Simple question: they lied about everything, why would they say the truth about what's in the injections?

Engineered protein crystals make cells magnetic -- ScienceDaily

Date: September 25, 2019
Source: American Chemical Society
Summary: If scientists could give living cells magnetic properties, they could perhaps manipulate cellular activities with external magnetic fields . But previous attempts to magnetize cells by producing iron-containing proteins inside them have resulted in only weak magnetic forces. Now, researchers have engineered genetically encoded protein crystals that can generate magnetic forces many times stronger than those already reported.

https://www.sciencedaily.com/releases/2019/09/190925083802.htm

Something is making those magnets stick. Montanari is a real scientist, he has seen it with his own eyes. If anything all the science I have shared is meant to show that it is scientifically entirely within the realm of possibility that the injections create a magnetic force at the site of injection, or at least some of them do.

If I were to hazard a guess ⬇️

"Biosynthesis of magnetic nanoparticles from nano-
degradation products revealed in human stem cells: This “remagnetiza-
tion” phenomenon is observed under specific pathways only,
involves the ferritin protein, and seems linked to a de-
toxification mechanism in case of iron excess . It also brings a
direct experimental proof that magnetic nanoparticles can be
synthesized by human cells."

"Selective activation of mechanosensitive ion channels using magnetic particles:

This study reports the preliminary development of a novel magnetic particle-based technique that permits the application of highly localized mechanical forces directly to specific regions of an ion-channel structure. 

The development of a technique that permits the direct manipulation of mechanosensitive ion channels in real time without the need for pharmacological drugs

has huge potential benefits not only for basic biological research of ion-channel gating mechanisms, but also potentially as a tool for the treatment of human diseases caused by ion-channel dysfunction."

https://pubmed.ncbi.nlm.nih.gov/18077244/

"Ion channel, protein expressed by virtually all living cells that creates a pathway for charged ions from dissolved salts, including sodium, potassium, calcium, and chloride ions, to pass through the otherwise impermeant lipid cell membrane."

Ion channel | biology | Britannica
https://www.britannica.com/science/ion-channel

"Several earlier studies have shown that nerve cell proteins which are activated by heat and mechanical pressure can be genetically engineered so that they become sensitive to radio waves and magnetic fields, by attaching them to an iron-storing protein called ferritin , or to inorganic paramagnetic particles . These methods represent an important advance – they have, for example, already been used to regulate blood glucose levels in mice – but involve multiple components which have to be introduced separately. "

⬆️ Boosters anyone?

"The new technique builds on this earlier work, and is based on a protein called TRPV4, which is sensitive to both temperature and stretching forces. These stimuli open its central pore, allowing electrical current to flow through the cell membrane; this evokes nervous impulses that travel into the spinal cord and then up to the brain ."

"Güler and his colleagues reasoned that magnetic torque (or rotating) forces might activate TRPV4 by tugging open its central pore, and so they used genetic engineering to fuse the protein to the paramagnetic region of ferritin , together with short DNA sequences that signal cells to transport proteins to the nerve cell membrane and insert them into it."

"When they introduced this genetic construct into human embryonic kidney cells growing in Petri dishes, the cells synthesized the ‘Magneto’ protein and inserted it into their membrane . Application of a magnetic field activated the engineered TRPV1 protein"

" Next, the researchers inserted the Magneto DNA sequence into the genome of a virus .. Using microelectrodes, they then showed that applying a magnetic field to the brain slices activated Magneto so that the cells produce nervous impulses."

⬆️ Do we even know whether this magneto DNA sequence has or has not been inserted into the genome of the SARSCoV2 virus? We don't. It could have been. The virus could be part 1, the injection part 2, the booster part 3.

“Previous attempts [ using magnets to control neuronal activity ] needed multiple components for the system to work – injecting magnetic particles [THE "VACCINE"?], injecting a virus that expresses a heat-sensitive channel [THE BOOSTER?], [or] head-fixing the animal so that a coil could induce changes in magnetism,” he explains. “The problem with having a multi-component system is that there’s so much room for each individual piece to break down.”

"This system is a single, elegant virus [SARSCoV2?] that can be injected anywhere in the brain [SPIKE CROSSES BLOOD BRAIN BARRIER?], which makes it technically easier and less likely for moving bells and whistles to break down,” he adds, “and their behavioral equipment was cleverly designed to contain magnets where appropriate [THE "VACCINE"?] so that the animals could be freely moving around"

WE ARE TALKING MAGNETOGENETICS HERE.
" Magnetogenetics ’ is therefore an important addition to neuroscientists’ tool box, which will undoubtedly be developed further, and provide researchers with new ways of studying brain development and function."
https://www.theguardian.com/science/neurophilosophy/2016/mar/24/magneto-remotely-controls-brain-and-behaviour

"Genetically targeted magnetic control of the nervous system - PubMed

We have overcome these disadvantages by synthesizing a single-component, magnetically sensitive actuator, "Magneto," comprising the cation channel TRPV4 [ ⚠️LOOK AT WHAT TRPV4 DOES IN THE NEXT ARTICLE⚠️ ] fused to the paramagnetic protein ferritin . We validated noninvasive magnetic control over neuronal activity by demonstrating remote stimulation of cells using in vitro calcium imaging assays, electrophysiological recordings in brain slices, in vivo electrophysiological recordings in the brains of freely moving mice, and behavioral outputs in zebrafish and mice. As proof of concept, we used Magneto to delineate a causal role of striatal dopamine receptor 1 neurons in mediating reward behavior in mice. Together our results present Magneto as an actuator capable of remotely controlling circuits associated with complex animal behaviors."
https://pubmed.ncbi.nlm.nih.gov/26950006/