Gigaohm Biological (July 28)

Gigaohm Biological (July 28)

Phoshpholipid

Another excellent presentation with Walter Chestnut discussing his latest findings, also commenting on a Robert Malone video who warns about the LNP delivery mechanism causing problems such as PEG micelles stimulating production of anti-PEG IgM, which led to accelerated clearance of subsequently administered PEGylated liposomes. According to A review on phospholipids and their main applications in drug delivery systems, Phoshpholipid–PE–PEG mixtures could form micelles rather than liposomes if PE–PEG content exceeds certain critical limit.  Of course the PEG  interests me because it is used along with surfactants for micelle formation in polymerisations.  I never thought something like that would be injected into people (lolz). Below is actually a good resource on Lipids (have a look at all the pages very informative):

 

Heavy metals play a role in neurodegeneration  but lipids are important as  Anticardiolipin and other antiphospholipid antibodies (are found) in critically ill COVID-19 positive and negative patients Antiphospholipid antibodies (APLAs) are biomarkers of a spectrum of clinical features observed in antiphospholipid syndrome (APS).1 Features of APS include venous and arterial thrombosis involving multiple organs and having various presentations. Positive APLA serology was associated with more severe disease regardless of COVID-19 status.  Moreover, Persistent lgG anticardiolipin autoantibodies are associated with post-COVID syndromePersistence of various symptoms in patients who have recovered from coronavirus disease 2019 (COVID-1 9) was recently defined as ‘long COVID’ or ‘post-COVID syndrome’ (PCS). They conclude that Immunoglobulin G (lgG) anticardiolipin autoantibodies (aCL) are associated with the severity of COVID-19.  In other words an allergic or inflammatory reaction to lipid (in the heart) but also “…persistence of the virus, especially in the nervous system, could be suggested with a post-infectious inflammatory or autoimmune reaction”.  Might this have something to do with pumping the body full of phoshpholipids and mRNA spikes? What do I know? (I am just a bucket chemist who used to mix this stuff in buckets not in human bodies).

Unfortunately, many of Walter’s hypothesis are proving to be correct. He is an avid reader of the medical literature and a talented dot-connecter with a big picture overview. His sub-stack is highly recommended.  In his latest article he shows how amyloid is a double-edged sword. A large build-up will cause problems, but amyloids also serve protective functions – against autoimmune attacks.  So, they are symptomatic rather than causal factors.

Comment: Repeated infection with covids is not good even for the unjabbed and even if they got over it before. A least the omicrons have the PrP silenced. But the HIV and the other nasties and all the humanized nucleic acid etc tacked into the spike yes, will be immune insults that will catch up with us the older we are. Shortened lifetimes, yes. The younger the less shortened. Of course, the jabbed are the ones who will suffer shortest lives.

More study is needed into the mutagenic properties of the spike-protein. Perhaps this explains Nucleic Acid Acid Based Therapeutics against Respiratory Infections?

Comment: The prion promoting sequence in the spike also promotes amyloidosis. They are seeing where there won't be a positive D-dimer test but when they put blood under the scope then you see the amyloid building up. The amyloid is causing the clotting, the heart damage, etc. They look for a test for amyloid in those "rare" pre-jab liver inflammation cases and they find amyloid build up and light chains. The hepatitis victims go on to be found Dx with myloid leukemia (if I have the name correct). The Chinese are making more targeted covid viruses - but it is US research over 25 years that developed those - there is research trail from Baric, Daszak and others and a lot of patents. Baric collaborated with Shi - he trained her! That enrichment is bad news - they did that in the jab for a lot of reasons - it throws off all kinds of cascades along with the defanging IFN-1. IFN-1 has all these cascades which include regulatory ones to down regulate inflammation. But that is all gone because of the jab made to evade being recognized and take IFN-1 out. Enriching with C-G over-glycosylates it possibly more than HIV is so it sails on by more so than the virus construct.

This is very complex and there is so much that we do not know. As someone commented.

Code that codes for multiple things depending happening on how it’s parsed with the folds everybody producing the spikes internally become a mini gain of function study. multiply by a billion consecutive studies running concurrently.

It is not just the structure of the protein but how it folds and polarity as in hydrophilic or hydrophobic nature and charge.  Who is to say that the same protein might not fold differently under other circumstances thereby acquiring different properties?  Repeat expansions have been proposed to cause disease by both the repeat RNA forming foci that sequester RNA-binding proteins and through toxic dipeptide repeat proteins generated by repeat-associated non-ATG translation discussed in the article  G-quadruplex-binding small molecules ameliorate C9orf72 FTD/ALS pathology in vitro and in vivo.  

