God genes, schizophrenia & worms🪱

Predicting psychotic mice and the coming zombie nation

Greg Reese’s intriguing new vid is warning us that we may have had our VMAT (vesicular monoamine transporter) genes intentionally deleted (knockout), causing the loss of ability to feel God. 4:30 min vid linked to image.

Many of you saw Greg’s vid, did any of you actually read the papers?

👉If not and you thought the content is true, then you have just learned something very serious about yourself. You may remember people who did not think and got jabbed.

He shows some studies showing that abnormal VMAT genes can cause a wide variety of neurologic disorders but does not provide a study showing if or how this is being done to humans. The logic of going from the never-proven, “God Gene” to a knockout of this gene causing schizophrenia, Parkinson’s, & other numerous neurologic disorders, and that the government is doing this to us is a scientific enigma.

👉The only conclusion about the God Gene narrative is that this is a psyop to discredit religion by the idea that “if a gene is needed to believe in God then you don’t need a God”. A subtle echo on the debauchery of society and New Age quasi-occult movements that were planned by Tavistock and other think tanks at the behest of the global controllers in the 60s and are still ongoing aimed to destabilize society and the family unit.

• Listening the video certainly gave me vertigo though my VMAT genes are intact I’m sure.

👉Now, impairment in cognitive function can clearly make people dazed and unable to conceptualize many things by giving them a dementia syndrome that can include trouble understanding spirituality, knowing who they and their family are etc., but that is not a “God gene” per se. The persons promoting knock-out of this gene in the video want you to think this could be a be a good thing to treat extremism, but it seems to me that the only extremists around are the people pushing this psyop.

Let’s look at a couple of the examples Reese gives. First this one on VMAT knockout and “schizophrenia in mice”.

Reese says mice are getting schizophrenia from VMAT deletion. Can a mouse really get a disease that is subjectively defined even in humans (generally requiring delusions, hallucinations, thought disorder, and blunted affect)? I guess Micky the mouse was delusional that Little Kitty is secretly filming him and heard Kitty whispering his name thru the wall. Micky reported his delusions to the researchers thru mouse talk of course. I’m new to this language but it seems simple enough, with only 2 vocab words and no grammar to master, the researchers could elucidate delusions and hallucinations with ease:

“Squeaking and chirping are common noises that mice make to communicate with one another.” Maybe they combine to make a Morse-mouse code? Well this little proton will just stick with the easy 2 -word mouse vocab model.

Here he is squeaking and chirping away: “shizo or bust”

Back to the paper:

In this study, “we aimed to anatomically and functionally probe the Calb2 subtype of monoaminergic neurons. We implemented histological and gene-targeting approaches [“Genotyping was performed by PCR”, ugh] followed through with behavioral assessments and pharmacological challenges. Upon confirmed deletion of Vmat2 gene expression...mice revealed significantly altered behaviors in terms of locomotion, anxiety, and responses to sucrose, ethanol, and amphetamine [that’s cool stuff but that’s not schizophrenia].

Following their important roles, compromised monoaminergic function is linked to several neurological and neuropsychiatric diseases such as Parkinson’s Disease, substance use disorder, depression, and schizophrenia.

👉This study didn’t actually look at mice getting “schizophrenia”, and “linked to” is not the same as “caused”. More importantly MICE CAN’T GET SCHIZOPHRENIA because it is a criteria set of symptoms that can only be evaluated (but never proven) in humans. Be clear, a list of symptoms in a book unconnected to a specific biologic parameter does not mean the name of a diagnosis is a valid label for an actual disease state, it is only a description (a syndrome with no proven causality or specificity that can overlap with other syndromes). Labels may be useful clinically to try to help patients and communicate a patient’s state to other persons, but that is not the same as proven. Even if mice could get schizophrenia, how would we evaluate that from their 2-word vocab? Ay Caramba!

What exactly is schizophrenia? It is fitting a specified number of patient’s symptoms to a list of behaviors and symptoms decided in board meeting and then put in a book called the DSM, there is no specific physical parameter that can be measured. The symptoms are subjective and can overlap with other symptom lists like that for bipolar disorder, psychotic depression, etc.

