNA of Hemagglutinin (https://www.uniprot.org/uniprotkb/O92929/entry), which probably will be the mass murder, one has to look at its amino acid sequence and its conserved motif in HIV-1 and partly in SARS-COV-2 Spike. and what one can see is disturbing, to say the least:

Query  312  PLTIGECPKYVKSNRLVLATGLRNTPQRERRRKKRGLFG  350 O92929
            P+  G C  Y             N+P+R R    + +  
Sbjct  665  PIGAGICASYQTQT---------NSPRRARSVASQSIIA  694 <==Spike FURIN SITE
a Spike homolog fragment in H5N1 is ~150 residues long(!!):

Query  23   YHANNSTEQVDTIMEKNVTVTHAQDILERTHNGKLCDLNGVKPLILRDCSVAGWXLGNPM  82
            YH NN +      ME    V  + +          C    V    L D         N  
Sbjct  145  YHKNNKSW-----MESEFRVYSSANN---------CTFEYVSQPFLMDLEGKQGNFKNLR  190

Query  83   CDEFLNVPEWSYIVEKTSPAN---DLCYPGHFNDYEELKHLLSRIN--HFEKIQIIPKSS  137
               F N+  +  I  K +P N   DL  P  F+  E L  L   IN   F+ +  + +S 
Sbjct  191  EFVFKNIDGYFKIYSKHTPINLVRDL--PQGFSALEPLVDLPIGINITRFQTLLALHRSY  248

Query  138  WSNHDASSG--VSSACPYLGRSSFFRNVVWLIKKN  170
             +  D+SSG    +A  Y+G   + +   +L+K N
Sbjct  249  LTPGDSSSGWTAGAAAYYVG---YLQPRTFLLKYN  280
and BLAST won't do it, again, so with no shifts, by hand, the fragment binding fats, like in the Spike, the cluster of cysteines at its C-terminal, every one conserved: 
GLSLWM---CSNGSLQ-CRICIYFCEF <= H5N1
 LCC-MTSCCS--CLKGCCSCGSCCKF <= SARS-CoV-2 Spike

all these similarities are extremely worrisome, given that SARS-CoV-2 is positively stranded RNA corona-virus, and H5N1 negatively…. What’s the implication of that???

BUT the last homology indicates at least this one (https://pubmed.ncbi.nlm.nih.gov/35336938/): “Identification of SARS-CoV-2 Spike Palmitoylation Inhibitors That Results in Release of Attenuated Virus with Reduced Infectivity“, that the saturated fat palmitate is a good start, the best possible the ascorbyl palmitate version, supporting the cell membranes with the fat soluble Vit C….

With the consequences of the past not even digested properly yet, VAERS system (https://www.medalerts.org/vaersdb/index.php) reports only 2 cases of prion disease after covid injections, one of then was fatal. Due to multiple names for one and the same or related disease (deceptive strategy) there are also ‘93 cases where Vaccine is COVID19 or COVID19-2 and Symptom is Creutzfeldt-Jakob disease’, 53 of which were fatal!!! That’s >50% fatality rate. This post below summarizes the cause of the covid crime related to just one of the diseases the gene therapies cause, but it does not mention that there is already a solution for the problem, by the same players, which indicates, that everything around covid injections is and was a PLAN, a PREMEDITATED MURDER.

UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases

Once again, both Pfizer and Mod-E-RNA covid19 gene based injection materials contain cholesterol in their LNP composition^3..*

A 2018 study (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984996/) titled “The Chemical Potential of Plasma Membrane Cholesterol: Implications for Cell Biology“ measured for the first time the chemical potential of the membrane bound cholesterol and related its increased chemical potential to the activation of transcription factor STAT3. This very same factor affects the pathogenesis of covid19, according to https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937040/, https://pubmed.ncbi.nlm.nih.gov/34626364/ and many more. The 2020 article at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545020/, indicates that STAT3 phosphorylation of one of its serines is the cause of the covid-19 pathogenicity (https://www.nature.com/articles/s41598-023-46628-5). What else the STAT3 gene is involved with? It is activated by a member of a large family of phosphatidylserine (PS)-dependent kinases (https://pubmed.ncbi.nlm.nih.gov/17583567/), which also contribute to many cancer types, among other skin cancers..