C9orf72 (chromosome 9 open reading frame 72) is a protein which in humans is encoded by the gene C9orf72. The protein is found in many regions of the brain, in the cytoplasm of neurons as well as in presynaptic terminals. The mutations in C9orf72 are significant because it is the first pathogenic mechanism identified to be a genetic link between familial frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). The mutation of C9ORF72 is a hexanucleotide repeat expansion of the six-letter string of nucleotides GGGGCC.

I wonder, I wonder if pumping the body full of mRNA instructions to make spike proteins will deliver the spike proteins that they want?  We know already that the mRNA vaccines are not pure but contain fragments.   The start codon of a gene is always “ATG” so repeat associated non-ATG translation means that it does not read the correct starting point, or you could say that it reads through the stop condon (runs the red light).  It looks like read-through can cause disease. Is that why the above experiment attempted to improve dementia using small peptides that stick to the G-quadruplex?

Walter Chesnut LIVE: Gigaohm Biological High Resistance Low Noise Information Brief (2:50)

Gigaohm Biological 10 July

Gigaohm Biological 10 July

Updated Version 1.2 (spelling corrections)

Scroll down to the bottom for video

Now uploaded to Odysee:

Gigaohm Biological. The Spike Protein and the brain-lung-gut nexus. Interview with Walter Chesnut and Zdogg review (3:30)

This was an excellent presentation. One of the best that Johnathan has given so far as it draws all the threads together and the interview with Walter is also top class.  I will save this video and upload it to different platforms.  Twitch only holds onto videos for a limited time therefore I have downloaded this one and will archive it.  I will also select some clips for tweeting.  Refresh your browser to check if the links have been added.

A holistic oversight is presented which explains the pathogenesis and the the gut-lungs-brain nexus  and insights into disease etiology and progression.  This explains why the Chinese were taking anal swabs.  To put it simply when someone is infected with a respiratory disease they cough up the virus and some of the antigens that get swallowed enter the stomach and are digested in the gut. This is normally not a problem because the gut is used to processing food and contains flora (the gut has a bacterial microbiome).   The T cells in the lung and the gut react differently.  The viral structural proteins that end up in the gut should not induce autoimmune inflammation.  It does not induce inflammation with other coronaviruses or a rhinovirus (cold). However the spike with it’s FCS is a synthetic (bioengineered) protein and if injected straight into the blood it bypasses the lung barrier and the T cell mediated intervention and memory function formation.   Children are now seeing   Multisystem inflammatory syndrome (MIS) or (MIS-C) and adults (MIS-A). MIS is a rare but serious condition associated with COVID-19 in which different body parts become inflamed, including the heart, lungs, kidneys, brain, skin, eyes, or gastrointestinal organs.

Multisystem inflammatory syndrome in children is driven by zonulin-dependent loss of gut mucosal barrier

Zonulin-dependent loss of gut mucosal barrier and MIS-C (10 min)

However, we must be very wary scrutinizing any data. Are we seeing misdiagnosis?  How was MIS-C diagnosed (PCR?).   What was the age distribution in this cohort?  Are the parents vaccinated?  Was the mother vaccinated during pregnancy? So many unknowns especially when there is a drive to vaccinate all children.

Rough Running Order:

24:00 In order to absorb nutrients and make memory to flora etc and make tolerant immunity – some of the antigens digested will be the structural proteins of the virus. You may make an inhibitory tolerant gut immune response which counterbalances any Tcells that attack the spike protein in the lungs -infection and learning in the lungs being counter balanced by processing in the gut but the vaccine (transfection) bypasses the lungs and goes straight to the blood.

 

The lung and gut are separate pathways, but they are linked. And the gut is linked to the brain. The vagus nerve carries an extensive range of signals from digestive system and organs to the brain and vice versa. So, you literally are what you eat. I have personally been stressing the importance of gut health and probiotics especially if you take Quercetin and Zinc etc. which may be harmful to good bacteria. You need to balance this with probiotics. They found covid in sewerage and many people have been having diarrhea for weeks. At one point the Chinese were taking anal swabs.

 

 

 

42:00 MHS3  Homology: The  discovery of a Moderna patent from 2017 that contained the FCS has confirmed the lab origins of the virus.  That can no longer be argued.  This was based on the blast work done by Arkmedic (Jikkileaks):

Blasted Liars

Johnathan asks the following questions: How would this have been the result of [natural???] recombination?  In what specific scenario? Was it standard procedure to create permissive cultures and thereby to enable viral infection (increasing yield)?  [If you increase attachment to ACE receptors you can make more virus to experiment with]. Is there data in the literature to suggest this could work?  

01:00 Walter Chestnut interview. 

Great Interview. This is Walter’s latest article:

Dysautonomia, palpitations, tremors, hyperactive immune system, autoimmune, hyperactivated T cells cause Cachexia. The spike is present in people with long covid causing metabolic issues. Autoimmune response hyperactivated amyloidosis causing fibrins etc. The spike protein activates T-cells in a non-specific way therefore no T cell memory is formed to sars-Cov-2. Three or more autoimmune responses can be formed at once…induces both autoimmunity and amyloidosis. It is possibly erasing previous T cell memory a re-programming points towards a “universal epitope”.