👉I suspect some of you will look up animal models of schizophrenia and try to correct me in the comments so I’ll do it for you. NO, nonspecific signs of increased locomotor activity, prepulse inhibition, etc. said to be connected to neurotransmitters thought to be disordered in schizophrenia are not actually a valid model of schizophrenia. First of all because as I noted above, there is no one physical parameter that the schizophrenia symptom list is actually connected to. These are interesting studies but do not prove anything besides that drug companies need some parameter to measure for pre-clinical drug testing, whether or not it really related to specific person with a nonspecific syndrome. No it’s not autism either, for the same reasons!

Micky was never the same after his VMAT knockout:

Poor guy doesn’t sing or dance anymore but that is NOT schizophrenia

So we don’t really know the cause of schizophrenia, but no, it is not caused by “Demons from CERN” either as Greg once opined, and even argued with me about in a thread  (screen shot below). Maybe these demons have knocked-out the VMAT genes in their victims? Greg seems to really be taken by the schizophrenic mystery.

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Reese’s next reference says this study of VMAT variant alleles showed that it caused “Parkinson’s Disease”.

First, variant alleles are not “knockout” genes, and not all the subjects in this study had the same variant alleles (assuming these alleles even exist). This means there was a variety of genetics and a variety of pathology (=too many variables). Nerds: please see this table.

The affected individuals typically showed global developmental delay, hypotonia, dystonia, oculogyric crisis, and autonomic nervous system involvement, and some had Parkinsonism [According to table 1 there were only about 10 subjects per allele group and about 70% in each group had Parkinson-like symptoms (rigidity, dystonia etc.) that are non-specific to different neurologic illnesses].

The subjects were normal at birth and developed the symptoms a few weeks to a few months after birth. Did they get injections in those few months? Probably, couldn’t find that in the paper (correct, the study isn’t controlled at all), but here is the CDC vax schedule you can reference. Even the Covid vax is recommended at 6 months. Well, we’ll need a cover for that sh*t won’t we?

👉 It’s all another model. Ahh, so many model toys in science.

The structure of human VMAT2 has not been experimentally determined. However, homology models of the rat protein (rVMAT2) have been constructed using related transporter structures as templates...These models agree well with a model created by an artificial intelligence-based structure prediction program...

Sounds just like a computer model of Sars-CoV-2! Now we should be really scared. OMG (sorry I forgot, there is no God allowed in this experiment).

They used exome sequencing (not exosome), homology matching to a data base, and PCR (where have we seen the latter two before). They also got into a worm hole of more genetic models based on the worm C. Elegans. This seems like a pet project of one of the over 60(!) authors, though it fits perfectly with the confusion-obtrusion nature of the paper.

Worm models of genetic diseases are useful for mechanistic studies of disease-related gene function and for drug repurposing screens [ah ha, the Pharma connection]. we attempted to develop a suitable C. elegans model to identify novel candidate treatments in vivo. Automated quantitative phenotyping was used to evaluate a consistent multidimensional behavioral phenotype of the disease model…

How could an artist draw something like this if it wasn’t true?

This study showed that abnormal genetics in the monoamine system caused loads of different neurologic problems (surprise?). Are we supposed to rally around gene knockout tech instead of the fake virus issue heating up again now with a never proven Avian flu virus?

Chick-Filet Virus Grips Wikistan🐦

Conclusions:

👉There are many injuries we can blame VMAT variants for.

👉A variety of illnesses can be made with “vaccines”, then we can pcr them to find what treatments people will need based on the worm model, and then finish them off with pin-point drug treatments, who could have guessed?

“This study was funded in part by the US National Human Genome Research Institute.” 👉 They want to find genetic causes for everything don’t they?

👉 With 349 likes and 7 dislikes, Greg’s video reminds us that people have limited bandwidth to question and investigate-that’s why 80% of them took fake shots. It only took me 10-min to peruse each paper to realize there was no actual study of schizophrenia in mice, nor Parkinson’s in persons with supposed VMAT variants.

• I vote that this video is a “disruption-confusion” PR piece aimed at keeping the masses in general fear and confusion about any and every illness and germ the government throws at us.

• It is also diverting from the multiple neuro injuries the childhood vax schedule and Covid shots can cause.

• Greg Reese is an intriguing researcher, writer, and narrator. Recommend you all subscribe to his bitchute and SS channels.

  👉Yes this little proton is fully and soundly banned from Greg Reese’s substack. My mentors roundly scolded me, “if you think less you will be banned less often”.

  📣Greg, please unban me. Don’t you appreciate researchers who can help you with these medical topics? Pretty please!

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Freedom fighters make us study things we would have never noticed on our own.

Yours Truly Proton Magic & Co.

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