When we talk SARS-CoV-2, we need to keep an eye on HIV-1 too, alone due to the repeatable character of the ‘covid19 infections’. So, generally, is HIV-1 involved in cholesterol issues? Yes, it is, NIH admits it at: https://hivinfo.nih.gov/understanding-hiv/fact-sheets/hiv-and-high-cholesterol. Is STAT3 involved in HIV-1? Yes, it is, here a AAAS report at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514100/ titled “Insertional activation of STAT3 and LCK by HIV-1 proviruses in T cell lymphomas“. How about Monkeypox, any cholesterol connection? Yes, there is, just one example at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10751291/. And Influenza, the most recent crystal ball prepared like covid19, by BARDA et al.? Also here, yes, there is, described in 2022 for example at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513517/ and titled “Modulating cholesterol-rich lipid rafts to disrupt influenza A virus infection“.

Oh, actually, just recently, the autopilot changed the direction, WHO decided to choose the Monkeypox as the next threat, again..

So why all these viral infections are so cholesterol dependent? Because many types of both DNA and RNA viruses have their GENETIC material protected by LIPID bilayers which have to fuse with human cells, thus interact with human cell membranes, which contain the essential cholesterol, which in turn regulates fluidity, dielectric properties, permeability, i.e. function of the natural human cellular borders. The average cell membrane contains 10-30% of cholesterol, the membranes within the cell (endoplasmic reticulum, Golgi apparatus, and mitochondria membranes) have less cholesterol, i.e. <10%, that’s in order to facilitate cholesterol sensing and homeostatic feedback.. The cell types with high cholesterol level of ~50% are red blood cells and the myelin membranes of Schwann cells isolating nerve axons, in which the ratio of cholesterol/phospholipids (PL) is >1. The highest level of Cholesterol is in eye lens (that’s why its UV spectrum is important), >50%. At ~66% of cholesterol content, crystals form, which can be seen in old individuals and in atherosclerotic arteries. The higher the cholesterol level in the membrane, the higher its hydrophobicity and rigidity ( https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645210/ ) and thus higher protection from synthetic lethal nanos.

One of the first known extremely cholesterol-lowering dipeptides was the in 2015 described simple Phenylalanine-Proline (FP in single amino acid code) (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469013/). How many of those dipeptides are in the Spike sequence encoded by the synthetic genes injected into billions? FOUR ‘FP’ cholesterol lowering dipeptides are being build from single amino acids phenylalanine (F) and proline (P) for the production of every single toxic patented Spike. It is almost as if the universally injected Spike production on its own supports the synthetic statins, once the Spike gets degraded back into those peptides.

STAT3 has a huge list of functions (https://www.uniprot.org/uniprotkb/P40763/entry), including synaptic plasticity and cognition, thus was found to be involved in Alzheimers (https://pubmed.ncbi.nlm.nih.gov/33859760/ , https://pubmed.ncbi.nlm.nih.gov/30617153/). When a mouse is missing one of the isoforms of STAT3 and apolipoprotein E, it ends up with an enhanced atherosclerotic plaque formation (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771242/). Further the ApoE protein transporting lipids in plasma and interstitial fluid, together with few other factors is also deeply involved in Alzheimers, and in the so called exotic ‘episotic memory’ issue. One of the best known experts on Alzheimers, Dr Rudolph E Tanzi (Harvard) worked for decades on genetics involved in that brain disorders. The following publications (available at https://scholar.google.com/citations?user=2Qlrv_cAAAAJ) by Rudolph E Tanzi point to the ‘other factors’ accompanying ApoE in episodic memory:

-Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory. S Barral, T Bird, A Goate, MR Farlow, R Diaz-Arrastia, DA Bennett, Neurology 78 (19), 1464-1471 also

-Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes G Jun, AC Naj, GW Beecham, LS Wang, J Buros, PJ Gallins, JD Buxbaum. Archives of neurology 67 (12), 1473-1484. 2010

Is covid19 involved in any of those APOE ‘episodic memory’ involved genes?? Here a small list of the studies and where they are located:

-”Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family”(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014500/)

-”ApoE4 associated with severe COVID-19 outcomes via downregulation of ACE2 and imbalanced RAS pathway” (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910247/)

-”APOE interacts with ACE2 inhibiting SARS-CoV-2 cellular entry and inflammation in COVID-19 patients” (https://www.nature.com/articles/s41392-022-01118-4)

-CLU→”Serum Clusterin Concentration and Its Glycosylation Changes as Potential New Diagnostic Markers of SARS-CoV-2 Infection and Recovery Process”(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11049940/)