 

01:09 Gut and lungs linked…you cough it out but also swallow and it enters your gut where you form tolerance regulatory T cells, but the engineered GOF Spike triggers an immune response. It is an immunogenic protein, and the gut is linked to the CNS. So, from respiratory (lungs) to the gut and via the vagal nerve to the brain.

DC-sign epitope and GP120 to attract the attract the attention of the immune system. 

DC-sign stands for Dendritic Cell-Specific Intercellular adhesion molecule-3 grabbing non-integrin. It makes cells “sticky” and promotes antigen (virus) uptake. Envelope glycoprotein GP120 (or gp120) is a glycoprotein exposed on the surface of the HIV envelope is essential for virus entry into cells as it plays a vital role in attachment to specific cell surface receptors.  I am sure that both of those epitopes found there way into the spike protein by accident.  I am sure that it only took a couple of months to make the “vaccine” (boy people are Stooopid).

01:21 The decrease is largely made in the gut and the expanding response made in the lungs; push and pull – the transfection (vaccine) wrecks the push and pull (interplay between gut and lung) by going directly into the blood.

There are no more fully vaccinated in Canada only up to date vaccinated.

01:31 End of Interview

01:40 Omicron Boosters, Kids’ Vaccine & More (w/Dr. Paul Offit)

Jonathan takes apart this Psy-op by Zdogg who belongs in the Doghouse.  The original interview is here  and our “hero” Paul Offit can be found here.

01:46 JC says, “the worst experiment I ever heard”, and he is correct

02:08 Zdogg a Monumental dumbass

CDC is investigating multisystem inflammatory syndrome in children and adults, a rare but serious condition associated with COVID-19.

02:26 MIS-C is being misclassified to confuse and force parents to vaccinate kids.

Multisystem inflammatory syndrome (MIS) can affect children (MIS-C) and adults (MIS-A). MIS is a rare but serious condition associated with COVID-19 in which different body parts become inflamed, including the heart, lungs, kidneys, brain, skin, eyes, or gastrointestinal organs.

02:34 HPV (Human papillomavirus): HPV is a common virus that is spread through sexual contact. HPV infection can be serious. It can cause cancers, including cancer of the cervix, vulva, vagina, penis and anus, and some head and neck cancers. Types 16 and 18 cause up to 80% of the cervical cancers in women and up to 90% of HPV-related cancers in men.  See how they throw that one in? (lolz)…but…. The Gardasil controversy: as reports of adverse effects increase, cervical cancer rates rise in HPV-vaccinated age groups

02:36 Lies, lies about the numbers

02:44 He is trying to say that the reason we have sterilizing immunity to things like measles is because the longer incubation period allows antibodies to develop (lolz)

02:46 Murder all animals

02:55 Autoimmunity heart

03:07 COMPLETE CONTRADICTION

03:16 Enriching for viral virulence =MAREK

End of Video Review

03:21 We build tolerance (not immunity) to the most functionally constrained proteins because they are processed by our gut   the transfection goes everywhere in your body and makes endothelial cells express spike activating neutrophils to destroy them producing an enzyme called elastase which makes fibrinogen which leads to amyloidosis and protein misfolding (prions)…

03:23 Gene therapy trials FAILED….they lie…it resulted in autoimmune liver failure

It is not an endogenous protein

This technology has never worked for an endogenous protein.

So why would it work with an alien protein?

Why would that be presumed safer?

03:24 modifying platelets with mRNA

paper from 2011 redundant genetic code being not so redundant, synonymous changes can affect protein folding and cause silent disease.

03:25 Condon optimization (such as they did by methylating the uracil to pseudouridine)

03:26 Quadruplex forming changing 3D shape etc; layers upon layers of unknowns introduced

Resources (not in order)

https://rumble.com/v1bh5ul-ny-mets-pitcher-chris-bassitt-slams-covid-protocols-stop-testing.html

Reference to Kevin McKernan (not Kevin McCairn) archived videos

Multisystem inflammatory syndrome in children is driven by zonulin-dependent loss of gut mucosal barrier

Sars-Cov-2 infection produces chronic pulmonary epithelial and immune cell dysfunction with fibrosis in mice

DNA repair in species with extreme lifespan differences

DNA mismatch repair controls the host innate response and cell fate after influenza virus infection

Anti–spike IgG causes severe acute lung injury by skewing macrophage responses during acute SARS-CoV infection

Plasma Markers of Disrupted Gut Permeability in Severe Covid 19 Patients

Breaking the Silence

Enhancing Transfusable Platelets Using mRNA Therapy to Produce Exogenous Proteins