-PCALM→”Paradoxical relationship between proton pump inhibitors and COVID-19: A systematic review and meta-analysis” (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058681/)

-BIN1→”BIN1 rs744373 SNP and COVID-19 mortality” (https://pubmed.ncbi.nlm.nih.gov/33521641/ )

If all the genes related to Alzheimers (oh, FDA blocked the ApoE4 genetic tests for early Alzheimers detection, because it was not a drug, how strange, and covid19 PCR tests are?) were investigated by Dr. Rudolph E Tanzi, and now they all also relate to the first universal gene therapy in form of covid19 injections, will there be a continuation of the scientific work by Dr. Tanzi? He connected Alzheimers with cholesterol and plaque buildup, he works in the same place where Dr. Rochelle Walensky does, and he does not mention in a single article among others the Alzheimers MERCURY or the ALUMINUM connection, but hey, he just published:

Gene therapy for CNS disorders: modalities, delivery and translational challenges. J Gao, S Gunasekar, Z Xia, K Shalin, C Jiang, H Chen, D Lee, S Lee. Nature Reviews Neuroscience, 1-20, 2024.

And will this plan fix the covid19 related episodic memories, lets be honest, most probably caused in part by the universal covid19 gene therapy injection and its shedding, also called ‘long covid19’? The german Dr. Tillenburg has the same opinion (https://report24.news/dr-tillenburg-long-covid-nur-ein-versuch-von-nebenwirkungen-der-impfung-abzulenken/). Just 2 reports on the memory issues during covid19 infection:

-”Episodic long-term memory in post-infectious SARS-CoV-2 patients.”(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598275/)

-”Rapid vigilance and episodic memory decrements in COVID-19 survivors”(https://pubmed.ncbi.nlm.nih.gov/35128398/)

Well, time will tell if the episodic memories, like ‘what did I want here?’, ‘where did I put it again?’, ‘is it mine or..?’, ‘where am I?” will disappear, even in case of the so fall prone Joe... The above could explain Biden’s bizarre 'freezing' episodes, Fauci’s et al. sudden memory loss in all the hearings, all in regard to details of covid19 operation. As a side note, was it a coincidence that the only two, so famous US presidential covid injected candidates, one of which isn’t any more, didn’t want the 3rd legitimate candidate, RFK in their debate?? Please, judge for yourself the quality of the answers to the same questions, by RFK, Jr.:

https://x.com/RobertKennedyJr/status/1806462171892895808

The mentioned APOE protein exists in few forms in human bodies which differ by just few amino acids, yet they play an essential role in specific diseases. That’s what official world data base on proteins states about one out of the three isoforms:”Thus APOE*4 gene dose is a major risk factor for late onset AD (Alzheimer Disease) and, in these families, homozygosity for APOE*4 was virtually sufficient to cause AD by age 80. The mechanism by which APOE*4 participates in pathogenesis is not known” (https://www.uniprot.org/uniprotkb/P02649/entry). What are the differences between APOE-4 and APOE-2? According to Prof. Boyd Haley (https://emeramed.com/boyd-haley-phd-curriculum-vitae/) people with APOE-2 isoform never have AD and the only difference between the two are cysteines in APOE-2 replaced with two arginines in APOE-4. The cysteines in APOE-2 are known to bind mercury (Hg), while arginines can’t. Prof. Haley was not able to get any NIH grants which would allow him investigating the mercury involvement in the Alzheimer disease while looking into this APOE-2,4 issue. The official explanation for that was always dodged. In the meantime EU team of scientist publishes “Mercury Ion Binding to Apolipoprotein E Variants ApoE2, ApoE3, and ApoE4: Similar Binding Affinities but Different Structure Induction Effects“ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404194/) and say quote “Hg(II) ions bind all three ApoE variants with approximately the same binding affinity, around 4–5 μM. This indicates similar binding sites with similar binding ligands in all protein variants.“ Thus no mercury involvement in Alzheimer, in contrary to what Prof Haley says for years! What does the EU team is using in order to determine whether Hg binds or not? Fluorescence and CD spectra, both sensitive only to global structural changes, nothing with absorption of heavy metal. So while the difference in isoforms is only Cys→Arg exchange in 2 positions, which the study says do not bind the Hg in both forms, instead histidine, still the question is why only the cysteine containing isoform is free of AD, exactly the isoform which contains cysteines? The histidines binding the Hg are both on the same positions in the pro-AD and non-AD patients, thus all this in fact indicates, Hg is not involved in AD… How clever. Also a new phenomenon is being introduced here namely, quote: ‘the differences in structure induction’ between the three ApoE variants might conceivably be connected to the APOE-ε4 gene being a risk factor in mercury intoxication… That’s a 2022 publication, where NOTHING in science makes sense any more. Equivalent to saying a 16-24 piece of DNA can detect infection caused by a virus consisting of 30,000 other pieces and that only in one of its components, because the PCR method doesn’t detect the lipids, proteins, metals, the water, all in a virus, normally!

It is literally a shame to be a ‘life sciences’ scientist, in particular in med-I-cin-e, ever since 2020….

Myeloperoxidase (https://www.uniprot.org/uniprotkb/P05164/entry) can influence the oxidation status of the LDL’s and it is equally capable of loosing its binding partner iron (Fe) to mercury (Hg). It was known for a long time, that oxidation of fats, lipids is influenced by chelating agents: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC345326/pdf/pnas00613-0283.pdf and that this process involves immune system (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC304787/) and it is connected with the earliest well-defined lesion in atherogenesis.

The war on cholesterol goes even into the chicken and eggs business, putting the cholin, the dietary cholesterol supply, in danger. It is thus not only because of the potential H5N1:

One Flew over the Chickens' Nest

Cholesterol structure in comparison of what Mod-E-RNA or Pfizer throw into their formulas looks following:

Please look above at the cholesterol and now at the testosterone and estrogen below:

and now at the pathway of testosterone production, from cholesterol (!)_

remember the direction of these arrows, meaning, the amount of testosterone is cholesterol dependent(!). Further down the line there is also DHEA and thyroid hormones, everything about human energy. And below just to throw in, how hydrogenated fats look like, in comparison with cholesterol (https://en.wikipedia.org/wiki/Fat_hydrogenation):

Cholesterol’s UV spectrum, ‘proceeds’ DNA/RNA/proteins in its wavelength absorption:

That above spectrum alone allows one to imagine a cellular cholesterol fortress surrounding all the essential building blocks of every cell and guiding those extremely energetic photons towards other pi-converting, properly positioned cell compounds, with the healthiest cells emitting the least amount of biophotons all the way down around (350-360)nm….

Over the years the officially ‘recognized as good’ cholesterol levels went from 280 or less, as normal, to 250, then to 220, now in 2024 the ‘new normal’ is ~200mg/dl, and according to some real sick fanatics, it should be even much less than that.. How about zero..? Since function of human livers didn’t change in those years, at least theoretically, sizes of human brains didn’t change/shrink, hopefully, there is a reason why these new cholesterol limit values are becoming constantly lower, and lower, and lower… This page https://www.ahajournals.org/doi/pdf/10.1161/CIR.0000000000000624 lists the names of MD’s, who made these guidelines and which drugs/statin manufacturers, among others Merck and Pfizer, possibly affected ‘their opinion’….

Statin drugs are not only neurotoxins but on top of it antibiotics (Dr. Thomas Lewis lecture, Harvard), which like glyphosate kill only special bacteria^1 leaving sometimes in peace the really bad ones, like the endotoxin producing strains, or diminishing the good Lacto and Bifido species. Also according to Dr. Lewis, the no 1 condition leading to mortality due to low cholesterol are the s.c. mood disorders ending in ‘violent deaths’, suicides.. In addition, the underlying infections in Alzheimers, are frequently connected to the presence of certain pathogens, 3 in particular: Herpes virus, Chlamydia Pneumonia and Spiroki. Judith Miklossy in her 2016 study at https://pubmed.ncbi.nlm.nih.gov/27314530/ titled “Bacterial Amyloid and DNA are Important Constituents of Senile Plaques: Further Evidence of the Spirochetal and Biofilm Nature of Senile Plaques“ points actually to the disease caused by presence of foreign DNA in human brain. That’s what happened in 1944 when Avery, MacLeod and McCarty, Rockefellers fellows, discovered how to transform a mixture of 2 types of pneumonia bacteria, one living type and one dead type, into just one type. All what was needed was to add the gene from the dead bacteria into the culture of the living ones, in order to transfer the living type into the dead type. Shocking but true, and T. Avery went unnoticed in the history for his discovery. Isaac Asimovs book ‘The Genetic Code’ describes these historical facts of molecular biology/genetics. ‘So what are the covid Mod-E-RNA and Pfizer shots again??? FOREIGN Genetic material containing TRANSLATION, affected by TRANSFORMATION information. The question is, transformation of humans into WHAT??? Genetic aspect of living nature is grounded on every specie having its own ‘footprint’, if left untouched, that footprint prevails, changing its appearance depending on the environment, but mixing different footprints of different species, that’s where eugenics comes in.