Delivery of mRNA to platelets using lipid nanoparticles

Mini Review Correspondence to: BNT162b2 Vaccine: Possible Codons Misreading, Errors in Protein Synthesis and Alternative Splicing’s Anomalies

Translation affects mRNA stability in a condon-dependent manner in human cells

Kevin McKernan: Differences in Vaccine and SARS-CoV-2 Replication Derived mRNA: Implications for Cell Biology and Future Disease

Colocalization of m 6 A and G-Quadruplex-Forming Sequences in Viral RNA (HIV, Zika, Hepatitis B, and SV40) Suggests Topological Control of Adenosine N 6-Methylation

Immunomythology Update: Gigaohm Biological High Resistance Low Noise Information Brief (3:30)

Kevin and Walter discuss amyloid

Kevin and Walter discuss amyloid

$3600/$5000 Raised

 

 

Highly recommended

Walter is a high IQ savant who reads medical and scientific papers and proposes hypotheses and Dr Kevin McCairn is a systems neuroscientist.  In this video they discuss amyloid and prion disease or protein misfolding.  It has been hypothesized for a long time that amyloid was the cause of dementia and other neurodegenerative  diseases. The aggregation of amyloid-β is thought to trigger a cascade of disease-causing processes such as inflammation, tau-tangle formation, synapse dysfunction and cell death, which ultimately leads to dementia. However….“The amyloid hypothesis has never been universally accepted, and the failed drug trials have only emboldened its critics”.  (The amyloid hypothesis on trial).  Basically, people who received treatments that dissolved the amyloid plaques did not show any improvement. This leads neuroscientists such as Dr McCairn to understand the amyloid as a signal or symptom of the disease rather than the causal factor.

Whatever the case might be, the Spike Protein is triggering problems all over the body particularly in high metabolic areas like the heart and brain and amyloid is at the very least a signal.

Dr McCairn has now raised $3600 towards lab work and that is about four days.  He is under DOS attack when he streams.  I have embedded the WTYL version and downloaded a version from Dlive and placed it on Odysee. The audio is slightly out of sync in that version and the frames freeze toward the back end but the audio is good.

WTYL version:

Kevin and Walter discuss Amyloid (2:20)

Odysee upload (embed):

Walter M Chestnut

Walter M Chestnut

This video features an interview with the Independent researcher and twitter phenomenon that is Walter Chestnut who is a composer by trade and who has a prodigious capacity to consume research articles and find links thus enabling him to suggest different hypotheses which are documented on his website https://wmcresearch.org/  and tweeted out. His work has already borne fruit as he made Kevin aware of the prion domain and prion genesis. He has however been dismissed by the likes of Kristian Andersen who wrote to Anthony Fauci about the possibility of an engineered coronavirus and then later back-tracked and participated in the cover-up.  As far as these people are concerned if you are not credentialed you should just shut-up and listen to your betters (while they screw you over). However, many of Walter’s theories have proven correct and it is refreshing to have someone with a sharp mind and unhindered by bias and preconception proposing hypotheses.  In case anyone has forgotten that is how science progresses.  It never progresses through consensus.

Kevin and Walter discuss a leaked report by  Acuitas Therapeutics on how testing LNP (Lipid nano-particles) caused damage to rats. Report: “[A Tissue Distribution Study of a [³H]-Labelled Lipid Nanoparticle-mRNA Formulation Containing ALC-0315 and ALC-0159 Following Intramuscular Administration in Wistar Han Rats]

The story of the therapeutics company Acuitas is interesting because the accusation went out on twitter that the Trudeau Foundation owned 40% of Acuitas.  That was quickly debunked as false and had the fact checkers crawling all over it.  However, is it false?

Is their evidence of malfeasance? I think their is and Trudeau has “form” with other scandals. This was the main chance to get in on the ground floor and make a killing on new technology. Acuitas Therapeutics is a private company and you will never prove it as their are multiple shell companies and no transparency.  Basically they are crooks. Malone certainly thinks it is true and he is (was) an insider:

Here then is the four hour stream with the Dojo links underneath.

Dojo links with timestamps:

  • 00:00:27 Start
  • 00:17:38 Report: “[A Tissue Distribution Study of a [³H]-Labelled Lipid Nanoparticle-mRNA Formulation Containing ALC-0315 and ALC-0159 Following Intramuscular Administration in Wistar Han Rats](https://phmpt.org/wp-content/uploads/2022/03/125742_S1_M4_4223_185350.pdf)”, “SPONSOR: Acuitas Therapeutics Inc. 6190 Agronomy Road, Suite 402, Vancouver, British Columbia, V6T 1Z3 Canada”
  • 00:21:50 Neurotoxins, MPTP, Parkinson’s