It is unfortunate that Alzheimers’ research money is favoring mainly plaque/amyloids related reasoning (being only diagnostic markers of the AD disease) leaving out some of the true actors on the AD scene, to comedians:

It is only little bit unsettling to hear from MIT researchers (again..) about their cell’s study^4 in which they report cholesterol-metabolising bacteria from Oscillibacter species, which encode the conserved cholesterol-metabolizing enzymes, lowering its levels and thus linking its absence with Cardio Vascular Disease. Bugs, good for the heart but what about the brain??? Maybe no more needed, and Elons chips instead??

So we know statin drugs lower VitK2 amounts, lower Testosterone, increase risk of type 2 diabetes, lower CoQ10, raise liver enzymes, lower the energy level, lower DHEA, worsen memory, increase shingle risk and also increase risk of erectile dysfunction, and since so many people are ‘on them’ while in the same time immense number of people have cardiovascular issues, now comes a solution^5: “How Gene Editing Could Help Solve the Problem of Poor Cholesterol“! Who owns the best-seller called lipitor? Pfizer. In the meantime all the good news about statins and covid19 were crashed by this short summary with 18 supporting citations: https://www.bmj.com/content/368/bmj.m1182/rr-21. It’s final sentence:”There are therefore good reasons to stop statin treatment of patients with severe Covid-9 infection, also because at least 20 statin trials have been unable to lower mortality with statistical significance (7) and because more than 20% of statin-treated people suffer from serious side effects (6,7).” Science is never settled, that’s for sure.

Despite of the huge statin dilemma, fraud actually, New Zealand got its first ‘edited’ patient^6 in 2022, a case reported in article titled “Edits to a cholesterol gene could stop the biggest killer on earth“!! A killer which is essential for brain survival, for every single cell in the body? Who is behind it? US biotechnology company Verve Therapeutics, which injected a version of the gene-editing tool CRISPR in order to modify a single letter of DNA in the patient’s liver cells. Sekar Kathiresan, is the geneticist who started Verve three years ago and is the company’s CEO, the same who worked at Broad Institute in Cambridge, Massachusetts, on heart issues… Verve’s plan is to test it on much more people. What the article says is, quote:
”One reason Verve’s base-editing technique is moving fast is that the technology is substantially similar to mRNA vaccines for covid-19. Just like the vaccines, the treatment consists of genetic instructions wrapped in a nanoparticle, which ferries everything into a cell.” WHAT? The ‘gene editing’ of now real humans is substantially similar to covid 'injections???

Further the article states:

“While the vaccine instructs cells to make a component of the SARS-CoV-2 virus, the particles in Verve’s treatment carry RNA directions for a cell to assemble and aim a base-editing protein, which then modifies that cell’s copy of PCSK9, introducing the tiny mistake.  In experiments on monkeys, Verve found that the treatment lowered bad cholesterol by 60%. The effect has lasted more than a year in the animals and could well be permanent.” Sir, and what happened to the monkey and its brain??? Silence.

Apr ‘24 news at https://www.biopharmadive.com/news/verve-pcsk-liver-enzyme-pause-trial/711936/ announce:”Verve pauses base editing trial, shifts strategy after treatment side effect”.. Is there a single healthy human on this planet with less than half of the necessary cholesterol in brain? The problem with all these trials is one never hears back from the participants personally… Maybe because they are gone???? Also, who gives the money like the $267 millions to this guy Kathiresan, so that he can shrink the human brain by 60% without telling what is he going to replace it with….??? Let’s calm down..

One of the largest human plasma proteins Apolipoprotein B (https://www.uniprot.org/uniprotkb/P04114/entry), among its countless functions, processes cholesterol efflux, homeostasis, metabolic process and its transport. It was THE PROTEIN of interest when in 1987 Baylor College of Medicine in Houston discovered organ specific in-frame stop codon (https://www.jstor.org/stable/1700694) in its mRNA, responsible for two forms of APOB: APOB100 (in liver) and the shorter APOB48 isoform (small intestine). That first in 2001 (!!) discovered RNA ‘editing’ resulted from the DEAMINATION of C → U at nucleotide position 6666 (C 6666 ) in the APOB mRNA, which causes the change of a glutamine to a translational stop codon ^7. The APOB sequence can be also found at https://www.ncbi.nlm.nih.gov/nuccore/NM_000384.3 . Just wonder, that natural ‘editing’ won’t exist when U is replaced with the synthetic N1-methypseudouridine..? Many thanks to 2 very kind ANL scientists who gave me the copy of that article describing the first RNA editing at the position C6666 (!), related to cholesterol… That number, 6666 position in mRNA sequence, how unique it is, like the earth speed around the sun 66,616 mph, or the tilt axis on its orbit of 90-23.4=66.6 or even the DNA tilt in the Polymerase-beta, equally ~22 deg…, and like the triangle on Trump Tower with 6x6x6 trees along its each side. How unique!

It is indisputable, that many people were put on statin drugs in recent years^8, more than two times, since 2017. Here another source on it^10. Was it all on purpose??

How all the cholesterol issues and covid gene modifying injections are reflected in VAERS system?A search in an expert mode of the VAERS data at: https://www.medalerts.org/vaersdb/findfield.php

indicates, that there is NO LLT SYMPTOM entry for anything cholesterol related, except for cholestasis and its related liver injury. Searching for those 3 cholestasis ‘allowable entries’ gives 6 deaths among 37,647 deceased victims in total as of 5/31/2024 (that’s how long I’m working on this post…). A manual search for the keyword ‘statin’ of the first 20 VAERS reports pages reveals total of 22 dead covid injected patients who were on some kind of statin drugs.. Assuming this trend over the rest of the data base, and given that each page contains ~10 entries with 1 death accompanied by statin drugs on each page, that can be extrapolated to ~10%, at least, of all covid injected and deceased, who died while being ‘on statin’ drugs. If that extrapolation is true, seems like the papers relating covid19 with supporting statin drugs, should be clarified, supporting in which direction, survival or death??

Vaers lists 17 deaths related to Antiphospholipid syndrome(APS) and the antibodies against this lipid, among in total 1008 registered cases. Early on in covid injection campaign Sep ‘21 paper titled: “Pfizer–biontech COVID-19 RNA vaccination induces phosphatidylserine autoantibodies, cryoglobulinemia, and digital necrosis in a patient with pre-existing autoimmunity“ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486180/) pointed out that autoantibodies to one of the most important cancer markers, phosphatidylserine (https://www.mdpi.com/2072-6694/14/10/2536) are the cause of that APS syndrome!! The studied case described a progression of the s/c digital necrosis within ~1 month pictured below_

Why would human body generate antibodies against one of the essential compounds in it??? A similar case in terms of symptoms, from 2017 though (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518967/) indicated a huge dose of norepinephrine, with the same outcome. This 2021 study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396423/ talks about ‘Vasopressor-Induced Digital Ischemia’ with the same outcome (be aware, pictures are terrifying). With that, a help is on its way: https://www.nature.com/articles/d41586-024-02157-3 “Bionic leg moves like a natural limb — without conscious thought“… How much cruelty the medical cartels need to possess in order first to mutilate the human being and then having the audacity to offer a fix for it, all the time?

Back to the APS cases, related to covid injections and also to overdose of the neurotransmitters, is it the antibodies or vasopressin (Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH₂ ) or norepinephrine, all ending with the same ‘black legs’ outcome? How many Spikes are being produced per second in the human body after the Mod-E-RNA and Pfizer injections? Trillions. Is the below homology maybe responsible for the ‘overproduction’ of vasopressin-like peptides after the Spike digestion? Maybe, or just a coincidence….?

CYFQNC--PR-G  VASOPRESSIN
C FQ C  P  G  <<IDENTITIES !!!
CEFQFCNDPFLGV  SPIKE 2020

That CYSTEINE-X-X-X-X-CYSTEINE sequence motif in vasopressin CYFQNCPRG , where X stands for any amino acid, represents Faucis’ favorite Jesuits HIV cure patented peptide, with the motif CxxxxC!

That ‘digital’ phenomenon involving autoimmune reaction, points also to now an impossible application, “Targeting phosphatidylserine for Cancer therapy: prospects and challenges’ (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415799/)/. Even more disturbing digital necrosis pictures are presented in this ‘22 study at https://www.emjreviews.com/hematology/article/digital-necrosis-as-initial-manifestation-of-multiple-myeloma-an-unusual-case-report/ titled “Digital Necrosis as Initial Manifestation of Multiple Myeloma: An Unusual Case Report“.

No wonder this report ‘predicts’ the future, its title: “2024—First Year the US Expects More than 2M New Cases of Cancer“ at : https://www.cancer.org/research/acs-research-news/facts-and-figures-2024.html

Phosphatidylserine supplement is also used for improving memory and cognitive function and now it is related to possible autoimmune reactions!?

Just recently I met a 65+ female, who after ONE covid injection, got the same issue, but, only the right leg became completely black, from toes to the knee. While in hospital, she got the message, amputation. That’s where her ‘inner voice’ came through, as a Christian, and she decided to go home and heal herself with her plants. After ~4 years, that leg which was supposed to be amputated is still there, grey in color though, but in much lesser extend it was at the begin. And she walks perfectly fine! The question left: how a greyish looking human body actually work???

Another recent victim: Wojcicki with small cell lung cancer (SCLC), which is known to be stimulated by a small peptide called bombesin with a sequence ‘QRLGNQWAVGHLM’ . Is it partly present in the injected genes encoding the Spike? A BLAST comparison indicates a presence of few bombesin homolog pieces in Spike:

That all what BLAST finds:
Query  5      QRLGNQWAVGHLM  9 Bombesin
                  NQ AV
Sbjct  606    TNTSNQVAVLYQD 610 Spike

and that's what eyes can see, i.e found 'by hand', almost 100% identity:
Query  1     QRL-GNQW--AVGHLM  13 Bombesin
             Q++ +NQ+  A+G++
             QKLIANQFNSAIGKIQ    Spike
and few more with less homology:
Query  1     QRLGNQWA--VGHLM   Bombesin
             QDVVNQNAQALNTLVK  Spike
QUERY  1     Q--RLGNQW-AVG-HLM  Bombesin
             QSKRV--DFCGKGYHLM  SPIKE

Can the expression of trillions of the injected Spike genes (initiated by covid genetically modifying injections), after their digestion, deliver countless bombesin homologs, and this somehow trigger and contribute to that pathogenic cancerous condition??? You be the judge. Is it unusual to see NOW BNT116 tests of a new ‘miracle’ cure for the non-SCLC cancers, by the same criminals who invented BNT162B2: https://www.annalsofoncology.org/article/S0923-7534(22)03170-2/fulltext ???

To all of these tragedies, we got some unpractical facts, for example the good healthy oils, olive oil for example, is now double the price in comparison to pre-covid times.. According to the Dr. Daniel Amen, healthy fat diet leads to 42% smaller chance of getting Alzheimers, with healthy protein diet that values sinks to 21%, a simple carbohydrate diet with bread, pasta, potatoes, sugar leads to 400% increased risk of getting Alzheimers…

Is that why Broad / MIT was preparing the crimes for quite a while already while giving the path to the first CRISPED patients with ‘too much cholesterol’? Only because among others, according to the late Dr. Pauling, they do not have enough VitC??? Is that why all the MD’s in USA (governed by Rockerfellers et al.) are calling the same type of product once like ‘vaccines’ (in order to get enough patients to be eliminated/injured) and once like ‘gene therapy’ for apparently trying to repair the collateral damages? I’d almost dare to say, covid injections purpose was to make the takers immune to almost anything human…, and that MD’s these days’ ‘vaccinate’ in order to CRISP the victims afterwards, whether they know it or not.

Never forget who introduced WAR(P) S(P)EED operation, all leading to the for decades prepared and now full employed erasing of the Creator given human genome and replacing it with CRISPED organoids, straight from the labs of the new false ‘creators’. Never forget the names which forced you to become genetically modified... How strange, all of the above was written BEFORE the 13th of July, the birthday of Julius Casear, or was something else there?

We were told to get genetically modified in order to get anti-bodies, and now:

https://www.nature.com/articles/d41586-024-02010-7 “What causes long COVID? Case builds for rogue antibodies“ with quote: ““The findings suggest that antibodies might drive some symptoms of long COVID — although how that process works is unclear, and the results will need to be replicated in larger studies.” How similar to the lack of protection during the transmission. As always, more funds are needed, to continue the research and buy more time for even larger collateral damage by keeping people in dark. And now, the casino house with the living roulette’s fights starts to fall apart, Plotkin admits issues with injections https://www.nejm.org/doi/full/10.1056/NEJMp2402379 .

Cholesterol issues go far deeper than all of this above. The literature below has a collection of papers, including Dr. Kariko’s work, connecting cholesterol with radioresistance of biological matter. Last but not least commercial cholesterol antibodies represented by short peptides, can be found these days in genetically modified tomatoes (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538285/) and of course are also partly embedded in Spike sequence. The evil never ends.

The US Disinformation Governance Board should consider a serious investigation into the hate/war of/on cholesterol!

Enjoy your eggs, butter, olive oil, fish oil, as long as you can;)

Closing this chaotic post with a link to Dr. Thomas Binder’s precious remarks on covid injections containing synthetic foreign genetic material: https://www.brighteon.com/04635967-e615-4c70-9fa0-19eae92d583d

and a link to extremely disturbing, just one out of many facts, leading to annihilation of police forces in US: https://www.brighteon.com/6a1631d9-16f4-4615-9e83-e68352c1fa56 . What are they going to replace it with? AI driven robots or young ‘illegal immigrants’ trained as special forces in communist countries???

Thank you for your patience and getting that far!

Literature.

1. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261966/pdf/PRP2-8-e00601.pdf

2. E. Canepa et al. “Cholesterol Hinders the Passive Uptake of Amphiphilic Nanoparticles into Fluid Lipid Membranes“ J. Phys. Chem. Lett. 2021, 12, 35, 8583–8590 https://pubs.acs.org/doi/10.1021/acs.jpclett.1c02077

3. Ewelina Musielak et al. “Synthesis and Potential Applications of Lipid Nanoparticles in Medicine“ Materials (Basel). 2022 Jan; 15(2): 682. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780297/

4. https://www.cell.com/cell/abstract/S0092-8674(24)00305-2

5. “How Gene Editing Could Help Solve the Problem of Poor Cholesterol“ https://time.com/6239076/high-cholesterol-crispr-gene-editing/

6. July 2022 “Edits to a cholesterol gene could stop the biggest killer on earth“ https://www.technologyreview.com/2022/07/12/1055773/crispr-gene-editing-cholesterol/

7. Liam P. Keegan et al. “THE MANY ROLES OF AN RNA EDITOR“ Nature Review. Genetics, Vol2, 2001. p. 869.

8. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203693/

9. Increased radioresistance of ejras‐transformed human osteosarcoma cells and its modulation by lovastatin, an inhibitor of p21ras isoprenylation

   AC Miller, K Kariko, CE Myers, EP Clark, D Samid

   International journal of cancer 53 (2), 302-307. https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.2910530222

   IN collection at https://scholar.google.com/citations?user=PS_CX0AAAAAJ

10. “US Trends in Cholesterol Screening, Lipid Levels, and Lipid‐Lowering Medication Use in US Adults, 1999 to 2018“ https://www.ahajournals.org/doi/10.1161/JAHA.122.028205

11. Dandan An et al. “The role of lipid metabolism in cancer radioresistance”

    Clinical and Translational Oncology Volume 25, pages 2332–2349, (2023)

    https://link.springer.com/article/10.1007/s12094-023-03134-4

12. “Cancer radioresistance is characterized by a differential lipid droplet content along the cell cycle“ https://celldiv.biomedcentral.com/articles/10.1186/s13008-024-00116-y

13. https://journals.lww.com/pn/fulltext/2024/06000/radioresistance_via_lipid_metabolism__intrinsic,.1.aspx

    GIGAVLKVLTTGLPALISWIKRKRQQX“Radioresistance via lipid metabolism: intrinsic, acquired, and tumor microenvironment.”

14. https://journals.lww.com/jno/fulltext/2023/09000/cholesterol_metabolism_and_tumor_radiotherapy.2.aspx

15. “Radioresistance of Human Cancers: Clinical Implications of Genetic Expression Signatures” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579106/

16. “Novel insight into metabolic reprogrammming in cancer radioresistance: A promising therapeutic target in radiotherapy” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910008/

17. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524424/pdf/canmedaj00414-0049.pdf

18. https://daveasprey.com/the-ultimate-biohacking-fat-c150-explained/

    https://www.greenvalleynaturals.com/learn/article/do-dairy-foods-contain-the-most-powerful-anti-aging-factor-yet-discovered?optout=1